Haploidentical bone marrow transplant with posttransplant cyclophosphamide for sickle cell disease: An update

Hematol Oncol Stem Cell Ther. 2020 Jun;13(2):91-97. doi: 10.1016/j.hemonc.2020.01.002. Epub 2020 Mar 12.

Abstract

Hematopoietic cell transplant (HCT) can cure both children and adults with sickle cell disease. Outcomes have historically been poor for the vast majority of patients who lack a matched sibling donor. However, the development of haploidentical HCT (haplo-HCT) with high doses of posttransplant cyclophosphamide (PTCy) has allowed for curative long-term potential with favorable transplant-related outcomes, though this has not obviated the potential for graft rejection from human leukocyte antigen mismatch and repeated red blood cell transfusions. Accordingly, multiple strategies have been developed to improve outcomes, the majority of which are based on the Johns Hopkins platform from 2012. Presently, we aim to discuss results from pertinent studies and compare outcomes with the two most recent approaches involving either thiotepa plus 200-cGy total body irradiation or 400-cGy total body irradiation. Direct comparisons are required to determine the optimized curative potential. Transplant-eligible patients must be referred to tertiary medical centers for consideration of haplo-HCT.

Keywords: Cyclophosphamide; Haploidentical transplant; Sickle cell disease; Thiotepa; Total body irradiation.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Anemia, Sickle Cell / drug therapy*
  • Anemia, Sickle Cell / therapy*
  • Bone Marrow Transplantation / methods*
  • Cyclophosphamide / pharmacology
  • Cyclophosphamide / therapeutic use*
  • Female
  • Humans
  • Male
  • Transplantation, Haploidentical / methods*
  • Young Adult

Substances

  • Cyclophosphamide