Clofarabine and busulfan conditioning facilitates engraftment and provides significant antitumor activity in nonremission hematologic malignancies.

Journal Article (Clinical Trial;Journal Article)

Patients with hematologic malignancies not in remission before allogeneic hematopoietic stem cell transplantation (HSCT) have a poor prognosis. To improve the antitumor activity of conditioning, we combined clofarabine with myeloablative doses of busulfan in a phase 1/2 study in nonremission hematologic malignancies. Forty-six patients were enrolled, including 31 patients with nonremission acute myelogenous leukemia (AML). Patients had a median age of 53 years, with a median comorbidity index of 3. Donors were unrelated, HLA mismatched, or both in 59% of patients. Common grade III to IV nonhematologic toxicities included transient transaminitis (50%), mucositis (24%), hand-foot syndrome (13%), transient hypoxia (13%), nausea/vomiting (9%), and diarrhea (9%). All patients engrafted. Complete remission was achieved in 80% of all patients by day +30 and in 100% of AML patients without prior hematopoietic stem cell transplantation. Two-year nonrelapse mortality for all patients was 31%, and overall survival was 28%. In AML, the overall survival was 48% at 1 year and 35% at 2 years. These data suggest that clofarabine combined with myeloablative doses of busulfan is well tolerated, secures engraftment, and possesses significant antitumor activity, particularly in nonremission AML. This study is registered at under identifier NCT00556452.

Full Text

Duke Authors

Cited Authors

  • Magenau, J; Tobai, H; Pawarode, A; Braun, T; Peres, E; Reddy, P; Kitko, C; Choi, S; Yanik, G; Frame, D; Harris, A; Erba, H; Kujawski, L; Elenitoba-Johnson, K; Sanks, J; Jones, D; Paczesny, S; Ferrara, J; Levine, J; Mineishi, S

Published Date

  • October 13, 2011

Published In

Volume / Issue

  • 118 / 15

Start / End Page

  • 4258 - 4264

PubMed ID

  • 21841163

Electronic International Standard Serial Number (EISSN)

  • 1528-0020

Digital Object Identifier (DOI)

  • 10.1182/blood-2011-06-358010


  • eng

Conference Location

  • United States