Outcomes of Patients with Non-Small Cell Lung Cancer and Brain Metastases Treated with the Upfront Single Agent Pembrolizumab: A Retrospective and Multicentric Study of the ESCKEYP GFPC Cohort.

brain metastasis central nervous system immunotherapy non-small cell lung cancer real-life data

Journal

Current oncology (Toronto, Ont.)
ISSN: 1718-7729
Titre abrégé: Curr Oncol
Pays: Switzerland
ID NLM: 9502503

Informations de publication

Date de publication:
21 Mar 2024
Historique:
received: 11 02 2024
revised: 10 03 2024
accepted: 20 03 2024
medline: 27 3 2024
pubmed: 27 3 2024
entrez: 27 3 2024
Statut: epublish

Résumé

Non-small cell lung cancer (NSCLC) is the most common cause of brain metastasis (BM). Little is known about immune checkpoint inhibitor activity in the central nervous system, especially in patients receiving monotherapy for tumors with a tumor proportion score (TPS) ≥ 50%. This noninterventional, retrospective, multicenter study, conducted with the GFPC, included treatment-naïve patients strongly positive for PD-L1 (TPS ≥ 50%) with BM receiving first-line single-agent pembrolizumab treatment between May 2017 and November 2019. The primary endpoints were centrally reviewed intracranial overall response rates (ORRs), centrally reviewed intracranial progression-free survival (cPFS), extracranial PFS, and overall survival were secondary endpoints. Forty-three patients from five centers were included. Surgical or local radiation therapy was administered to 31 (72%) patients, mostly before initiating ICI therapy (25/31). Among 38/43 (88.4%) evaluable patients, the intracranial ORR was 73%. The median PFS was 8.3 months. The cerebral and extracerebral median PFS times were 9.2 and 5.3 months, respectively. The median OS was 25.5 months. According to multivariate analysis, BM surgery before ICI therapy was the only factor significantly associated with both improved PFS (HR = 0.44) and OS (HR = 0.45). This study revealed the feasibility and outcome of front-line pembrolizumab treatment in this population with BM.

Identifiants

pubmed: 38534959
pii: curroncol31030126
doi: 10.3390/curroncol31030126
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1656-1666

Auteurs

Simon Nannini (S)

Department of Oncology, Institut de Cancérologie Strasbourg Europe, 67200 Strasbourg, France.

Florian Guisier (F)

Department of Pneumology, UNIROUEN, LITIS Lab QuantIF Team EA4108, CHU Rouen, Normandie University, Rouen and Inserm CIC-CRB 1404, 76000 Rouen, France.

Hubert Curcio (H)

Department of Pneumology, Centre Régionale de Lutte Contre le Cancer François Baclesse, 14000 Caen, France.

Charles Ricordel (C)

Department of Pneumology, Centre Hospitalier Universitaire, 35000 Rennes, France.

Pierre Demontrond (P)

Department of Pneumology, Centre Régionale de Lutte Contre le Cancer François Baclesse, 14000 Caen, France.

Safa Abdallahoui (S)

Department of Oncology, Institut de Cancérologie Strasbourg Europe, 67200 Strasbourg, France.

Seyyid Baloglu (S)

Department of Radiological, Centre Hospitalier Universitaire de Strasbourg, 67200 Strasbourg, France.

Laurent Greillier (L)

Multidisciplinary Oncology and Therapeutic Innovations, APHM, INSERM, CNRS, CRCM, Hôpital Nord, Aix Marseille University, 13015 Marseille, France.

Christos Chouaid (C)

Department of Pneumology, Centre Hospitalier, 94000 Créteil, France.

Roland Schott (R)

Department of Oncology, Institut de Cancérologie Strasbourg Europe, 67200 Strasbourg, France.

Classifications MeSH