Efficacy of Immune Checkpoint Inhibitors in Lung Sarcomatoid Carcinoma

Charlotte Domblides, Karen Leroy, Isabelle Monnet, Julien Mazières, Fabrice Barlesi, Valérie Gounant, Simon Baldacci, Bertrand Mennecier, Anne Claire Toffart, Clarisse Audigier-Valette, Ludovic Doucet, Etienne Giroux-Leprieur, Florian Guisier, Charles Ricordel, Olivier Molinier, Maurice Perol, Eric Pichon, Gilles Robinet, Dorine Templement-Grangerat, Anne Marie RuppertNathalie Rabbe, Martine Antoine, Marie Wislez

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

92 Citations (Scopus)

Résumé

Introduction: Immune checkpoint inhibitors (ICIs) have improved cancer prognosis but have not been evaluated specifically in sarcomatoid carcinoma (SC), a rare lung cancer subtype with poor prognosis. As such, our study sought to retrospectively assess the efficacy of ICI in SC. Methods: All consecutive patients with centrally confirmed SC treated using ICI as a second-line treatment or beyond between 2011 and 2017 were enrolled. Programmed death-ligand 1 (PD-L1) tumor expression was assessed using immunohistochemistry (SP263 clone) and the tumor mutational burden (TMB) with the Foundation One panel. TMB was considered high if it was greater than or equal to 10 mutations per megabase. Results: Overall, 37 patients with SC were evaluated, predominantly men (73%) with a median age of 63.2 years (36.8–79.7) and who were current or former smokers (94.6%). Immunotherapy (nivolumab, 86.5% of cases) was given as a second-line treatment in 54% of the patients and as third-line treatment or beyond in 46% of the patients. The objective response rate was 40.5% and disease control rate was 64.8%, regardless of PD-L1 status. Median overall survival was 12.7 months (range: 0.3–45.7). One-third of patients exhibited early progression. The median PD-L1 expression was 70% (0–100). There was a trend toward higher PD-L1 expression in responsive diseases, with an objective response rate of 58.8% in patients with PD-L1+ and 0% in the one patient with PD-L1- (p = 0.44). The median TMB was 18 (4–39) mutations per megabase, with 87.5% of the cases displaying a high TMB. There was a trend toward higher TMB in responders versus stable or progressive diseases (p = 0.2). Conclusions: Patients with SC exhibited high response rates and prolonged overall survival under ICI treatment. These data support the prospective investigation of ICI in patients with SC who are under first-line treatment.

langue originaleAnglais
Pages (de - à)860-866
Nombre de pages7
journalJournal of Thoracic Oncology
Volume15
Numéro de publication5
Les DOIs
étatPublié - 1 mai 2020
Modification externeOui

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