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      The EBMT Handbook : Hematopoietic Cell Transplantation and Cellular Therapies 

      Selection of Stem Cell Source

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      Springer International Publishing

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          Abstract

          Selection of stem cell source is an important consideration for any physician planning an allogeneic haematopoietic cell transplant (HCT) and has evolved considerably since bone marrow (BM) was used as the stem cell source in the first successful allogeneic HCT in 1968 (Gatti et al. 1968). BM remained the only source of stem cells for the two decades that followed until experimental work demonstrating that peripheral blood (PB) stem cells can be enriched by pre-treatment with certain chemotherapy agents and haematopoietic growth factors (Richman et al. 1976; Socinski et al. 1988; Duhrsen et al. 1988) resulted in the first peripheral blood stem cell transplant in 1986 (Korbling and Freireich 2011). Alongside this, the recognition of cord blood (CB) as a rich source of stem cells (Prindull et al. 1978) led to the successful use of cord blood as a third stem cell source in allogeneic HCT in the late 80s (Gluckman et al. 1989).

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          Most cited references32

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          HLA match likelihoods for hematopoietic stem-cell grafts in the U.S. registry.

          Hematopoietic stem-cell transplantation (HSCT) is a potentially lifesaving therapy for several blood cancers and other diseases. For patients without a suitable related HLA-matched donor, unrelated-donor registries of adult volunteers and banked umbilical cord-blood units, such as the Be the Match Registry operated by the National Marrow Donor Program (NMDP), provide potential sources of donors. Our goal in the present study was to measure the likelihood of finding a suitable donor in the U.S. registry. Using human HLA data from the NMDP donor and cord-blood-unit registry, we built population-based genetic models for 21 U.S. racial and ethnic groups to predict the likelihood of identifying a suitable donor (either an adult donor or a cord-blood unit) for patients in each group. The models incorporated the degree of HLA matching, adult-donor availability (i.e., ability to donate), and cord-blood-unit cell dose. Our models indicated that most candidates for HSCT will have a suitable (HLA-matched or minimally mismatched) adult donor. However, many patients will not have an optimal adult donor--that is, a donor who is matched at high resolution at HLA-A, HLA-B, HLA-C, and HLA-DRB1. The likelihood of finding an optimal donor varies among racial and ethnic groups, with the highest probability among whites of European descent, at 75%, and the lowest probability among blacks of South or Central American descent, at 16%. Likelihoods for other groups are intermediate. Few patients will have an optimal cord-blood unit--that is, one matched at the antigen level at HLA-A and HLA-B and matched at high resolution at HLA-DRB1. However, cord-blood units mismatched at one or two HLA loci are available for almost all patients younger than 20 years of age and for more than 80% of patients 20 years of age or older, regardless of racial and ethnic background. Most patients likely to benefit from HSCT will have a donor. Public investment in donor recruitment and cord-blood banks has expanded access to HSCT. (Funded by the Office of Naval Research, Department of the Navy, and the Health Resources and Services Administration, Department of Health and Human Services.).
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            Hematopoietic reconstitution in a patient with Fanconi's anemia by means of umbilical-cord blood from an HLA-identical sibling.

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              Cord-Blood Transplantation in Patients with Minimal Residual Disease

              The majority of patients in need of a hematopoietic-cell transplant do not have a matched related donor. Data are needed to inform the choice among various alternative donor-cell sources.
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                Book Chapter
                2024
                April 11 2024
                : 135-141
                10.1007/978-3-031-44080-9_14
                d1314d16-e670-4b17-9a85-39b08c2b82f3
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