Pembrolizumab Plus Ipilimumab or Placebo for Metastatic Non-Small-Cell Lung Cancer With PD-L1 Tumor Proportion Score ≥ 50%: Randomized, Double-Blind Phase III KEYNOTE-598 Study.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 07 2021
Historique:
pubmed: 30 1 2021
medline: 11 11 2021
entrez: 29 1 2021
Statut: ppublish

Résumé

Pembrolizumab monotherapy is standard first-line therapy for metastatic non-small-cell lung cancer (NSCLC) with programmed death ligand 1 (PD-L1) tumor proportion score (TPS) ≥ 50% without actionable driver mutations. It is not known whether adding ipilimumab to pembrolizumab improves efficacy over pembrolizumab alone in this population. In the randomized, double-blind, phase III KEYNOTE-598 trial (ClinicalTrials.gov identifier: NCT03302234), eligible patients with previously untreated metastatic NSCLC with PD-L1 TPS ≥ 50% and no sensitizing Of the 568 participants, 284 were randomly allocated to each group. Median overall survival was 21.4 months for pembrolizumab-ipilimumab versus 21.9 months for pembrolizumab-placebo (hazard ratio, 1.08; 95% CI, 0.85 to 1.37; Adding ipilimumab to pembrolizumab does not improve efficacy and is associated with greater toxicity than pembrolizumab monotherapy as first-line treatment for metastatic NSCLC with PD-L1 TPS ≥ 50% and no targetable

Identifiants

pubmed: 33513313
doi: 10.1200/JCO.20.03579
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
B7-H1 Antigen 0
CD274 protein, human 0
Ipilimumab 0
pembrolizumab DPT0O3T46P

Banques de données

ClinicalTrials.gov
['NCT03302234']

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

2327-2338

Commentaires et corrections

Type : CommentIn

Auteurs

Michael Boyer (M)

Chris O'Brien Lifehouse, Camperdown, NSW, Australia.

Mehmet A N Şendur (MAN)

Ankara Yıldırım Beyazıt University, Faculty of Medicine and Ankara City Hospital, Ankara, Turkey.

Delvys Rodríguez-Abreu (D)

Complejo Hospitalario Universitario Insular Materno-Infantil de Gran Canaria, Universidad de Las Palmas de Gran Canaria, Las Palmas de Gran Canaria, Spain.

Keunchil Park (K)

Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Dae Ho Lee (DH)

Asan Medical Center, Seoul, South Korea.

Irfan Çiçin (I)

Trakya University, Erdine, Turkey.

Perran Fulden Yumuk (PF)

Marmara University School of Medicine, Istanbul, Turkey.

Francisco J Orlandi (FJ)

Orlandi-Oncología, Providencia, Chile.

Ticiana A Leal (TA)

University of Wisconsin Carbone Cancer Center, Madison, WI.

Olivier Molinier (O)

Hospital of Le Mans, Le Mans, France.

Nopadol Soparattanapaisarn (N)

Mahidol University, Sriraj Hospital, Bangkok, Thailand.

Adrian Langleben (A)

St Mary's Hospital - ODIM, McGill University Department of Oncology, Montreal, QC, Canada.

Raffaele Califano (R)

The Christie NHS Foundation Trust, and Division of Cancer Sciences, The University of Manchester, Manchester, UK.

Balazs Medgyasszay (B)

Veszprém Megyei Tüdőgyógyintézet Farkasgyepű, Farkasgyepű, Hungary.

Te-Chun Hsia (TC)

China Medical University and China Medical University Hospital, Taichung, Taiwan.

Gregory A Otterson (GA)

The Ohio State University-James Comprehensive Cancer Center, Columbus, OH.

Lu Xu (L)

Merck & Co, Inc, Kenilworth, NJ.

Bilal Piperdi (B)

Merck & Co, Inc, Kenilworth, NJ.

Ayman Samkari (A)

Merck & Co, Inc, Kenilworth, NJ.

Martin Reck (M)

LungenClinic, Airway Research Center North, German Center for Lung Research, Grosshansdorf, Germany.

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Classifications MeSH