PMID- 36961333 OWN - NLM STAT- MEDLINE DCOM- 20230511 LR - 20230624 IS - 1537-2995 (Electronic) IS - 0041-1132 (Linking) VI - 63 IP - 5 DP - 2023 May TI - Modeling unrelated blood stem cell donor recruitment using simulated registrant cohorts: Assessment of human leukocyte antigen matching across ethnicity groups. PG - 1060-1066 LID - 10.1111/trf.17310 [doi] AB - BACKGROUND: Human leukocyte antigen (HLA)-matched unrelated donors are not available for some patients considered for allogeneic hematopoietic cell transplantation, particularly among certain ethnic groups. Simulated recruitment modeling can inform efforts to find new matches for more patients. METHODS: Simulated recruits were generated by assigning a pair of donor HLA haplotypes from historical data files and matched against HLA data of patient searches in the Canadian Blood Services Stem Cell Registry. Recruitment cohorts reflected the proportion of five specific ethnic groups in the 2016 Canadian census data. RESULTS: Novel 8/8 HLA matches between simulated recruits and patients increased linearly with larger recruitment cohorts. The proportion of novel 8/8 HLA matches from Caucasian, Hispanic, and Native American/First Nations recruits was equal to or greater than their relative proportion in the recruited cohort (match to: recruit ratio (MRR) >/= 1). In contrast, African American and Asian & Pacific Islander recruits represented a smaller proportion of novel matches relative to their percentage of the recruited cohort (MRR <1). The proportion of novel 7/8 HLA-matches from each ethnic group was approximately the same as their proportion in the recruited cohort (MRR ~ 1) and high rates of 7/8 HLA-matching already exist within the Canadian Blood Services registry for all ethnic groups. CONCLUSION: Continued large recruitment cohorts are needed to add new 8/8 HLA matches to registry inventories. Likelihoods of novel HLA matches varied across ethnic groups, reflecting varied HLA haplotype frequencies across groups. Simulated cohort modeling can inform recruitment strategies that will generate new donor options for patients. CI - (c) 2023 The Authors. Transfusion published by Wiley Periodicals LLC on behalf of AABB. FAU - Blake, John T AU - Blake JT AUID- ORCID: 0000-0003-0617-8996 AD - Stem Cells, Canadian Blood Services, Ottawa, Ontario, Canada. AD - Department of Industrial Engineering, Faculty of Engineering, Dalhousie University, Halifax, Nova Scotia, Canada. FAU - Parmar, Gaganvir AU - Parmar G AD - Stem Cells, Canadian Blood Services, Ottawa, Ontario, Canada. FAU - Ganz, Kathy AU - Ganz K AD - Stem Cells, Canadian Blood Services, Ottawa, Ontario, Canada. FAU - Seftel, Matthew D AU - Seftel MD AD - Stem Cells, Canadian Blood Services, Ottawa, Ontario, Canada. AD - Department of Medicine, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada. FAU - Allan, David S AU - Allan DS AUID- ORCID: 0000-0003-3261-8289 AD - Stem Cells, Canadian Blood Services, Ottawa, Ontario, Canada. AD - Department of Medicine, and Biochemistry, Microbiology & Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada. AD - Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20230324 PL - United States TA - Transfusion JT - Transfusion JID - 0417360 RN - 0 (HLA Antigens) RN - 0 (Histocompatibility Antigens Class I) RN - 0 (Histocompatibility Antigens Class II) SB - IM MH - Humans MH - *Unrelated Donors MH - Ethnicity MH - Histocompatibility Testing MH - Canada MH - *Hematopoietic Stem Cell Transplantation MH - HLA Antigens/genetics MH - Histocompatibility Antigens Class I MH - Haplotypes MH - Histocompatibility Antigens Class II MH - Stem Cells MH - Registries OTO - NOTNLM OT - HLA-matching OT - allogeneic OT - hematopoietic cell transplant OT - simulated recruitment OT - stem cell registry EDAT- 2023/03/25 06:00 MHDA- 2023/05/11 06:42 CRDT- 2023/03/24 10:12 PHST- 2023/02/10 00:00 [revised] PHST- 2022/12/12 00:00 [received] PHST- 2023/02/12 00:00 [accepted] PHST- 2023/05/11 06:42 [medline] PHST- 2023/03/25 06:00 [pubmed] PHST- 2023/03/24 10:12 [entrez] AID - 10.1111/trf.17310 [doi] PST - ppublish SO - Transfusion. 2023 May;63(5):1060-1066. doi: 10.1111/trf.17310. Epub 2023 Mar 24.