CheckMate 73L: A Phase 3 Study Comparing Nivolumab Plus Concurrent Chemoradiotherapy Followed by Nivolumab With or Without Ipilimumab Versus Concurrent Chemoradiotherapy Followed by Durvalumab for Previously Untreated, Locally Advanced Stage III Non-Small-Cell Lung Cancer.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
05 2022
Historique:
received: 14 05 2021
revised: 28 06 2021
accepted: 04 07 2021
pubmed: 8 9 2021
medline: 18 5 2022
entrez: 7 9 2021
Statut: ppublish

Résumé

The 5 year survival rate for patients with locally advanced non-small-cell lung cancer (NSCLC) not amenable for definitive resection with historical standard-of-care concurrent chemoradiotherapy (cCRT) ranges from 15% to 32%. cCRT primes anti-tumor immunity and also upregulates programmed death ligand-1 (PD-L1), providing a rationale for combining an immune checkpoint inhibitor with cCRT to improve outcomes. In the PACIFIC trial, consolidation therapy with the PD-L1 inhibitor durvalumab improved progression-free survival (PFS) and overall survival (OS) vs. placebo in patients with stage III NSCLC who did not have disease progression after cCRT. CheckMate73L (NCT04026412), a randomized phase 3 study, evaluates the efficacy of nivolumab plus cCRT followed by nivolumab with or without ipilimumab vs. cCRT followed by durvalumab for untreated, stage III NSCLC. Patients with untreated, stage III NSCLC will be randomized 1:1:1 to nivolumab plus cCRT followed by nivolumab in combination with ipilimumab (Arm A) or nivolumab alone (Arm B); or cCRT followed by durvalumab (Arm C). Primary endpoints are PFS and OS (Arm A vs. Arm C). Secondary endpoints include additional analyses of PFS and OS (Arm A vs. Arm B; Arm B vs. Arm C), as well as objective response rate, complete response rate, time to response, duration of response, time to death or distant metastases, and safety and tolerability. Recruitment began on August 20, 2019, and the estimated primary completion date is October 17, 2022.

Identifiants

pubmed: 34489161
pii: S1525-7304(21)00186-8
doi: 10.1016/j.cllc.2021.07.005
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
Ipilimumab 0
durvalumab 28X28X9OKV
Nivolumab 31YO63LBSN

Banques de données

ClinicalTrials.gov
['NCT04026412']

Types de publication

Clinical Trial, Phase III Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e264-e268

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Dirk De Ruysscher (D)

Department of Radiation Oncology (Maastro), Maastricht University Medical Center, GROW School for Oncology and Developmental Biology, The Netherlands. Electronic address: dirk.deruysscher@maastro.nl.

Suresh Ramalingam (S)

Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.

James Urbanic (J)

Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA.

David E Gerber (DE)

Division of Hematology Oncology, Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX.

Daniel S W Tan (DSW)

Division of Medical Oncology, National Cancer Centre Singapore, Singapore.

Junliang Cai (J)

Oncology Clinical Development, Biometrics and Data Sciences, Bristol Myers Squibb, Lawrenceville, NJ.

Ang Li (A)

Oncology Clinical Development, Biometrics and Data Sciences, Bristol Myers Squibb, Lawrenceville, NJ.

Solange Peters (S)

Oncology Department, Centre hospitalier universitaire vaudois (CHUV), Lausanne University, Switzerland.

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Classifications MeSH