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(A) Start at two months and (B) fifth-month follow-up.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "M.S. Zegpi-Trueba, Á. Abarzúa-Araya, S. Silva-Valenzuela, C. Navarrete-Dechent, P. Uribe-González, C. Nicklas-Díaz" "autores" => array:6 [ 0 => array:2 [ "nombre" => "M.S." "apellidos" => "Zegpi-Trueba" ] 1 => array:2 [ "nombre" => "Á." "apellidos" => "Abarzúa-Araya" ] 2 => array:2 [ "nombre" => "S." "apellidos" => "Silva-Valenzuela" ] 3 => array:2 [ "nombre" => "C." "apellidos" => "Navarrete-Dechent" ] 4 => array:2 [ "nombre" => "P." "apellidos" => "Uribe-González" ] 5 => array:2 [ "nombre" => "C." 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Izu-Belloso, J.C. García-Ruiz" "autores" => array:2 [ 0 => array:4 [ "nombre" => "R.M." "apellidos" => "Izu-Belloso" "email" => array:1 [ 0 => "rizu@ya.com" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">¿</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "J.C." "apellidos" => "García-Ruiz" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] ] "afiliaciones" => array:2 [ 0 => array:3 [ "entidad" => "Servicio de Dermatología, Hospital de Basurto, Bilbao, Spain" "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Hematología y Hemoterapia, Hospital de Cruces, Barakaldo, Bizkaia, Spain" "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Coorresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Actualización terapéutica en linfomas cutáneos" ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Primary cutaneous lymphomas (PCLs) are a heterogeneous group of lymphoid malignancies that originate primarily in the skin.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Most (75%) are derived from T cells (primary cutaneous T-cell lymphoma [CTCL]) while 20% to 25% are derived from B cells (primary cutaneous B-cell lymphoma [CBCL]). Mycosis fungoides (MF) and Sézary syndrome (SS) are the most common such PCLs. It is important to differentiate PCLs from their equivalent lymph node disease, given that they show clinical and histopathologic differences and have different immunophenotypes and a different molecular biology. Most importantly, PCLs have a more indolent course in most cases and different treatment regimens are used.</p><p id="par0010" class="elsevierStylePara elsevierViewall">For a correct diagnosis and hence appropriate treatment, it is necessary to be familiar with the latest classifications such as those of the European Organisation for Research and Treatment of Cancer (EORTC)/World Health Organization (WHO)<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>) and the WHO (2008).<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,3</span></a> PCLs have a very low incidence,<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> and most patients survive for a long time. It is therefore difficult to assess the impact of a given treatment on outcome and there are almost no case-control studies to guide us. The levels of evidence are therefore low. Ideally, all patients with PCLs would be included in a clinical trial.</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Many therapeutic options are available for the management of PCL.<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,6</span></a> The choice of treatment should be based mainly on the clinical stage, but other factors should also be considered such as access to treatments, age and general health of the patient, and cost-benefit ratio. In the initial stages of the disease, no data are available to demonstrate the superiority of systemic treatment (the more aggressive option) over local treatment targeting the skin lesions. A conservative approach is therefore recommended.</p><p id="par0020" class="elsevierStylePara elsevierViewall">The treatments can be divided into 2 broad groups:<ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">1</span><p id="par0025" class="elsevierStylePara elsevierViewall">Treatments that target the skin and act only on the population of neoplastic cells in the skin. In this case, the adverse effects are usually less severe than those arising with systemic treatments. This type of treatment is in practice the only one recommended for first-line treatment of early phases of MF. In advanced stages, it is still an important option, forming part of combination therapies. Such treatments include:<ul class="elsevierStyleList" id="lis0010"><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">-</span><p id="par0030" class="elsevierStylePara elsevierViewall">Topical corticosteroids</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">-</span><p id="par0035" class="elsevierStylePara elsevierViewall">Alkylating agents: topical nitrogen mustard (mechlorethamine) and carmustine</p></li><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel">-</span><p id="par0040" class="elsevierStylePara elsevierViewall">Narrow-band UV-B phototherapy, psoralens<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>UV-A (PUVA), and other types of phototherapy</p></li><li class="elsevierStyleListItem" id="lsti0025"><span class="elsevierStyleLabel">-</span><p id="par0045" class="elsevierStylePara elsevierViewall">Radiotherapy (conventional and electron beam)</p></li></ul></p></li><li class="elsevierStyleListItem" id="lsti0030"><span class="elsevierStyleLabel">2</span><p id="par0050" class="elsevierStylePara elsevierViewall">Systemic treatments, which include biological response modifiers (such as retinoids, cytokines, immunotoxins and vaccines, monoclonal antibodies, and histone deacetylase inhibitors), chemotherapy (traditional single- or multiagent chemotherapy or polychemotherapy, new chemotherapies), and allogeneic stem cell transplantation.</p></li></ul></p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Treatments That Target the Skin</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Topical Corticosteroids</span><p id="par0055" class="elsevierStylePara elsevierViewall">Corticosteroids are able to induce apoptosis in most neoplastic lymphocytes in the skin and reduce the number of Langerhans cells, thereby interfering with the stimulation of neoplastic cells. Although such treatments have been in use for years, there are few studies of their use.<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7,8</span></a> Zackheim et al.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> reported their experience in 79 patients with MF in the form of patches or plaques. Patients received medium- and high-potency corticosteroids (class I-III), sometimes with an occlusive dressing. In patients with stage T1 disease, 63% had complete response (CR) and 31% had partial response (PR), while in patients with stage T2 disease, 25% had CR and 57% had PR. The adverse effects observed were adrenal suppression in 10 patients, skin irritation in 2, and skin atrophy with stretch marks in 1 patient. The authors concluded that the treatment is well tolerated and effective in the very incipient stages of the disease.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Alkylating Agents</span><p id="par0060" class="elsevierStylePara elsevierViewall">Alkylating agents are drugs that act on different mechanisms and functions of DNA, thereby finally inducing cell death.</p><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Topical Mechlorethamine (Nitrogen Mustard)</span><p id="par0065" class="elsevierStylePara elsevierViewall">Although the exact mechanism of action of mechlorethamine is unknown, when administered systematically, it acts as an alkylating agent with an antimitotic effect. Its topical activity, however, appears to be mediated by immune mechanisms or by interaction with Langerhans cells. The drug is usually used as an aqueous solution with a strength of 10-20<span class="elsevierStyleHsp" style=""></span>mg/100<span class="elsevierStyleHsp" style=""></span>mL or as a gel (10-20<span class="elsevierStyleHsp" style=""></span>mg/100<span class="elsevierStyleHsp" style=""></span>g petroleum jelly).<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9–15</span></a> An ongoing randomized, double-blind, multicenter trial is comparing the safety and efficacy of 2 preparations of nitrogen mustard (0.02% in propylene glycol and 0.02% in petroleum jelly) in patients with stage I or IIA MF refractory to topical corticosteroids.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> The preliminary results have shown similar efficacy (overall response rate [ORR] of around 70%) and a good safety profile (no systemic absorption was seen) for both preparations. In clinical practice, the drug is initially applied daily until the lesions have cleared (in 3 to 6 months with the solution and 6 to 12 months with the gel). An intermittent maintenance regimen is followed thereafter. Application to the entire body surface is usually recommended, though avoiding intertriginous areas. However, the need to treat unaffected areas is not very clear. Response varies between 50% and 75% in stage T1 and 25% and 50% in stage T2. Contact dermatitis (allergic or irritant) may arise, particularly when using the aqueous solution (30% vs <span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>5% with the gel). Urticaria and anaphylactic reactions have also been reported. Prolonged use increases the risk of nonmelanoma skin cancer, particularly if the patients have received prior PUVA or total skin electron beam therapy. In general, myelosuppression or other systemic effects do not occur. Efficacy appears to be similar for the 2 preparations (solution and gel), although prospective studies comparing the 2, other than the one described above,<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> have not been undertaken. In recent years, the availability of mechlorethamine in hospital pharmacies has been limited, and so it is unfortunately being used less and less despite its efficacy.</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Carmustine</span><p id="par0070" class="elsevierStylePara elsevierViewall">Carmustine is an alkylating agent that induces cell death through inhibition of DNA synthesis. It is used as an alcohol solution (2<span class="elsevierStyleHsp" style=""></span>mg/mL) or as an ointment.<a class="elsevierStyleCrossRefs" href="#bib0085"><span class="elsevierStyleSup">17–20</span></a> It should be applied daily to the lesioned skin, and the clearance time is similar to that of mechlorethamine. Response rates vary from 86% in stage T1 to 48% in stage T2. Most patients experience erythema, sometimes followed by persistent telangiectasia, and approximately 3% to 5% develop mild leukopenia due to myelosuppression. The agent can be used as an alternative in patients who are allergic to mechlorethamine, although the availability of carmustine is also limited.