Immune-Checkpoint Inhibitors in Advanced Non-Small Cell Lung Cancer With Uncommon Histology

•Efficacy of Immune-checkpoint inhibitors (ICIs) in non-small cell lung cancer with uncommon histology is an unmet need.•Our findings highlight no progression-free survival and overall survival difference compared to common histotypes•Further prospective trials are needed to clarify ICIs role in unc...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical lung cancer 2022-01, Vol.23 (1), p.e17-e28
Hauptverfasser: Manglaviti, Sara, Brambilla, Marta, Signorelli, Diego, Ferrara, Roberto, Lo Russo, Giuseppe, Proto, Claudia, Galli, Giulia, De Toma, Alessandro, Occhipinti, Mario, Viscardi, Giuseppe, Beninato, Teresa, Zattarin, Emma, Bini, Marta, Lobefaro, Riccardo, Massa, Giacomo, Bottiglieri, Achille, Apollonio, Giulia, Sottotetti, Elisa, Di Mauro, Rosa Maria, Trevisan, Benedetta, Ganzinelli, Monica, Fabbri, Alessandra, de Braud, Filippo G.M., Garassino, Marina Chiara, Prelaj, Arsela
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•Efficacy of Immune-checkpoint inhibitors (ICIs) in non-small cell lung cancer with uncommon histology is an unmet need.•Our findings highlight no progression-free survival and overall survival difference compared to common histotypes•Further prospective trials are needed to clarify ICIs role in uncommon histotypes.•Combination of ICIs and chemotherapy should be explored in uncommon histologies with a more aggressive behavior. Immune-checkpoint inhibitors (ICIs) have significantly improved outcome of advanced non-small cell lung cancer (aNSCLC) patients. However, their efficacy remains uncertain in uncommon histologies (UH). Data from ICI treated aNSCLC patients (April,2013-January,2021) in one Institution were retrospectively collected. Univariate and multivariate survival analyses were estimated by Kaplan-Meier and Cox proportional hazards regression model, respectively. Objective response rate (ORR) and disease control rate (DCR) were assessed. Of 375 patients, 79 (21.1%) had UH: 19 (24.1%) sarcomatoid carcinoma, 15 (19.0%) mucinous adenocarcinoma, 10 (12.6%) enteric adenocarcinoma, 8 (10.1%) adenocarcinoma not otherwise specified, 7 (8.9%) large-cell neuroendocrine carcinoma, 6 (7.6%) mixed histology non-adenosquamous, 5 (6.3%) adenosquamous carcinoma, 9 (11.4%) other UH. In UH group, programmed death-ligand 1 (PD-L1)
ISSN:1525-7304
1938-0690
DOI:10.1016/j.cllc.2021.06.013