| Literature DB >> 27377901 |
Gheath Alatrash1, Peter F Thall2, Benigno C Valdez1, Patricia S Fox2, Jing Ning2, Haven R Garber1, Selma Janbey1, Laura L Worth3, Uday Popat1, Chitra Hosing1, Amin M Alousi1, Partow Kebriaei1, Elizabeth J Shpall1, Roy B Jones1, Marcos de Lima4, Gabriela Rondon1, Julianne Chen1, Richard E Champlin1, Borje S Andersson5.
Abstract
Pretransplant conditioning regimens critically determine outcomes in the setting of allogeneic stem cell transplantation (allo-SCT). The use of nucleoside analogs such as fludarabine (Flu) in combination with i.v. busulfan (Bu) has been shown to be highly effective as a pretransplant conditioning regimen in acute myeloid leukemia (AML), chronic myeloid leukemia (CML), and myelodysplastic syndrome (MDS). Because leukemia relapse remains the leading cause of death after allo-SCT, we studied whether clofarabine (Clo), a nucleoside analog with potent antileukemia activity, can be used to complement Flu. In a preliminary report, we previously showed the safety and efficacy of Clo ± Flu with i.v. Bu in 51 patients with high-risk AML, CML, and MDS. The study has now been completed, and we present long-term follow-up data on the entire 70-patient population, which included 49 (70%), 8 (11%), and 13 (19%) patients with AML, MDS, and CML, respectively. Thirteen patients (19%) were in complete remission, and 41 patients (59%) received matched unrelated donor grafts. Engraftment was achieved in all patients. Sixty-three patients (90%) achieved complete remission. There were no deaths reported at day +30, and the 100-day nonrelapse mortality rate was 4% (n = 3). Thirty-one percent of patients (n = 22) developed grades II to IV acute graft-versus-host disease, and the median overall survival and progression-free survival times were 2.4 years and .9 years, respectively. Our results confirm the safety and overall and progression-free survival advantage of the arms with higher Clo doses and lower Flu doses, which was most prominent in the AML/MDS group.Entities:
Keywords: Allogeneic stem cell transplantation; Busulfan; Clofarabine; Conditioning regimen; Fludarabine
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Year: 2016 PMID: 27377901 PMCID: PMC5026955 DOI: 10.1016/j.bbmt.2016.06.023
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742