AI Article Synopsis

  • The study investigates the role of ABO blood group compatibility in outcomes following umbilical cord blood transplantation (UCBT) for nonmalignant disorders, finding no significant impact on survival or complications related to ABO mismatches.
  • Researchers analyzed data from 270 patients and observed only a minor trend toward worse acute graft-versus-host disease (GVHD) in cases of major incompatibility.
  • The findings suggest that when choosing UCB for treating nonmalignant disorders, ABO compatibility may not be a critical factor.

Article Abstract

Existing literature shows mixed conclusions regarding the impact of ABO incompatibility on outcomes after hematopoietic stem cell transplantation. Because the future for umbilical cord blood (UCB) expansion technologies is bright, we assessed whether this typically overlooked graft characteristic impacted various outcomes after UCB transplantation (UCBT) for nonmalignant disorders (NMDs). A prospectively maintained institutional blood and marrow transplant program database was queried for all patients undergoing first UCBT for NMDs. UCB and recipient ABO compatibility was considered as matched, major mismatched, minor mismatched, or bidirectional mismatched. The impact of ABO incompatibility was assessed on overall survival, graft failure, acute and chronic graft-versus-host disease (GVHD), time to neutrophil and platelet recovery, day 0 to day 100 RBC transfusion burden, and donor hematopoietic chimerism. Through December 2014, 270 patients have undergone first UCBT for various NMDs. In both univariable and multivariable analyses, ABO compatibility status did not appear to impact any outcomes assessed, although a trend toward increased grades III to IV acute GVHD was seen in recipients of major mismatched units. When considering UCBT for treatment of NMDs, ABO compatibility between the donor unit and intended recipient does not appear to be an important consideration in the UCB unit choice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067229PMC
http://dx.doi.org/10.1016/j.bbmt.2016.07.019DOI Listing

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