| Literature DB >> 26132980 |
Udo Holtick1, Alexander Shimabukuro-Vornhagen1, Geothy Chakupurakal1, Sebastian Theurich1, Silke Leitzke1, Anke Burst1, Michael Hallek1, Michael von Bergwelt-Baildon1, Christof Scheid1, Jens M Chemnitz1.
Abstract
Reduced-intensity conditioning regimens have demonstrated lower toxicity but increased relapse rates in the context of allogeneic hematopoietic stem cell transplantation (aSCT) for patients with acute myelogenous leukemia (AML). The FLAMSA- reduced-intensity conditioning (RIC) regimen, combining a cytoreductive and a transplant-conditioning part, has been described to be efficacious in patients with refractory disease. We retrospectively analyzed clinical data of 130 patients with AML after aSCT following FLAMSA RIC at our center. The median follow-up was 37 (10-125) months. The 4-yr overall and disease-free survival rates of the whole cohort were 45% and 40%. Cumulative incidence of relapse was 29%, 35%, and 40% at 1, 2, and 4 yr. There were no significant differences regarding overall and disease-free survival for patients transplanted in CR1, CR2, or primary induction failure (PIF). Patients with refractory disease after salvage therapy had significantly lower disease-free and overall survival (OS). Disease-free and OS rates were also significantly decreased in patients with 10% or more BLASTS at transplant. non-relapse mortality was 15%, 19%, and 20% at 1, 2, and 4 yr and similar in all cohorts. These data underscore the potency of the FLAMSA RIC regimen for patients with AML especially with PIF. The decision for re-induction therapy prior to aSCT in relapsed patients has to be weighed against the potential toxicity of this approach and might be influenced by the amount of leukemic BLASTS present. Only randomised trials will answer this important question.Entities:
Keywords: FLAMSA; acute myeloid leukemia; allogeneic stem cell transplantation; conditioning
Mesh:
Year: 2015 PMID: 26132980 DOI: 10.1111/ejh.12615
Source DB: PubMed Journal: Eur J Haematol ISSN: 0902-4441 Impact factor: 2.997