Reduced-Intensity Hematopoietic Cell Transplantation for Patients with Primary Myelofibrosis: A Cohort Analysis from the Center for International Blood and Marrow Transplant Research
- Vikas Gupta(corresponding author),
- Adriana K. Malone,
- Parameswaran N. Hari,
- Kwang Woo Ahn,
- Zhen Huan Hu,
- Robert Peter Gale
- University of Toronto,
- Icahn School of Medicine at Mount Sinai,
- Medical College of Wisconsin,
- Imperial College London,
- Massachusetts General Hospital,
- West Virginia University
Open access
Abstract
We evaluated outcomes and associated prognostic factors in 233 patients undergoing allogeneic hematopoietic cell transplantation (HCT) for primary myelofibrosis (MF) using reduced-intensity conditioning (RIC). The median age at RIC HCT was 55 yr. Donors were a matched sibling donor (MSD) in 34% of RIC HCTs, an HLA well-matched unrelated donor (URD) in 45%, and a partially matched/mismatched URD in 21%. Risk stratification according to the Dynamic International Prognostic Scoring System (DIPSS) was 12% low, 49% intermediate-1, 37% intermediate-2, and 1% high. The probability of survival at 5 yr was 47% (95% confidence interval [CI], 40% to 53%). In a multivariate analysis, donor type was the sole independent factor associated with survival. Adjusted probabilities of survival at 5-yr were 56% (95% CI, 44% to 67%) for MSD, 48% (95% CI, 37% to 58%) for well-matched URD, and 34% (95% CI, 21% to 47%) for partially matched/mismatched URD (P=002). The relative risk (RR) for NRM was 3.92 (P= .006) for well-matched URD and 9.37 (P < .0001) for partially matched/mismatched URD. Trends toward increased NRM (RR, 1.7; P= .07) and inferior survival (RR, 1.37; P= .10) were observed in DIPSS intermediate-2/high-risk patients compared with DIPSS low/intermediate-1 risk patients. Our data indicate that RIC HCT is a potentially curative option for patients with MF, and that donor type is the most important factor influencing survival in these patients.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 89-97 (9 pages)Journal (Volume, Issue Number)
Biology of Blood and Marrow Transplantation (Volume 20, Issue 1)Publication milestones
- Published - 01/2014
Publication status
ISSN
1083-8791Publication IDs
- Scopus: 84890911661
- PubMed: 24161923
- ORCID: /0000-0002-8636-1071/work/68811328
