TY - JOUR
T1 - Efficacy of Immune Checkpoint Inhibitors in Lung Sarcomatoid Carcinoma
AU - Domblides, Charlotte
AU - Leroy, Karen
AU - Monnet, Isabelle
AU - Mazières, Julien
AU - Barlesi, Fabrice
AU - Gounant, Valérie
AU - Baldacci, Simon
AU - Mennecier, Bertrand
AU - Toffart, Anne Claire
AU - Audigier-Valette, Clarisse
AU - Doucet, Ludovic
AU - Giroux-Leprieur, Etienne
AU - Guisier, Florian
AU - Ricordel, Charles
AU - Molinier, Olivier
AU - Perol, Maurice
AU - Pichon, Eric
AU - Robinet, Gilles
AU - Templement-Grangerat, Dorine
AU - Ruppert, Anne Marie
AU - Rabbe, Nathalie
AU - Antoine, Martine
AU - Wislez, Marie
N1 - Publisher Copyright:
© 2020 International Association for the Study of Lung Cancer
PY - 2020/5/1
Y1 - 2020/5/1
N2 - 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.
AB - 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.
KW - Immune check point inhibitor
KW - PD-L1
KW - Pulmonary sarcomatoid carcinoma
KW - Tumor mutational burden
UR - http://www.scopus.com/inward/record.url?scp=85079902167&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2020.01.014
DO - 10.1016/j.jtho.2020.01.014
M3 - Article
C2 - 31991225
AN - SCOPUS:85079902167
SN - 1556-0864
VL - 15
SP - 860
EP - 866
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 5
ER -