Ethical Challenges in Hematopoietic Cell Transplantation for Sickle Cell Disease

Biol Blood Marrow Transplant. 2018 Feb;24(2):219-227. doi: 10.1016/j.bbmt.2017.08.034. Epub 2017 Sep 1.

Abstract

Hematopoietic cell transplantation (HCT) using an HLA-identical sibling donor offers a very high likelihood of cure with good outcomes for patients with sickle cell disease (SCD), and alternative donor HCT for SCD is an area of active clinical research. Thus, HCT is a potential option for a growing number of patients with SCD. This expanded use of HCT has raised several ethical questions. Who is eligible for HCT, in terms of both disease severity and psychosocial factors? Should affected children with matched sibling donors undergo HCT only when they have declared themselves as having significant symptomatology? Regarding donors, special ethical challenges include the use of preimplantation genetic diagnosis to conceive an HLA-identical sibling. In this review, we critically analyze various ethical challenges related to HCT for SCD, and offer recommendations to guide clinical care.

Keywords: Bone marrow transplant; Donor; Eligibility; Ethics; Hematopoietic stem cell transplantation; Sickle cell disease.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Anemia, Sickle Cell / therapy*
  • Child
  • Hematopoietic Stem Cell Transplantation / ethics*
  • Hematopoietic Stem Cell Transplantation / methods
  • Humans
  • Preimplantation Diagnosis
  • Psychology
  • Tissue Donors / ethics
  • Young Adult