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
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
5345-5352Informations 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.
Références
J Invest Dermatol. 2017 Aug;137(8):1792-1795
pubmed: 28442307
J Invest Dermatol. 2015 Aug;135(8):1929-1933
pubmed: 26174532
Curr Oncol Rep. 2016 Sep;18(9):56
pubmed: 27475805
Eur J Cancer. 2019 Dec;123:58-71
pubmed: 31670077
Br J Cancer. 2018 Mar 20;118(6):777-784
pubmed: 29438370
Curr Treat Options Oncol. 2019 Nov 18;20(11):81
pubmed: 31741065
Melanoma Res. 2019 Feb;29(1):65-69
pubmed: 30376465
J Clin Oncol. 2011 Apr 1;29(10):1239-46
pubmed: 21343559
Cancer Med. 2019 Dec;8(18):7637-7643
pubmed: 31677253
Medicine (Baltimore). 2019 Jul;98(28):e16328
pubmed: 31305421
Mod Pathol. 2018 Jan;31(1):24-38
pubmed: 29148538
Br J Dermatol. 2018 Aug;179(2):544
pubmed: 29738075
MMWR Morb Mortal Wkly Rep. 2015 Jun 5;64(21):591-6
pubmed: 26042651
AIDS. 2002 Mar 8;16(4):605-13
pubmed: 11873004
Lancet Oncol. 2018 Mar;19(3):310-322
pubmed: 29449192
PLoS Med. 2016 Aug 16;13(8):e1002081
pubmed: 27529652
Br J Cancer. 2016 Mar 29;114(7):801-8
pubmed: 26924424
Front Oncol. 2018 Jun 12;8:202
pubmed: 29946532
N Engl J Med. 2011 Jun 30;364(26):2507-16
pubmed: 21639808
Future Oncol. 2019 Sep 1;15(25):2933-2942
pubmed: 30799646
J Clin Oncol. 2009 Dec 20;27(36):6199-206
pubmed: 19917835
N Engl J Med. 2003 Apr 24;348(17):1625-38
pubmed: 12711737
Ther Adv Med Oncol. 2016 Jan;8(1):48-56
pubmed: 26753005
Clin Cancer Res. 2021 Jun 22;:
pubmed: 34158360