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               <dc:title>Induced Vitiligo due to Talimogene Laherparepvec Injection for Metastatic Melanoma Associated with Long-term Complete Response</dc:title>
               <dc:creator>Iglesias, Pablo</dc:creator>
               <dc:creator>Ribero, Simone</dc:creator>
               <dc:creator>Barreiro Capurro, Alicia</dc:creator>
               <dc:creator>Podlipnik, Sebastian</dc:creator>
               <dc:creator>Carrera Álvarez, Cristina</dc:creator>
               <dc:creator>Malvehy, J. (Josep)</dc:creator>
               <dc:creator>Puig i Sardà, Susana</dc:creator>
               <dc:subject>Càncer de pell</dc:subject>
               <dc:subject>Vitiligen</dc:subject>
               <dc:subject>Melanoma</dc:subject>
               <dc:subject>Skin cancer</dc:subject>
               <dc:subject>Vitiligo</dc:subject>
               <dc:subject>Melanoma</dc:subject>
               <dc:description>Talimogene laherparepvec (T-VEC) (Imlygic, Amgen) is the first oncolytic virus approved for use in therapy for metastatic melanoma. T-VEC provides a treatment option for patients with limited metastatic disease. T-VEC is a genetically modified, live, attenuated herpes simplex virus type 1 designed to replicate in tumour cells and promote an enhanced anti-tumour response (1) T-VEC is administered by injection into cutaneous, subcutaneous or nodal lesions, which are visible and/or palpable and/ or visualized by ultrasonography (2). Other local management options have been used to control metastatic disease in stage IIIB, but almost all have shown only a local effect and rapid disease relapse (3, 4). With T-VEC, responses occurred in injected and uninjected lesions, including a greater than 50% decrease in size in 15% of uninjected visceral lesions. The appearance of vitiligo has been described as an adverse event after administration of immune checkpoint inhibitors (5, 6). It has been reported as a marker of activity of the drug and long-term results, inducing clinicians to use it as a predictor of drug response (7). A T-VEC phase II study has reported 85% adverse events, all of which were grade 1 or 2. The appearance of vitiligo has been described in 3 patients out of 50 (8), although no details regarding duration and appearance have been reported.</dc:description>
               <dc:date>2020-06-09T11:38:34Z</dc:date>
               <dc:date>2020-06-09T11:38:34Z</dc:date>
               <dc:date>2019-02-01</dc:date>
               <dc:date>2020-06-09T11:38:34Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.2340/00015555-3061</dc:relation>
               <dc:relation>Acta Dermato-Venereologica, 2019, vol. 99, num. 2, p. 232-233</dc:relation>
               <dc:relation>https://doi.org/10.2340/00015555-3061</dc:relation>
               <dc:rights>(c) Iglesias, Pablo et al., 2019</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Society for the Publication of Acta Dermato-Venereologica</dc:publisher>
               <dc:source>Articles publicats en revistes (Medicina)</dc:source>
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