</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Phototherapy</span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Narrow-Band UV-B Phototherapy (311-312<span class="elsevierStyleHsp" style=""></span>nm)</span><p id="par0075" class="elsevierStylePara elsevierViewall">Several studies have shown the usefulness of narrow-band UV-B phototherapy in the initial stages of MF (CR rates of around 75%, with a mean response duration of 51 months).<a class="elsevierStyleCrossRefs" href="#bib0105"><span class="elsevierStyleSup">21–26</span></a> The risk of skin cancer is increased, however, and therapy is only effective in MF with incipient lesions with little or no infiltration, given the limited penetration of the radiation. This type of therapy is considered particularly useful in those patients who do not tolerate psoralens, those with very light skin, and those with very incipient lesions.<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a></p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Psoralens Plus UV (320-400<span class="elsevierStyleHsp" style=""></span>nm)</span><p id="par0080" class="elsevierStylePara elsevierViewall">PUVA is the classic treatment in the early stages of lymphatic disease.<a class="elsevierStyleCrossRefs" href="#bib0100"><span class="elsevierStyleSup">20,29–34</span></a> Usually, the patient starts with 2 to 3 weekly sessions, with the interval between sessions being reduced according to response. There is no consensus about whether it is necessary to follow a maintenance regimen once CR has been achieved.<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> In a study of 82 patients with MF in the form of superficial plaques and/or palpable plaques, CR was obtained in 65% and PR in 30%, with a mean response duration of 43 months.<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> Chronic actinic damage was observed in 10% of the patients, with the appearance of carcinomas in 6 patients: 3 with basal cell carcinoma and 3 with squamous cell carcinoma. Although there are studies that show a statistically significant increase in carcinogenesis, including melanoma, we believe that this risk is more theoretical than real, at least in this group of patients. According to the most recent studies, the disease-free interval is related to a higher cumulative dose of PUVA and longer treatment times.<a class="elsevierStyleCrossRefs" href="#bib0135"><span class="elsevierStyleSup">27,35</span></a> Although late recurrences are seen, between 30% and 50% of patients in stages IA, IB, and IIA can maintain CR for periods of up to 10 years. The disease-free survival at 5 and 10 years for patients in stage IA was 56% and 30%, respectively. For those patients in stages IB/IIA, 5- and 10-year disease-free survival was 74% and 50%, respectively. However, the overall survival did not vary significantly between those with recurrences and those without.</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Others Types of Phototherapy</span><p id="par0085" class="elsevierStylePara elsevierViewall"><ul class="elsevierStyleList" id="lis0015"><li class="elsevierStyleListItem" id="lsti0035"><span class="elsevierStyleLabel">-</span><p id="par0090" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Extracorporeal photopheresis.</span><a class="elsevierStyleCrossRefs" href="#bib0180"><span class="elsevierStyleSup">36–39</span></a> In a modification of PUVA, after ingestion of psoralen, circulating mononuclear cells from the patient are exposed to UV-A. The main drawback of this approach is the high cost and, in addition, efficacy is no better than other treatments. The best responses are obtained in patients with early-stage SS who have normal CD8 counts and have not received prior aggressive therapies.</p></li><li class="elsevierStyleListItem" id="lsti0040"><span class="elsevierStyleLabel">-</span><p id="par0095" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Hypericin</span>. This new photodynamic plant derivative induces T-lymphocyte apoptosis in association with visible or UV-A light. If preliminary results are confirmed, this option could be better than the other forms of phototherapy,<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a> as visible light does not increase the risk of skin cancer.</p></li><li class="elsevierStyleListItem" id="lsti0045"><span class="elsevierStyleLabel">-</span><p id="par0100" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Photodynamic therapy</span>. The use of photodynamic therapy with derivatives of 5-aminolevulinic acid could be particularly appropriate in patients with few lesions or lesions on the scalp.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a></p></li><li class="elsevierStyleListItem" id="lsti0050"><span class="elsevierStyleLabel">-</span><p id="par0105" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Monochromatic excimer laser light</span>. Excimer lasers at a wavelength of 308<span class="elsevierStyleHsp" style=""></span>nm have also been used and are approved by the US Food and Drug Administration (FDA) for psoriasis and vitiligo. Passeron et al.<a class="elsevierStyleCrossRefs" href="#bib0210"><span class="elsevierStyleSup">42,43</span></a> have performed a clinical trial in which good responses were obtained in very incipient lesions. This approach can therefore be considered in areas that are not usually accessible with phototherapy.</p></li></ul></p><p id="par0110" class="elsevierStylePara elsevierViewall">The evidence to support these approaches is, however, limited. Likewise, there is little evidence with regard to other therapeutic options.</p></span></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Radiotherapy</span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conventional (Orthovoltage)</span><p id="par0115" class="elsevierStylePara elsevierViewall">Conventional radiotherapy is used for highly infiltrated plaques or localized MF tumors refractory to other treatments.<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">44</span></a> It is particularly indicated as front-line treatment of cutaneous marginal zone B-cell lymphoma and follicle center lymphoma along with excision.<a class="elsevierStyleCrossRefs" href="#bib0225"><span class="elsevierStyleSup">45,56</span></a> The recurrence rate is higher if doses less than 30<span class="elsevierStyleHsp" style=""></span>Gy are used. Local radiotherapy has also been used in solitary MF lesions with impressive results.<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">47</span></a></p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Total Skin Electron Radiation (Electron Beam Therapy)</span><p id="par0120" class="elsevierStylePara elsevierViewall">An electron beam is the treatment of choice for patients with MF with infiltrated plaques or small generalized tumors. The most widely used voltage is 6 MeV, and therapy is applied 4 days per week for a total dose of 3600 cGy in 10 weeks.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">48</span></a> The treatment can be repeated several times if reduced doses are used. Adverse effects include generalized erythema, edema, scaling and exudation, apparent worsening of existing lesions, total loss of skin appendages, transverse melanonychia and, less frequently, blistering. Hair loss is usually reversible if the total dose administered has not exceeded 2500 cGy. In the longer term, patients may develop edema, hyperpigmentation, telangiectasia, and persistent xerosis, while men may become sterile.<a class="elsevierStyleCrossRefs" href="#bib0240"><span class="elsevierStyleSup">48–50</span></a></p><p id="par0125" class="elsevierStylePara elsevierViewall">The disease-free interval can be extended according to some authors by subsequent maintenance therapy, either with mustard derivatives or PUVA.<a class="elsevierStyleCrossRefs" href="#bib0240"><span class="elsevierStyleSup">48,49,51,52</span></a> The recommendations of the EORTC on total skin electron radiation in MF were published in 2002.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> The procedure is not recommended for erythrodermic CTCL (T3) given the risk of severe scaling and because the CR rates are higher in the earlier stages (CR of 90% in T1 and 70% in T2 disease) than in the more advanced stages, where the effect is only palliative.</p><p id="par0130" class="elsevierStylePara elsevierViewall">It is known that CR rate depends on the stage of the disease, the dose applied, and the electron energy.<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">51</span></a> Overall, CR rates of 96% are obtained in patients with stage IA, IB, and IIA disease; of 36% in those with stage IIB disease; and of 60% or less in patients with stage III disease. CR rates are also related to total dose (32-36<span class="elsevierStyleHsp" style=""></span>Gy) and electron energy (4-6 MeV).<a class="elsevierStyleCrossRefs" href="#bib0260"><span class="elsevierStyleSup">52,53</span></a></p></span></span></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Systemic Treatments</span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Biological Response Modifiers</span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Retinoids</span><p id="par0135" class="elsevierStylePara elsevierViewall">Isotretinoin and etretinate have been used in the treatment of MF to similar effect. Their usefulness as monotherapy is limited, as it was seen that atypical cells were still present according to the pathology study even though the lesions had apparently healed. These agents have been combined with PUVA and interferon alfa (IFN-α). When combined with PUVA, they seem to be able to reduce the UV-A dose while with IFN-α they seem to enhance the response to interferon in early but not late disease stages. However, there are no randomized studies that compare IFN-α and IFN-α in combination with retinoids.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a></p><p id="par0140" class="elsevierStylePara elsevierViewall">Bexarotene is a new retinoid (more specifically a rexinoid) whose exact mechanism of action is unknown although it inhibits growth of tumor lymphocytes and also enhances apoptosis in vitro.