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Volume 13, Issue 12, Pages 1499-1507 (December 2007)


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Comparable Outcomes after Nonmyeloablative Hematopoietic Cell Transplantation with Unrelated and Related Donors

Marco MielcarekacCorresponding Author Informationemail address, Barry E. Storerabd, Brenda M. Sandmaierac, Mohamed L. Sorrora, David G. Maloneyac, Effie Petersdorfac, Paul J. Martinac, Rainer Storbc

Received 6 July 2007; accepted 2 September 2007.

Abstract 

We sought to determine whether patients with hematologic malignancies treated by nonmyeloablative hematopoietic cell transplantation (HCT) at a single institution between December 1997 and June 2006 had worse outcomes with grafts from unrelated donors (URDs) (n = 184) compared with HLA-identical related donors (n = 221). The nonmyeloablative preparative regimen consisted of 2 Gy of total body irradiation (TBI) with (78%) or without (22%) fludarabine, along with posttransplantation mycophenolate mofetil (MMF) and cyclosporine (CSa). After adjusting for the HCT comorbidity index, relapse risk, patient age, stem cell source, preparative regimen, previous cytomegalovirus (CMV) infection, and sex mismatch of donor and recipient in multivariate analysis, we found no statistically significant differences between unrelated and related HCT recipients in terms of risk of nonrelapse mortality (NRM; hazard ratio [HR] = 0.98; 95% confidence interval = 0.6-1.6; P = .94), relapse (HR = 1.04; 95% confidence interval = 0.7-1.5; P = .82), or overall mortality (HR = 0.99; 95% confidence interval = 0.7-1.4; P = .94). Overall rates of severe acute and extensive chronic graft-versus-host disease (aGVHD, cGVHD) also were not significantly different between the 2 groups. We conclude that within the limitations of a retrospective study, these results indicate that candidates for nonmyeloablative HCT without suitable related donors may expect similar outcomes with grafts from URDs.

a Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington

b Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington

c Department of Medicine, University of Washington School of Medicine, Seattle, Washington

d Department of Biostatistics, University of Washington School of Medicine, Seattle, Washington

Corresponding Author InformationCorrespondence and reprint requests: Marco Mielcarek, MD, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N, D1-100, PO Box 19024, Seattle, WA 98109-1024. Tel: 206-667-2827; Fax: 206-667-6124.

PII: S1083-8791(07)00441-7

doi:10.1016/j.bbmt.2007.09.004


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