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

BACKGROUND: The combination of BRAF and MEK inhibitors delays the onset of resistance and provides more sustained and dramatic responses in comparison with a BRAF inhibitor in monotherapy. The objective of the study was to evaluate the effectiveness of the combination therapy with vemurafenib/cobime...

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Autores principales: Álamo, Mª del Carmen, Ochenduszko, Sebastian, Crespo, Guillermo, Corral, Mónica, Oramas, Juana, Sancho, Pilar, Medina, Javier, Garicano, Fernando, López, Pedro, Campos Balea, Begoña, Rodríguez Garzotto, Analia, Muñoz-Couselo, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636950/
https://www.ncbi.nlm.nih.gov/pubmed/34866914
http://dx.doi.org/10.2147/OTT.S325208
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author Álamo, Mª del Carmen
Ochenduszko, Sebastian
Crespo, Guillermo
Corral, Mónica
Oramas, Juana
Sancho, Pilar
Medina, Javier
Garicano, Fernando
López, Pedro
Campos Balea, Begoña
Rodríguez Garzotto, Analia
Muñoz-Couselo, Eva
author_facet Álamo, Mª del Carmen
Ochenduszko, Sebastian
Crespo, Guillermo
Corral, Mónica
Oramas, Juana
Sancho, Pilar
Medina, Javier
Garicano, Fernando
López, Pedro
Campos Balea, Begoña
Rodríguez Garzotto, Analia
Muñoz-Couselo, Eva
author_sort Álamo, Mª del Carmen
collection PubMed
description BACKGROUND: The combination of BRAF and MEK inhibitors delays the onset of resistance and provides more sustained and dramatic responses in comparison with a BRAF inhibitor in monotherapy. The objective of the study was to evaluate the effectiveness of the combination therapy with vemurafenib/cobimetinib in terms of durability, and to describe differential characteristics in patients associated to durable responses in real-world settings. PATIENTS AND METHODS: Retrospective, observational, cross-sectional, multicenter study involving 41 patients with advanced melanoma harboring a BRAF(V600) mutation who initiated a combination therapy with vemurafenib/cobimetinib between May 2018 and March 2019. Participants were differentiated regarding the durability of the response: durable (complete response, CR, or a partial response, PR, for at least 12 months) and non-durable (stable disease, SD, progressive disease, PD, or CR/PR <12 months). Secondary endpoints included treatment adherence, labor productivity, anxiety/depression, and safety profile. 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: 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.
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spelling pubmed-86369502021-12-03 Durable Response to Vemurafenib and Cobimetinib for the Treatment of BRAF-Mutated Metastatic Melanoma in Routine Clinical Practice Álamo, Mª del Carmen Ochenduszko, Sebastian Crespo, Guillermo Corral, Mónica Oramas, Juana Sancho, Pilar Medina, Javier Garicano, Fernando López, Pedro Campos Balea, Begoña Rodríguez Garzotto, Analia Muñoz-Couselo, Eva Onco Targets Ther Original Research BACKGROUND: The combination of BRAF and MEK inhibitors delays the onset of resistance and provides more sustained and dramatic responses in comparison with a BRAF inhibitor in monotherapy. The objective of the study was to evaluate the effectiveness of the combination therapy with vemurafenib/cobimetinib in terms of durability, and to describe differential characteristics in patients associated to durable responses in real-world settings. PATIENTS AND METHODS: Retrospective, observational, cross-sectional, multicenter study involving 41 patients with advanced melanoma harboring a BRAF(V600) mutation who initiated a combination therapy with vemurafenib/cobimetinib between May 2018 and March 2019. Participants were differentiated regarding the durability of the response: durable (complete response, CR, or a partial response, PR, for at least 12 months) and non-durable (stable disease, SD, progressive disease, PD, or CR/PR <12 months). Secondary endpoints included treatment adherence, labor productivity, anxiety/depression, and safety profile. 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: 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. Dove 2021-11-27 /pmc/articles/PMC8636950/ /pubmed/34866914 http://dx.doi.org/10.2147/OTT.S325208 Text en © 2021 Álamo et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Álamo, Mª del Carmen
Ochenduszko, Sebastian
Crespo, Guillermo
Corral, Mónica
Oramas, Juana
Sancho, Pilar
Medina, Javier
Garicano, Fernando
López, Pedro
Campos Balea, Begoña
Rodríguez Garzotto, Analia
Muñoz-Couselo, Eva
Durable Response to Vemurafenib and Cobimetinib for the Treatment of BRAF-Mutated Metastatic Melanoma in Routine Clinical Practice
title Durable Response to Vemurafenib and Cobimetinib for the Treatment of BRAF-Mutated Metastatic Melanoma in Routine Clinical Practice
title_full Durable Response to Vemurafenib and Cobimetinib for the Treatment of BRAF-Mutated Metastatic Melanoma in Routine Clinical Practice
title_fullStr Durable Response to Vemurafenib and Cobimetinib for the Treatment of BRAF-Mutated Metastatic Melanoma in Routine Clinical Practice
title_full_unstemmed Durable Response to Vemurafenib and Cobimetinib for the Treatment of BRAF-Mutated Metastatic Melanoma in Routine Clinical Practice
title_short Durable Response to Vemurafenib and Cobimetinib for the Treatment of BRAF-Mutated Metastatic Melanoma in Routine Clinical Practice
title_sort durable response to vemurafenib and cobimetinib for the treatment of braf-mutated metastatic melanoma in routine clinical practice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636950/
https://www.ncbi.nlm.nih.gov/pubmed/34866914
http://dx.doi.org/10.2147/OTT.S325208
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