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"apellidos" => "Puig" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S1578219014001462" "doi" => "10.1016/j.adengl.2014.05.011" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219014001462?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731012005765?idApp=UINPBA000044" "url" => "/00017310/0000010500000006/v1_201406280127/S0001731012005765/v1_201406280127/es/main.assets" ] ] "itemSiguiente" => array:19 [ "pii" => "S1578219014001528" "issn" => "15782190" "doi" => "10.1016/j.adengl.2014.05.017" "estado" => "S300" "fechaPublicacion" => "2014-07-01" "aid" => "939" "copyright" => "Elsevier España, S.L. and AEDV" "documento" => "article" "crossmark" => 0 "subdocumento" => "fla" "cita" => "Actas Dermosifiliogr. 2014;105:590-6" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 1554 "formatos" => array:3 [ "EPUB" => 39 "HTML" => 1130 "PDF" => 385 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original Article</span>" "titulo" => "Allergic Contact Dermatitis due to Nickel: Descriptive Study in a Tertiary Hospital, 2000-2010" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "590" "paginaFinal" => "596" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Dermatitis alérgica de contacto a níquel. Estudio descriptivo en un hospital terciario en la década del 2000 al 2010" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1080 "Ancho" => 1447 "Tamanyo" => 244511 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">A-D. Metal objects causing nickel-induced allergic contact dermatitis. Note the positive result in the dimethylglyoxime spot test.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "A.E. García-Rabasco, V. Zaragozá-Ninet, R. García-Ruíz, J. de la Cuadra-Oyanguren" "autores" => array:4 [ 0 => array:2 [ "nombre" => "A.E." "apellidos" => "García-Rabasco" ] 1 => array:2 [ "nombre" => "V." "apellidos" => "Zaragozá-Ninet" ] 2 => array:2 [ "nombre" => "R." "apellidos" => "García-Ruíz" ] 3 => array:2 [ "nombre" => "J." "apellidos" => "de la Cuadra-Oyanguren" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0001731014000040" "doi" => "10.1016/j.ad.2013.12.003" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731014000040?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219014001528?idApp=UINPBA000044" "url" => "/15782190/0000010500000006/v1_201406280124/S1578219014001528/v1_201406280124/en/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S1578219014001504" "issn" => "15782190" "doi" => "10.1016/j.adengl.2014.05.015" "estado" => "S300" "fechaPublicacion" => "2014-07-01" "aid" => "873" "copyright" => "Elsevier España, S.L. and AEDV" "documento" => "article" "crossmark" => 0 "subdocumento" => "ssu" "cita" => "Actas Dermosifiliogr. 2014;105:574-82" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 2618 "formatos" => array:3 [ "EPUB" => 40 "HTML" => 1911 "PDF" => 667 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Controversies in Dermatology</span>" "titulo" => "Circumscribed Palmar or Plantar Hypokeratosis 10 Years After the First Description: What Is Known and the Issues Under Discussion" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "574" "paginaFinal" => "582" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Hipoqueratosis circunscrita palmar o plantar. Conocimientos y controversias tras 10 años de su descripción" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 695 "Ancho" => 981 "Tamanyo" => 92269 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Circumscribed plantar hypokeratosis. A lesion with similar characteristics to those of Fig.<span class="elsevierStyleHsp" style=""></span>1, but in a much less common site (source, Dr. Arno Rütten, with permission).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "F. Urbina, A. Pérez, L. Requena, A. Rütten" "autores" => array:4 [ 0 => array:2 [ "nombre" => "F." "apellidos" => "Urbina" ] 1 => array:2 [ "nombre" => "A." "apellidos" => "Pérez" ] 2 => array:2 [ "nombre" => "L." "apellidos" => "Requena" ] 3 => array:2 [ "nombre" => "A." "apellidos" => "Rütten" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0001731013002627" "doi" => "10.1016/j.ad.2013.05.011" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731013002627?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219014001504?idApp=UINPBA000044" "url" => "/15782190/0000010500000006/v1_201406280124/S1578219014001504/v1_201406280124/en/main.assets" ] "en" => array:19 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Novelties in Dermatology</span>" "titulo" => "Methotrexate: New Therapeutic Approaches" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "583" "paginaFinal" => "589" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "L. Puig" "autores" => array:1 [ 0 => array:3 [ "nombre" => "L." "apellidos" => "Puig" "email" => array:1 [ 0 => "lpuig@santpau.cat" ] ] ] "afiliaciones" => array:1 [ 0 => array:2 [ "entidad" => "Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain" "identificador" => "aff0005" ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Metotrexato: novedades terapéuticas" ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Methotrexate (MTX, <span class="elsevierStyleItalic">4-amino-4-deoxy-N10</span>-methyl pteroylglutamic acid) is an analog of aminopterin (<span class="elsevierStyleItalic">4-amino</span>-pteroylglutamic acid), a folic acid antagonist that was introduced in 1948 to treat acute leukemia in children but later replaced by MTX as this had a more favorable toxicity profile. The first study of the efficacy of MTX in the treatment of psoriasis was published in 1958,<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> and the first guidelines on its use in dermatology appeared in 1972.