Efficacy and Safety of Anti-PD-1 Immunotherapy in Patients Aged ≥ 75 Years With Non-small-cell Lung Cancer (NSCLC): An Italian, Multicenter, Retrospective Study.


Journal

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

Informations de publication

Date de publication:
11 2020
Historique:
received: 28 10 2019
revised: 28 03 2020
accepted: 06 05 2020
pubmed: 28 6 2020
medline: 12 10 2021
entrez: 28 6 2020
Statut: ppublish

Résumé

Non-small-cell lung cancer (NSCLC) is predominantly a disease of the elderly population. Over the past few years, immunotherapy with monoclonal antibodies named checkpoint inhibitors (ICIs) greatly improved the clinical management of a significant proportion of patients with metastatic NSCLC. However, pivotal trials excluded older patients, although, given the favorable clinical profile of ICIs, this treatment may be revealed to be a most valuable option also for these patients. To this aim, a multicenter retrospective analysis was performed on patients aged ≥ 75 years with NSCLC treated with anti-programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) immunotherapy. Inclusion criteria were: diagnosis of locally advanced or metastatic NSCLC (stage IIIB or IV, according to the American Joint Committee on Cancer (AJCC) classification system, version 8.0); age ≥ 75 years; treatment with anti-PD-1/PD-L1 monoclonal antibodies in first or subsequent lines of treatment; absence of epidermal growth factor receptor-activating mutations or anaplastic lymphoma kinase and ROS-1 rearrangements. The primary endpoints of the study were the efficacy, in terms of overall response rate, progression-free survival, and overall survival, and safety, by means of evaluations of the incidence of immune-related adverse events. Eighty-six patients were considered for the final analysis; 71 (82.6%) were male. The mean age was 78.5 years (range, 75-86 years; SD, 3.12 years). Of the 86 patients, 69 (80.2%) of patients had a performance status of 0 or 1. The overall median progression-free survival was 5.6 months (range 1-36 months; SD, 7.5 months,) whereas the median overall survival was 10.1 months (range, 1.7-34.8 months; SD, 8 months). At the Cox regression analysis, the only parameter significantly associated with survival was the smoking status (P = .008). No difference in survival was found between patients younger and older than 80 years. In the present real-world retrospective cohort, efficacy and toxicity profiles of ICIs in older patients with advanced NSCLC were comparable with those observed in younger patients enrolled in clinical trials.

Identifiants

pubmed: 32591311
pii: S1525-7304(20)30144-3
doi: 10.1016/j.cllc.2020.05.004
pii:
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
B7-H1 Antigen 0
CD274 protein, human 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e567-e571

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Andrea Luciani (A)

Medical Oncology Unit, ASST Santi Paolo e Carlo, Università̀ di Milano, Milan, Italy. Electronic address: andrea.luciani@asst.santipaolocarlo.it.

Antonio Marra (A)

Medical Oncology Unit, ASST Santi Paolo e Carlo, Università̀ di Milano, Milan, Italy.

Luca Toschi (L)

Medical Oncology Unit, Humanitas Cancer Center, Rozzano, Italy.

Diego Cortinovis (D)

Medical Oncology Unit, ASST Monza, Ospedale San Gerardo, Monza, Italy.

Sergio Fava (S)

Medical Oncology Unit, ASST Ovest Milanese, Legnano, Milan, Italy.

Virginio Filipazzi (V)

Medical Oncology Unit, ASST FBF-Sacco, Milan, Italy.

Alessandro Tuzi (A)

Medical Oncology Unit, ASST Settelaghi, Varese, Italy.

Giulio Cerea (G)

Medical Oncology, Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, Milan, Italy; Dipartimento di Oncologia e Emato-Oncologia, Università degli Studi di Milano, Milan, Italy.

Sabrina Rossi (S)

Medical Oncology Unit, Humanitas Cancer Center, Rozzano, Italy.

Vittorio Perfetti (V)

Internal Medicine Unit, Oncologia Oltrepò, Ospedale di Varzi, ASST Pavia, Pavia, Italy.

Antonio Rossi (A)

Medical Oncology Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo (FG), Italy.

Laura Giannetta (L)

Medical Oncology, Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, Milan, Italy; Dipartimento di Oncologia e Emato-Oncologia, Università degli Studi di Milano, Milan, Italy.

Luca Sala (L)

Medical Oncology Unit, ASST Monza, Ospedale San Gerardo, Monza, Italy.

Giovanna Finocchiaro (G)

Medical Oncology Unit, Humanitas Cancer Center, Rozzano, Italy.

Elio Gregory Pizzutilo (EG)

Medical Oncology, Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, Milan, Italy; Dipartimento di Oncologia e Emato-Oncologia, Università degli Studi di Milano, Milan, Italy.

Stephana Carelli (S)

Department of Pharmacology, University of Milan, Milan Italy.

Francesco Agustoni (F)

Medical Oncology Unit, ASST Monza, Ospedale San Gerardo, Monza, Italy.

Massimiliano Cergnul (M)

Medical Oncology Unit, ASST Ovest Milanese, Legnano, Milan, Italy.

Sabrina Zonato (S)

Medical Oncology Unit, ASST Santi Paolo e Carlo, Università̀ di Milano, Milan, Italy.

Salvatore Siena (S)

Medical Oncology, Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, Milan, Italy; Dipartimento di Oncologia e Emato-Oncologia, Università degli Studi di Milano, Milan, Italy.

Paolo Bidoli (P)

Medical Oncology Unit, ASST Monza, Ospedale San Gerardo, Monza, Italy.

Daris Ferrari (D)

Medical Oncology Unit, ASST Santi Paolo e Carlo, Università̀ di Milano, Milan, Italy.

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