Outcomes to first-line pembrolizumab in patients with PD-L1-high (≥50%) non-small cell lung cancer and a poor performance status.


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
08 2020
Historique:
accepted: 27 06 2020
entrez: 6 8 2020
pubmed: 6 8 2020
medline: 16 9 2021
Statut: ppublish

Résumé

Patients with non-small cell lung cancer (NSCLC) and a poor Eastern Cooperative Oncology Group Performance Status (ECOG PS) have been excluded from phase III immunotherapy clinical trials. We sought to evaluate clinical outcomes to first-line pembrolizumab in patients with advanced NSCLC, a PD-L1 Tumor Proportion Score (TPS) of ≥50%, and an ECOG PS of 2. We performed a multicenter retrospective analysis of patients with metastatic NSCLC and a PD-L1 TPS of ≥50% (negative for genomic alterations in Among the 234 patients, 83.3% (n=195) had an ECOG PS of 0 or 1, and 16.7% (n=39) had an ECOG PS of 2. The baseline clinicopathological characteristics were balanced between the ECOG PS 0-1 vs 2 groups in terms of age, sex, tobacco use, histology, A subset of patients with NSCLC and an ECOG PS of 2 can respond to first-line pembrolizumab. However, clinical outcomes in this population are often poor and use of second-line systemic therapy is infrequent.

Sections du résumé

BACKGROUND
Patients with non-small cell lung cancer (NSCLC) and a poor Eastern Cooperative Oncology Group Performance Status (ECOG PS) have been excluded from phase III immunotherapy clinical trials. We sought to evaluate clinical outcomes to first-line pembrolizumab in patients with advanced NSCLC, a PD-L1 Tumor Proportion Score (TPS) of ≥50%, and an ECOG PS of 2.
METHODS
We performed a multicenter retrospective analysis of patients with metastatic NSCLC and a PD-L1 TPS of ≥50% (negative for genomic alterations in
RESULTS
Among the 234 patients, 83.3% (n=195) had an ECOG PS of 0 or 1, and 16.7% (n=39) had an ECOG PS of 2. The baseline clinicopathological characteristics were balanced between the ECOG PS 0-1 vs 2 groups in terms of age, sex, tobacco use, histology,
CONCLUSIONS
A subset of patients with NSCLC and an ECOG PS of 2 can respond to first-line pembrolizumab. However, clinical outcomes in this population are often poor and use of second-line systemic therapy is infrequent.

Identifiants

pubmed: 32753547
pii: jitc-2020-001007
doi: 10.1136/jitc-2020-001007
pmc: PMC7406027
pii:
doi:

Substances chimiques

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

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCI NIH HHS
ID : R25 CA020449
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL111024
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009207
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002384
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA209414
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA203636
Pays : United States

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MMA serves as a consultant to Merck, Bristol-Myers Squibb, Genentech, AstraZeneca, Nektar, Ariad, Maverick, Blueprint Medicine, Syndax, Abbvie, and Gridstone. Research Funding: Bristol-Myers Squibb, Lilly, Genentech and AstraZeneca. MA serves as scientific advisory boards for GSK and Shattuck Lab. Research funding: GSK, Bristol-Myers Squibb, Genentech, Nektar, Jounce, Lilly, Adaptimmune, Novartis. FH: consultant to Merck. JVH serves as consultant to AstraZeneca, Bristol-Myers Squibb, GlaxoSmithKline, Guardant Health, Kairos Venture Investments, BrightPath Biotherapeutics, Hengrui Therapeutics, Eli Lilly, Spectrum, EMD Serono, Roche, Foundation One Medicine. Research grant from NIH/NCI, American Cancer Society, Cancer Prevention & Research Institute of Texas, AACR Johnson & Johnson Lung Cancer, AstraZeneca, Spectrum, Checkmate Pharmaceuticals. Royalties from Bio-Tree Systems, Inc. In addition, Dr Heymach has a patent held by Spectrum with royalties paid. MN serves as consultant to Daiichi Sankyo. Research grant from Merck and AstraZeneca. Honorarium from Roche. NIH funding (R01CA203636, U01CA209414, R01HL111024). MDH: research funding from Bristol-Myers Squibb. Consultant to Merck, Bristol-Myers Squibb, AstraZeneca, Genentech/Roche, Immunai, Syndax, Mirati, Nektar, Blueprint, Archilles, Arcus, Pact Pharma and Shattuck Labs. A patent has been filed by MSK related to the use of tumor mutation burden to predict response to immunotherapy (PCT/US2015/062208), which has received licensing fees from PGDx.

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Auteurs

Joao V Alessi (JV)

Lowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.

Biagio Ricciuti (B)

Lowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.

Elizabeth Jiménez-Aguilar (E)

Department of Medical Oncology, Hospital Universitario 12 de Octubre, Madrid, Comunidad de Madrid, Spain.

Fangxin Hong (F)

Department of Data Sciences, Dana Farber Cancer Institute, Boston, Massachusetts, USA.

Zihan Wei (Z)

Department of Data Sciences, Dana Farber Cancer Institute, Boston, Massachusetts, USA.

Mizuki Nishino (M)

Department of Radiology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.

Andrew J Plodkowski (AJ)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Peter Sawan (P)

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Jia Luo (J)

Thoracic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Hira Rizvi (H)

Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Brett W Carter (BW)

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

John V Heymach (JV)

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

Mehmet Altan (M)

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

Matthew Hellmann (M)

Thoracic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Mark Awad (M)

Lowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA mark_awad@dfci.harvard.edu.

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Classifications MeSH