Fluoropyrimidine (FP) plus platinum chemotherapy has been recently established as a second-line (L2) preferred option in advanced biliary tract cancer (aBTC) (ABC-06 phase III trial). However, the overall survival (OS) benefit was limited and comparison with FP monotherapy was not available. Our aim was to assess the OS of patients treated with a FP monotherapy compared to a doublet with irinotecan or platinum in L2. We performed a retrospective analysis of two large multicenter prospective cohorts: a French cohort (28 centers) and an Italian cohort (9 centers). All consecutive patients with aBTC receiving FP-based L2 after gemcitabine plus cisplatin/gemcitabine plus oxaliplatin L1 between 2003 and 2016 were included. A subgroup analysis according to performance status (PS) and an exploratory analysis according to platinum sensitivity in L1 were planned. In the French cohort (n = 351), no significant OS difference was observed between the FP monotherapy and doublet groups (median OS: 5.6 vs 6.8 months,P= .65). Stratification on Eastern Cooperative Oncology Group (ECOG) PS showed similar results in PS 0-1 and 2. Median OS was not different between FP monotherapy, platinum- and irinotecan-based doublets (5.6 vs 7.1 vs 6.7 months,P= .68). Similar findings were observed in the Italian cohort (n = 174) and in the sensitivity analysis in pooled cohorts (n = 525). No L2 regimen seemed superior over others in the platinum resistant/refractory or sensitive subgroups. Our results suggest that FP monotherapy is as active as FP doublets in aBTC in L2, regardless of the patient PS and country, and could be a therapeutic option in this setting.
Fluropyrimidine single agent or doublet chemotherapy as second line treatment in advanced biliary tract cancer / Neuzillet, C; Casadei-Gardini, A; Brieau, B; Vivaldi, C; Brandi, G; Tougeron, D; Filippi, R; Vienot, A; Silvestris, N; Pointet, Al; Lonardi, S; Rousseau, B; Scartozzi, M; Dahan, L; Aprile, G; Le Sourd, S; Evesque, L; Meurisse, A; Lievre, A; Vernerey, D; Boussaha, T; Heurgue, A; Desrame, J; Lecomte, T; Cacheux, W; Bachet, Jb; Phelip, Jm; Hautefeuille, V; Mary, F; Locher, C; Bidault-Thirot, A; Marthey, L; Touchefeu, Y; Moulin, V; Zaanan, A; Taieb, J; Casagrande, M; Murgioni, S; Santini, D; Fornaro, L; Montagnani, F; Leone, F; Faloppi, L; Giommoni, E; Lutrino, Se; Palloni, A; Brunetti, O; Argentiero, A; Bergamo, F; Vasile, E; Lai, E; Ziranu, P; Dadduzio, V; Rizzato, M; Pellino, A; Aglietta, M; Cappetta, A; Garattini, Sk; Basile, D; Hammoudi, N; Puzzoni, M. - In: INTERNATIONAL JOURNAL OF CANCER. - ISSN 0020-7136. - 147:11(2020), pp. 3177-3188. [10.1002/ijc.33146 EA JUL 2020]
Fluropyrimidine single agent or doublet chemotherapy as second line treatment in advanced biliary tract cancer
Santini D;
2020
Abstract
Fluoropyrimidine (FP) plus platinum chemotherapy has been recently established as a second-line (L2) preferred option in advanced biliary tract cancer (aBTC) (ABC-06 phase III trial). However, the overall survival (OS) benefit was limited and comparison with FP monotherapy was not available. Our aim was to assess the OS of patients treated with a FP monotherapy compared to a doublet with irinotecan or platinum in L2. We performed a retrospective analysis of two large multicenter prospective cohorts: a French cohort (28 centers) and an Italian cohort (9 centers). All consecutive patients with aBTC receiving FP-based L2 after gemcitabine plus cisplatin/gemcitabine plus oxaliplatin L1 between 2003 and 2016 were included. A subgroup analysis according to performance status (PS) and an exploratory analysis according to platinum sensitivity in L1 were planned. In the French cohort (n = 351), no significant OS difference was observed between the FP monotherapy and doublet groups (median OS: 5.6 vs 6.8 months,P= .65). Stratification on Eastern Cooperative Oncology Group (ECOG) PS showed similar results in PS 0-1 and 2. Median OS was not different between FP monotherapy, platinum- and irinotecan-based doublets (5.6 vs 7.1 vs 6.7 months,P= .68). Similar findings were observed in the Italian cohort (n = 174) and in the sensitivity analysis in pooled cohorts (n = 525). No L2 regimen seemed superior over others in the platinum resistant/refractory or sensitive subgroups. Our results suggest that FP monotherapy is as active as FP doublets in aBTC in L2, regardless of the patient PS and country, and could be a therapeutic option in this setting.| File | Dimensione | Formato | |
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