Atezolizumab Plus Chemotherapy for First-Line Treatment of Nonsquamous NSCLC: Results From the Randomized Phase 3 IMpower132 Trial.


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:
04 2021
Historique:
received: 30 09 2020
revised: 16 11 2020
accepted: 26 11 2020
pubmed: 18 12 2020
medline: 22 4 2021
entrez: 17 12 2020
Statut: ppublish

Résumé

We report the final results of the phase 3 IMpower132 study evaluating atezolizumab plus carboplatin or cisplatin plus pemetrexed (APP) in patients with nonsquamous NSCLC. Chemotherapy-naive patients with stage IV nonsquamous NSCLC without sensitizing EGFR or ALK genetic alterations were randomized in a one-to-one ratio to receive four or six cycles of carboplatin or cisplatin plus pemetrexed (PP) or APP every 3 weeks, followed by maintenance therapy with atezolizumab plus pemetrexed or pemetrexed alone. Co-primary end points were overall survival (OS) and investigator-assessed progression-free survival (PFS). The intention-to-treat population included 578 patients (APP, n = 292; PP, n = 286). At the primary PFS analysis (May 22, 2018; median follow-up, 14.8 mo), APP exhibited significant PFS improvement versus PP (median = 7.6 versus 5.2 mo, stratified hazard ratio [HR] = 0.60, 95% confidence interval [CI]: 0.49-0.72, p < 0.0001). OS for the APP group was numerically better but not statistically significant at the interim (May 22, 2018; median = 18.1 versus 13.6 mo, stratified HR = 0.81, 95% CI: 0.64-1.03, p = 0.0797) and final analyses (July 18, 2019; median = 17.5 versus 13.6 mo; stratified HR = 0.86, 95% CI: 0.71-1.06, p = 0.1546). The OS and PFS results favored APP versus PP across subgroups. Grade 3 or 4 treatment-related adverse events occurred in 54.6% (APP) and 40.1% (PP) of patients; grade 5 treatment-related events occurred in 3.8% and 2.9%, respectively. IMpower132 met its co-primary PFS end point but not its co-primary OS end point, with numerical improvement for OS in the APP arm. APP had a manageable safety profile, with no new or unexpected safety signals identified.

Identifiants

pubmed: 33333328
pii: S1556-0864(20)31100-X
doi: 10.1016/j.jtho.2020.11.025
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Pemetrexed 04Q9AIZ7NO
atezolizumab 52CMI0WC3Y
Carboplatin BG3F62OND5
Cisplatin Q20Q21Q62J

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

653-664

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

Makoto Nishio (M)

The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan. Electronic address: mnishio@jfcr.or.jp.

Fabrice Barlesi (F)

Department of Medical Oncology, Cancer Research Center of Marseille, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Assistance Publique-Hopitaux de Marseille, Campus Timone, Centres Hospitaliers et Universitaires Nord, Aix Marseille University, Marseille, France; Department of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.

Howard West (H)

Department of Medical Oncology and Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, California.

Simon Ball (S)

Department of Oncology, Queen's Hospital, Rom Valley Way, Romford, United Kingdom.

Rodolfo Bordoni (R)

Northside Hospital Cancer Institute, Atlanta, Georgia.

Manuel Cobo (M)

Unidad de Gestión Clínica Intercentros de Oncología Médica. Hospitales Universitarios Regional y Virgen de la Victoria, Málaga, Spain.

Pascale Dubray Longeras (PD)

Department of Medical Oncology, Centre Jean Perrin, Clermont-Ferrand, France.

Jerome Goldschmidt (J)

Blue Ridge Cancer Care, Blacksburg, Virginia.

Silvia Novello (S)

Department of Oncology, University of Turin, Orbassano, Italy.

Francisco Orlandi (F)

Department of Medical Oncology, Instituto Nacional del Tόrax, Santiago, Chile.

Rachel E Sanborn (RE)

Earle A. Chiles Research Institute, Providence Cancer Institute, Portland, Oregon.

Zsuzsanna Szalai (Z)

Department of Pulmonology, Petz Aladár County Teaching Hospital, Vasvári Pál, Hungary.

Grigoriy Ursol (G)

Acinus, Karla Marksa Kirovograd, Ukraine.

Diana Mendus (D)

Genentech, Inc., South San Francisco, California.

Lijia Wang (L)

Genentech, Inc., South San Francisco, California.

Xiaohui Wen (X)

Genentech, Inc., South San Francisco, California.

Mark McCleland (M)

Genentech, Inc., South San Francisco, California.

Tien Hoang (T)

Genentech, Inc., South San Francisco, California.

See Phan (S)

Genentech, Inc., South San Francisco, California.

Mark A Socinski (MA)

Department of Medical Oncology, AdventHealth Cancer Institute, Orlando, Florida.

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Classifications MeSH