The ethics of a proposed study of hematopoietic stem cell transplant for children with "less severe" sickle cell disease

被引:22
|
作者
Nickel, Robert S. [1 ]
Hendrickson, Jeanne E. [2 ]
Haight, Ann E. [1 ]
机构
[1] Emory Univ, Childrens Healthcare Atlanta, Aflac Canc & Blood Disorders Ctr, Atlanta, GA 30322 USA
[2] Yale Univ, New Haven, CT USA
关键词
BONE-MARROW-TRANSPLANTATION; VERSUS-HOST DISEASE; SILENT CEREBRAL INFARCTS; RISK-FACTORS; CORD BLOOD; ADVERSE OUTCOMES; DONOR; ANEMIA; SURVIVAL; HYDROXYUREA;
D O I
10.1182/blood-2014-05-575209
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hematopoietic stem cell transplant (HSCT) is the only cure for sickle cell disease (SCD). HSCT using an HLA-identical sibling donor is currently an acceptable treatment option for children with severe SCD, with expected HSCT survival >95% and event-free survival >85%. HSCT for children with less severe SCD (children who have not yet suffered overt disease complications or only had mild problems) is controversial. It is important to consider the ethical issues of a proposed study comparing HLA-identical sibling HSCT to best supportive care for children with less severe SCD. In evaluating the principles of nonmaleficence, respect for individual autonomy, and justice, we conclude that a study of HLA-identical sibling HSCT for all children with SCD, particularly hemoglobin SS and S beta(0)-thalassemia disease, is ethically sound. Future work should explore the implementation of a large trial to help determine whether HSCT is a beneficial treatment of children with less severe SCD.
引用
收藏
页码:861 / 866
页数:6
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