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Until quite recently, however, there was relatively little evidence to support the use of MTX in the treatment of psoriasis.</p><p id="par0010" class="elsevierStylePara elsevierViewall">Among the advances that justify this review are new efficacy data that have led MTX to be considered the first-line therapy among the classic systemic treatments for psoriasis and new subcutaneous formulations that offer improved bioavailability and convenience of administration.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Pharmacokinetics</span><p id="par0015" class="elsevierStylePara elsevierViewall">MTX can be administered orally, subcutaneously, intramuscularly, or intravenously. In the case of psoriasis, the standard dose (7.5-25<span class="elsevierStyleHsp" style=""></span>mg/wk) is nearly always administered orally or subcutaneously. The bioavailability of low-dose oral MTX is high (70%),<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> although it varies from patient to patient. At doses of more than 15<span class="elsevierStyleHsp" style=""></span>mg/wk bioavailability drops to 30%, as the uptake of MTX by the gastrointestinal tract is mediated by a saturable transporter, reduced folate carrier 1 (RFC1).<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> The preferred route of administration in such cases is thus generally parenteral, which is also associated with better gastrointestinal tolerability,<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> although the use of split doses of oral MTX can improve bioavailability.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> The absorption of oral MTX, which primarily occurs in the proximal jejunum, is not affected by food intake, but is decreased in cases of malabsorption or inflammatory bowel disease. The bioavailability of parenteral MTX is similar regardless of the administration route used.</p><p id="par0020" class="elsevierStylePara elsevierViewall">Once absorbed, 10% of MTX is converted in the liver to its partly inactive metabolite, 7-hydroxymethotrexate (7-OH-MTX), thereby reducing plasma MTX concentrations. The ability to convert MTX to 7-OH-MTX via aldehyde oxidase varies greatly—relative interindividual differences ranging from 1 to 14 have been described—and exhibits a bimodal distribution in the population. Rapid metabolizers have a poorer therapeutic response to MTX; additionally, folic acid (unlike folinic acid) blocks the production of 7-OH-MTX and could therefore contribute to higher levels of MTX in these patients.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> 7-OH-MTX competes with MTX for cellular uptake via RFCs, which also internalize reduced folates and folic acid, albeit with low affinity. Quantitative or qualitative alterations in RFCs, similarly to high levels of exogenous folates competing for the receptor, can result in transport-related resistance to the therapeutic action of MTX. A recent study described a single nucleotide polymorphism in the <span class="elsevierStyleItalic">RCF1</span> gene that predicts therapeutic response to MTX in Japanese patients with rheumatoid arthritis,<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> illustrating the role that pharmacogenetics may come to play in improving treatment outcomes.</p><p id="par0025" class="elsevierStylePara elsevierViewall">MTX, like 7-OH-MTX, is metabolized intracellularly to produce monoglutamates and polyglutamates, which are the main inhibitors of a range of enzymes; the intracellular levels of these metabolites correlate with the therapeutic efficacy of MTX (which is actually a prodrug).<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Both the bioavailability of MTX and its intracellular conjugation are partly determined by the administration route. In one study of patients with rheumatoid arthritis, switching from oral to subcutaneous administration resulted in a 37% increase in the concentration of very long-chain polyglutamates and a 31% reduction in disease activity.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Polyglutamates are released slowly from the interior of the cell by the action of active efflux carriers, which may contribute to prolonging the elimination of the drug and also reflect pharmacogenetic differences.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> While no studies have demonstrated that genetic variability in the enzymes involved in MTX metabolism is of clinical relevance in psoriasis,<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> variations in the genes involved in polyglutamate efflux transporters have been associated with differences in treatment efficacy and the risk of toxicity.<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">11</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Between 35% and 50% of circulating MTX binds to albumin (compared with 91%-95% of 7-OH-MTX) and peak concentrations are reached in the kidneys, liver, gallbladder, spleen, skin, and red blood cells (RBCs). RBC MTX levels may indicate possible hematologic toxicity and hepatic accumulation of the drug. MTX tends to accumulate in the extravascular compartment, and therefore extra caution should be exercised in patients with pleural effusion, ascites, or massive edema due to the risk of toxicity from reabsorption of extravascular fluid.