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

  • Jae Sook Ahn
  • , Yeo Kyeoung Kim
  • , Yoo Hong Min
  • , June Won Cheong
  • , Jun Ho Jang
  • , Chul Won Jung
  • , In Ho Kim
  • , Hwi Joong Yoon
  • , Hong Ghi Lee
  • , Sang Kyun Sohn
  • , Joon Ho Moon
  • , Hawk Kim
  • , Yoo Jin Kim
  • , Jong Ho Won
  • , Joo Seop Chung
  • , Yeung Chul Mun
  • , Je Hwan Lee
  • , Hyeoung Joon Kim
  • Chonnam National University
  • Yonsei University
  • Sungkyunkwan University
  • Seoul National University
  • Kyung Hee University
  • Konkuk University
  • Kyungpook National University
  • University of Ulsan
  • The Catholic University of Korea
  • Soonchunhyang University
  • Pusan National University
  • Ewha Womans University

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Pages (from-to)40-48
Number of pages9
JournalActa Haematologica
Volume134
Issue number1
DOIs
StatePublished - 22 Jul 2015
Externally publishedYes

Keywords

  • Allogeneic stem cell transplantation
  • Azacitidine
  • Myelodysplastic syndrome

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