Pembrolizumab for advanced nonsmall cell lung cancer: Efficacy and safety in everyday clinical practice.


Journal

Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805

Informations de publication

Date de publication:
07 2019
Historique:
received: 11 02 2019
revised: 26 04 2019
accepted: 05 05 2019
entrez: 16 6 2019
pubmed: 16 6 2019
medline: 7 3 2020
Statut: ppublish

Résumé

While pembrolizumab improves overall survival (OS) in a subset of advanced nonsmall cell lung cancer (aNSCLC) patients (pts) in clinical trials, individuals with poor Eastern Cooperative Oncology Group performance status (ECOG PS) were excluded. Furthermore, some studies have identified a potential link between improved pt outcomes and development of immune related adverse events (irAE.) In a large provincial cohort, we studied the efficacy and safety of pembrolizumab for poor ECOG PS pts and whether irAE correlate with improved OS. aNSCLC pts treated with pembrolizumab between 06/2015 and 08/2018 at BC Cancer were retrospectively identified. Kaplan-Meier curves of OS from initiation of pembrolizumab were plotted. 3-, 6-, and 9- month landmark Kaplan-Meier analysis was performed and log-rank tests used to determine an association of irAE subtypes with OS. Multivariable logistic regression identified variables associated with grade ≥3 irAE within 3 months of pembrolizumab initiation. Of 190 pts, 74.2% were treatment naïve and 92.6% had PD-L1 expression ≥ 50%. Median OS in the 1st line and ≥2nd line settings were 24.3 months (95% CI, 9.7-not reached, NR) and 13.4 months (95% CI, 8.1-NR), respectively. Pts with ECOG PS 2/3 had lower median OS than if ECOG PS 0/1 (5.8 months vs. 16.7 months, p < 0.0001). In multivariable analysis, the odds of grade ≥ 3 irAE within 3 months was 6.3 fold higher if ECOG PS 2/3 versus 0/1 (p = 0.05). Development of pneumonitis at the 9 month landmark weakly correlated with decreased OS (p = 0.09). In the studied cohort, ECOG PS 2/3 pts had a significantly lower OS and greater odds of experiencing high-grade irAE than if ECOG PS 0/1. Development of irAE did not result in improved OS. Randomized trials to determine benefit of pembrolizumab for poor ECOG PS pts are needed.

Identifiants

pubmed: 31200816
pii: S0169-5002(19)30446-5
doi: 10.1016/j.lungcan.2019.05.005
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
pembrolizumab DPT0O3T46P

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

110-116

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Doran Ksienski (D)

BC Cancer- Victoria, British Columbia, Canada. Electronic address: dksienski@bccancer.bc.ca.

Elaine S Wai (ES)

BC Cancer- Victoria, British Columbia, Canada.

Nicole Croteau (N)

University of Victoria, British Columbia, Canada.

Ashley T Freeman (AT)

BC Cancer- Victoria, British Columbia, Canada.

Angela Chan (A)

BC Cancer- Surrey, British Columbia, Canada.

Leathia Fiorino (L)

BC Cancer- Victoria, British Columbia, Canada.

Edward G Brooks (EG)

BC Cancer- Victoria, British Columbia, Canada.

Zia Poonja (Z)

BC Cancer- Victoria, British Columbia, Canada.

David Fenton (D)

BC Cancer- Victoria, British Columbia, Canada.

Georgia Geller (G)

BC Cancer- Victoria, British Columbia, Canada.

Sarah Irons (S)

BC Cancer- Victoria, British Columbia, Canada.

Mary Lesperance (M)

University of Victoria, British Columbia, Canada.

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Classifications MeSH