Five-Year Outcomes With Nivolumab in Patients With Wild-Type


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
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

3937-3946

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Auteurs

Caroline Robert (C)

Gustave Roussy, Villejuif, France.
Université Paris-Saclay, Le Kremlin-Bicêtre, France.

Georgina V Long (GV)

Melanoma Institute Australia, University of Sydney, and Royal North Shore and Mater Hospitals, Sydney, New South Wales, Australia.

Benjamin Brady (B)

Cabrini Health, Melbourne, Victoria, Australia.

Caroline Dutriaux (C)

Hôpital Saint André Centre Hospitalier Universitaire, Bordeaux, France.

Anna Maria Di Giacomo (AM)

Center for Immuno-Oncology, University Hospital of Siena, Siena, Italy.

Laurent Mortier (L)

University of Lille, INSERM U1189, Service de Dermatologie, Chu Lille, Lille, France.

Piotr Rutkowski (P)

Maria Skłodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Jessica C Hassel (JC)

National Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany.

Catriona M McNeil (CM)

Chris O'Brien Lifehouse, Melanoma Institute Australia, and Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.

Ewa Anna Kalinka (EA)

Polish Mother's Memorial Hospital-Research Institute, Lodz, Poland.

Céleste Lebbé (C)

Université de Paris, INSERM U976, and Dermatology and CIC, AP-HP, Saint Louis Hospital, Paris, France.

Julie Charles (J)

Grenoble Alpes University Hospital, INSERM U1209, Grenoble Alpes University, Grenoble, France.

Micaela M Hernberg (MM)

Helsinki University Hospital, Helsinki, Finland.

Kerry J Savage (KJ)

British Columbia Cancer Agency, University of British Columbia, Vancouver, British Columbia, Canada.

Vanna Chiarion-Sileni (V)

Oncology Institute of Veneto Istituto di Ricovero e Cura a Carattere Scientifico, Padua, Italy.

Catalin Mihalcioiu (C)

Royal Victoria Hospital, McGill University, Montreal, Quebec, Canada.

Cornelia Mauch (C)

University Hospital Cologne and Centrum für Integrierte Onkologie Köln, Bonn, Germany.

Ana Arance (A)

Hospital Clínic Barcelona, Barcelona, Spain.

Francesco Cognetti (F)

Regina Elena Institute, Rome, Italy.

Lars Ny (L)

Department of Oncology, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden.

Henrik Schmidt (H)

Aarhus University Hospital, Aarhus, Denmark.

Dirk Schadendorf (D)

Department of Dermatology, Comprehensive Cancer Center, University Hospital Essen, Essen, Germany.
German Cancer Consortium, Heidelberg, Germany.

Helen Gogas (H)

National and Kapodistrian University of Athens, Athens, Greece.

Jesús Zoco (J)

Syneos Health, Braine l'Alleud, Belgium.

Sandra Re (S)

Bristol Myers Squibb, Princeton, NJ.

Paolo A Ascierto (PA)

Istituto Nazionale Tumori IRCCS Fondazione Pascale, Naples, Italy.

Victoria Atkinson (V)

Princess Alexandra Hospital, Woolloongabba, and Gallipoli Medical Research Foundation, Greenslopes Private Hospital, Greenslopes, Queensland, Australia.

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Classifications MeSH