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a> Bexarotene selectively activates RXR receptors (a type of nuclear receptor activated by retinoic acid), acting as a regulator of cell differentiation and proliferation. In 2002, the FDA approved the compound, both for topical use as a 1% gel (which has so far not been marketed in Spain but can be obtained as an imported medicine) and for systemic use at an optimum dose of 300<span class="elsevierStyleHsp" style=""></span>mg/m<span class="elsevierStyleSup">2</span>/d. Regular laboratory testing should be performed during treatment, focusing mainly on triglyceride levels and thyroid hormones. Bexarotene induces hypertriglyceridemia, which can be marked at times. Preventive treatment should therefore be given the preceding week with statins or a fenofibrate but not with gemfibrozil as this fibrate increases the levels of bexarotene in blood, probably through inhibition of cytochrome P450. Hypothyroidism is another common adverse effect that can be controlled with administration of thyroid hormone. Bexarotene can be combined with other treatments such as PUVA or IFN-α. It may also find uses in a maintenance regimen after more aggressive therapies in patients with more advanced disease. As with other retinoids, it requires contraceptive measures in view of the risk of malformations.<a class="elsevierStyleCrossRefs" href="#bib0280"><span class="elsevierStyleSup">56–61</span></a></p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Interferon-alfa</span><p id="par0145" class="elsevierStylePara elsevierViewall">IFN-α is used as monotherapy administered subcutaneously (although intramuscular and intralesional administration is also possible) at a dose of 3 to 20 million units per day, 3 days a week, with a good (dose-dependent) response, particularly in early-stage disease (ORR of approximately 70%) or in combination with other therapies such as PUVA (apparently the most effective combination), retinoids, or purine analogs (fludarabine) with apparent benefit (studies that compare these options with IFN-α monotherapy are lacking). Adverse effects include flu-like syndrome, gastrointestinal disorders, bone marrow suppression, and elevated transaminases. The agent can be used for years as maintenance in patients who showed a good response and are at risk of relapse, although there is a risk of developing autoimmune diseases such as diabetes mellitus, thyroiditis, or hemolytic anemia.<a class="elsevierStyleCrossRefs" href="#bib0310"><span class="elsevierStyleSup">62–64</span></a></p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Immunotoxins</span><p id="par0150" class="elsevierStylePara elsevierViewall">Denileukin diftitox (DAB<span class="elsevierStyleInf">389</span>-interleukin 2 [IL-2]) is the first fusion cytotoxin approved by the FDA for the treatment of CTCL.<a class="elsevierStyleCrossRefs" href="#bib0325"><span class="elsevierStyleSup">65,66</span></a> It acts as a specific cytotoxin for cells that express the IL-2 receptor. It is obtained by expression in <span class="elsevierStyleItalic">Escherichia coli</span> of the product of fusion of the human IL-2 receptor genes with cytotoxic sequences of diphtheria toxin. The agent binds to the IL-2 receptor (CD25) of T lymphocytes, thereby inhibiting protein synthesis, and is administered intravenously at a dose of 9 or 18<span class="elsevierStyleHsp" style=""></span>mg/kg/d in 5-day cycles every 3 weeks. It has been shown to be particularly effective in stage IIB MF (response rate, 38%). Transient flu-like syndrome is reported in 60% to 70% of the patients, a similar figure to that seen with IFN-α. Other adverse effects such as urticaria, anaphylaxis, or vascular leak syndrome have also been reported. Some patients developed anti-DAB<span class="elsevierStyleInf">389</span> or anti-IL-2 antibodies in the first cycle, but there was no correlation with either toxicity or response. Efficacy has been boosted in recent studies through the concomitant use of oral bexarotene, particularly in patients with low or nonexistent expression of the IL-2 receptor.<a class="elsevierStyleCrossRefs" href="#bib0335"><span class="elsevierStyleSup">67,68</span></a> Combination therapy enabled lower doses of the 2 treatments to be used. The agent has been used in monotherapy in CTCLs other than MF,<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a> and in combination with radiotherapy.<a class="elsevierStyleCrossRef" href="#bib0350"><span class="elsevierStyleSup">70</span></a></p></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Monoclonal Antibodies</span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Alemtuzumab</span><p id="par0155" class="elsevierStylePara elsevierViewall">Alemtuzumab is a humanized monoclonal antibody that targets the CD52 glycoprotein expressed on the surface of T and B lymphocytes, natural killer (NK) cells, and to a lesser extent on monocytes and macrophages. The mechanism of action has not been fully elucidated but involves direct complement-mediated cell lysis and also antibody-dependent cytotoxicity and apoptosis. In 2003, its usefulness was demonstrated in 22 patients with pretreated MF/SS, most of whom had advanced disease (86%<span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>stage III and 36% with B symptoms) and a general poor state of health. The ORR was 55% (32% CR) and the mean response duration was 12 months.<a class="elsevierStyleCrossRef" href="#bib0355"><span class="elsevierStyleSup">71</span></a> Recently, these encouraging outcomes have been reproduced.<a class="elsevierStyleCrossRef" href="#bib0360"><span class="elsevierStyleSup">72</span></a> Alemtuzumab-induced cytopenia is potentially the most serious complication reported. Although different degrees of anemia and/or thrombocytopenia may develop due to mechanisms that are not well understood, T- and B-cell lymphopenia is a generalized finding in all patients. This predisposes them to serious opportunistic infections (particularly by cytomegalovirus and <span class="elsevierStyleItalic">Pneumocystis jirovecii</span>).<a class="elsevierStyleCrossRef" href="#bib0365"><span class="elsevierStyleSup">73</span></a> Alemtuzumab seems especially useful in the management of pruritus associated with the erythrodermic forms (SS).<a class="elsevierStyleCrossRefs" href="#bib0370"><span class="elsevierStyleSup">74,75</span></a></p></span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Zanolimumab</span><p id="par0160" class="elsevierStylePara elsevierViewall">Zanolimumab is another monoclonal antibody, which targets the CD4 receptor expressed on T lymphocytes and macrophages. It interferes with T-cell activation by impeding the interaction of CD4 with class II molecules of the major histocompatibility complex and also induces cell lysis through antibody-mediated cytotoxicity rather than by complement-mediated effects as is the case with alemtuzumab.<a class="elsevierStyleCrossRefs" href="#bib0380"><span class="elsevierStyleSup">76,77</span></a> Zanolimumab has been shown to be effective in 2 phase II multicenter studies of 47 patients with heavily pretreated persistent and refractory CTCL (38 MF and 9 SS).<a class="elsevierStyleCrossRef" href="#bib0390"><span class="elsevierStyleSup">78</span></a> The arms in which high doses of zanolimumab were administered (560<span class="elsevierStyleHsp" style=""></span>mg/wk for early stages [MF, stages IB-IIA] and 980<span class="elsevierStyleHsp" style=""></span>mg/wk for advanced stages [MF, stages IIB-IVB, and SS]) achieved an ORR of 56% with an impressive mean duration of response of 81 weeks (particularly in MF). Overall, zanolimumab has an acceptable safety profile with moderate adverse effects such as dermatitis, eczemas, and infections limited to the skin and upper respiratory tract despite the severe CD4 cell depletion associated with its use. No differences were observed in the incidence of infection between the 2 different dose groups. Although a more marked CD4 cell depletion was observed among patients treated at the higher dose (560-980 vs 280<span class="elsevierStyleHsp" style=""></span>mg/wk), of note was that there were no statistically significant differences in CD4 cell recovery once treatment had finished. On the basis of these findings, a pivotal phase III study was started and is currently in progress.</p></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Rituximab</span><p id="par0165" class="elsevierStylePara elsevierViewall">Rituximab is a chimeric (human-murine) anti-C20 monoclonal antibody that is used as monotherapy or in combination with other agents mainly for the treatment of systemic non-Hodgkin B-cell lymphoma. Several studies have found it to be effective when administered intralesionally in patients with CBCL (marginal zone and follicle center cell types).<a class="elsevierStyleCrossRefs" href="#bib0225"><span class="elsevierStyleSup">45,46,79,80</span></a> It is considered particularly useful in patients with multiple lesions or those with a high risk of recurrence, as well as in areas where we wish to avoid the unsightly sequelae of surgery and/or radiotherapy. It is also used in combination with cyclophosphamide, vincristine, and prednisone with doxorubicin (CHOP) for CBCL, leg-type.</p></span><span id="sec0115" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histone Deacetylase Inhibitors</span><p id="par0170" class="elsevierStylePara elsevierViewall">Histones are proteins present in abundance in cell nuclei, where they form the chromatin of eukaryotic cells along with other types of proteins and DNA. In recent years, several molecules within the pharmacologic group of histone deacetylase inhibitors have been developed, encouraged by different experimental findings that suggest that excess histone acetylation occurs in most cancers.<a class="elsevierStyleCrossRefs" href="#bib0405"><span class="elsevierStyleSup">81,82</span></a> Four histone deacetylase inhibitors have been studied in the treatment of CTCL: vorinostat, romidepsin, panobinostat, and belinostat.</p></span><span id="sec0120" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Vorinostat</span><p id="par0175" class="elsevierStylePara elsevierViewall">Vorinostat has been authorized by the FDA for the treatment of skin manifestations of patients with CTCL which persist, progress, or recur after at least 2 systemic treatments.<a class="elsevierStyleCrossRef" href="#bib0415"><span class="elsevierStyleSup">83</span></a> However, the drug has not been marketed in Europe. The indication was established after a phase II study of 74 patients with MF/SS.<a class="elsevierStyleCrossRef" href="#bib0420"><span class="elsevierStyleSup">84</span></a> Most of these patients had advanced disease stages (61 patients with <span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>IIB disease and 30 patients with SS, while 22 patients had clinically abnormal lymph nodes). All patients had received intensive treatment (96% with bexarotene, 63% with IFN-α, 61% with chemotherapy, 36% with photophoresis, and 31% with denileukin diftitox). The dose was 400<span class="elsevierStyleHsp" style=""></span>mg/d, administered orally, with adjustment or suspension according to toxicity or adverse effects. Overall, 29.7% achieved response. Among patients with advanced disease (IIB or worse), 29.5% achieved response. Among patients with SS, 33.3% achieved response. Vorinostat was generally well tolerated and the adverse effects observed most frequently were gastrointestinal (nausea, diarrhea) and constitutional (asthenia, anorexia, and weight loss). Cytopenias (thrombocytopenias and anemia) were also frequently reported. Neutropenia was not observed. Fewer than 15% of the patients required a reduction in vorinostat dose and 11% had serious adverse effects, which were mainly thromboembolic phenomena. QT prolongation was only observed in 3 patients.