TY - JOUR
T1 - Race as a factor in donor selection and survival of children with hematologic malignancies undergoing hematopoietic stem cell transplant in Florida
AU - Horn, Biljana
AU - Lamba, Nikhil
AU - Chellapandian, Deepak
AU - Sunkersett, Gauri
AU - Silva, Jorge Galvez
AU - Ziga, Edward
AU - Alperstein, Warren
AU - Joyce, Michael
AU - Castillo, Paul
AU - Fort, John
AU - Zhao, Jing
AU - Oshrine, Benjamin
N1 - Funding Information:
informationChildren's Miracle NetworkWe gratefully acknowledge the support of Dr. Douglas Rizzo, Senior Scientific Director from CIBMTR, who introduced us to the eDBtC platform. We thank the nonprofit Children's Miracle Network for their 2018 and 2020 grants in support of FPBCC.
Publisher Copyright:
© 2021 Wiley Periodicals LLC
PY - 2021/10
Y1 - 2021/10
N2 - Background: Previous studies have explored posthematopoietic cell transplant (HCT) outcomes by race in adults; however, pediatric data addressing this topic are scarce. Procedure: This retrospective registry study included 238 White (W) and 57 Black (B) children with hematologic malignancies (HM) receiving first allogeneic HCT between 2010 and 2019 at one of the five Florida pediatric HCT centers. Results: We found no differences between W and B children in transplant characteristics, other than donor type. There was a significant difference in use of human leukocyte antigen (HLA)-mismatched donors (HLA-MMD) (53% W, 71% B, p =.01). When comparing HLA-MMD use to fully HLA-matched donors, B had relative risk (RR) of 1.47 (95% CI 0.7–3) of receiving a mismatched unrelated donor (MMUD), RR of 2.34 (95% CI 1.2–4.4) of receiving a mismatched related donor (MMRD), and RR of 1.9 (95% CI 0.99–3.6) of receiving a mismatched cord blood donor (MMCBD) HCT, respectively. There was no significant difference in the incidence of aGVHD (48% W, 35% B), p =.1, or cGVHD (19% W, 28% B, p =.1), or primary cause of death. Overall 24-month survival was 61% (95% CI 55%–68%) for W, and 60% (95% CI 48–75) for B children, log-rank p =.7. While HLA matching improved survival in W children, the number of B children receiving HLA-matched HCT was too small to identify the impact of HLA matching on survival. Conclusions: In this contemporary cohort of children with HM, we found that B children were more likely to receive HLA-MMD transplants, but this did not adversely affect survival or GVHD rates.
AB - Background: Previous studies have explored posthematopoietic cell transplant (HCT) outcomes by race in adults; however, pediatric data addressing this topic are scarce. Procedure: This retrospective registry study included 238 White (W) and 57 Black (B) children with hematologic malignancies (HM) receiving first allogeneic HCT between 2010 and 2019 at one of the five Florida pediatric HCT centers. Results: We found no differences between W and B children in transplant characteristics, other than donor type. There was a significant difference in use of human leukocyte antigen (HLA)-mismatched donors (HLA-MMD) (53% W, 71% B, p =.01). When comparing HLA-MMD use to fully HLA-matched donors, B had relative risk (RR) of 1.47 (95% CI 0.7–3) of receiving a mismatched unrelated donor (MMUD), RR of 2.34 (95% CI 1.2–4.4) of receiving a mismatched related donor (MMRD), and RR of 1.9 (95% CI 0.99–3.6) of receiving a mismatched cord blood donor (MMCBD) HCT, respectively. There was no significant difference in the incidence of aGVHD (48% W, 35% B), p =.1, or cGVHD (19% W, 28% B, p =.1), or primary cause of death. Overall 24-month survival was 61% (95% CI 55%–68%) for W, and 60% (95% CI 48–75) for B children, log-rank p =.7. While HLA matching improved survival in W children, the number of B children receiving HLA-matched HCT was too small to identify the impact of HLA matching on survival. Conclusions: In this contemporary cohort of children with HM, we found that B children were more likely to receive HLA-MMD transplants, but this did not adversely affect survival or GVHD rates.
KW - Florida consortium
KW - malignant disorders
KW - pediatric HCT
KW - race disparities
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U2 - 10.1002/pbc.29180
DO - 10.1002/pbc.29180
M3 - Article
C2 - 34121322
AN - SCOPUS:85107895585
SN - 1545-5009
VL - 68
JO - Medical and Pediatric Oncology
JF - Medical and Pediatric Oncology
IS - 10
M1 - e29180
ER -