</p><p id="par0035" class="elsevierStylePara elsevierViewall">Between 65% and 80% of MTX is eliminated unaltered by the kidneys (mainly in the first 12<span class="elsevierStyleHsp" style=""></span>hours after administration) and 20% to 35% undergoes biliary secretion and is metabolized or transferred to other compartments. Glomerular filtration is the main pathway of renal elimination; tubular secretion and reabsorption are also involved but to a lesser extent. Biliary secretion is an important factor in patents with renal insufficiency, who have reduced drug clearance and an increased risk of toxicity. Hemodialysis and peritoneal dialysis result in limited and transient reductions in serum MTX levels due to the drug's low-to-medium protein binding and high tissue distribution.</p><p id="par0040" class="elsevierStylePara elsevierViewall">The terminal half-life of MTX in serum is approximately 7 to 10 hours, but it can be as long as 26 hours in some patients. RBC MTX concentrations remain stable for 9 days, while serum levels become undetectable after 52<span class="elsevierStyleHsp" style=""></span>hours.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">12</span></a> Although individual MTX clearance rates can be established with just 2 tests (at 30 and 120<span class="elsevierStyleHsp" style=""></span>minutes after administration), they have not been found to be useful for defining an optimal treatment regimen in rheumatoid arthritis.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a> While many drugs interact with MTX, the use of various nonsteroidal anti-inflammatory drugs (NSAIDs) was not found to significantly alter MTX serum levels, as compared with levels in patients not treated with NSAIDs.<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a> Nevertheless, it is very important to remember that dose reductions are necessary in older patients (><span class="elsevierStyleHsp" style=""></span>65 years) and patients with renal insufficiency.<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a></p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Mechanisms of Action</span><p id="par0045" class="elsevierStylePara elsevierViewall">Various mechanisms of action have been proposed for MTX. The most relevant in the case of inflammatory diseases is the promotion of adenosine release with subsequent suppression of inflammation.<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">MTX inhibits the proliferation of neoplastic cells, blocking the de novo synthesis of purines and pyrimidines by irreversibly inhibiting dihydrofolate reductase, which is responsible for the production of tetrahydrofolate. Although high doses of folic or folinic acid can reverse this effect, folic and folinic acid supplementation in inflammatory diseases is not used for this purpose but rather to prevent MTX toxicity without significantly reducing treatment efficacy.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The most important mechanism of action of MTX in inflammatory diseases is probably related to the recently described anti-inflammatory activity of adenosine through specific receptors.<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">17</span></a> In both animal models of inflammation and patients with rheumatoid arthritis, MTX induces the extracellular release of adenosine, which acts as an anti-inflammatory agent through specific type A<span class="elsevierStyleInf">2</span> receptors<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> that also participate in the pathogenesis of hepatic fibrosis.<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">19</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">MTX, especially in its polyglutamate form—which accumulates in the interior of cells—inhibits AICAR (5-aminoimidazole-4-carboxamide ribonucleotide) transformylase.<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">20</span></a> This results in the intracellular accumulation of AICAR, which competitively inhibits adenosine monophosphate desaminase. The increased intracellular levels of AICAR would then induce the release of adenine nucleotides and their conversion to adenosine by ecto-5’-nucleotidase (CD73).<a class="elsevierStyleCrossRefs" href="#bib0105"><span class="elsevierStyleSup">21,22</span></a> Adenosine has a very short half-life (of just seconds) in peripheral blood and body fluids, and it is therefore extremely difficult to measure its levels. Most of the studies published have based their measurements on the inhibition of the biological effects of adenosine using drugs that inhibit the metabolism or receptors of MTX<a class="elsevierStyleCrossRefs" href="#bib0115"><span class="elsevierStyleSup">23,24</span></a> or on animal models such as the CD73-deficient mouse<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">21</span></a> and other mouse strains.<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">Caffeine, a nonselective adenosine receptor antagonist, blocks the anti-inflammatory effects of MTX in vitro and in animal models of arthritis<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a>; it is therefore possible that coffee and other caffeine drinks interfere with the therapeutic (and perhaps toxic) activity of MTX. This hypothesis is supported by the findings of several studies<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> but was not corroborated in a retrospective study of patients with rheumatoid artritis.