Long-Term Overall Survival From KEYNOTE-021 Cohort G: Pemetrexed and Carboplatin With or Without Pembrolizumab as First-Line Therapy for Advanced Nonsquamous NSCLC.


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:
01 2021
Historique:
received: 21 08 2020
revised: 11 09 2020
accepted: 20 09 2020
pubmed: 19 10 2020
medline: 2 4 2021
entrez: 18 10 2020
Statut: ppublish

Résumé

In cohort G of KEYNOTE-021 (NCT02039674), first-line pembrolizumab plus pemetrexed-carboplatin significantly improved the objective response rate and progression-free survival versus chemotherapy alone with manageable toxicity in advanced nonsquamous NSCLC. We report the long-term outcomes from this study. Patients with previously untreated advanced nonsquamous NSCLC without sensitizing EGFR or ALK alterations were randomly assigned 1:1 to receive open-label pemetrexed 500 mg/m After the median time of 49.4 months from randomization to data cutoff, objective response rate (58% versus 33%) and progression-free survival (median: 24.5 versus 9.9 mo; hazard ratio: 0.54; 95% confidence interval: 0.35‒0.83) remained improved with pembrolizumab combination (n = 60) versus chemotherapy (n = 63), regardless of programmed death ligand 1 status. Median overall survival was 34.5 versus 21.1 months (hazard ratio: 0.71; 95% confidence interval: 0.45‒1.12), despite a 70% crossover rate from chemotherapy alone to anti‒programmed death (ligand) 1 therapy. Among the 12 patients who completed 2 years of pembrolizumab, 92% were alive at data cutoff; the estimated 3-year duration of response rate was 100%. Grade 3 to 5 treatment-related adverse events occurred in 39% of patients receiving pembrolizumab combination and 31% receiving chemotherapy. First-line pembrolizumab plus pemetrexed-carboplatin continued to show improved response and survival versus chemotherapy alone in advanced nonsquamous NSCLC, with durable clinical benefit in patients who completed 2 years of therapy. No new safety signals were observed with longer follow-up.

Identifiants

pubmed: 33069888
pii: S1556-0864(20)30761-9
doi: 10.1016/j.jtho.2020.09.015
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Pemetrexed 04Q9AIZ7NO
Carboplatin BG3F62OND5
pembrolizumab DPT0O3T46P

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

162-168

Informations de copyright

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

Auteurs

Mark M Awad (MM)

Medical Oncology, Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts. Electronic address: mark_awad@dfci.harvard.edu.

Shirish M Gadgeel (SM)

Thoracic Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, Michigan.

Hossein Borghaei (H)

Hematology and Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.

Amita Patnaik (A)

Clinical Research, START Center for Cancer Care, San Antonio, Texas.

James Chih-Hsin Yang (JC)

Department of Oncology, National Taiwan University Hospital and National Taiwan University Cancer Center, Taipei, Republic of China.

Steven F Powell (SF)

Oncology, Sanford Health, Sioux Falls, South Dakota.

Ryan D Gentzler (RD)

Hematology/Oncology, University of Virginia Cancer Center, Charlottesville, Virginia.

Renato G Martins (RG)

Department of Medicine, University of Washington, Seattle, Washington.

James P Stevenson (JP)

Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

Mehmet Altan (M)

Thoracic/Head and Neck Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Shadia I Jalal (SI)

Indiana University School of Medicine, Indianapolis, Indiana.

Amit Panwalkar (A)

Hematology/Oncology, Sanford Roger Maris Cancer Center, Fargo, North Dakota.

Matthew Gubens (M)

Medical Oncology, University of California San Francisco, San Francisco, California.

Lecia V Sequist (LV)

Hematology/Oncology, Massachusetts General Hospital, Boston, Massachusetts.

Sanatan Saraf (S)

Merck & Co., Inc., Kenilworth, New Jersey.

Bin Zhao (B)

Merck & Co., Inc., Kenilworth, New Jersey.

Bilal Piperdi (B)

Merck & Co., Inc., Kenilworth, New Jersey.

Corey J Langer (CJ)

Department of Medicine, Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH