Impact of donor source on hematopoietic cell transplantation outcomes for patients with myelodysplastic syndromes (MDS)
- Wael Saber(corresponding author),
- Corey S. Cutler,
- Ryotaro Nakamura,
- Mei Jie Zhang,
- Ehab Atallah,
- J. Douglas Rizzo
- Medical College of Wisconsin,
- Dana-Farber Cancer Institute,
- City of Hope National Med Center,
- Oregon Health and Science University,
- University of Texas MD Anderson Cancer Center,
- Cleveland Clinic Foundation
Sustainable Development Goals
- SDG 3 Good Health and Well
Abstract
Allogeneic hematopoietic cell transplantation (HCT) from human leukocyte antigen (HLA) matched related donor (MRD) and matched unrelated donors (MUD) produces similar survival for patients with acute myelogenous leukemia.Whether these results can be extended to patientswithmyelodysplastic syndromes (MDS) is unknown. Therefore, analysis of post-HCT outcomes for MDS was performed. Outcomes of 701 adult MDS patients who underwent HCT between 2002 and 2006 were analyzed (MRD [n 5 176], 8 of 8 HLA-A, -B, -C, -DRB1 allele matchedMUD [n 5 413], 7 of 8 MUD [ n 5 112]). Median agewas 53 years (range, 22-78 years). In multivariate analyses, MRD HCT recipients had similar disease free survival (DFS) and survival rates compared with 8 of 8 MUD HCT recipients (relative risk [RR] 1.13 [95% confidence interval (CI) 0.91-1.42] and 1.24 [95% CI 0.98-1.56], respectively), and both MRD and 8 of 8MUD had superior DFS(RR1.47 [95%CI 1.10-1.96] and 1.29 [95%CI 1.00-1.66], respectively) and survival (RR 1.62 [95% CI 1.21-2.17] and 1.30 [95% CI 1.01-1.68], respectively) compared with 7 of 8 MUDHCT recipients. In patients with MDS, MRD remains the best stem cell source followed by 8 of 8 MUD. Transplantation from 7 of 8 MUD is associated with significantly poorer outcomes.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 1974-1982 (9 pages)Journal (Volume, Issue Number)
Blood (Volume 122, Issue 11)Publication milestones
- Published - 09/12/2013
Publication status
ISSN
0006-4971Publication IDs
- Scopus: 84887389178
- PubMed: 23847196
- ORCID: /0000-0002-8636-1071/work/68888069