<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> Moreover, no relationship was found between MTX at a maintenance dose and coffee consumption in patients with psoriasis or psoriatic arthritis.<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">Although the antiproliferative action of MTX explains stomatitis, anemia, leukopenia, and alopecia, the release of adenosine could help to explain other adverse effects of this drug. Adenosine binding to A<span class="elsevierStyleInf">1</span> and A<span class="elsevierStyleInf">2B</span> receptors induces hepatic steatosis,<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> while binding to A<span class="elsevierStyleInf">2A</span> receptors plays a role in the development of fibrosis<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a> and hepatic cirrhosis.<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a> Some patients have reported marked asthenia on the day they take MTX. This may be related to the release of adenosine into the central nervous system<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a> and could be improved with the administration of aminophylline.<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">Another possible mechanism of action of MTX may involve its inhibitory effect on the proliferation of antigen-stimulated T cells, which has been reported both in vitro and in patients receiving MTX,<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a> or the induction of apoptosis in activated T cells,<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a> which may also be mediated by adenosine receptors.<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">Finally, the action of MTX in psoriasis could be mediated by the suppression of T-cell activation (through folate-dependent mechanisms) and the altered expression of adhesion molecules; adenosine would also have a role in this mechanism.<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a></p><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Efficacy in Psoriasis</span><p id="par0085" class="elsevierStylePara elsevierViewall">A number of clinical trials in recent years have explored the efficacy of MTX in psoriasis and compared it with other options.<a class="elsevierStyleCrossRefs" href="#bib0185"><span class="elsevierStyleSup">37–42</span></a><a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> summarizes the findings.</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0090" class="elsevierStylePara elsevierViewall">Various regimens can produce a 75% improvement in the Psoriasis Area and Severity Index (PASI 75) in up to 40% of patients by week 24, although in most cases PASI response at week 12 is a good indicator of whether treatment should be continued or not.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a></p><p id="par0095" class="elsevierStylePara elsevierViewall">Experience with combination regimens of MTX and diverse biologics to treat moderate to severe psoriasis has shown improved patient responses and treatment adherence. The possible mechanisms underlying these effects include reduced clearance of the biologic agent and reduced production of antibodies against the agent.<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">43</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">The results of a clinical trial comparing etanercept monotherapy and etanercept plus MTX in 239 patients per arm were recently published.<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">44</span></a> Patients in the monotherapy arm received 50<span class="elsevierStyleHsp" style=""></span>mg twice weekly for 12 weeks followed by 50<span class="elsevierStyleHsp" style=""></span>mg weekly for 12 weeks, while those in the combination therapy group received 7.5<span class="elsevierStyleHsp" style=""></span>mg weekly for the first 2 weeks, 10<span class="elsevierStyleHsp" style=""></span>mg weekly for the next 2 weeks, and up to 15<span class="elsevierStyleHsp" style=""></span>mg weekly up to week 24. Combination therapy with etanercept plus MTX was superior to etanercept alone, with PASI 75 responses observed in 70% of patients at week 12 (vs 54% in the monotherapy group) and in 77% of patients (vs 60%) at week 24. The corresponding rates of PASI 90 responses were 34% vs 23% and 54% vs 34%, respectively.</p></span></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Patterns of Use and Administration Routes</span><p id="par0105" class="elsevierStylePara elsevierViewall">Patterns of MTX use by both rheumatologists and dermatologists have changed somewhat in recent years. One recent review concluded that the bioavailability of oral MTX decreases at doses above 17.5<span class="elsevierStyleHsp" style=""></span>mg,<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">45</span></a> indicating that parenteral administration is preferable. In a clinical trial comparing the efficacy and safety of oral and subcutaneous MTX in patients with rheumatoid arthritis, 78% of patients treated with subcutaneous MTX and 70% of those treated with oral MTX achieved the treatment goal of a 20% improvement in the American College of Rheumatology criteria (ACR20) by week 48.