Nivolumab Monotherapy and Nivolumab Plus Ipilimumab in Recurrent Small Cell Lung Cancer: Results From the CheckMate 032 Randomized Cohort.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
03 2020
Historique:
received: 30 07 2019
revised: 03 10 2019
accepted: 04 10 2019
pubmed: 21 10 2019
medline: 7 1 2021
entrez: 21 10 2019
Statut: ppublish

Résumé

Nivolumab monotherapy is approved in the United States for third-line or later metastatic small cell lung cancer based on pooled data from nonrandomized and randomized cohorts of the multicenter, open-label, phase 1/2 trial of nivolumab ± ipilimumab (CheckMate 032; NCT01928394). We report updated results, including long-term overall survival (OS), from the randomized cohort. Patients with small cell lung cancer and disease progression after one to two prior chemotherapy regimens were randomized 3:2 to nivolumab 3 mg/kg every 2 weeks or nivolumab 1 mg/kg plus ipilimumab 3 mg/kg every 3 weeks for four cycles followed by nivolumab 3 mg/kg every 2 weeks. Patients were stratified by number of prior chemotherapy regimens and treated until disease progression or unacceptable toxicity. The primary endpoint was objective response rate (ORR) by blinded independent central review. Overall, 147 patients received nivolumab and 96 nivolumab plus ipilimumab. Minimum follow-up for ORR/progression-free survival/safety was 11.9 months (nivolumab) and 11.2 months (nivolumab plus ipilimumab). ORR increased with nivolumab plus ipilimumab (21.9% versus 11.6% with nivolumab; odds ratio: 2.12; 95% confidence interval: 1.06-4.26; p = 0.03). For long-term OS, minimum follow-up was 29.0 months (nivolumab) versus 28.4 months (nivolumab plus ipilimumab); median (95% confidence interval) OS was 5.7 (3.8-7.6) versus 4.7 months (3.1-8.3). Twenty-four-month OS rates were 17.9% (nivolumab) and 16.9% (nivolumab plus ipilimumab). Grade 3 to 4 treatment-related adverse event rates were 12.9% (nivolumab) versus 37.5% (nivolumab plus ipilimumab), and treatment-related deaths were n =1 versus n = 3, respectively. Whereas ORR (primary endpoint) was higher with nivolumab plus ipilimumab versus nivolumab, OS was similar between groups. In each group, OS remained encouraging with long-term follow-up. Toxicities were more common with combination therapy versus nivolumab monotherapy.

Identifiants

pubmed: 31629915
pii: S1556-0864(19)33531-2
doi: 10.1016/j.jtho.2019.10.004
pii:
doi:

Substances chimiques

Ipilimumab 0
Nivolumab 31YO63LBSN

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

426-435

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

Neal E Ready (NE)

Duke University Medical Center, Durham, North Carolina. Electronic address: neal.ready@duke.edu.

Patrick A Ott (PA)

Dana Farber Cancer Institute, Boston, Massachusetts.

Matthew D Hellmann (MD)

Memorial Sloan-Kettering Cancer Center, New York, New York; Weill Cornell Medical College, New York, New York.

Jon Zugazagoitia (J)

University Hospital 12 de Octubre, Madrid, Spain.

Christine L Hann (CL)

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland.

Filippo de Braud (F)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan; University of Milan, Milan, Italy.

Scott J Antonia (SJ)

H. Lee Moffitt Cancer Center, Tampa, Florida.

Paolo A Ascierto (PA)

Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", Naples, Italy.

Victor Moreno (V)

START Madrid - FJD, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.

Akin Atmaca (A)

Department of Oncology and Hematology, Krankenhaus Nordwest, UCT-University Cancer Center, Frankfurt, Germany.

Stefania Salvagni (S)

Policlinico S.Orsola-Malpighi, Azienda Ospedaliero Universitaria, Bologna, Italy.

Matthew Taylor (M)

Oregon Health & Science University, Portland, Oregon.

Asim Amin (A)

Levine Cancer Institute, Atrium Healthcare System, Charlotte, North Carolina.

D Ross Camidge (DR)

University of Colorado Denver, Aurora, Colorado.

Leora Horn (L)

Vanderbilt Ingram Cancer Center, Nashville, Tennessee.

Emiliano Calvo (E)

START Madrid - CIOCC, Centro Integral Oncológico Clara Campal, Madrid, Spain.

Ang Li (A)

Bristol-Myers Squibb, Lawrenceville, New Jersey.

Wen Hong Lin (WH)

Bristol-Myers Squibb, Lawrenceville, New Jersey.

Margaret K Callahan (MK)

Memorial Sloan-Kettering Cancer Center, New York, New York.

David R Spigel (DR)

Sarah Cannon Research Institute/Tennessee Oncology Nashville, Nashville, Tennessee.

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Classifications MeSH