: In the registration clinical trial 301 (NCT01696084), CPX-351 has shown to be superior to conventional 3 + 7 in secondary AML (s-AML). However, the optimal duration of treatment, the best timing for allogeneic stem cell transplantation (allo-HSCT), and the activity of CPX-351 in specific s-AML subgroups are unclear. To evaluate these aspects, a total of 513 s-AML patients (median age 65.6 years, 19-79) treated with CPX-351 were retrospectively analyzed. Complete remission (CR) rate after induction was 297/513 (58%), increasing to 340/513 (66%) after cycle 2. Among the 340 responding patients, 118 (34.7%), 137 (40.3%), and 85 (25%) received none, one, or two consolidation cycles of CPX-351, respectively. Overall, 230/513 patients (48.8%) received allo-HSCT. Median follow up was 23.66 months and median overall survival (OS) was 16.23 months. Patients with mutated NPM1 or with ELN 2017 favorable risk (p < 0.05) had a significantly longer OS (p < 0.05). In a landmark analysis, receiving allo-HSCT was associated with a longer survival (Median OS not reached vs. 16.3 months for patients receiving or not receiving allo-HSCT, p < 0.05). Completion of all allowed CPX-351 cycles was beneficial only in patients not proceeding to transplant (p < 0.05), whereas in transplanted patients additional CPX-351 cycles did not improve outcome. Our analysis suggests that also s-AML patients with NPM1 mutations and those belonging to the ELN 2017 favorable risk category benefit from CPX-351. In eligible patients, allo-HSCT should be performed as soon as a CR is achieved, whereas patients not undergoing transplant benefit from a complete CPX-351 schedule.
Real World Study on the Best CPX‐351 Treatment Duration and Timing for Allogeneic Stem Cell Transplantation / Guolo, Fabio; Fianchi, Luana; Martelli, Maria Paola; Lussana, Federico; Grimaldi, Francesco; Pilo, Federica; Rondoni, Michela; Filì, Carla; Minetto, Paola; Capelli, Debora; Chiusolo, Patrizia; Breccia, Massimo; Mastaglio, Sara; Bernardi, Massimo; Bocchia, Monica; Fumagalli, Monica; Galimberti, Sara; Mancini, Valentina; Piccioni, Anna Lisa; Maurillo, Luca; Fracchiolla, Nicola Stefano; Palmieri, Raffaele; Vetro, Calogero; Papayannidis, Cristina; Brunetti, Lorenzo; Sperotto, Alessandra; Gigli, Federica; Zappasodi, Patrizia; Mulé, Antonino; Patti, Caterina; Borlenghi, Erika; Dargenio, Michelina; Lessi, Federica; Cerrano, Marco; Cilloni, Daniela; Isidori, Alessandro; Lunghi, Monia; Alati, Caterina; Gurrieri, Carmela; Riva, Carola; Marconi, Giovanni; Lotesoriere, Ivana; Gatani, Samuele; Scattolin, Anna Maria; Caizzi, Manuela; Perrone, Salvatore; Billio, Atto; Gherlinzoni, Filippo; Mannelli, Francesco; Gottardi, Michele; Cairoli, Roberto; Candoni, Anna; Ferrara, Felicetto; Pagano, Livio; Lemoli, Roberto Massimo; Venditti, Adriano; Todisco, Elisabetta. - In: AMERICAN JOURNAL OF HEMATOLOGY. - ISSN 0361-8609. - (2025), pp. 1-10. [10.1002/ajh.70083]
Real World Study on the Best CPX‐351 Treatment Duration and Timing for Allogeneic Stem Cell Transplantation
Candoni, Anna;
2025
Abstract
: In the registration clinical trial 301 (NCT01696084), CPX-351 has shown to be superior to conventional 3 + 7 in secondary AML (s-AML). However, the optimal duration of treatment, the best timing for allogeneic stem cell transplantation (allo-HSCT), and the activity of CPX-351 in specific s-AML subgroups are unclear. To evaluate these aspects, a total of 513 s-AML patients (median age 65.6 years, 19-79) treated with CPX-351 were retrospectively analyzed. Complete remission (CR) rate after induction was 297/513 (58%), increasing to 340/513 (66%) after cycle 2. Among the 340 responding patients, 118 (34.7%), 137 (40.3%), and 85 (25%) received none, one, or two consolidation cycles of CPX-351, respectively. Overall, 230/513 patients (48.8%) received allo-HSCT. Median follow up was 23.66 months and median overall survival (OS) was 16.23 months. Patients with mutated NPM1 or with ELN 2017 favorable risk (p < 0.05) had a significantly longer OS (p < 0.05). In a landmark analysis, receiving allo-HSCT was associated with a longer survival (Median OS not reached vs. 16.3 months for patients receiving or not receiving allo-HSCT, p < 0.05). Completion of all allowed CPX-351 cycles was beneficial only in patients not proceeding to transplant (p < 0.05), whereas in transplanted patients additional CPX-351 cycles did not improve outcome. Our analysis suggests that also s-AML patients with NPM1 mutations and those belonging to the ELN 2017 favorable risk category benefit from CPX-351. In eligible patients, allo-HSCT should be performed as soon as a CR is achieved, whereas patients not undergoing transplant benefit from a complete CPX-351 schedule.Pubblicazioni consigliate

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