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a> There were also differences in the frequency of adverse effects between the groups (66% vs 62%) but these were not statistically significant. Thirty percent of the patients who did not respond to oral MTX 15<span class="elsevierStyleHsp" style=""></span>mg achieved an ACR20 response when they were switched to subcutaneous MTX. The study is the first to provide formal proof that subcutaneous MTX has superior clinical efficacy to oral MTX,<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">47</span></a> and one would expect these results to be extrapolated to the treatment of psoriasis, despite the current lack of scientific evidence in this setting. The main advantage of the subcutaneous route is the superior bioavailability of MTX. It has been demonstrated that the increased effectiveness seen in rheumatoid arthritis patients following a switch from oral to subcutaneous MTX without a change in dose is accompanied by an increase in RBC MTX polyglutamate concentrations, although it may take 6 months for the new steady-state concentrations to be reached.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">48</span></a></p><p id="par0110" class="elsevierStylePara elsevierViewall">Data on the superior clinical efficacy of subcutaneous MTX in the treatment of rheumatoid arthritis were used as the starting point for a pharmacoeconomic analysis conducted in Spain that concluded that the additional cost associated with the use of the subcutaneous route would be offset by improved effectivness.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">49</span></a><a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> summarizes the results of an incremental cost-effectiveness analysis of subcutaneous MTX and several alternatives based on data from comparative clinical trials. The results show that subcutaneous MTX has a higher incremental cost-effectiveness ratio to ciclosporin, adalimumab, and infliximab in the treatment of moderate to severe psoriasis. (We have omitted the sensitivity analysis and confidence intervals due to space constraints.)</p><p id="par0115" class="elsevierStylePara elsevierViewall">A study of MTX use among dermatologists and rheumatologists in Canada reported that most dermatologists (97%) and rheumatologists (80%) start treating psoriasis with oral MTX and that fewer dermatologists subsequently switch to parenteral MTX (49% vs 96% of rheumatologists); of the dermatologists that do switch 63% choose the subcutaneous route (vs 98% of the rheumatologists).<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">50</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">Considering that the usefulness of test doses of MTX in psoriasis is still being questioned (treatment is commonly initiated with a dose of 10 to 15<span class="elsevierStyleHsp" style=""></span>mg in selected patients),<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">51</span></a> the advantages of subcutaneous MTX in rheumatoid arthritis (greater efficacy<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">45</span></a> and fewer gastrointestinal problems<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">52</span></a>) could probably be extrapolated to psoriasis, and it would appear reasonable to assume that subcutaneous MTX will be increasingly used in dermatology. Greater familiarity with subcutaneous injections among dermatology patients will undoubtedly contribute to this increased use, as will the introduction of higher-concentration formulations (50<span class="elsevierStyleHsp" style=""></span>mg/mL) in prefilled syringes, as these offer greater tolerability and convenience<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> and are preferred to the 10-mg/mL formulations by the majority of patients treated with 20<span class="elsevierStyleHsp" style=""></span>mg per week.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a> Single-dose formulations also have environmental and safety benefits as they eliminate the need to handle and discard unused portions of vials or syringes.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a></p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Ethical Disclosures</span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Protection of humans and animals</span><p id="par0125" class="elsevierStylePara elsevierViewall">The authors declare that no tests were carried out in humans or animals for the purpose of this study.</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Confidentiality of data</span><p id="par0130" class="elsevierStylePara elsevierViewall">The authors declare that they have followed their hospital's protocol on the publication of data concerning patients and that all patients included in the study have received sufficient information and have given their written informed consent to participate in the study.</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Right to privacy and informed consent</span><p id="par0135" class="elsevierStylePara elsevierViewall">The authors declare that no private patient data appear in this article.</p></span></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Conflicts of Interest</span><p id="par0140" class="elsevierStylePara elsevierViewall">The author has received speakers and/or consultancy and/or clinical trial investigator fees from Gebro Pharma and Pfizer; he has also received fees from Marge Medica Books for coordinating and co-authoring <span class="elsevierStyleItalic">Methotraxate and psoriasis. Barcelona: Marge Medica Books; 2012</span>, sponsored by Gebro Pharma.