RASopathic skin eruptions during vemurafenib therapy.

Vemurafenib is a potent inhibitor of V600 mutant BRAF with significant impact on progression-free and overall survival in advanced melanoma. Cutaneous side effects are frequent. This single-center observational study investigates clinical and histological features of these class-specific cutaneous a...

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Main Authors: Jeannine D Rinderknecht, Simone M Goldinger, Sima Rozati, Jivko Kamarashev, Katrin Kerl, Lars E French, Reinhard Dummer, Benedetta Belloni
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3597638?pdf=render
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spelling doaj-3e4e094b49e342bca75f899402e95c682020-11-24T22:21:32ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5872110.1371/journal.pone.0058721RASopathic skin eruptions during vemurafenib therapy.Jeannine D RinderknechtSimone M GoldingerSima RozatiJivko KamarashevKatrin KerlLars E FrenchReinhard DummerBenedetta BelloniVemurafenib is a potent inhibitor of V600 mutant BRAF with significant impact on progression-free and overall survival in advanced melanoma. Cutaneous side effects are frequent. This single-center observational study investigates clinical and histological features of these class-specific cutaneous adverse reactions.Patients were all treated with Vemurafenib 960 mg b.i.d. within local ethic committees approved clinical trials. All skin reactions were collected and documented prospectively. Cutaneous reactions were classified by reaction pattern as phototoxic and inflammatory, hair and nail changes, keratinocytic proliferations and melanocytic disorders.Vemurafenib was well tolerated, only in two patients the dose had to be reduced to 720 mg due to arthralgia. 26/28 patients (93%) experienced cutaneous side effects. Observed side effects included UVA dependent photosensitivity (n = 16), maculopapular exanthema (n = 14), pruritus (n = 8), folliculitis (n = 5), burning feet (n = 3), hair thinning (mild alopecia) (n = 8), curly hair (n = 2) and nail changes (n = 2). Keratosis pilaris and acanthopapilloma were common skin reactions (n = 12/n = 13), as well as plantar hyperkeratosis (n = 4), keratoacanthoma (n = 5) and invasive squamous cell carcinoma (n = 4). One patient developed a second primary melanoma after more than 4 months of therapy (BRAF and RAS wild type).Vemurafenib has a broad and peculiar cutaneous side effect profile involving epidermis and adnexa overlapping with the cutaneous manifestations of genetic diseases characterized by activating germ line mutations of RAS (RASopathy). They must be distinguished from allergic drug reaction. Regular skin examination and management by experienced dermatologists as well as continuous prophylactic photo protection including an UVA optimized sun screen is mandatory.http://europepmc.org/articles/PMC3597638?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jeannine D Rinderknecht
Simone M Goldinger
Sima Rozati
Jivko Kamarashev
Katrin Kerl
Lars E French
Reinhard Dummer
Benedetta Belloni
spellingShingle Jeannine D Rinderknecht
Simone M Goldinger
Sima Rozati
Jivko Kamarashev
Katrin Kerl
Lars E French
Reinhard Dummer
Benedetta Belloni
RASopathic skin eruptions during vemurafenib therapy.
PLoS ONE
author_facet Jeannine D Rinderknecht
Simone M Goldinger
Sima Rozati
Jivko Kamarashev
Katrin Kerl
Lars E French
Reinhard Dummer
Benedetta Belloni
author_sort Jeannine D Rinderknecht
title RASopathic skin eruptions during vemurafenib therapy.
title_short RASopathic skin eruptions during vemurafenib therapy.
title_full RASopathic skin eruptions during vemurafenib therapy.
title_fullStr RASopathic skin eruptions during vemurafenib therapy.
title_full_unstemmed RASopathic skin eruptions during vemurafenib therapy.
title_sort rasopathic skin eruptions during vemurafenib therapy.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Vemurafenib is a potent inhibitor of V600 mutant BRAF with significant impact on progression-free and overall survival in advanced melanoma. Cutaneous side effects are frequent. This single-center observational study investigates clinical and histological features of these class-specific cutaneous adverse reactions.Patients were all treated with Vemurafenib 960 mg b.i.d. within local ethic committees approved clinical trials. All skin reactions were collected and documented prospectively. Cutaneous reactions were classified by reaction pattern as phototoxic and inflammatory, hair and nail changes, keratinocytic proliferations and melanocytic disorders.Vemurafenib was well tolerated, only in two patients the dose had to be reduced to 720 mg due to arthralgia. 26/28 patients (93%) experienced cutaneous side effects. Observed side effects included UVA dependent photosensitivity (n = 16), maculopapular exanthema (n = 14), pruritus (n = 8), folliculitis (n = 5), burning feet (n = 3), hair thinning (mild alopecia) (n = 8), curly hair (n = 2) and nail changes (n = 2). Keratosis pilaris and acanthopapilloma were common skin reactions (n = 12/n = 13), as well as plantar hyperkeratosis (n = 4), keratoacanthoma (n = 5) and invasive squamous cell carcinoma (n = 4). One patient developed a second primary melanoma after more than 4 months of therapy (BRAF and RAS wild type).Vemurafenib has a broad and peculiar cutaneous side effect profile involving epidermis and adnexa overlapping with the cutaneous manifestations of genetic diseases characterized by activating germ line mutations of RAS (RASopathy). They must be distinguished from allergic drug reaction. Regular skin examination and management by experienced dermatologists as well as continuous prophylactic photo protection including an UVA optimized sun screen is mandatory.
url http://europepmc.org/articles/PMC3597638?pdf=render
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