ORIGINAL ARTICLE
Cytoreductive treatment with clofarabine/ara-C combined with reduced-intensity conditioning and allogeneic stem cell transplantation in patients with high-risk, relapsed, or refractory acute myeloid leukemia and advanced myelodysplastic syndrome
Article first published online: 17 NOV 2011
DOI: 10.1111/j.1600-0609.2011.01703.x
© 2011 John Wiley & Sons A/S
Additional Information
How to Cite
Buchholz, S., Dammann, E., Stadler, M., Krauter, J., Beutel, G., Trummer, A., Eder, M. and Ganser, A. (2012), Cytoreductive treatment with clofarabine/ara-C combined with reduced-intensity conditioning and allogeneic stem cell transplantation in patients with high-risk, relapsed, or refractory acute myeloid leukemia and advanced myelodysplastic syndrome. European Journal of Haematology, 88: 52–60. doi: 10.1111/j.1600-0609.2011.01703.x
Publication History
- Issue published online: 13 DEC 2011
- Article first published online: 17 NOV 2011
- Accepted manuscript online: 31 AUG 2011 03:14AM EST
- Accepted for publication 24 August 2011
- Abstract
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Keywords:
- clofarabine;
- stem cell transplantation;
- leukemia;
- myelodysplastic syndrome
Abstract
The combination of cytoreductive chemotherapy with reduced-intensity conditioning (RIC) is a highly effective antileukemic therapy. Purpose of this retrospective analysis was to evaluate the antileukemic efficacy and toxicity of clofarabine-based chemotherapy followed by RIC and allogeneic stem cell transplantation (SCT) for high-risk, relapsed, or refractory acute myeloid leukemia (AML) or myelodysplastic syndromes (MDS). From May 2007 until October 2009, a total of 27 patients underwent allogeneic SCT after treatment with clofarabine and ara-C for 5 d and RIC (4 Gy TBI/cyclophosphamide/ATG). Prophylaxis of graft-versus-host disease (GvHD) consisted of cyclosporine and mycophenolate mofetil. Unmanipulated G-CSF mobilized PBSC (n = 26) or bone marrow cells (n = 1) were transplanted from unrelated (n = 21) or matched related (n = 6) donors. Non-hematological toxicities of this regimen mainly affected liver and skin and were all reversible. Seven patients relapsed within a median time of 5.7 months. The overall survival (OS) and relapse-free survival rates were 56% and 52% at 2 yr, respectively. In this cohort of patients, cytoreduction with clofarabine/ara-C (ClAraC) followed by RIC allogeneic SCT was well tolerated and showed good antileukemic efficacy even in patients with high-risk AML or MDS, with engraftment and GvHD-incidence comparable to other RIC regimens.

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