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:11 [ 0 => array:2 [ "identificador" => "xres349093" "titulo" => "Abstract" ] 1 => array:2 [ "identificador" => "xpalclavsec330760" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xres349094" "titulo" => "Resumen" ] 3 => array:2 [ "identificador" => "xpalclavsec330759" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "Pharmacokinetics" ] 6 => array:3 [ "identificador" => "sec0015" "titulo" => "Mechanisms of Action" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "sec0020" "titulo" => "Efficacy in Psoriasis" ] ] ] 7 => array:2 [ "identificador" => "sec0025" "titulo" => "Patterns of Use and Administration Routes" ] 8 => array:3 [ "identificador" => "sec0030" "titulo" => "Ethical Disclosures" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0035" "titulo" => "Protection of humans and animals" ] 1 => array:2 [ "identificador" => "sec0040" "titulo" => "Confidentiality of data" ] 2 => array:2 [ "identificador" => "sec0045" "titulo" => "Right to privacy and informed consent" ] ] ] 9 => array:2 [ "identificador" => "sec0050" "titulo" => "Conflicts of Interest" ] 10 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2012-10-12" "fechaAceptado" => "2012-11-29" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec330760" "palabras" => array:6 [ 0 => "Psoriasis" 1 => "Methotrexate" 2 => "Clinical trials" 3 => "Pharmacokinetics" 4 => "Mechanism of action" 5 => "Cost-effectiveness" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec330759" "palabras" => array:6 [ 0 => "Psoriasis" 1 => "Metotrexato" 2 => "Ensayos clínicos" 3 => "Farmacocinética" 4 => "Mecanismo de acción" 5 => "Coste-eficacia" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Although the first study on the efficacy of methotrexate in the treatment of psoriasis was reported in 1958, scientific evidence for this indication has been scant until quite recently. We now have new data on the pharmacokinetics and mechanism of action of methotrexate and new subcutaneous formulations that have improved the bioavailability, efficacy, and ease of administration of the drug. The results of recent clinical trials comparing methotrexate with several biologic agents have shown it to be the first-line therapy among the classic systemic treatments for psoriasis. Moreover, the incremental cost-effectiveness ratio for subcutaneous methotrexate has been shown to be superior to that of ciclosporin, adalimumab, and infliximab.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Pese a que el primer estudio sobre la eficacia de metotrexato en el tratamiento de la psoriasis se remonta a 1958, hasta no hace mucho ha sido escasa la evidencia científica disponible sobre su uso en esta indicación.</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Disponemos de nuevos datos acerca de la farmacocinética y el mecanismo de acción del metotrexato, así como de nuevas presentaciones por vía subcutánea que mejoran la biodisponibilidad, la eficacia y la conveniencia de la administración de este fármaco. La reciente publicación de ensayos clínicos comparativos con diversos biológicos permite considerar al metotrexato como el estándar terapéutico dentro de los tratamientos sistémicos clásicos de la psoriasis, con un cociente coste-eficacia incremental favorable al metotrexato subcutáneo si se compara con ciclosporina, adalimumab o infliximab.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0015">Please cite this article as: Puig L. Metotrexato: novedades terapéuticas. Actas Dermosifiliogr. 2014;105:583–589.</p>" ] ] "multimedia" => array:1 [ 0 => array:7 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:3 [ "leyenda" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: ALT, alanine aminotransferase; PASI, Psoriasis Area and Severity Index; PASI 50, ≥<span class="elsevierStyleHsp" style=""></span>50% improvement in PASI score with respect to baseline; PASI 75, ≥<span class="elsevierStyleHsp" style=""></span>75% improvement in PASI score with respect to baseline; PASI 90, ≥<span class="elsevierStyleHsp" style=""></span>90% improvement in PASI score with respect to baseline; PGA, physician's global assessment.</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">MTX Regimen \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">Comparator \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">No. Treated (MTX) \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">PASI 75 \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">ICER<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a> PASI 75 \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">PASI 90 \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">Observations \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">Study \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">15<span class="elsevierStyleHsp" style=""></span>mg/wk \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">Ciclosporin \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">43 \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">60% wk 16 \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">691.52–390.88/0.71–0.60<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>€2733.09 in favor of subcutaneous MTX \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">40% wk 16 \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">12 patients had to stop taking MTX due to an increase in transanimase levels (max. ALT level, 198/mL) \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">Heydendael et al.