</p><p id="par0180" class="elsevierStylePara elsevierViewall">Recent studies are using these agents in combination with other therapies such as bexarotene<a class="elsevierStyleCrossRef" href="#bib0425"><span class="elsevierStyleSup">85</span></a> or IFN-α.<a class="elsevierStyleCrossRef" href="#bib0430"><span class="elsevierStyleSup">86</span></a></p></span><span id="sec0125" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Romidepsin</span><p id="par0185" class="elsevierStylePara elsevierViewall">Romidepsin is a new and potent histone deacetylase inhibitor that has been used in patients with CTCL and peripheral T-cell lymphomas. Several studies have demonstrated its usefulness,<a class="elsevierStyleCrossRefs" href="#bib0435"><span class="elsevierStyleSup">87–90</span></a> with an ORR of 41% (7% with CR and 33% with PR), a median response duration of 14.9 months, and a median time to progression of 8.3 months. The most frequently observed adverse effects were nausea, asthenia, and vomiting. Adverse effects grade 3 or worse were only observed in 33% of the patients. The most frequently observed adverse effects were disease progression (6%), fever (3%), sepsis (2%), tumor lysis syndrome (2%), and hypotension (2%). Six patients died, one possibly of treatment-related causes. QT prolongation was only observed in 2% of the patients (patients with significant cardiac abnormalities and/or those in treatment with QT prolonging agents or inhibitors of cytochrome P3A4 were excluded from the study).</p></span><span id="sec0130" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Panobinostat</span><p id="par0190" class="elsevierStylePara elsevierViewall">The new histone deacetylase inhibitor, panobinostat, not only produces histone acetylation but also induces p21, cell cycle arrest, apoptosis, and HSP90 (pan-histone deacetylase inhibitor) acetylation. Its usefulness and safety profile have been demonstrated recently in a phase II study performed in 40 patients with CTCL refractory to at least 2 prior treatments (mean of 5 prior treatments per patient).<a class="elsevierStyleCrossRef" href="#bib0455"><span class="elsevierStyleSup">91</span></a> Patients received 20<span class="elsevierStyleHsp" style=""></span>mg/d of panobinostat orally on days 1, 3, and 5 of each week until disease progression or intolerance. The response rates were poor. In patients who had received prior treatment with bexarotene (group 1, 25 patients), PR was obtained in 3 and 4 had stable disease. Three patients had progression. Thirty patients could not be evaluated because of limited follow-up at the time of publication. The most frequently observed adverse effects were diarrhea, thrombocytopenia, fatigue, asthenia, hypertriglyceridemia, taste alterations, nausea, and pruritus (15% of all patients). No significant QT prolongations were observed.</p></span><span id="sec0135" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Belinostat</span><p id="par0195" class="elsevierStylePara elsevierViewall">Belinostat is another pan-histone deacetylase inhibitor that has been tested in a phase II clinical trial with 29 patients (15 with MF, 7 with SS, 5 without either MF or SS, and 2 with unclassified disease).<a class="elsevierStyleCrossRef" href="#bib0460"><span class="elsevierStyleSup">92</span></a> The participants received 1000<span class="elsevierStyleHsp" style=""></span>mg/m<span class="elsevierStyleSup">2</span> in a 30-minute infusion from day 1 to 5 of each cycle, every 3 weeks. Seventeen patients achieved stable disease for longer than 127 days. There were 2 PR and 2 CR with a median response duration of 273 days. It is important to note that the time to response was very short: 16 days (range, 14-35 days) with a substantial improvement in pruritus. There were no reports of grade 4 hematologic toxicity or cases of grade 3 QT prolongation. Four grade 3 or 4 adverse effects were observed: pruritus, erythema, edema, and adynamic ileus.</p></span></span><span id="sec0140" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Others</span><span id="sec0145" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Bortezomib</span><p id="par0200" class="elsevierStylePara elsevierViewall">Bortezomib is a drug indicated as first-line treatment in patients with multiple myeloma who are not candidates for hematopoietic stem cell transplantation and in patients with a relapse after prior treatment. The group at the Hematology Institute of the University of Bologna in Italy conducted a phase II study of 12 patients (10 with advanced MF and 2 with peripheral T-cell lymphomas with isolated cutaneous involvement).<a class="elsevierStyleCrossRef" href="#bib0465"><span class="elsevierStyleSup">93</span></a> They reported an ORR of 67%, including 2 CR (17%) and 6 PR (50%). One patient with MF and 1 with peripheral T-cell lymphoma achieved CR (10% and 50%, respectively). CR lasted for more than 1 year after the last study dose in the patient with MF while relapse was observed 10 months later in the patient with peripheral T-cell lymphoma. The regimen of bortezomib used was the same as for multiple myeloma: 1.3<span class="elsevierStyleHsp" style=""></span>mg/m<span class="elsevierStyleSup">2</span>, given intravenously on days 1, 4, 8, and 11 of each 21-day cycle up to a total of 6 cycles. The adverse effects observed most frequently were neutropenia (2 patients [17%], WHO grade 3), thrombocytopenia (2 patients [17%], WHO grade 3), and sensory neuropathy (2 patients [17%], WHO grade 3). No infections or treatment-related deaths were reported during the study. The rationale for using bortezomib is that it can act as an inhibitor of nuclear factor κB (NF-κB), which is constitutively activated in CTCL cell lines, and induce apoptosis.<a class="elsevierStyleCrossRef" href="#bib0470"><span class="elsevierStyleSup">94</span></a> NF-κB is a transcriptional factor implicated in the generation of inflammatory responses, regulation of the cell cycle, and protection against apoptosis.</p></span><span id="sec0150" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Lenalidomide</span><p id="par0205" class="elsevierStylePara elsevierViewall">The antitumor effects of lenalidomide are attributed to several mechanisms of action: inhibition of the production of proinflammatory mediators by monocytes (tumor necrosis factor α, IL-1, IL-6, IL-12), enhancement of IL-2 and IFN-γ production by T lymphocytes, and enhancement of the cytotoxic activity of these cytokines and NK cells. In a phase II study, lenalidomide was administered at a dose of 10 to 25<span class="elsevierStyleHsp" style=""></span>mg/d for 21 days in cycles of 28 days to 25 patients with extensively pretreated CTCL (mean of 6 prior regimens).<a class="elsevierStyleCrossRef" href="#bib0475"><span class="elsevierStyleSup">95</span></a> Seven patients achieved PR after a mean of 9 cycles of treatment. The adverse effects observed most frequently were anemia, scaling, pruritus, and leg edema. In the high-dose group, intense neutropenia was observed in 2 patients while 1 patient discontinued treatment due to dysarthria.</p></span></span></span><span id="sec0155" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Chemotherapy</span><p id="par0210" class="elsevierStylePara elsevierViewall">Chemotherapy should only be used in CTCL in advanced stages of the disease, as it is no more effective than conservative treatment in the early phases. Almost all chemotherapy agents used for systemic lymphomas have also been used in advanced CTCL: alkylating agents, methotrexate, cisplatin, etoposide, bleomycin, vinblastine, cyclophosphamide. It is not clear whether one agent is any better than another and, in general, responses are short-lasting. The most effective combination, and therefore the most widely used one, is CHOP or CHOP without doxorubicin (CVP), but randomized studies have not been undertaken that demonstrate increased survival with any of these regimens.</p><span id="sec0160" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Methotrexate</span><p id="par0215" class="elsevierStylePara elsevierViewall">Methotrexate is the first-choice treatment in CD30<span class="elsevierStyleSup">+</span> CTCL, particularly when the patient has multiple lesions (radiotherapy is the best alternative in solitary lesions).<a class="elsevierStyleCrossRef" href="#bib0480"><span class="elsevierStyleSup">96</span></a> High weekly doses are required in some cases to achieve CR, with a higher risk of adverse effects.</p><p id="par0220" class="elsevierStylePara elsevierViewall">Recently, 2 other chemotherapies (gemcitabine and pegylated liposomal doxorubicin [DOX-PEG]) have been shown to be useful in monotherapy.</p></span><span id="sec0165" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Gemcitabine</span><p id="par0225" class="elsevierStylePara elsevierViewall">Gemcitabine is a pyrimidine antimetabolite indicated for solid tumors traditionally considered resistant to conventional treatment such as lung cancer, ovarian cancer, pancreatic cancer, and urinary bladder cancer. Its effectiveness in cutaneous lymphomas has been investigated in 2 studies. The first to these was a series of 32 patients (mostly with MF).<a class="elsevierStyleCrossRef" href="#bib0485"><span class="elsevierStyleSup">97</span></a> CR was achieved by 22% (7 patients) while PR was achieved by 53% (17 patients). Unfortunately, the study used standard criteria for assessing response as if the patients had common forms of non-Hodgkin lymphoma and not specifically cutaneous lymphoma (severity-weighted assessment tool). Response was achieved by 73% of those with MF (26 patients), with 23% with CR and 50% with PR. The only patient included with SS did not respond. The median duration of CR was 10 months (range, 4-22 months). Gemcitabine was administered as an intravenous infusion at a dose of 1200 <span class="elsevierStyleHsp" style=""></span>mg/m<span class="elsevierStyleSup">2</span> for 30<span class="elsevierStyleHsp" style=""></span>minutes in cycles of 28 days (total of 6 cycles) on days 1, 8, and 15 of each cycle. The most frequently reported adverse effects were cytopenias. Reversible liver toxicity was the most frequently reported nonhematologic adverse effect (13 patients, 40%). No treatment-related deaths were reported. The second study was a series of 33 patients, most of whom had heavily pretreated MF (median of 5 prior regimens) (31 patients).