Immune Checkpoint Inhibitors Rechallenge Efficacy in Non-Small-Cell Lung Cancer Patients.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
09 2020
Historique:
received: 30 01 2020
revised: 26 03 2020
accepted: 23 04 2020
pubmed: 2 7 2020
medline: 12 10 2021
entrez: 2 7 2020
Statut: ppublish

Résumé

Immune checkpoint inhibitor (ICPi) rechallenge could represent an attractive option in non-small-cell lung cancer (NSCLC), yet no sufficient data supporting this strategy are available. This retrospective observational multicenter national study explored the efficacy of anti-programmed cell death 1 (PD-1)/programmed death ligand 1 (PD-L1) rechallenge in advanced NSCLC patients, looking for potential clinical features associated with greater outcomes. We retrospectively collected data from 144 advanced NSCLC patients whose disease was rechallenged with ICPis after ≥ 12 weeks of discontinuation. The progression-free survival (PFS) and overall survival (OS) were calculated from first or second ICPi initiation to disease progression (PFS1 and PFSR, respectively), death, or last follow-up (OS1, OSR), respectively. The median (interquartile range) age was 63 (58-70) years. Most patients were male (67%) and smokers (87%). Most had adenocarcinomas (62%) and/or stage IV disease at diagnosis (66%). The best response at rechallenge was not associated with that under the first ICPi (P = 1.10 Patients discontinuing first ICPi because of toxicity or clinical decision, those able to maintain a treatment-free period, and those with good performance status may be potential candidates for rechallenge.

Sections du résumé

BACKGROUND
Immune checkpoint inhibitor (ICPi) rechallenge could represent an attractive option in non-small-cell lung cancer (NSCLC), yet no sufficient data supporting this strategy are available. This retrospective observational multicenter national study explored the efficacy of anti-programmed cell death 1 (PD-1)/programmed death ligand 1 (PD-L1) rechallenge in advanced NSCLC patients, looking for potential clinical features associated with greater outcomes.
PATIENTS AND METHODS
We retrospectively collected data from 144 advanced NSCLC patients whose disease was rechallenged with ICPis after ≥ 12 weeks of discontinuation. The progression-free survival (PFS) and overall survival (OS) were calculated from first or second ICPi initiation to disease progression (PFS1 and PFSR, respectively), death, or last follow-up (OS1, OSR), respectively.
RESULTS
The median (interquartile range) age was 63 (58-70) years. Most patients were male (67%) and smokers (87%). Most had adenocarcinomas (62%) and/or stage IV disease at diagnosis (66%). The best response at rechallenge was not associated with that under the first ICPi (P = 1.10
CONCLUSION
Patients discontinuing first ICPi because of toxicity or clinical decision, those able to maintain a treatment-free period, and those with good performance status may be potential candidates for rechallenge.

Identifiants

pubmed: 32605892
pii: S1525-7304(20)30136-4
doi: 10.1016/j.cllc.2020.04.013
pii:
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e497-e510

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Elisa Gobbini (E)

Thoracic Oncology Unit SHUPP, CHU Grenoble-Alpes, Grenoble, France; Cancer Research Center Lyon, Center Léon Bérard, Lyon, France. Electronic address: EGobbini@chu-grenoble.fr.

Anne Claire Toffart (AC)

Thoracic Oncology Unit SHUPP, CHU Grenoble-Alpes, Grenoble, France.

Maurice Pérol (M)

Department of Medical Oncology, Léon Bérard Cancer Center, Lyon, France.

Jean-Baptiste Assié (JB)

Thoracic Oncology Unit, CHU Créteil, Paris, France.

Michaël Duruisseaux (M)

Unité de Recherche Commune en Oncologie Thoracique (URCOT), Hospices Civils de Lyon Cancer Institute, Lyon, France; Anticancer Antibodies Laboratory, Cancer Research Center of Lyon, Inserm 1052, CNRS 5286, Lyon, France; Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France.

Dahna Coupez (D)

Thoracic Oncology Unit, CHU Nantes, Nantes, France.

Catherine Dubos (C)

Thoracic Oncology Unit, Center François Baclesse, Caen, France.

Virginie Westeel (V)

Thoracic Oncology Unit, CH Besançon, Besançon, France.

Myriam Delaunay (M)

Pulmonology Department, CHU Toulouse, Toulouse, France.

Florian Guisier (F)

Pneumology, Thoracic Oncology, and Respiratory Intensive Care Unit, CHU Rouen, Rouen, France.

Rémi Veillon (R)

Respiratory Diseases Department, F-33000, CHU Bordeaux, Bordeaux, France.

Valérie Gounant (V)

Thoracic Oncology Department, CIC 1425 INSERM, Center Bichat, Paris, France.

Etienne Giroux Leprieur (E)

Department of Respiratory Diseases and Thoracic Oncology, APHP-Hôpital Ambroise Pare, Paris, France.

François-Roger Vanel (FR)

Thoracic Oncology Unit, CHU Strasbourg, Strasbourg, France.

Nouha Chaabane (N)

Pulmonology Service, AP-HP Paris Center University Hospitals, Cochin Hospital, Paris, France.

Eric Dansin (E)

Thoracic Oncology Unit, Center Oscar Lambret, Lille, France.

Hélène Babey (H)

Thoracic Oncology Unit, CHRU Brest, Brest, France.

Chantal Decroisette (C)

Pulmonology and Thoracic Oncology Unit, CH Annecy-Genevois, Annecy, France.

Fabrice Barlesi (F)

Aix-Marseille Université, CNRS, INSERM, CRCM, APHM, Marseille, France.

Catherine Daniel (C)

Thoracic Oncology Unit, Institute Curie, Paris/Saint Cloud, France.

Pierre Fournel (P)

Medical Oncology Department, Institut de Cancérologie de la Loire, Saint, France.

Laura Mezquita (L)

Department of Medical Oncology, Thoracic Group, Gustave Roussy, Villejuif, France.

Youssef Oulkhouir (Y)

Pulmonology and Thoracic Oncology Unit, CHU Caen, Caen, France.

Anthony Canellas (A)

Pulmonology Unit, APHP Hôpital Tenon and GRC 04 Theranoscan Sorbonne University, Paris, France.

Boris Duchemann (B)

Thoracic Oncology Unit, Center Bobigny, Paris, France.

Olivier Molinier (O)

Thoracic Oncology Unit, CH Le Mans, Le Mans, France.

Vincent Alcazer (V)

Cancer Research Center Lyon, Center Léon Bérard, Lyon, France.

Denis Moro-Sibilot (D)

Thoracic Oncology Unit SHUPP, CHU Grenoble-Alpes, Grenoble, France.

Matteo Giaj Levra (MG)

Thoracic Oncology Unit SHUPP, CHU Grenoble-Alpes, Grenoble, France.

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