Immunotherapy rechallenge after nivolumab treatment in advanced non-small cell lung cancer in the real-world setting: A national data base analysis.


Journal

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

Informations de publication

Date de publication:
02 2020
Historique:
received: 24 10 2019
revised: 20 12 2019
accepted: 30 12 2019
pubmed: 9 1 2020
medline: 7 4 2021
entrez: 9 1 2020
Statut: ppublish

Résumé

Nivolumab is now a reference treatment for patients with advanced non-small cell lung cancer (NSCLC) after failure of prior platinum-based chemotherapy. Little data are available on treatment approaches following discontinuation of nivolumab and on the interest of a second course of immunotherapy after nivolumab discontinuation. The aims of this study were to describe treatment pathways following nivolumab discontinuation and to describe survival following retreatment with immunotherapy. The analysis includes all patients with NSCLC recorded in a national hospital database, starting nivolumab in 2015-2016. Nivolumab treatment was considered discontinued if ≥3 infusions were missed. Patients starting a second course of PD-1 inhibitor following nivolumab discontinuation were analysed according to the duration of their initial nivolumab treatment course. 10,452 patients were included (71 % men; mean age: 63.8 ± 9.6 years; squamous histology: 44 %). Median nivolumab treatment duration was 2.8 months [IQR :1.4-6.9]. Median OS was 11.5 months [95 %CI: 11.1-11.9]; 5118 (53.4 %) patients received post nivolumab therapy lines: 1517 (29.6 %) of these received a second course of PD-1 inhibitor, either after a treatment-free interval (resumption: n = 1127) or after intervening chemotherapy (rechallenge: n = 390). Median OS after nivolumab discontinuation was 15.0 months [13.9-16.7] in the resumption group and 18.4 months [14.8-21.9] in the rechallenge group. Median OS was significantly longer in patients with an initial nivolumab treatment duration ≥3 months. In this real-world setting, outcome after retreatment with a PD-1 inhibitor following a first course of nivolumab was significantly better in patients with a longer duration of initial nivolumab treatment.

Identifiants

pubmed: 31911324
pii: S0169-5002(19)30785-8
doi: 10.1016/j.lungcan.2019.12.017
pii:
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Nivolumab 31YO63LBSN

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

99-106

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Matteo Giaj Levra (M)

Thoracic Oncology Unit, Centre Hospitalier Universitaire Grenoble Alpes (CHUGA), Grenoble, France; Institute For Advanced Biosciences INSERM U1209 CNRS UMR5309 Université Grenoble Alpes, Grenoble, France.

François-Emery Cotté (FE)

Bristol-Myers Squibb France, Rueil Malmaison, France. Electronic address: Francois-Emery.Cotte@bms.com.

Romain Corre (R)

CHU Rennes Hôpital Pontchaillou, Rennes, France.

Christophe Calvet (C)

Bristol-Myers Squibb France, Rueil Malmaison, France.

Anne-Françoise Gaudin (AF)

Bristol-Myers Squibb France, Rueil Malmaison, France.

John R Penrod (JR)

Bristol-Myers Squibb France, Rueil Malmaison, France.

Valentine Grumberg (V)

Pharmacy Faculty Université Grenoble Alpes, Grenoble, France.

Baptiste Jouaneton (B)

HEVA, Lyon, France.

Ronan Jolivel (R)

HEVA, Lyon, France.

Jean-Baptiste Assié (JB)

GRC OncoThoParisEst, Service de Pneumologie, CHI Créteil, UPEC, Créteil, France; Centre de Recherche des Cordeliers, Sorbonne Universités, Inserm, UMRS-1138, Paris, France.

Christos Chouaïd (C)

GRC OncoThoParisEst, Service de Pneumologie, CHI Créteil, UPEC, Créteil, France.

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Classifications MeSH