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

  • Fabio Guolo*
  • , Luana Fianchi
  • , Paola Minetto
  • , Marino Clavio
  • , Michele Gottardi
  • , Sara Galimberti
  • , Giuliana Rizzuto
  • , Michela Rondoni
  • , Giambattista Bertani
  • , Michela Dargenio
  • , Atto Bilio
  • , Barbara Scappini
  • , Patrizia Zappasodi
  • , Anna Maria Scattolin
  • , Francesco Grimaldi
  • , Giuseppe Pietrantuono
  • , Pellegrino Musto
  • , Marco Cerrano
  • , Stefano D'Ardia
  • , Ernesta Audisio
  • Alessandro Cignetti, Crescenza Pasciolla, Francesca Pavesi, Anna Candoni, Carmela Gurreri, Monica Morselli, Caterina Alati, Nicola Fracchiolla, Giovanni Rossi, Manuela Caizzi, Fabrizio Carnevale-Schianca, Agostino Tafuri, Giuseppe Rossi, Felicetto Ferrara, Livio Pagano, Roberto Massimo Lemoli
*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivistaArticolo

1 Citazioni (Scopus)

Abstract

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.
Lingua originaleInglese
pagine (da-a)96-104
Numero di pagine9
RivistaBlood Cancer Journal
Volume10
Numero di pubblicazione10
DOI
Stato di pubblicazionePubblicato - 2020

All Science Journal Classification (ASJC) codes

  • Ematologia
  • Oncologia

Keywords

  • Leukemia

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