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a> \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">7.5<span class="elsevierStyleHsp" style=""></span>mg/wk with gradual increments up to 15<span class="elsevierStyleHsp" style=""></span>mg/wk in patients who did not achieve PASI 50. \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">Ciclosporin \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">41 \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">24% wk 12 \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">518.64–293.16/0.58–0.60<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>€633.18 in favor of subcutaneous MTX \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">11% wk 12 \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><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">Flytström et al.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> \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">Initial dose of 7.5<span class="elsevierStyleHsp" style=""></span>mg/wk, 10<span class="elsevierStyleHsp" style=""></span>mg from wk 2, 15<span class="elsevierStyleHsp" style=""></span>mg from wk 4. Increase to 20<span class="elsevierStyleHsp" style=""></span>mg in patients who did not achieve PASI 50 by wk 8; increase to 25<span class="elsevierStyleHsp" style=""></span>mg in patients who did not achieve PASI 50 by wk 12. \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">Adalimumab \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">110 \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">36% wk 16 \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">6355.96–390.88/0.80–0.36<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>€13 557 in favor of subcutaneous MTX \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">14% wk 16 \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">Treatment discontinuation recommended if no response by wk 12<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</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">Saurat et al.<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a> \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">15<span class="elsevierStyleHsp" style=""></span>mg/wk for first 6 wk; thereafter, dose increments up to 20<span class="elsevierStyleHsp" style=""></span>mg/wk if PASI improvement was <<span class="elsevierStyleHsp" style=""></span>25%. Patients who did not achieve PASI 50 or who did not tolerate treatment were able to change treatment arm at wk 16. \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">Infliximab \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">215 \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">42% wk 1631% wk 26 \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">8006.44–390.88/0.78–0.42<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>€21 154.33 in favor of subcutaneous MTX \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">19% wk 1615% wk 26 \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><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">Barker et al.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> \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">Initial dose of 5<span class="elsevierStyleHsp" style=""></span>mg/wk, 10<span class="elsevierStyleHsp" style=""></span>mg/wk for 1 wk, 15<span class="elsevierStyleHsp" style=""></span>mg up to wk 9; 20<span class="elsevierStyleHsp" style=""></span>mg after wk 10, and 25<span class="elsevierStyleHsp" style=""></span>mg after wk 16 in patients who did not achieve PASI 75 or a PGA score of 0 or 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="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Briakinumab \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">163 \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">36% wk 1240% wk 2424% wk 52 \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><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>14% wk 12<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a>≈<span class="elsevierStyleHsp" style=""></span>23% wk 24<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a>≈<span class="elsevierStyleHsp" style=""></span>17% wk 52<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</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="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \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">Reich et al.<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab521000.png" ] ] ] "notaPie" => array:2 [ 0 => array:3 [ "identificador" => "tblfn0005" "etiqueta" => "a" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">ICER, incremental cost-effectiveness ratio (cost of alternative−cost of subcutaneous MTX)/(efficacy alternative−efficacy subcutaneous MTX). Recommended retail prices as of October 2012. Metoject: €19.36<span class="elsevierStyleHsp" style=""></span>€/wk (7.5<span class="elsevierStyleHsp" style=""></span>mg); €24.43/wk (15<span class="elsevierStyleHsp" style=""></span>mg) (based on maximum dose). Sandimmun Neoral 100<span class="elsevierStyleHsp" style=""></span>mg/mL suspension: €128.62/50<span class="elsevierStyleHsp" style=""></span>mL; €43.22/wk based on starting dose of 3<span class="elsevierStyleHsp" style=""></span>mg/kg/d for a patient weighing 80<span class="elsevierStyleHsp" style=""></span>kg. Remicade: 80<span class="elsevierStyleHsp" style=""></span>kg, 4 vials of 100<span class="elsevierStyleHsp" style=""></span>mg (€615.88) × 3.25 doses (16 wk)<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>€8006.44. Humira: €1127.57/2 × 9.5 doses (16 wk)<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>€5355.96.