| Literature DB >> 27561720 |
Mohamad Mohty1,2,3,4,5, Florent Malard6,3,4,5, Didier Blaise7, Noel Milpied8, Gérard Socié9, Anne Huynh10, Oumédaly Reman11, Ibrahim Yakoub-Agha12, Sabine Furst7, Thierry Guillaume6, Resa Tabrizi8, Stéphane Vigouroux8, Pierre Peterlin6, Jean El-Cheikh7, Philippe Moreau6,2, Myriam Labopin5, Patrice Chevallier6,2.
Abstract
The prognosis of patients with acute myeloid leukemia in whom primary treatment fails remains very poor. In order to improve such patients' outcome, we conducted a phase 2, prospective, multicenter trial to test the feasibility of a new sequential regimen, combining a short course of intensive chemotherapy and a reduced intensity-conditioning regimen, before allogeneic stem-cell transplantation. Twenty-four patients (median age, 47 years) with acute myeloid leukemia in primary treatment failure were included. Cytogenetic risk was poor in 15 patients (62%) and intermediate in nine (38%). The sequential regimen consisted of clofarabine (30 mg/m2/day) and cytosine arabinoside (1 g/m2/day) for 5 days, followed, after a 3-day rest, by reduced-intensity conditioning and allogeneic stem-cell transplantation combining cyclophosphamide (60 mg/kg), intravenous busulfan (3.2 mg/kg/day) for 2 days and anti-thymocyte globulin (2.5 mg/kg/day) for 2 days. Patients in complete remission at day +120 received prophylactic donor lymphocyte infusion. Eighteen patients (75%) achieved complete remission. With a median follow-up of 24.6 months, the Kaplan-Meier estimate of overall survival was 54% (95% CI: 33-71) at 1 year and 38% (95% CI: 18-46) at 2 years. The Kaplan-Meier estimate of leukemia-free survival was 46% (95% CI: 26-64) at 1 year and 29% (95% CI: 13-48) at 2 years. The cumulative incidence of non-relapse mortality was 8% (95% CI: 1-24) at 1 year and 12% (95% CI: 3-19) at 2 years. Results from this phase 2 prospective multicenter trial endorsed the safety and efficacy of a clofarabine-based sequential reduced-toxicity conditioning regimen, which warrants further investigation. This study was registered at www.clinicaltrials.gov, identifier number: NCT01188174. Copyright© Ferrata Storti Foundation.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27561720 PMCID: PMC5210249 DOI: 10.3324/haematol.2016.150326
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941