Donor, recipient, and transplant characteristics as risk factors after unrelated donor PBSC transplantation: beneficial effects of higher CD34+ cell dose

Author:

Pulsipher Michael A.1,Chitphakdithai Pintip2,Logan Brent R.3,Leitman Susan F.4,Anderlini Paolo5,Klein John P.3,Horowitz Mary M.3,Miller John P.6,King Roberta J.2,Confer Dennis L.6

Affiliation:

1. University of Utah School of Medicine, Primary Children's Hospital, Salt Lake City;

2. Center for International Blood and Marrow Transplant Research, Minneapolis, MN;

3. Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee;

4. National Institutes of Health, Clinical Center, Bethesda, MD;

5. University of Texas M. D. Anderson Cancer Center, Houston; and

6. National Marrow Donor Program, Minneapolis, MN

Abstract

AbstractWe report outcomes of 932 recipients of unrelated donor peripheral blood stem cell hematopoietic cell transplantation (URD-PBSC HCT) for acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelogenous leukemia, and myelodysplastic syndrome enrolled on a prospective National Marrow Donor Program trial from 1999 through 2003. Preparative regimens included myeloablative (MA; N = 611), reduced-intensity (RI; N = 160), and nonmyeloablative (NMA; N = 161). For MA recipients, CD34+ counts greater than 3.8 × 106/kg improved neutrophil and platelet engraftment, whereas improved overall survival (OS) and reduced transplant-related mortality (TRM) were seen for all preparative regimens when CD34+ cell doses exceeded 4.5 × 106/kg. Higher infused doses of CD34+ cell dose did not result in increased rates of either acute or chronic graft-versus-host disease (GVHD). Three-year OS and disease-free survival (DFS) of recipients of MA, RI, and NMA approaches were similar (33%, 35%, and 32% OS; 33%, 30%, and 29% DFS, respectively). In summary, recipients of URD-PBSC HCT receiving preparative regimens differing in intensity experienced similar survival. Higher CD34+ cell doses resulted in more rapid engraftment, less TRM, and better 3-year OS (39% versus 25%, MA, P = .004; 38% versus 21% RI/NMA, P = .004) but did not increase the risk of GVHD. This trial was registered at www.clinicaltrials.gov as #NCT00785525.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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