TY - JOUR
T1 - Chemotherapy in non-small cell lung cancer patients after prior immunotherapy: The multicenter retrospective CLARITY study
AU - Bersanelli, Melissa
AU - Buti, Sebastiano
AU - Giannarelli, Diana
AU - Leonetti, Alessandro
AU - Cortellini, Alessio
AU - Russo, Giuseppe Lo
AU - Signorelli, Diego
AU - Toschi, Luca
AU - Milella, Michele
AU - Pilotto, Sara
AU - Bria, Emilio
AU - Proto, Claudia
AU - Marinello, Arianna
AU - Randon, Giovanni
AU - Rossi, Sabrina
AU - Vita, Emanuele
AU - Sartori, Giulia
AU - D'Argento, Ettore
AU - Qako, Eva
AU - Giaiacopi, Elisa
AU - Ghilardi, Laura
AU - Bettini, Anna Cecilia
AU - Rapacchi, Elena
AU - Mazzoni, Francesca
AU - Lavacchi, Daniele
AU - Scotti, Vieri
AU - Ciccone, Lucia Pia
AU - De Tursi, Michele
AU - Di Marino, Pietro
AU - Santini, Daniele
AU - Russano, Marco
AU - Bordi, Paola
AU - Di Maio, Massimo
AU - Audisio, Marco
AU - Filetti, Marco
AU - Giusti, Raffaele
AU - Berardi, Rossana
AU - Fiordoliva, Ilaria
AU - Cerea, Giulio
AU - Pizzutilo, Elio Gregory
AU - Bearz, Alessandra
AU - De Carlo, Elisa
AU - Cecere, Fabiana
AU - Renna, Davide
AU - Camisa, Roberta
AU - Caruso, Giuseppe
AU - Ficorella, Corrado
AU - Banna, Giuseppe Luigi
AU - Cortinovis, Diego
AU - Brighenti, Matteo
AU - Garassino, Marina Chiara
AU - Tiseo, Marcello
N1 - Place: Ireland
PY - 2020/12/1
Y1 - 2020/12/1
N2 - OBJECTIVES: In the most of cases, for non-small cell lung cancer (NSCLC) patients who progressed to previous immune checkpoint inhibitors (CKI) administered as first- or as second-line therapy, chemotherapy (CT) remains the only viable options in the absence of "druggable" mutations. We aimed to explore the efficacy of salvage chemotherapy after immunotherapy (SCAI) in advanced NSCLC patients. MATERIALS AND METHODS: We designed a retrospective, multicenter study, involving 20 Italian centers, with the primary objective of describing the clinical outcome of advanced NSCLC patients treated with SCAI at the participating institutions from November 2013 to July 2019. The primary endpoint of the study was represented by overall survival (OS), defined as the time from CT initiation to death. Secondary outcome endpoints of the SCAI (progression free survival, PFS, objective response rate, ORR and toxicity) and explorative biomarkers (lactate dehydrogenase, LDH, and neutrophil-to-lymphocyte ratio, NLR during immunotherapy) were also analyzed. RESULTS: In our study population of 342 NSCLC patients, SCAI obtained a median OS of 6.8 months (95 CI 5.5-8.1), median PFS of 4.1 months (95 .4-4.8) and ORR of 22.8 CKI score" was constructed by combining significant predictors of OS at the multivariate analyses (sex, ECOG PS, disease control with prior immunotherapy), Harrell'C was 0.65, (95 0.59-0.71). CONCLUSIONS: Despite the late-line settings, our findings support the hypothesis that previous immunotherapy might increase the sensitivity of the tumor to the subsequent chemotherapy. The "Post-CKI score" was clinically effective in successfully discriminating three distinct prognostic subgroups of patients after the failure of CKI, representing a possibly useful tool for the tailored decision-making process of advanced treatment-line settings in NSCLC.
AB - OBJECTIVES: In the most of cases, for non-small cell lung cancer (NSCLC) patients who progressed to previous immune checkpoint inhibitors (CKI) administered as first- or as second-line therapy, chemotherapy (CT) remains the only viable options in the absence of "druggable" mutations. We aimed to explore the efficacy of salvage chemotherapy after immunotherapy (SCAI) in advanced NSCLC patients. MATERIALS AND METHODS: We designed a retrospective, multicenter study, involving 20 Italian centers, with the primary objective of describing the clinical outcome of advanced NSCLC patients treated with SCAI at the participating institutions from November 2013 to July 2019. The primary endpoint of the study was represented by overall survival (OS), defined as the time from CT initiation to death. Secondary outcome endpoints of the SCAI (progression free survival, PFS, objective response rate, ORR and toxicity) and explorative biomarkers (lactate dehydrogenase, LDH, and neutrophil-to-lymphocyte ratio, NLR during immunotherapy) were also analyzed. RESULTS: In our study population of 342 NSCLC patients, SCAI obtained a median OS of 6.8 months (95 CI 5.5-8.1), median PFS of 4.1 months (95 .4-4.8) and ORR of 22.8 CKI score" was constructed by combining significant predictors of OS at the multivariate analyses (sex, ECOG PS, disease control with prior immunotherapy), Harrell'C was 0.65, (95 0.59-0.71). CONCLUSIONS: Despite the late-line settings, our findings support the hypothesis that previous immunotherapy might increase the sensitivity of the tumor to the subsequent chemotherapy. The "Post-CKI score" was clinically effective in successfully discriminating three distinct prognostic subgroups of patients after the failure of CKI, representing a possibly useful tool for the tailored decision-making process of advanced treatment-line settings in NSCLC.
M3 - Article
JO - Lung Cancer
JF - Lung Cancer
SN - 0169-5002
ER -