A Randomized, Placebo-Controlled Trial of Pembrolizumab Plus Chemotherapy in Patients With Metastatic Squamous NSCLC: Protocol-Specified Final Analysis of KEYNOTE-407.


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:
10 2020
Historique:
received: 05 05 2020
revised: 10 06 2020
accepted: 16 06 2020
pubmed: 1 7 2020
medline: 2 2 2021
entrez: 30 6 2020
Statut: ppublish

Résumé

In the randomized KEYNOTE-407 study (ClinicalTrials.gov, NCT02775435), pembrolizumab plus carboplatin and paclitaxel/nab-paclitaxel (chemotherapy) significantly improved overall survival (OS) and progression-free survival (PFS) compared with placebo plus chemotherapy in patients with previously untreated metastatic squamous NSCLC. We report updated efficacy outcomes from the protocol-specified final analysis and, for the first time, progression on next line of treatment. Eligible patients were randomized to chemotherapy plus either pembrolizumab (n = 278) or placebo (n = 281). After positive results from the second interim analysis, patients still receiving placebo could cross over to pembrolizumab monotherapy at the time of confirmed progressive disease. The primary end points were OS and PFS. PFS-2 (time from randomization to progression on next-line treatment/death, whichever occurred first) was an exploratory end point. After median (range) follow-up of 14.3 (0.1-31.3) months, pembrolizumab plus chemotherapy continued to exhibit a clinically meaningful improvement over placebo plus chemotherapy in OS (median, 17.1 mo [95% confidence interval (CI): 14.4‒19.9] versus 11.6 mo [95% CI: 10.1‒13.7]; hazard ratio [HR], 0.71 [95% CI: 0.58‒0.88]) and PFS (median, 8.0 mo [95% CI: 6.3‒8.4] versus 5.1 mo [95% CI: 4.3‒6.0]; HR, 0.57 [95% CI: 0.47‒0.69]). PFS-2 was longer for patients randomized to first-line pembrolizumab plus chemotherapy (HR, 0.59 [95% CI: 0.49‒0.72]). Grade 3 to 5 adverse events occurred in 74.1% and 69.6% of patients receiving pembrolizumab plus chemotherapy and placebo plus chemotherapy, respectively. Pembrolizumab plus chemotherapy continued to exhibit substantially improved OS and PFS in patients with metastatic squamous NSCLC. The PFS-2 outcomes support pembrolizumab plus chemotherapy as a standard first-line treatment in patients with metastatic squamous NSCLC.

Identifiants

pubmed: 32599071
pii: S1556-0864(20)30500-1
doi: 10.1016/j.jtho.2020.06.015
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
pembrolizumab DPT0O3T46P

Banques de données

ClinicalTrials.gov
['NCT02775435']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1657-1669

Informations de copyright

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

Auteurs

Luis Paz-Ares (L)

Department of Medical Oncology, Hospital Universitario 12 de Octubre, H12o-CNIO Lung Cancer Unit, Universidad Complutense & Ciberonc, Madrid, Spain. Electronic address: lpazaresr@seom.org.

David Vicente (D)

Department of Clinical Oncology, Hospital Universitario Virgen Macarena, Sevilla, Spain.

Ali Tafreshi (A)

Wollongong Oncology, Wollongong Private Hospital, Wollongong, New South Wales, Australia.

Andrew Robinson (A)

Cancer Centre of Southeastern Ontario, Kingston General Hospital, Kingston, Ontario, Canada.

Hector Soto Parra (H)

Azienda Ospedaliero Universitaria Policlinico Vittorio Emanuele, Catania, Italy.

Julien Mazières (J)

Hôpital Larrey, Centre Hospitalier Universitaire Toulouse, Toulouse, France.

Barbara Hermes (B)

Universitätskinikum Tübingen, Tuebingen, Germany.

Irfan Cicin (I)

Department of Medical Oncology, Trakya University, Edirne, Turkey.

Balazs Medgyasszay (B)

Veszprém Megyei Tüdőgyógyintézet Farkasgyepű, Farkasgyepű, Hungary.

Jerónimo Rodríguez-Cid (J)

Oncology Center, Medica Sur Hospital, Mexico City, Mexico.

Isamu Okamoto (I)

Department of Medicine and Surgery, Kyushu University Hospital, Fukuoka, Japan.

SungSook Lee (S)

Department of Hematology-Oncology, Inje University College of Medicine, Busan, South Korea.

Rodryg Ramlau (R)

Department of Oncology, Poznan University of Medical Sciences, Poznan, Poland.

Vladimir Vladimirov (V)

Pyatigorsk Oncology Dispensary, State Healthcare Institute, Pyatigorsk, Russia.

Ying Cheng (Y)

Department of Oncology, Cancer Hospital of Jilin Province, Changchun, People's Republic of China.

Xuan Deng (X)

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

Ying Zhang (Y)

HTA Statistics Europe, Merck Sharp & Dohme, Brussels, Belgium.

Tuba Bas (T)

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

Bilal Piperdi (B)

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

Balazs Halmos (B)

Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York.

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Classifications MeSH