Five-Year Outcomes With Nivolumab in Patients With Wild-Type
Antineoplastic Agents, Alkylating
/ administration & dosage
Antineoplastic Agents, Immunological
/ administration & dosage
Dacarbazine
/ administration & dosage
Humans
Melanoma
/ drug therapy
Nivolumab
/ administration & dosage
Progression-Free Survival
Proto-Oncogene Proteins B-raf
/ genetics
Survival Rate
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333
Informations de publication
Date de publication:
20 11 2020
20 11 2020
Historique:
pubmed:
1
10
2020
medline:
26
3
2021
entrez:
30
9
2020
Statut:
ppublish
Résumé
The CheckMate 066 trial investigated nivolumab monotherapy as first-line treatment for patients with previously untreated In this multicenter, double-blind, phase III study, 418 patients with previously untreated, unresectable, stage III/IV, wild-type Patients were followed for a minimum of 60 months from the last patient randomly assigned (median follow-up, 32.0 months for nivolumab and 10.9 months for dacarbazine). Five-year OS rates were 39% with nivolumab and 17% with dacarbazine; PFS rates were 28% and 3%, respectively. Five-year OS was 38% in patients randomly assigned to dacarbazine who had subsequent therapy, including nivolumab (n = 37). ORR was 42% with nivolumab and 14% with dacarbazine; among patients alive at 5 years, ORR was 81% and 39%, respectively. Of 42 patients treated with nivolumab who had a complete response (20%), 88% (37 of 42) were alive as of the 5-year analysis. Among 75 nivolumab-treated patients alive and evaluable at the 5-year analysis, 83% had not received subsequent therapy; 23% were still on study treatment, and 60% were treatment free. Safety analyses were similar to the 3-year report. Results from this 5-year analysis confirm the significant benefit of nivolumab over dacarbazine for all end points and add to the growing body of evidence supporting long-term survival with nivolumab mono-therapy. Survival is strongly associated with achieving a durable response, which can be maintained after treatment discontinuation, even without subsequent systemic therapies.
Identifiants
pubmed: 32997575
doi: 10.1200/JCO.20.00995
pmc: PMC7676881
doi:
Substances chimiques
Antineoplastic Agents, Alkylating
0
Antineoplastic Agents, Immunological
0
Nivolumab
31YO63LBSN
Dacarbazine
7GR28W0FJI
BRAF protein, human
EC 2.7.11.1
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
Banques de données
ClinicalTrials.gov
['NCT01721772']
Types de publication
Clinical Trial, Phase III
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
3937-3946Références
JAMA Oncol. 2019 Feb 1;5(2):187-194
pubmed: 30422243
Pigment Cell Melanoma Res. 2016 Sep;29(5):572-7
pubmed: 27333363
J Immunother Cancer. 2018 Jan 15;6(1):2
pubmed: 29332608
N Engl J Med. 2019 Oct 17;381(16):1535-1546
pubmed: 31562797
Oncology (Williston Park). 2009 May;23(6):488-96
pubmed: 19544689
Nat Med. 2019 Mar;25(3):454-461
pubmed: 30804515
N Engl J Med. 2017 Oct 5;377(14):1345-1356
pubmed: 28889792
N Engl J Med. 2015 Jul 2;373(1):23-34
pubmed: 26027431
Ann Oncol. 2018 Oct 1;29(10):2115-2120
pubmed: 30137228
N Engl J Med. 2015 Jun 25;372(26):2521-32
pubmed: 25891173
Lancet Oncol. 2018 Nov;19(11):1480-1492
pubmed: 30361170
Ann Oncol. 2019 Apr 1;30(4):582-588
pubmed: 30715153
J Clin Oncol. 2018 Jun 10;36(17):1668-1674
pubmed: 29283791
J Thorac Oncol. 2017 Feb;12(2):208-222
pubmed: 27913228
Lancet Oncol. 2019 Sep;20(9):1239-1251
pubmed: 31345627
Br J Cancer. 2016 Nov 22;115(11):1280-1284
pubmed: 27711085
N Engl J Med. 2015 Jan 22;372(4):320-30
pubmed: 25399552