Real-world multicentre cohort of first-line pembrolizumab alone or in combination with platinum-based chemotherapy in non-small cell lung cancer PD-L1 ≥ 50.


Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 11 08 2022
accepted: 23 12 2022
medline: 22 5 2023
pubmed: 24 1 2023
entrez: 23 1 2023
Statut: ppublish

Résumé

Pembrolizumab alone (IO-mono) or in combination with platinum-based chemotherapy (CT-IO) is first-line standard of care for advanced non-small cell lung cancer (NSCLC) patients with PD-L1 ≥ 50%. This retrospective multicentre study assessed real-world use and efficacy of both strategies. Patients with advanced NSCLC PD-L1 ≥ 50% from eight hospitals who had received at least one cycle of IO-mono or CT-IO were included. Overall survival (OS) and real-word progression-free-survival were estimated using Kaplan-Meier methodology. Cox proportional hazards regression models were used to estimate hazard ratios (HRs) and 95% CIs, and a Cox model with inverse propensity treatment weighting was carried out. Among the 243 patients included, 141 (58%) received IO-mono and 102 (42%) CT-IO. Younger patients, those with symptomatic disease and brain metastases were more likely to be proposed CT-IO. With a median follow-up of 11.5 months (95% CI 10.4-13.3), median OS was not reached, but no difference was observed between groups (p = 0.51). Early deaths at 12 weeks were 11% (95% CI 4.6-16.9) and 15.2% (95% CI 9.0-20.9) in CT-IO and IO groups (p = 0.32). After adjustment for age, gender, performance status, histology, brain metastases, liver metastases and tobacco status, no statistically significant difference was found for OS between groups, neither in the multivariate adjusted model [HR 1.07 (95% CI 0.61-1.86), p = 0.8] nor in propensity adjusted analysis [HR 0.99 (95% CI 0.60-1.65), p = 0.99]. Male gender (HR 2.01, p = 0.01) and PS ≥ 2 (HR 3.28, p < 0.001) were found to be negative independent predictive factors for OS. Younger patients, those with symptomatic disease and brain metastases were more likely to be proposed CT-IO. However, sparing the chemotherapy in first-line does not appear to impact survival outcomes, even regarding early deaths.

Identifiants

pubmed: 36690799
doi: 10.1007/s00262-022-03359-2
pii: 10.1007/s00262-022-03359-2
pmc: PMC10198917
doi:

Substances chimiques

pembrolizumab DPT0O3T46P
Platinum 49DFR088MY
B7-H1 Antigen 0
Antineoplastic Agents, Immunological 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1881-1890

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2023. The Author(s).

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Auteurs

E Pons-Tostivint (E)

Centre Hospitalier Universitaire Nantes, Medical Oncology, Nantes University, 44000, Nantes, France. elvire.pons@chu-nantes.fr.

P Hulo (P)

Medical Oncology Unit, Clinique Mutualiste de L'Estuaire, Saint-Nazaire, France.

V Guardiolle (V)

Centre Hospitalier Universitaire Nantes, Institute of Health and Medical Research, Santé Publique, Clinique Des Données, Inserm CIC 1413, Centre Hospitalier Universitaire de Nantes, Nantes University, 44000, Nantes, France.

L Bodot (L)

Thoracic Oncology Department, Hôpital Larrey, CHU Toulouse, 31000, Toulouse, France.

A Rabeau (A)

Thoracic Oncology Department, Hôpital Larrey, CHU Toulouse, 31000, Toulouse, France.

M Porte (M)

Department of Medical Oncology, Comprehensive Cancer Center, Institut de Cancérologie de L'Ouest, Saint-Herblain, France.

S Hiret (S)

Department of Medical Oncology, Comprehensive Cancer Center, Institut de Cancérologie de L'Ouest, Saint-Herblain, France.

P Demontrond (P)

Department of Pneumology, Centre François Baclesse, Caen, France.

H Curcio (H)

Department of Pneumology, Centre François Baclesse, Caen, France.

A Boudoussier (A)

Department of Pneumology, University Hospital of Bordeaux, Pessac, France.

R Veillon (R)

Department of Pneumology, University Hospital of Bordeaux, Pessac, France.

M Mayenga (M)

Department of Medical Oncology, Hospital Foch, Suresnes, France.

C Dumenil (C)

Department of Respiratory Diseases and Thoracic Oncology, APHP-Hopital Ambroise Pare, 92100, Boulogne-Billancourt, France.

T Chatellier (T)

Medical Oncology Unit, Clinique Mutualiste de L'Estuaire, Saint-Nazaire, France.

P A Gourraud (PA)

Centre Hospitalier Universitaire Nantes, Institute of Health and Medical Research, Santé Publique, Clinique Des Données, Inserm CIC 1413, Centre Hospitalier Universitaire de Nantes, Nantes University, 44000, Nantes, France.

J Mazieres (J)

Thoracic Oncology Department, Hôpital Larrey, CHU Toulouse, 31000, Toulouse, France.

J Bennouna (J)

Department of Medical Oncology, Hospital Foch, Suresnes, France.

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Classifications MeSH