| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2101409 | Biology of Blood and Marrow Transplantation | 2016 | 6 Pages |
•Reduced-intensity conditioning allogeneic hematopoietic cell transplantation with busulfan and clofarabine is safe and well tolerated.•Clofarabine/busulfan leads to successful engraftment and acceptable rates of nonrelapse mortality.•Clofarabine/busulfan show promising preliminary efficacy, especially in acute myeloid leukemia in first complete remission.
Clofarabine has potent antileukemia activity and its inclusion in reduced-intensity conditioning (RIC) allogeneic hematopoietic stem cell transplantation (HSCT) for acute leukemia could potentially improve outcomes. We conducted a phase II study of busulfan (.8 mg/kg i.v. twice daily on days −5, −4, −3, and −2) with clofarabine (40 mg/m2 i.v. daily on days −5, −4, −3, and −2) conditioning before allogeneic 8/8 HLA–matched related or unrelated HSCT. The primary endpoint was donor neutrophil engraftment by day +40. Secondary endpoints included nonrelapse mortality (NRM), acute and chronic graft-versus-host disease (GVHD), progression-free survival (PFS), and overall survival (OS). Thirty-four patients (acute myeloid leukemia [AML], n = 25; myelodysplastic syndromes, n = 5; and acute lymphoid leukemia, n = 4) were enrolled. Day 40+ engraftment with donor chimerism was achieved in 33 of 34 patients with 1 patient dying before count recovery. Day 100 and 1-year NRM were 5.9% (95% confidence interval [CI], 1.0 to 17.4) and 24% (95% CI, 11 to 39), respectively. The 2-year relapse rate was 26% (95% CI, 13 to 42). Cumulative incidences of acute and chronic GVHD were 21% and 44%, respectively. The 2-year PFS was 50% (95% CI, 32 to 65) and OS was 56% (95% CI, 38 to 71). For patients with AML in first complete remission, 2-year PFS and OS were both 82% (95% CI, 55 to 94). RIC with busulfan and clofarabine leads to successful engraftment with acceptable rates of NRM and GVHD.
