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RF-Topical Rapamycin as an Adjuvant to Laser Treatment in Capillary Malformations
FR- Rapamicina tópica adyuvante al tratamiento con láser en malformaciones capilares
A. Alegre-Sánchez
Corresponding author
adrian.alegresanchez@gmail.com

Corresponding author.
, P. Boixeda
Unidad de Láser, Departamento de Dermatología, Hospital Ramón y Cajal, Madrid, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">To date&#44; the gold-standard treatment for capillary malformations &#40;CM&#41; is pulsed dye laser &#40;PDL&#41;&#46; The lightening achieved is&#44; however&#44; incomplete and persistence or redarkening of the malformation appears to be the norm&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Revascularization of the lesions after laser treatment appears to be the reason for the varying efficacy of PDL in CM&#46; Different topical antiangiogenic molecules have been tried in an attempt to halt this revascularization&#46; Of these molecules&#44; the most widely studied is rapamycin &#40;RPM&#41;&#44; for which studies of different kinds and with different results are available&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The antiangiogenic action of RPM works by inhibiting its specific target &#40;mTOR&#41;&#46; This action is conditioned by a reduction of vascular endothelial growth factor &#40;VEGF&#41; and other proangiogenic signals&#46; RPM is known in dermatology for its considerable efficacy&#44; when applied topically&#44; in managing facial angiofibromas characteristic of tuberous sclerosis&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">1</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">Experiments with mouse models have shown strong induction of proangiogenic genes between 3 and 7 days after exposure in conjunction with PDL&#46; Application of 1&#37; topical RPM appears to systematically reverse this induction&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Initial trials in healthy human skin with histologic monitoring showed that the combination of topical RPM once daily for 14 days&#44; following the PDL session&#44; inhibited normal vascular repair in the superficial and middle dermis&#44; measured using immunohistochemical markers &#40;CD31&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The first randomized&#44; double-blind&#44; intraindividual placebo-controlled clinical trial was carried out by a Spanish multicenter group&#46; Twenty-three patients were enrolled in this trial&#46; The combination of PDL &#40;2 sessions&#41; and 1&#37; topical RPM &#40;once daily for 12 weeks&#41; showed greater clearance than the other combinations &#40;PDL alone&#44; topical placebo alone&#44; and PDL with placebo&#41;&#46; A limitation of that study is that PDL was only applied to the sides of the face&#44; which are areas that generally respond better to PDL&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">4</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">In more recent placebo-controlled trials&#44; however&#44; the combination of PDL and RPM has shown no greater efficacy of statistical significance than PDL alone&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">5&#44;6</span></a> One of these studies included 13 patients with nonfacial CM and the other study included 6 such patients&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">In terms of the safety profile&#44; only 1 case of allergic contact dermatitis has been reported in association with the use of RPM as an adjuvant to PDL&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">7</span></a> No cases of systemic toxicity have been reported&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">In light of the available evidence&#44; the use of RPM as an adjuvant to PDL in CM appears to have a solid foundation supported by quality research&#46; Nevertheless&#44; its real efficacy and optimum recommended dosage and formulation have yet to be determined&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Another factor to be taken into account is the fact that RPM is not yet available for sale in Spain&#44; which means that its use would be off-label&#46; Furthermore&#44; its formulation is expensive for patients and complicated for pharmacists&#46;</p></span>"
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Article information
ISSN: 15782190
Original language: English
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