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Azacitidine Pre-Treatment Followed by Reduced-Intensity Stem Cell Transplantation in Patients with Higher-Risk Myelodysplastic Syndrome.

Authors :
ahn, Jae-Sook
Kim, Yeo-Kyeoung
Min, Yoo Hong
Cheong, June-Won
Jang, Jun Ho
Jung, Chul Won
Kim, In Ho
Yoon, Hwi-Joong
Lee, Hong Ghi
Sohn, Sang Kyun
Moon, Joon Ho
Kim, Hawk
Kim, Yoo-Jin
Won, Jong-Ho
Chung, Joo-Seop
Mun, Yeung Chul
Lee, Je-Hwan
Kim, Hyeoung-Joon
Source :
Acta Haematologica; Jun2015, Vol. 134 Issue 1, p40-48, 9p, 2 Charts, 3 Graphs
Publication Year :
2015

Abstract

Azacitidine (AZA) is commonly used in patients with myelodysplastic syndrome (MDS). To determine the role of AZA before allogeneic stem cell transplantation (allo-SCT), we conducted a prospective study of AZA pre-treatment followed by allo-SCT in patients with higher-risk MDS. Twenty-one patients who were scheduled for their third to sixth cycle of AZA pre-treatment followed by allo-SCT were enrolled. AZA pre-treatment was interrupted early in 3 patients (14.3%) because of leukaemic transformation or death. The overall response rate to AZA pre-treatment was 57.1%. There were 2 cases of complete remission, 1 case of partial remission, and 9 cases of haematologic improvement. Fourteen patients (66.7%) received the planned allo-SCT and 5 patients were alive at the last follow-up. Three-year progression-free survival (PFS) and 3-year overall survival (OS) in the 14 patients who received allo-SCT were 30.0% (95% CI 3.3-56.7) and 42.9% (95% CI 17.1-68.7), respectively. PFS and OS were not influenced by response to AZA pre-treatment (p > 0.05). In this study, AZA had a role as a bridge therapy to prevent leukaemic transformation prior to selection of a donor for allo-SCT and showed low toxicity. It may be considered in patients with higher-risk MDS. © 2015 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00015792
Volume :
134
Issue :
1
Database :
Complementary Index
Journal :
Acta Haematologica
Publication Type :
Academic Journal
Accession number :
103427876
Full Text :
https://doi.org/10.1159/000368711