Pembrolizumab Plus Chemotherapy for Metastatic Non-Small-Cell Lung Cancer With Programmed Cell Death Ligand 1 Tumor Proportion Score Less Than 1%: Pooled Analysis of Outcomes After 5 Years of Follow-Up.

PD-L1–negative non‒small-cell lung cancer pembrolizumab pooled analysis

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:
18 Apr 2024
Historique:
received: 26 02 2024
revised: 11 04 2024
accepted: 14 04 2024
medline: 21 4 2024
pubmed: 21 4 2024
entrez: 20 4 2024
Statut: aheadofprint

Résumé

We report long-term outcomes from a pooled analysis of patients with previously untreated metastatic non‒small-cell lung cancer (NSCLC) with programmed cell death ligand 1 (PD-L1) tumor proportion score (TPS) <1% enrolled in phase 3 studies of pembrolizumab plus chemotherapy versus placebo plus chemotherapy. This exploratory pooled analysis included individual patient data from the KEYNOTE-189 global (NCT02578680) and Japan extension (NCT03950674) studies of metastatic nonsquamous NSCLC without EGFR or ALK alterations and the KEYNOTE-407 global (NCT02775435) and China extension (NCT03875092) studies of metastatic squamous NSCLC. Patients received pembrolizumab or placebo plus pemetrexed and cisplatin or carboplatin in KEYNOTE-189 and pembrolizumab or placebo plus carboplatin and paclitaxel or nab-paclitaxel in KEYNOTE-407. PD-L1 TPS was centrally assessed using PD-L1 IHC 22C3 pharmDX (Agilent Technologies, Carpinteria, CA). Overall, 442 patients were included in this analysis (pembrolizumab plus chemotherapy, n=255; chemotherapy, n=187). Median follow-up was 60.7 (range, 49.9‒72.0) months. Pembrolizumab plus chemotherapy improved overall survival (OS; hazard ratio [HR], 0.64; 95% CI, 0.51‒0.79) and progression-free survival (HR, 0.66; 95% CI, 0.54‒0.81) versus chemotherapy. Five-year OS rates (95% CI) were 12.5% (8.6%‒17.3%) versus 9.3% (5.6%‒14.1%). Grade 3‒5 treatment-related adverse events occurred in 59.1% of patients for pembrolizumab plus chemotherapy and 61.3% for chemotherapy. With ∼5 years of follow-up, pembrolizumab plus chemotherapy provided clinically meaningful and durable improvements in survival outcomes versus chemotherapy alone in patients with previously untreated metastatic NSCLC with PD-L1 TPS <1%. These results continue to support pembrolizumab plus chemotherapy as a standard of care in this patient population.

Sections du résumé

BACKGROUND BACKGROUND
We report long-term outcomes from a pooled analysis of patients with previously untreated metastatic non‒small-cell lung cancer (NSCLC) with programmed cell death ligand 1 (PD-L1) tumor proportion score (TPS) <1% enrolled in phase 3 studies of pembrolizumab plus chemotherapy versus placebo plus chemotherapy.
METHODS METHODS
This exploratory pooled analysis included individual patient data from the KEYNOTE-189 global (NCT02578680) and Japan extension (NCT03950674) studies of metastatic nonsquamous NSCLC without EGFR or ALK alterations and the KEYNOTE-407 global (NCT02775435) and China extension (NCT03875092) studies of metastatic squamous NSCLC. Patients received pembrolizumab or placebo plus pemetrexed and cisplatin or carboplatin in KEYNOTE-189 and pembrolizumab or placebo plus carboplatin and paclitaxel or nab-paclitaxel in KEYNOTE-407. PD-L1 TPS was centrally assessed using PD-L1 IHC 22C3 pharmDX (Agilent Technologies, Carpinteria, CA).
RESULTS RESULTS
Overall, 442 patients were included in this analysis (pembrolizumab plus chemotherapy, n=255; chemotherapy, n=187). Median follow-up was 60.7 (range, 49.9‒72.0) months. Pembrolizumab plus chemotherapy improved overall survival (OS; hazard ratio [HR], 0.64; 95% CI, 0.51‒0.79) and progression-free survival (HR, 0.66; 95% CI, 0.54‒0.81) versus chemotherapy. Five-year OS rates (95% CI) were 12.5% (8.6%‒17.3%) versus 9.3% (5.6%‒14.1%). Grade 3‒5 treatment-related adverse events occurred in 59.1% of patients for pembrolizumab plus chemotherapy and 61.3% for chemotherapy.
CONCLUSION CONCLUSIONS
With ∼5 years of follow-up, pembrolizumab plus chemotherapy provided clinically meaningful and durable improvements in survival outcomes versus chemotherapy alone in patients with previously untreated metastatic NSCLC with PD-L1 TPS <1%. These results continue to support pembrolizumab plus chemotherapy as a standard of care in this patient population.

Identifiants

pubmed: 38642841
pii: S1556-0864(24)00169-2
doi: 10.1016/j.jtho.2024.04.011
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Shirish M Gadgeel (SM)

Karmanos Cancer Institute, Detroit, MI, USA;. Electronic address: sgadgee1@hfhs.org.

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;. Electronic address: delvysra@yahoo.com.

Balazs Halmos (B)

Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY, USA;. Electronic address: bahalmos@montefiore.org.

Marina C Garassino (MC)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy;. Electronic address: mgarassino@medicine.bsd.uchicago.edu.

Takayasu Kurata (T)

Department of Thoracic Oncology, Kansai Medical University Hospital, Osaka, Japan;. Electronic address: kuratat@hirakata.kmu.ac.jp.

Ying Cheng (Y)

Department of Oncology, Jilin Cancer Hospital, Changchun, China;. Electronic address: jl.cheng@163.com.

Erin Jensen (E)

Merck & Co., Inc., Rahway, NJ, USA;. Electronic address: erin_jensen2@merck.com.

Mark Shamoun (M)

Merck & Co., Inc., Rahway, NJ, USA;. Electronic address: mark.shamoun@merck.com.

Kumar Rajagopalan (K)

Merck & Co., Inc., Rahway, NJ, USA;. Electronic address: kumar.rajagopalan@merck.com.

Luis Paz-Ares (L)

Medical Oncology Department, Hospital Universitario 12 de Octubre, Universidad Complutense & Ciberonc, Madrid, Spain. Electronic address: lpazaresr@seom.org.

Classifications MeSH