Reduced toxicity (FluBu3) versus myeloablative (BuCy) conditioning in acute myeloid leukemia patients who received first allogeneic hematopoietic stem cell transplantation in measurable residual disease-negative CR1

  • Silvia Park
  • , Su Yeon Bang
  • , Daehun Kwag
  • , Jong Hyuk Lee
  • , Tong Yoon Kim
  • , Joonyeop Lee
  • , Gi June Min
  • , Sung Soo Park
  • , Seung Ah Yahng
  • , Young Woo Jeon
  • , Seung Hwan Shin
  • , Jae Ho Yoon
  • , Sung Eun Lee
  • , Byung Sik Cho
  • , Ki Seong Eom
  • , Yoo Jin Kim
  • , Seok Lee
  • , Chang Ki Min
  • , Seok Goo Cho
  • , Jong Wook Lee
  • Hee Je Kim

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

In the present study, reduced toxicity (FluBu3) and myeloablative (BuCy) conditioning were compared in patients with AML who received first allogeneic HSCT in MRD-negative CR1. The study included 124 adult patients who underwent HSCT from an HLA-matched (8/8) sibling, unrelated, or 1-locus mismatched (7/8) unrelated donor (MMUD). The median age was 45 years and intermediate cytogenetics comprised majority (71.8%). The 2-year OS, RFS, CIR and NRM for BuCy (n = 78, 62.9%) and FluBu3 (n = 46, 37.1%) groups were 78.3% and 84.5% (p = 0.358), 78.0% and 76.3% (p = 0.806), 7.7% and 21.5% (p = 0.074) and 14.3% and 2.2% (p = 0.032), respectively. At the time of data cut-off, relapse and NRM were the main causes of HSCT failure in each of the FluBu3 and BuCy arms. Among patients, 75% of relapsed FluBu3 patients had high-risk features of either poor cytogenetics or FLT3-ITD mutation compared with 16.7% of BuCy patients. The majority of NRM in the BuCy group was due to GVHD (73%), half of whom received MMUD transplantation. To conclude, the FluBu3 reduced toxicity conditioning showed comparable post-transplant OS and RFS to BuCy and was associated with significantly reduced NRM that was offset by a trend towards higher risk of relapse even in MRD-negative CR1 population.

Original languageEnglish
Pages (from-to)813-823
Number of pages11
JournalBone Marrow Transplantation
Volume59
Issue number6
DOIs
StatePublished - Jun 2024

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© The Author(s), under exclusive licence to Springer Nature Limited 2024.

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