</p>" ] 1 => array:3 [ "identificador" => "tblfn0010" "etiqueta" => "b" "nota" => "<p class="elsevierStyleNotepara" id="npar0010">Obtained by interpolation from graph.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Summary of Comparative Clinical Trials of Methotrexate (MTX) in Psoriasis.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:55 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Treatment of psoriasis with folic acid antagonists" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "W.F. Edmundson" 1 => "W.B. 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Arai" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:3 [ "tituloSerie" => "Drug Metab Pharmacokinet" "fecha" => "2012" "volumen" => "11" ] ] ] ] ] ] 7 => array:3 [ "identificador" => "bib0040" "etiqueta" => "8" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Red blood cell methotrexate polyglutamates emerge as a function of dosage intensity and route of administration during pulse methotrexate therapy in rheumatoid arthritis" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "T. Dervieux" 1 => "R. Zablocki" 2 => "J. Kremer" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "Rheumatology (Oxford)" "fecha" => "2010" "volumen" => "49" "paginaInicial" => "2337" "paginaFinal" => "2345" ] ] ] ] ] ] 8 => array:3 [ "identificador" => "bib0045" "etiqueta" => "9" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "The pharmacogenetics of methotrexate" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "S.L. Hider" 1 => "I.N. Bruce" 2 => "W. 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año/Mes | Html | Total | |
---|---|---|---|
2024 Noviembre | 17 | 18 | 35 |
2024 Octubre | 104 | 49 | 153 |
2024 Septiembre | 113 | 42 | 155 |
2024 Agosto | 132 | 62 | 194 |
2024 Julio | 107 | 35 | 142 |
2024 Junio | 142 | 55 | 197 |
2024 Mayo | 131 | 51 | 182 |
2024 Abril | 119 | 39 | 158 |
2024 Marzo | 106 | 34 | 140 |
2024 Febrero | 91 | 52 | 143 |
2024 Enero | 74 | 47 | 121 |
2023 Diciembre | 90 | 33 | 123 |
2023 Noviembre | 103 | 53 | 156 |
2023 Octubre | 123 | 48 | 171 |
2023 Septiembre | 92 | 44 | 136 |
2023 Agosto | 79 | 16 | 95 |
2023 Julio | 98 | 40 | 138 |
2023 Junio | 103 | 31 | 134 |
2023 Mayo | 110 | 30 | 140 |
2023 Abril | 107 | 41 | 148 |
2023 Marzo | 115 | 59 | 174 |
2023 Febrero | 69 | 35 | 104 |
2023 Enero | 91 | 43 | 134 |
2022 Diciembre | 68 | 60 | 128 |
2022 Noviembre | 66 | 46 | 112 |
2022 Octubre | 41 | 43 | 84 |
2022 Septiembre | 74 | 62 | 136 |
2022 Agosto | 54 | 49 | 103 |
2022 Julio | 51 | 75 | 126 |
2022 Junio | 47 | 43 | 90 |
2022 Mayo | 73 | 62 | 135 |
2022 Abril | 114 | 60 | 174 |
2022 Marzo | 79 | 72 | 151 |
2022 Febrero | 85 | 30 | 115 |
2022 Enero | 75 | 56 | 131 |
2021 Diciembre | 86 | 52 | 138 |
2021 Noviembre | 154 | 80 | 234 |
2021 Octubre | 79 | 84 | 163 |
2021 Septiembre | 56 | 51 | 107 |
2021 Agosto | 57 | 29 | 86 |
2021 Julio | 91 | 55 | 146 |
2021 Junio | 73 | 62 | 135 |
2021 Mayo | 80 | 41 | 121 |
2021 Abril | 135 | 87 | 222 |
2021 Marzo | 98 | 32 | 130 |
2021 Febrero | 83 | 41 | 124 |
2021 Enero | 89 | 47 | 136 |
2020 Diciembre | 55 | 24 | 79 |
2020 Noviembre | 53 | 40 | 93 |
2020 Octubre | 60 | 26 | 86 |
2020 Septiembre | 43 | 18 | 61 |
2020 Agosto | 52 | 20 | 72 |
2020 Julio | 31 | 14 | 45 |
2020 Junio | 50 | 25 | 75 |
2020 Mayo | 58 | 38 | 96 |
2020 Abril | 54 | 23 | 77 |
2020 Marzo | 46 | 27 | 73 |
2020 Febrero | 7 | 7 | 14 |
2020 Enero | 5 | 4 | 9 |
2019 Diciembre | 8 | 4 | 12 |
2019 Noviembre | 4 | 6 | 10 |
2019 Octubre | 0 | 1 | 1 |
2019 Septiembre | 4 | 0 | 4 |
2019 Agosto | 4 | 3 | 7 |
2019 Julio | 4 | 10 | 14 |
2019 Junio | 6 | 21 | 27 |
2019 Mayo | 4 | 39 | 43 |
2019 Abril | 2 | 14 | 16 |
2019 Marzo | 4 | 6 | 10 |
2019 Febrero | 1 | 12 | 13 |
2019 Enero | 4 | 0 | 4 |
2018 Diciembre | 2 | 7 | 9 |
2018 Noviembre | 1 | 0 | 1 |
2018 Octubre | 6 | 0 | 6 |
2018 Septiembre | 1 | 0 | 1 |
2018 Marzo | 2 | 0 | 2 |
2018 Febrero | 152 | 2 | 154 |
2018 Enero | 118 | 5 | 123 |
2017 Diciembre | 155 | 9 | 164 |
2017 Noviembre | 73 | 6 | 79 |
2017 Octubre | 25 | 8 | 33 |
2017 Septiembre | 34 | 6 | 40 |
2017 Agosto | 41 | 11 | 52 |
2017 Julio | 31 | 6 | 37 |
2017 Junio | 39 | 16 | 55 |
2017 Mayo | 27 | 12 | 39 |
2017 Abril | 30 | 10 | 40 |
2017 Marzo | 22 | 23 | 45 |
2017 Febrero | 30 | 9 | 39 |
2017 Enero | 19 | 7 | 26 |
2016 Diciembre | 29 | 21 | 50 |
2016 Noviembre | 36 | 27 | 63 |
2016 Octubre | 47 | 22 | 69 |
2016 Septiembre | 46 | 14 | 60 |
2016 Agosto | 58 | 18 | 76 |
2016 Julio | 46 | 14 | 60 |
2016 Junio | 4 | 6 | 10 |
2016 Mayo | 5 | 17 | 22 |
2016 Abril | 3 | 9 | 12 |
2016 Marzo | 9 | 11 | 20 |
2016 Febrero | 6 | 11 | 17 |
2016 Enero | 26 | 10 | 36 |
2015 Diciembre | 16 | 0 | 16 |
2015 Noviembre | 9 | 2 | 11 |
2015 Octubre | 9 | 0 | 9 |
2015 Septiembre | 7 | 7 | 14 |
2015 Agosto | 14 | 2 | 16 |
2015 Julio | 44 | 5 | 49 |
2015 Junio | 37 | 8 | 45 |
2015 Mayo | 40 | 11 | 51 |
2015 Abril | 31 | 9 | 40 |
2015 Marzo | 39 | 5 | 44 |
2015 Febrero | 24 | 9 | 33 |
2015 Enero | 31 | 5 | 36 |
2014 Diciembre | 14 | 5 | 19 |
2014 Noviembre | 16 | 6 | 22 |
2014 Octubre | 17 | 13 | 30 |
2014 Septiembre | 5 | 4 | 9 |
2014 Agosto | 3 | 8 | 11 |
2014 Julio | 8 | 3 | 11 |