Durable Response to Vemurafenib and Cobimetinib for the Treatment of BRAF-Mutated Metastatic Melanoma in Routine Clinical Practice.

BRAF clinical practice cobimetinib durable response metastatic melanoma vemurafenib

Journal

OncoTargets and therapy
ISSN: 1178-6930
Titre abrégé: Onco Targets Ther
Pays: New Zealand
ID NLM: 101514322

Informations de publication

Date de publication:
2021
Historique:
received: 17 06 2021
accepted: 21 10 2021
entrez: 6 12 2021
pubmed: 7 12 2021
medline: 7 12 2021
Statut: epublish

Résumé

The combination of Retrospective, observational, cross-sectional, multicenter study involving 41 patients with advanced melanoma harboring a During the combination therapy, 12 patients (29.3%) had a CR, 19 a PR (46.3%), 5 showed SD (12.2%), and 5 had PD. A total of 12 patients (29.3%) were considered as achieving a durable response and 29 (70.7%) as a non-durable one. Practically all sociodemographic and clinical characteristics were similar between patients. Body mass index was the only differential factor (with higher body mass index achieving a non-durable response). The treatment adherence was 100% in patients with durable response and 66.7% in those with non-durable. The combination treatment with vemurafenib/cobimetinib results in an important impact on long-term survival, leading to a steady CR in one-third of the patients.

Sections du résumé

BACKGROUND BACKGROUND
The combination of
PATIENTS AND METHODS METHODS
Retrospective, observational, cross-sectional, multicenter study involving 41 patients with advanced melanoma harboring a
RESULTS RESULTS
During the combination therapy, 12 patients (29.3%) had a CR, 19 a PR (46.3%), 5 showed SD (12.2%), and 5 had PD. A total of 12 patients (29.3%) were considered as achieving a durable response and 29 (70.7%) as a non-durable one. Practically all sociodemographic and clinical characteristics were similar between patients. Body mass index was the only differential factor (with higher body mass index achieving a non-durable response). The treatment adherence was 100% in patients with durable response and 66.7% in those with non-durable.
CONCLUSION CONCLUSIONS
The combination treatment with vemurafenib/cobimetinib results in an important impact on long-term survival, leading to a steady CR in one-third of the patients.

Identifiants

pubmed: 34866914
doi: 10.2147/OTT.S325208
pii: 325208
pmc: PMC8636950
doi:

Types de publication

Journal Article

Langues

eng

Pagination

5345-5352

Informations de copyright

© 2021 Álamo et al.

Déclaration de conflit d'intérêts

BCB declares that has received consulting honoraria from Boehringer and Sanofi and is on the speaker’s bureau of Roche, Novartis, Merck Sharp & Dohme, Bristol-Myers Squibb, Rovi, Leopharma, Astra Zeneca, Leo-Pharma, and Sanofi. EMC declares that has received consulting honoraria, including travel and accommodation paid, and is on the speaker’s bureau of Novartis, Bristol-Myers Squibb, Merck Sharp & Dohme, Sanofi, Roche and Pierre Fabre. FG declares that has received consulting honoraria from Amgen, Merck Sharp & Dohme, Bristol-Myers Squibb and Roche. GC declares that has received consulting honoraria, including travel and accommodation paid, from Janssen, IPSEN, Novartis, Roche, Pierre Fabre, Bristol-Myers Squibb, Sanofi, and EISAI, and is on the speaker’s bureau of Roche, Merck, EVSA Pharma, EISAI, and Merck Sharp & Dohme. JM declares that has received consulting honoraria, including travel and accommodation paid, from Roche, Bristol-Myers Squibb, and Novartis, and is on the speaker’s bureau of Roche, Bristol-Myers Squibb, Novartis, Merck Sharp & Dohme, and Pierre Fabre. MC declares that received consulting honoraria, including travel and accommodation paid, from Novartis, Roche, Pierre Fabre, and Merck Sharp & Dohme. SO declares that has received consulting honoraria from Roche, Novartis, Merck Sharp & Dohme, and Bristol-Myers Squibb. The authors report no other conflicts of interest in this work.

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Auteurs

Mª Del Carmen Álamo (MDC)

Oncology Department, Hospital Universitario Virgen Macarena, Sevilla, Spain.

Sebastian Ochenduszko (S)

Oncology Department, Hospital Universitario Dr. Peset, Valencia, Spain.

Guillermo Crespo (G)

Oncology Department, Hospital Universitario de Burgos, Burgos, Spain.

Mónica Corral (M)

Oncology Department, Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.

Juana Oramas (J)

Oncology Department, Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain.

Pilar Sancho (P)

Oncology Department, Hospital Universitario Virgen del Rocío, Sevilla, Spain.

Javier Medina (J)

Oncology Department, Hospital Universitario Virgen de la Salud, Toledo, Spain.

Fernando Garicano (F)

Oncology Department, Hospital de Galdakao, Bizkaia, Spain.

Pedro López (P)

Oncology Department, Complejo Hospitalario General de Jaén, Jaén, Spain.

Begoña Campos Balea (B)

Oncology Department, Hospital Lucus Augusti, Lugo, Spain.

Analia Rodríguez Garzotto (A)

Medical Department and Strategy, Roche S.A, Madrid, Spain.

Eva Muñoz-Couselo (E)

Oncology Department, Hospital Universitario Vall d´Hebron, Barcelona, Spain.
VHIO Vall d'Hebron Institute on Oncology, Barcelona, Spain.

Classifications MeSH