<a class="elsevierStyleCrossRef" href="#bib0490"><span class="elsevierStyleSup">98</span></a> Two patients had anaplastic CD30<span class="elsevierStyleSup">+</span> T-cell lymphoma. Compared to the first study, a higher dose of gemcitabine was used (1000<span class="elsevierStyleHsp" style=""></span>mg/m<span class="elsevierStyleSup">2</span>) but the schedule of administration and number of cycles were the same. Response was assessed using variables that included the area of skin involved, size of lymph nodes, and peripheral blood cytometry. Response was achieved by 68% of the patients (2 with CR). Myelosuppression was the most frequently observed adverse effect (grade 3 in 8 of the 33 patients) and 2 characteristic uremic hemolytic syndromes were diagnosed in patients with SS. Other adverse effects were elevated transaminase liver enzymes, mucositis, lethargy, fever, hyperpigmentation, infusion-related maculopapular rash, and different types of cardiovascular events. Another more recent multicenter study reported similar outcomes to the studies already discussed, but with significantly greater toxicity.<a class="elsevierStyleCrossRef" href="#bib0495"><span class="elsevierStyleSup">99</span></a></p></span><span id="sec0170" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Pegylated Liposomal Doxorubicin</span><p id="par0230" class="elsevierStylePara elsevierViewall">DOX-PEG is approved for the treatment of advanced ovarian cancer, relapsed multiple myeloma after hematopoietic stem cell transplantation, and AIDS-associated Kaposi sarcoma. The usefulness of DOX-PEG has also been demonstrated in patients with CTCL in observational and retrospective studies. Recently, a prospective, multicenter study analyzed use of this agent in 25 patients with MF and/or SS in stages ≥<span class="elsevierStyleHsp" style=""></span>II refractory to at least 2 prior lines of treatment and in patients with CD30<span class="elsevierStyleSup">+</span> large-cell CTCL.<a class="elsevierStyleCrossRef" href="#bib0500"><span class="elsevierStyleSup">100</span></a> DOX-PEG was administered intravenously every 4 weeks at a dose of 40<span class="elsevierStyleHsp" style=""></span>mg/m<span class="elsevierStyleSup">2</span>/d for up to 8 cycles. An objective ORR of 56% was reported (14/25 patients with CR and 9/25 with PR). Response rates were high in patients with SS, with 6 of the 10 (60%) responding. One of these responses was a CR. Response rates were also high in transformed CTCL, and 50% of these responses were a CR. In general, more adverse effects were seen than in the previous studies, with 4 episodes of serious infection and some cardiac events. DOX-PEG has also been shown to have good activity in 5 CBCLs (1 with marginal zone disease and 4 diffuse large-cell lymphomas, leg-type) in an Italian phase II pilot study (dose of 20<span class="elsevierStyleHsp" style=""></span>mg/m<span class="elsevierStyleSup">2</span> every 3 or 4 weeks). An impressive prolonged CR was obtained in 4 of these patients (80%).<a class="elsevierStyleCrossRef" href="#bib0505"><span class="elsevierStyleSup">101</span></a> In another study published recently, excellent outcomes were obtained with DOX-PEG in combination with bleomycin, vinblastine, and dacarbazine (CBVD regimen) in 37 patients with advanced PCL, both of T-cell origin (19 patients) and B-cell origin (18 patients).<a class="elsevierStyleCrossRef" href="#bib0510"><span class="elsevierStyleSup">102</span></a> CR rates of 88.8% and 100%, respectively, were obtained. Between 4 and 6 cycles of CBVD were administered in the group of CTCL whereas those with CBCL received between 2 and 6 cycles (with rituximab added to the chemotherapy: R-CBVD). The safety profile was good. Subsequent allogeneic hematopoietic stem cell transplantation was performed in 3 patients (2 with CTCL and 1 with CBCL).</p></span><span id="sec0175" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Other Chemotherapies</span><span id="sec0180" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Forodesine</span><p id="par0235" class="elsevierStylePara elsevierViewall">Forodesine is a purine analog that inhibits purine nucleoside phosphorylase. Recruitment of patients with MF/SS with refractory disease in stages ≥<span class="elsevierStyleHsp" style=""></span>IB to a phase II pivotal study was completed in 2010. The preliminary results of this multicenter study have been published recently.<a class="elsevierStyleCrossRef" href="#bib0515"><span class="elsevierStyleSup">103</span></a> The overall response rate was around 30%. The most frequently observed adverse effects were nausea, tiredness, edema, dyspnea, and urinary calculi.</p></span><span id="sec0185" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Pralatrexate</span><p id="par0240" class="elsevierStylePara elsevierViewall">The cytotoxicity induced by pralatrexate can be 10 times greater than that of methotrexate, allowing acquired tumor resistances to be overcome. The agent has been shown to be active in advanced T-cell lymphomas and it is a promising drug for maintenance therapies in CTCL.<a class="elsevierStyleCrossRefs" href="#bib0520"><span class="elsevierStyleSup">104,105</span></a></p></span></span></span></span><span id="sec0190" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Stem Cell Transplantation</span><p id="par0245" class="elsevierStylePara elsevierViewall">Autologous stem cell transplantation can achieve high response rates but with immediate relapse (mean time to relapse, <<span class="elsevierStyleHsp" style=""></span>100 days).<a class="elsevierStyleCrossRefs" href="#bib0530"><span class="elsevierStyleSup">106,107</span></a> This approach is therefore only useful in certain patients as a means to improve quality of life or as a way to buy some time before moving on to other therapies.</p><p id="par0250" class="elsevierStylePara elsevierViewall">Long-term CR has been achieved with allogeneic stem cell transplantation, although mortality is high due mainly to graft-vs-host disease.<a class="elsevierStyleCrossRefs" href="#bib0540"><span class="elsevierStyleSup">108,109</span></a> Indeed, the efficacy of the technique is linked to the appearance of this event, known as a graft-vs-lymphoma effect,<a class="elsevierStyleCrossRef" href="#bib0550"><span class="elsevierStyleSup">110</span></a> in which the donor lymphocytes attack the tumor lymphocytes of the receptor, thereby eliminating them. Currently, regimens are used that are not myeloablative but that are nevertheless cytoreductive prior to transplant, in an attempt to improve response and reduce complications. A recent study lends support to the role of this treatment for tumoral MF (stage IIB) and SS.<a class="elsevierStyleCrossRef" href="#bib0555"><span class="elsevierStyleSup">111</span></a> The survival rates are significantly higher in patients with second CR, PR, or progression with 3 or fewer lines of prior systemic therapy. Administration of this therapy should therefore not be left too late in the course of the disease. In the short term, it may be the only curative treatment available.</p></span><span id="sec0195" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conclusions</span><p id="par0255" class="elsevierStylePara elsevierViewall">Currently, the aim in the treatment of PCL is to avoid progression to more advanced stages of the disease as, at present, there is no curative treatment available. There are no comparative studies between different systemic treatments in patients with advanced PCL, and so treatment in these patients is not at all protocolized. There is still much debate concerning the management of this disease, and so a conservative or <span class="elsevierStyleItalic">start low go slow</span> approach is recommended.<a class="elsevierStyleCrossRefs" href="#bib0560"><span class="elsevierStyleSup">112,113</span></a><a class="elsevierStyleCrossRefs" href="#tbl0010">Tables 2–8</a> summarize the recommendations of the EORTC consensus on treatment as well as staging.<a class="elsevierStyleCrossRefs" href="#bib0100"><span class="elsevierStyleSup">20,46</span></a> The recommendations of the EORTC for treatment of CTCL should be reviewed in the light of new emerging therapies.<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">20</span></a></p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><elsevierMultimedia ident="tbl0015"></elsevierMultimedia><elsevierMultimedia ident="tbl0020"></elsevierMultimedia><elsevierMultimedia ident="tbl0025"></elsevierMultimedia><elsevierMultimedia ident="tbl0030"></elsevierMultimedia><elsevierMultimedia ident="tbl0035"></elsevierMultimedia><elsevierMultimedia ident="tbl0040"></elsevierMultimedia></span><span id="sec0200" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflicts of Interest</span><p id="par0260" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:11 [ 0 => array:2 [ "identificador" => "xres96458" "titulo" => "Abstract" ] 1 => array:2 [ "identificador" => "xpalclavsec83619" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xres96459" "titulo" => "Resumen" ] 3 => array:2 [ "identificador" => "xpalclavsec83618" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:3 [ "identificador" => "sec0010" "titulo" => "Treatments That Target the Skin" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "sec0015" "titulo" => "Topical Corticosteroids" ] 1 => array:3 [ "identificador" => "sec0020" "titulo" => "Alkylating Agents" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "sec0025" "titulo" => "Topical Mechlorethamine (Nitrogen Mustard)" ] ] ] 2 => array:2 [ "identificador" => "sec0030" "titulo" => "Carmustine" ] 3 => array:3 [ "identificador" => "sec0035" "titulo" => "Phototherapy" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0040" "titulo" => "Narrow-Band UV-B Phototherapy (311-312 nm)" ] 1 => array:2 [ "identificador" => "sec0045" "titulo" => "Psoralens Plus UV (320-400 nm)" ] 2 => array:2 [ "identificador" => "sec0050" "titulo" => "Others Types of Phototherapy" ] ] ] 4 => array:3 [ "identificador" => "sec0055" "titulo" => "Radiotherapy" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0060" "titulo" => "Conventional (Orthovoltage)" ] 1 => array:2 [ "identificador" => "sec0065" "titulo" => "Total Skin Electron Radiation (Electron Beam Therapy)" ] ] ] ] ] 6 => array:3 [ "identificador" => "sec0070" "titulo" => "Systemic Treatments" "secciones" => array:2 [ 0 => array:3 [ "identificador" => "sec0075" "titulo" => "Biological Response Modifiers" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "sec0080" "titulo" => "Retinoids" ] 1 => array:2 [ "identificador" => "sec0085" "titulo" => "Interferon-alfa" ] 2 => array:2 [ "identificador" => "sec0090" "titulo" => "Immunotoxins" ] 3 => array:3 [ "identificador" => "sec0095" "titulo" => "Monoclonal Antibodies" "secciones" => array:8 [ 0 => array:2 [ "identificador" => "sec0100" "titulo" => "Alemtuzumab" ] 1 => array:2 [ "identificador" => "sec0105" "titulo" => "Zanolimumab" ] 2 => array:2 [ "identificador" => "sec0110" "titulo" => "Rituximab" ] 3 => array:2 [ "identificador" => "sec0115" "titulo" => "Histone Deacetylase Inhibitors" ] 4 => array:2 [ "identificador" => "sec0120" "titulo" => "Vorinostat" ] 5 => array:2 [ "identificador" => "sec0125" "titulo" => "Romidepsin" ] 6 => array:2 [ "identificador" => "sec0130" "titulo" => "Panobinostat" ] 7 => array:2 [ "identificador" => "sec0135" "titulo" => "Belinostat" ] ] ] 4 => array:3 [ "identificador" => "sec0140" "titulo" => "Others" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0145" "titulo" => "Bortezomib" ] 1 => array:2 [ "identificador" => "sec0150" "titulo" => "Lenalidomide" ] ] ] ] ] 1 => array:3 [ "identificador" => "sec0155" "titulo" => "Chemotherapy" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "sec0160" "titulo" => "Methotrexate" ] 1 => array:2 [ "identificador" => "sec0165" "titulo" => "Gemcitabine" ] 2 => array:2 [ "identificador" => "sec0170" "titulo" => "Pegylated Liposomal Doxorubicin" ] 3 => array:3 [ "identificador" => "sec0175" "titulo" => "Other Chemotherapies" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0180" "titulo" => "Forodesine" ] 1 => array:2 [ "identificador" => "sec0185" "titulo" => "Pralatrexate" ] ] ] ] ] ] ] 7 => array:2 [ "identificador" => "sec0190" "titulo" => "Stem Cell Transplantation" ] 8 => array:2 [ "identificador" => "sec0195" "titulo" => "Conclusions" ] 9 => array:2 [ "identificador" => "sec0200" "titulo" => "Conflicts of Interest" ] 10 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2011-08-10" "fechaAceptado" => "2012-01-29" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec83619" "palabras" => array:4 [ 0 => "Cutaneous lymphoma" 1 => "Treatment" 2 => "Update" 3 => "Review" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec83618" "palabras" => array:4 [ 0 => "Linfoma cutáneo" 1 => "Tratamiento" 2 => "Actualización" 3 => "Revisión" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Primary cutaneous lymphomas (PCLs) are a heterogeneous group of lymphoid tumors that originate primarily in the skin. Most PCLs (75%) are T-cell lymphomas and only 20% to 25% involve B cells. It is important to differentiate between cutaneous lymphomas and lymph node tumors given the differences in their molecular biology and clinical, histopathologic, and immunophenotypic features. Moreover, PCLs generally follow a more indolent course and require different treatments.</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Many treatment options are available for managing PLC's. The choice should be based primarily on the clinical stage of disease but must also take into consideration other factors, such as the patient's age and general health, the availability and accessibility of the treatment, and the cost-benefit ratio. It will be important to use a multidisciplinary approach, involving a team of expert dermatologists, hematologist-oncologists, and radiotherapists who are familiar with this rare disease. Recent years have seen the emergence of many new therapies, particularly for advanced stages of the disease and for patients whose tumors have proven refractory to treatment. The objective of this article is to review all the treatment options available to us.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Los linfomas cutáneos primarios (LCP) constituyen un grupo heterogéneo de neoplasias linfoides que se originan primariamente en la piel. La mayoría (75%) son linfomas de células T y solo un 20-25% se originan a partir de los linfocitos B. Es importante diferenciar los LCP de sus equivalentes ganglionares, dado que presentan características clínicas, histopatológicas, inmunofenotípicas y de biología molecular diferentes con un pronóstico en la mayoría de los casos más indolente y tratamientos diferentes.</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Existen múltiples opciones terapéuticas en el manejo de los LCP. La elección del tratamiento debe basarse principalmente en el estadio clínico del paciente, pero deben considerarse también otros factores, como la accesibilidad a los tratamientos, la edad y el estado general del paciente o el coste-beneficio. Además es importante el abordaje multidisciplinar de estos pacientes, formando un equipo experto entre dermatólogos, hematooncólogos y radioterapeutas que conozcan bien esta infrecuente patología. En los últimos años asistimos a la aparición de múltiples terapias nuevas, especialmente para el tratamiento de los estadios avanzados o de pacientes refractarios a tratamientos previos. El motivo de este artículo es revisar todas las alternativas terapéuticas a nuestro alcance.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara">Please cite this article as: Izu-Belloso RM, García-Ruiz JC. Actualización terapéutica en linfomas cutáneos. Actas Dermosifiliogr.2012;103:694-707.</p>" ] ] "multimedia" => array:8 [ 0 => array:7 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: BCL, B-cell lymphoma; MF, mycosis fungoides; NK, natural killer.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Cutaneous T-cell Lymphomas</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">MF and variants</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Folliculotropic MF \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Pagetoid reticulosis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Granulomatous slack skin \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Sézary syndrome</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">CD30</span><span class="elsevierStyleSup"><span class="elsevierStyleItalic">+</span></span><span class="elsevierStyleItalic">lymphoproliferative disorders</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Lymphomatoid papulosis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>CD30<span class="elsevierStyleSup">+</span> anaplastic lymphoma \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Adult T-cell leukemia/lymphoma</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Panniculitis-like T-cell lymphoma</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Extranodal NK/T-cell lymphoma, nasal-type</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Peripheral T-cell lymphoma, unspecified</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>CD8<span class="elsevierStyleSup">+</span> epidermotropic lymphoma \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Cutaneous T-cell lymphoma \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>CD4<span class="elsevierStyleSup">+</span> small/medium-sized pleomorphic T-cell lymphoma \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">B-Cell Cutaneous Lymphomas</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Primary cutaneous marginal zone BCL</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Cutaneous follicle center BCL</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Diffuse large BCL, leg-type</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Cutaneous diffuse large BCL, other</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Intravascular diffuse large BCL</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Neoplastic Disease With Hematologic Precursors</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">CD4</span><span class="elsevierStyleSup"><span class="elsevierStyleItalic">+</span></span><span class="elsevierStyleItalic">CD56</span><span class="elsevierStyleSup"><span class="elsevierStyleItalic">+</span></span><span class="elsevierStyleItalic">hematodermic neoplasm</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab182525.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">World Health Organization/European Organisation for Research and Treatment of Cancer Classification of Primary Cutaneous Lymphomas (2005).</p>" ] ] 1 => array:7 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">In blood, Sézary cells are defined as lymphocytes with highly convoluted cerebriform nuclei. If Sézary cells cannot be used establish the tumor level B<span class="elsevierStyleInf">2</span>, then 1 of the following modified criteria of the ISCL can be used along with a positive clonal rearrangement in the T-cell receptor: <span class="elsevierStyleItalic">1)</span> CD4<span class="elsevierStyleSup">+</span> or C3<span class="elsevierStyleSup">+</span> expansion with a CD4/CD8 ratio of 10 or more; <span class="elsevierStyleItalic">2)</span> CD4<span class="elsevierStyleSup">+</span> expansion with abnormal immunophenotype including loss of CD7 or CD26.</p><p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">T-cell clonality is defined by a polymerase chain reaction analysis or southern blotting of the gene that encodes the T-cell receptor.</p><p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Abbreviations and definitions: Dutch, criteria established by the Dutch Cutaneous Lymphomas Group; ISCL, International Society of Cutaneous Lymphoma.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Skin</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>T<span class="elsevierStyleInf">1</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Limited patches, papules, and/or plaques covering <<span class="elsevierStyleHsp" style=""></span>10% of the body surface area. Can be staged as T<span class="elsevierStyleInf">1a</span> (only patches) vs T<span class="elsevierStyleInf">1b</span> (plaques<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>patches) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>T<span class="elsevierStyleInf">2</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Patches, papules, and/or plaques covering ≥<span class="elsevierStyleHsp" style=""></span>10% of the body surface area. Can be staged as T<span class="elsevierStyleInf">2a</span> (only patches) vs T<span class="elsevierStyleInf">2b</span> (plaques<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>patches) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>T<span class="elsevierStyleInf">3</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">One or more tumors (≥<span class="elsevierStyleHsp" style=""></span>1<span class="elsevierStyleHsp" style=""></span>cm in diameter) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>T<span class="elsevierStyleInf">4</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Confluence of erythema covering ≥<span class="elsevierStyleHsp" style=""></span>80% of the body surface area \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Lymph nodes</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">0</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">No abnormal peripheral lymph nodes. Biopsy not required \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">1</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Enlarged peripheral lymph nodes, Dutch gr 1 or NCI LN<span class="elsevierStyleInf">0,2</span> histology \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">1a</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Negative clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">1b</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Positive clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">2</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Enlarged peripheral lymph nodes, Dutch gr 2 or NCI LN<span class="elsevierStyleInf">3</span> histology \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">2a</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Negative clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">2b</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Positive clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">3</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Enlarged peripheral lymph nodes, Dutch gr 3-4, or NCI LN<span class="elsevierStyleInf">4</span> positive or negative clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>N<span class="elsevierStyleInf">x</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Enlarged peripheral lymph nodes, without histologic confirmation \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Visceral</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>M<span class="elsevierStyleInf">o</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">No visceral involvement \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>M<span class="elsevierStyleInf">1</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Visceral involvement (histologic confirmation needed and the affected organ should be specified) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="2" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Hematologic</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>B<span class="elsevierStyleInf">0</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Absence of significant hematologic involvement ≤<span class="elsevierStyleHsp" style=""></span>5% atypical lymphocytes (Sézary cells) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>B<span class="elsevierStyleInf">0a</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Negative clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>B<span class="elsevierStyleInf">0b</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Positive clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>B<span class="elsevierStyleInf">1</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Low hematologic involvement: ><span class="elsevierStyleHsp" style=""></span>5% peripheral lymphocytes are atypical (Sézary cells) but do not meet the criterion for B<span class="elsevierStyleInf">2</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>B<span class="elsevierStyleInf">1a</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Negative clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>B<span class="elsevierStyleInf">1b</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Positive clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>B<span class="elsevierStyleInf">2</span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Extensive hematologic involvement: ≥<span class="elsevierStyleHsp" style=""></span>1000/mm<span class="elsevierStyleSup">3</span> Sézary cells with positive clonality \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab182521.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">TNMB Staging for Mycosis Fungoides/Sézary Syndrome.</p>" ] ] 2 => array:7 [ "identificador" => "tbl0015" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">T \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">N \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">M \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">B \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IA \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0,1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0,1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">II \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1-2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1,2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0,1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IIB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0-2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0,1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">III \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0-2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0,1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IIIA \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0-2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IIIB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0-2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IVA1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1-4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0-2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">2 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IVA2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1-4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0-2 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IVB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1-4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0-3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0-2 \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab182523.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Clinical Staging and Classification of Mycosis Fungoides and Sézary Syndrome.</p>" ] ] 3 => array:7 [ "identificador" => "tbl0020" "etiqueta" => "Table 4" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">T</span><span class="elsevierStyleItalic">T</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">1</span></span>: solitary skin lesionT<span class="elsevierStyleInf">1a</span>: solitary lesion<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>5<span class="elsevierStyleHsp" style=""></span>cm diameterT<span class="elsevierStyleInf">1b</span>: solitary lesion<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>5<span class="elsevierStyleHsp" style=""></span>cm diameter<span class="elsevierStyleItalic">T</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">2</span></span>: multiple skin lesions in 1 body region or 2 contiguous regionsT<span class="elsevierStyleInf">2a</span>: all disease encompassed in 1 body region<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>15<span class="elsevierStyleHsp" style=""></span>cm diameterT<span class="elsevierStyleInf">2b</span>: all disease encompassed in 1 body region ><span class="elsevierStyleHsp" style=""></span>15<span class="elsevierStyleHsp" style=""></span>cm and <span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>30<span class="elsevierStyleHsp" style=""></span>cm in diameterT<span class="elsevierStyleInf">2c</span>: all disease encompassed in 1 body region <span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>30<span class="elsevierStyleHsp" style=""></span>cm diameter<span class="elsevierStyleItalic">T</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">3</span></span>: generalized cutaneous involvementT<span class="elsevierStyleInf">3a</span>: multiple lesions affecting 2 noncontiguous body regionsT<span class="elsevierStyleInf">3b</span>: multiple lesions affecting more than 3 body regions \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">N</span><span class="elsevierStyleItalic">N</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">0</span></span>: no clinical or pathologic lymph node involvement<span class="elsevierStyleItalic">N</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">1</span></span>: involvement of 1 peripheral lymph node region that drains a region of skin involvement<span class="elsevierStyleItalic">N</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">2</span></span>: involvement of 2 or more peripheral lymph node regions or a lymph node region that does not drain a region of skin involvement<span class="elsevierStyleItalic">N</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">3</span></span>: involvement of central lymph nodes \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">M</span><span class="elsevierStyleItalic">M</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">0</span></span>: no evidence of extracutaneous non-lymph-node disease<span class="elsevierStyleItalic">M</span><span class="elsevierStyleInf"><span class="elsevierStyleItalic">1</span></span>: extracutaneous non-lymph-node disease \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab182520.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">TNM Classification for Lymphomas Other Than Mycosis Fungoides/Sézary Syndrome.</p>" ] ] 4 => array:7 [ "identificador" => "tbl0025" "etiqueta" => "Table 5" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: ECP, extracorporeal photophoresis; IFN-α: interferon alfa; MTX, methotrexate; PUVA, psoralen + UV-A; TSEB, total skin electron beam.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">MF IA-IIA \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">MF IIB \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">MF III \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">MF IVA-IVB \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">First-line \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">PUVAUV-B (patch lesions)Topical CorticosteroidsLocal radiotherapyTSEB (<<span class="elsevierStyleHsp" style=""></span> 3 treatments)CarmustineNitrogen mustard \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IFN-α<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>PUVATSEB, radiotherapyIFN-α<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>retinoidsBexarotene<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>PUVA \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IFN-α<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>PUVAIFN-αMTXTSEB, radiotherapyCarmustineNitrogen mustardECBPUVA<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>retinoid \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">ChemotherapyTSEB, radiotherapyOral bexaroteneDenileukin diftitoxIFN-αAlemtuzumabLow-dose MTX \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Second-line \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Oral bexaroteneIFN-αIFN-α<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>retinoidsDenileukin diftitoxLow-dose MTXIFN-α<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>PUVARetinoid<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>PUVABexarotene<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>PUVA \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Oral bexaroteneChemotherapyDenileukin diftitox \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Oral bexaroteneChemotherapy \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Inclusion in clinical trials \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab182522.