TY - JOUR
T1 - CPX-351 treatment in secondary acute myeloblastic leukemia is effective and improves the feasibility of allogeneic stem cell transplantation: results of the Italian compassionate use program
AU - Guolo, Fabio
AU - Fianchi, Luana
AU - Minetto, Paola
AU - Clavio, Marino
AU - Gottardi, Michele
AU - Galimberti, Sara
AU - Rizzuto, Giuliana
AU - Rondoni, Michela
AU - Bertani, Giambattista
AU - Dargenio, Michela
AU - Bilio, Atto
AU - Scappini, Barbara
AU - Zappasodi, Patrizia
AU - Scattolin, Anna Maria
AU - Grimaldi, Francesco
AU - Pietrantuono, Giuseppe
AU - Musto, Pellegrino
AU - Cerrano, Marco
AU - D’Ardia, Stefano
AU - Audisio, Ernesta
AU - Cignetti, Alessandro
AU - Pasciolla, Crescenza
AU - Pavesi, Francesca
AU - Candoni, Anna
AU - Gurreri, Carmela
AU - Morselli, Monica
AU - Alati, Caterina
AU - Fracchiolla, Nicola
AU - Rossi, Giovanni
AU - Caizzi, Manuela
AU - Carnevale-Schianca, Fabrizio
AU - Tafuri, Agostino
AU - Rossi, Giuseppe
AU - Ferrara, Felicetto
AU - Pagano, Livio
AU - Lemoli, Roberto Massimo
PY - 2020
Y1 - 2020
N2 - Secondary acute myeloid leukemia (sAML) poorly responds to conventional treatments and allogeneic stem cell transplantation (HSCT). We evaluated toxicity and efficacy of CPX-351 in 71 elderly patients (median age 66 years) with sAML enrolled in the Italian Named (Compassionate) Use Program. Sixty days treatment-related mortality was 7% (5/71). The response rate at the end of treatment was: CR/CRi in 50/71 patients (70.4%), PR in 6/71 (8.5%), and NR in 10/71 (19.7%). After a median follow-up of 11 months relapse was observed in 10/50 patients (20%) and 12 months cumulative incidence of relapse (CIR) was 23.6%. Median duration of response was not reached. In competing risk analysis, CIR was reduced when HSCT was performed in first CR (12 months CIR of 5% and 37.4%, respectively, for patients receiving (=20) or not (=30) HSCT, p = 0.012). Twelve-months OS was 68.6% (median not reached). In landmark analysis, HSCT in CR1 was the only significant predictor of longer survival (12 months OS of 100 and 70.5%, for patients undergoing or not HSCT in CR1, respectively, p = 0.011). In conclusion, we extend to a real-life setting, the notion that CPX is an effective regimen for high risk AML patients and may improve the results of HSCT.
AB - Secondary acute myeloid leukemia (sAML) poorly responds to conventional treatments and allogeneic stem cell transplantation (HSCT). We evaluated toxicity and efficacy of CPX-351 in 71 elderly patients (median age 66 years) with sAML enrolled in the Italian Named (Compassionate) Use Program. Sixty days treatment-related mortality was 7% (5/71). The response rate at the end of treatment was: CR/CRi in 50/71 patients (70.4%), PR in 6/71 (8.5%), and NR in 10/71 (19.7%). After a median follow-up of 11 months relapse was observed in 10/50 patients (20%) and 12 months cumulative incidence of relapse (CIR) was 23.6%. Median duration of response was not reached. In competing risk analysis, CIR was reduced when HSCT was performed in first CR (12 months CIR of 5% and 37.4%, respectively, for patients receiving (=20) or not (=30) HSCT, p = 0.012). Twelve-months OS was 68.6% (median not reached). In landmark analysis, HSCT in CR1 was the only significant predictor of longer survival (12 months OS of 100 and 70.5%, for patients undergoing or not HSCT in CR1, respectively, p = 0.011). In conclusion, we extend to a real-life setting, the notion that CPX is an effective regimen for high risk AML patients and may improve the results of HSCT.
KW - Leukemia
KW - Leukemia
UR - http://hdl.handle.net/10807/167068
U2 - 10.1038/s41408-020-00361-8
DO - 10.1038/s41408-020-00361-8
M3 - Article
SN - 2044-5385
VL - 10
SP - 96
EP - 104
JO - Blood Cancer Journal
JF - Blood Cancer Journal
ER -