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Blood, 1 November 2004, Vol. 104, No. 9, pp. 2976-2980.
Prepublished online as a Blood First Edition Paper on July 13, 2004; DOI 10.1182/blood-2004-04-1674.
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Submitted April 30, 2004
Accepted May 28, 2004
Limits of HLA Mismatching in Unrelated Hematopoietic Cell Transplantation
Effie W Petersdorf*, Claudio Anasetti, Paul J Martin, Ted Gooley, Jerald Radich, Mari Malkki, Ann Woolfrey, Anajane Smith, Eric Mickelson, and John A Hansen
Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Medicine, University of Washington, Seattle, WA, USA
H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA
Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA, USA
The Seattle Cancer Care Alliance, Seattle, WA, USA
* Corresponding author; email: epetersd{at}fhcrc.org.
HLA matching between the donor and recipient improves the success of unrelated hematopoietic cell transplantation (HCT). Matched donors are available for only a minority of patients. Further information is needed to evaluate the limits of HLA mismatching. We examined the association of mortality with HLA-A, B, C, DRB1 and DQB1 mismatching in 948 patients who received a T-replete unrelated HCT for treatment of a marrow disorder. A single HLA allele or antigen mismatch was associated with increased mortality among patients with chronic myeloid leukemia (CML) within 2 years after diagnosis compared to patients with no HLA mismatch, but not among those with more advanced malignancy. In particular, a single HLA-C mismatch conferred increased risk of mortality compared to matches. There was a suggestion for increased mortality with multiple mismatches involving HLA-DQB1 compared to multiple mismatches not involving HLA-DQB1. Donors with a single HLA allele or antigen mismatch may be used for HCT when a fully matched donor is not available for patients with diseases that do not permit time for a lengthy search. Whenever possible, HLA-C mismatches should be avoided for patients with early stage CML, and HLA-DQB1 mismatches should be avoided for patients with multiple mismatches.

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