| Literature DB >> 28890406 |
Koji Kawamura1, Shinichi Kako1, Shuichi Mizuta2, Ken Ishiyama3, Jun Aoki4, Shingo Yano5, Takahiro Fukuda6, Naoyuki Uchida7, Yukiyasu Ozawa8, Tetsuya Eto9, Koji Iwato10, Heiwa Kanamori4, Kaoru Kahata11, Tadakazu Kondo12, Masashi Sawa13, Tatsuo Ichinohe14, Yoshiko Atsuta15, Yoshinobu Kanda16.
Abstract
The optimal conditioning regimen for elderly patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HCT) remains unclear. We retrospectively analyzed 1607 patients aged 50 years or older with acute myeloid leukemia (AML), acute lymphoblastic leukemia, or myelodysplastic syndrome (MDS) who underwent allo-HCT using fludarabine/busulfan (FB) or fludarabine/melphalan (FM) between 2007 and 2014. We compared the clinical outcomes among FB2 (busulfan at 6.4 mg/kg iv, n = 463), FB4 (busulfan at 12.8 mg/kg iv, n = 721), and FM140 (melphalan at 140 mg/m2, n = 423). The nonrelapse mortality (NRM) rates in the FB4 and FM140 groups were higher than that in the FB2 group (hazard ratio [HR], 1.63 [P < .001]; and HR, 1.71 [P < .001], respectively). Conversely, the relapse rates in the FB4 and FM140 groups were lower than that in the FB2 group (HR, .73 [P = .011]; and HR, .56 [P < .001], respectively). There were no significant differences in overall survival (OS) among the FB2, FB4, and FM140 groups. The 3-year OS in patients with high-risk AML and MDS in the FM140 group (37.0% and 60.2%) were superior to those in the FB2 group (24.4% and 45.5%) and the FB4 group (24.6% and 40.6%) (P = .016 and P = .023), whereas there were no differences in OS in the other patients among the 3 groups. In conclusion, the lower rates of relapse in the FB4 and FM140 groups were largely offset by a worse NRM. However, FM140 might be associated with better OS in patients with high-risk AML and MDS.Entities:
Keywords: Allogeneic transplantation; Fludarabine/busulfan; Fludarabine/melphalan; Reduced-intensity conditioning regimen; Reduced-toxicity conditioning regimen
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Year: 2017 PMID: 28890406 DOI: 10.1016/j.bbmt.2017.09.003
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742