KEYNOTE-025: Phase 1b study of pembrolizumab in Japanese patients with previously treated programmed death ligand 1-positive advanced non-small-cell lung cancer.


Journal

Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 05 09 2018
revised: 19 12 2018
accepted: 24 12 2018
pubmed: 9 1 2019
medline: 9 3 2019
entrez: 9 1 2019
Statut: ppublish

Résumé

Pembrolizumab, a humanized monoclonal antibody against programmed death 1 (PD-1), has been shown to improve overall survival (OS) in patients with previously treated advanced non-small-cell lung cancer (NSCLC) with programmed death ligand 1 (PD-L1) tumor proportion score (TPS) ≥1%. We report safety and efficacy results from the phase 1b KEYNOTE-025 study, which evaluated pembrolizumab in Japanese patients with previously treated NSCLC. Eligible patients had histologically/cytologically confirmed advanced NSCLC with PD-L1 TPS ≥1% and had received ≥1 platinum-doublet chemotherapy. Patients received pembrolizumab 10 mg/kg once every 3 weeks for 2 years or until disease progression/unacceptable toxicity. Primary objectives were to evaluate the safety of pembrolizumab in patients with PD-L1 TPS ≥1% and the objective response rate (ORR) per RECIST version 1.1 in patients with PD-L1 TPS ≥50%. Thirty-eight patients were enrolled and received ≥1 pembrolizumab dose. The median (range) age was 66.0 (41-78) years, and 61% had received ≥2 prior systemic therapies. Eleven patients (29%) experienced grade 3-5 treatment-related adverse events (AE); 9 patients (24%) experienced immune-mediated AE and infusion reactions, with pneumonitis (11%; any grade) being most common. Among evaluable patients with PD-L1 TPS ≥50% (n = 11), ORR was 27% (95% CI, 6-61). Among evaluable patients with PD-L1 TPS ≥1% (n = 37), ORR was 22% (95% CI, 10-38). Median (95% CI) progression-free survival and OS were 3.9 (2.0-6.2) months and 19.2 (8.0-26.7) months, respectively. In summary, pembrolizumab was generally well tolerated and showed promising antitumor activity in Japanese patients with previously treated PD-L1-expressing NSCLC. Outcomes were consistent with those from the phase 3 KEYNOTE-010 study. (Trial registration number: ClinicalTrials.gov, NCT02007070.).

Identifiants

pubmed: 30618179
doi: 10.1111/cas.13932
pmc: PMC6398876
doi:

Substances chimiques

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

Banques de données

ClinicalTrials.gov
['NCT02007070']

Types de publication

Clinical Trial, Phase I Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1012-1020

Informations de copyright

© 2019 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.

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Auteurs

Makoto Nishio (M)

Department of Thoracic Medical Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.

Toshiaki Takahashi (T)

Division of Thoracic Oncology, Shizuoka Cancer Center, Suntogun, Japan.

Hiroshige Yoshioka (H)

Department of Respiratory Medicine, Kurashiki Central Hospital, Kurashiki, Japan.

Kazuhiko Nakagawa (K)

Department of Medical Oncology, Faculty of Medicine, Kindai University, Osaka-Sayama, Japan.

Tatsuro Fukuhara (T)

Department of Respiratory Medicine, Miyagi Cancer Center, Natori, Japan.

Kazuhiko Yamada (K)

Department of Internal Medicine, Division of Respirology, Neurology, and Rheumatology, Kurume University, Kurume, Japan.

Masao Ichiki (M)

Respiratory Medicine, Kyushu Medical Center, Fukuoka, Japan.

Hiroshi Tanaka (H)

Department of Internal Medicine (Pulmonology), Niigata Cancer Center Hospital, Niigata, Japan.

Takashi Seto (T)

Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka, Japan.

Hiroshi Sakai (H)

Thoracic Oncology, Saitama Cancer Center, Saitama, Japan.

Kazuo Kasahara (K)

Respiratory Medicine, Kanazawa University Hospital, Kanazawa, Japan.

Miyako Satouchi (M)

Department of Thoracic Oncology, Hyogo Cancer Center, Akashi, Japan.

Shi Rong Han (SR)

Oncology Science Unit, MSD K.K., Tokyo, Japan.

Kazuo Noguchi (K)

Oncology Science Unit, MSD K.K., Tokyo, Japan.

Takashi Shimamoto (T)

Oncology Science Unit, MSD K.K., Tokyo, Japan.

Terufumi Kato (T)

Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Yokohama, Japan.

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Classifications MeSH