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Recommendations of the European Organisation for Treatment and Research of Cancer on the Treatment of Mycosis Fungoides (MF).</p>" ] ] 5 => array:7 [ "identificador" => "tbl0030" "etiqueta" => "Table 6" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: IFN-α, interferon alfa; MTX, methotrexate.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">First-line</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Extracorporeal photophoresis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>IFN-α \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Denileukin diftitox \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Chlorambucil<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>prednisone \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Second-line</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Oral bexarotene \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Chemotherapy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Alemtuzumab \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>MTX \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab182519.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Recommendations of the European Organisation for Treatment and Research of Cancer on the Treatment of Sézary Syndrome.</p>" ] ] 6 => array:7 [ "identificador" => "tbl0035" "etiqueta" => "Table 7" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:3 [ "leyenda" => "<p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: CHOP, cyclophosphamide, vincristine, prednisone, and doxorubicin; CVP, cyclophosphamide, vincristine, and prednisone; IFN-α, interferon alfa; IL, intralesional; IV, intravenous; MZ, mantle-zone.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Type of CBCL/Extension \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">First-Line Treatment \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Alternative Treatment \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Solitary/localized MZ CBCL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Local radiotherapyExcisionAntibiotics<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IFN-α ILRituximab ILCorticosteroides IL \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Multifocal MZ CBCL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Watchful waitingLocal radiotherapyChlorambucil<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a>Rituximab IVAntibiotics<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IFN-α ILRituximab ILCorticosteroides IL ortopical \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Solitary/localized FC CBCL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Local radiotherapyExcision \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IFN-α ILRituximab IL \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Multifocal FC CBCL \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Watchful waitingLocal radiotherapyRituximab IV \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Chemotherapy(R-CVP/CHOP) inexceptional casesor extracutaneous diseases \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Solitary/localized CBCL, leg-type \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">R-CHOP<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>radiotherapy \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Local radiotherapyRituximab IV \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Multifocal CBCL, leg-type \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">R-CHOP \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Rituximab IV \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab182524.png" ] ] ] "notaPie" => array:2 [ 0 => array:3 [ "identificador" => "tblfn0005" "etiqueta" => "a" "nota" => "<p class="elsevierStyleNotepara">In the event of evidence of <span class="elsevierStyleItalic">Borrelia burgdorferi</span> infection.</p>" ] 1 => array:3 [ "identificador" => "tblfn0010" "etiqueta" => "b" "nota" => "<p class="elsevierStyleNotepara">Other appropriate single-agent or combined chemotherapies for low-grade B-cell lymphomas.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Recommendations of the European Organisation for Research and Treatment of Cancer on the Treatment of Cutaneous B-Cell Lymphoma (CBCL).</p>" ] ] 7 => array:7 [ "identificador" => "tbl0040" "etiqueta" => "Table 8" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0100" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: BCNU, carmustine; CHOP, cyclophosphamide, vincristine, prednisone, and doxorubicin; HDAC, histone deacetylase inhibitors; IFN-α, interferon alfa; MTX, methotrexate; NH<span class="elsevierStyleInf">2</span>, nitrogen mustard; PUVA, psoralen + UV-A.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">First-Line \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Second-Line \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="3" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Lymphomatoid papulosis</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Solitary lesion or limited number of lesions \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">No treatment (watchful waiting)Topical corticosteroids \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Generalized lesions \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">MTXNH<span class="elsevierStyleInf">2</span>, BCNU \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">PUVAIFN-αBexarotene \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="3" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">CD30</span><span class="elsevierStyleSup"><span class="elsevierStyleItalic">+</span></span><span class="elsevierStyleItalic">anaplastic large cell lymphoma</span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Solitary lesion \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">ExcisionRadiotherapyMTX \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IFN-α \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Multiple lesions \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">MTXRadiotherapy \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">IFN-αBexaroteneDoxorubicin, CHOP, HDACDenileukin diftitox \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab182518.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0095" class="elsevierStyleSimplePara elsevierViewall">Treatment of CD30<span class="elsevierStyleSup">+</span> Cutaneous T-Cell 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Year/Month | Html | Total | |
---|---|---|---|
2024 November | 16 | 12 | 28 |
2024 October | 107 | 43 | 150 |
2024 September | 88 | 45 | 133 |
2024 August | 126 | 68 | 194 |
2024 July | 85 | 30 | 115 |
2024 June | 95 | 36 | 131 |
2024 May | 93 | 38 | 131 |
2024 April | 92 | 24 | 116 |
2024 March | 69 | 32 | 101 |
2024 February | 71 | 32 | 103 |
2024 January | 75 | 48 | 123 |
2023 December | 71 | 8 | 79 |
2023 November | 54 | 39 | 93 |
2023 October | 46 | 39 | 85 |
2023 September | 52 | 34 | 86 |
2023 August | 53 | 25 | 78 |
2023 July | 51 | 48 | 99 |
2023 June | 49 | 24 | 73 |
2023 May | 64 | 29 | 93 |
2023 April | 41 | 22 | 63 |
2023 March | 40 | 20 | 60 |
2023 February | 52 | 20 | 72 |
2023 January | 64 | 35 | 99 |
2022 December | 51 | 46 | 97 |
2022 November | 26 | 20 | 46 |
2022 October | 20 | 29 | 49 |
2022 September | 21 | 39 | 60 |
2022 August | 41 | 30 | 71 |
2022 July | 21 | 38 | 59 |
2022 June | 27 | 37 | 64 |
2022 May | 29 | 35 | 64 |
2022 April | 69 | 50 | 119 |
2022 March | 73 | 53 | 126 |
2022 February | 52 | 20 | 72 |
2022 January | 33 | 46 | 79 |
2021 December | 61 | 46 | 107 |
2021 November | 64 | 55 | 119 |
2021 October | 44 | 60 | 104 |
2021 September | 33 | 54 | 87 |
2021 August | 39 | 25 | 64 |
2021 July | 27 | 37 | 64 |
2021 June | 31 | 35 | 66 |
2021 May | 41 | 38 | 79 |
2021 April | 80 | 54 | 134 |
2021 March | 51 | 31 | 82 |
2021 February | 42 | 26 | 68 |
2021 January | 41 | 18 | 59 |
2020 December | 35 | 16 | 51 |
2020 November | 23 | 22 | 45 |
2020 October | 32 | 16 | 48 |
2020 September | 64 | 21 | 85 |
2020 August | 34 | 17 | 51 |
2020 July | 25 | 16 | 41 |
2020 June | 42 | 24 | 66 |
2020 May | 30 | 14 | 44 |
2020 April | 31 | 19 | 50 |
2020 March | 39 | 12 | 51 |
2020 February | 7 | 1 | 8 |
2020 January | 4 | 1 | 5 |
2019 December | 8 | 0 | 8 |
2019 November | 4 | 4 | 8 |
2019 October | 0 | 4 | 4 |
2019 September | 8 | 4 | 12 |
2019 August | 4 | 0 | 4 |
2019 July | 2 | 8 | 10 |
2019 June | 6 | 23 | 29 |
2019 May | 1 | 23 | 24 |
2019 April | 0 | 17 | 17 |
2019 March | 2 | 11 | 13 |
2019 February | 0 | 5 | 5 |
2019 January | 1 | 0 | 1 |
2018 December | 4 | 0 | 4 |
2018 October | 3 | 0 | 3 |
2018 September | 4 | 0 | 4 |
2018 March | 1 | 1 | 2 |
2018 February | 26 | 3 | 29 |
2018 January | 37 | 8 | 45 |
2017 December | 41 | 7 | 48 |
2017 November | 26 | 4 | 30 |
2017 October | 37 | 5 | 42 |
2017 September | 45 | 12 | 57 |
2017 August | 51 | 7 | 58 |
2017 July | 48 | 6 | 54 |
2017 June | 69 | 12 | 81 |
2017 May | 65 | 4 | 69 |
2017 April | 67 | 14 | 81 |
2017 March | 47 | 51 | 98 |
2017 February | 33 | 4 | 37 |
2017 January | 23 | 9 | 32 |
2016 December | 48 | 3 | 51 |
2016 November | 46 | 19 | 65 |
2016 October | 55 | 23 | 78 |
2016 September | 52 | 12 | 64 |
2016 August | 55 | 17 | 72 |
2016 July | 52 | 11 | 63 |
2016 June | 11 | 9 | 20 |
2016 May | 8 | 11 | 19 |
2016 April | 7 | 13 | 20 |
2016 March | 9 | 1 | 10 |
2016 February | 11 | 13 | 24 |
2016 January | 10 | 11 | 21 |
2015 December | 10 | 11 | 21 |
2015 November | 18 | 1 | 19 |
2015 October | 14 | 23 | 37 |
2015 September | 13 | 4 | 17 |
2015 August | 16 | 1 | 17 |
2015 July | 66 | 5 | 71 |
2015 June | 64 | 8 | 72 |
2015 May | 84 | 12 | 96 |
2015 April | 77 | 13 | 90 |
2015 March | 71 | 11 | 82 |
2015 February | 60 | 12 | 72 |
2015 January | 68 | 28 | 96 |
2014 December | 36 | 10 | 46 |
2014 November | 36 | 18 | 54 |
2014 October | 53 | 27 | 80 |
2014 September | 7 | 5 | 12 |
2014 August | 18 | 9 | 27 |
2014 July | 7 | 10 | 17 |
2014 June | 25 | 6 | 31 |
2014 May | 26 | 3 | 29 |
2014 April | 25 | 2 | 27 |
2014 March | 20 | 15 | 35 |
2014 February | 27 | 11 | 38 |
2014 January | 25 | 7 | 32 |
2013 December | 31 | 9 | 40 |
2013 November | 30 | 10 | 40 |
2013 October | 19 | 10 | 29 |
2013 September | 16 | 5 | 21 |
2013 August | 15 | 16 | 31 |
2013 July | 11 | 16 | 27 |
2013 June | 6 | 26 | 32 |
2013 May | 13 | 12 | 25 |
2013 April | 11 | 24 | 35 |
2013 March | 20 | 17 | 37 |
2013 February | 33 | 8 | 41 |
2013 January | 29 | 4 | 33 |
2012 December | 24 | 6 | 30 |
2012 November | 2 | 3 | 5 |