Skip to main content
. Author manuscript; available in PMC: 2013 Oct 1.
Published in final edited form as: Pediatr Blood Cancer. 2011 Dec 19;59(4):725–731. doi: 10.1002/pbc.24036

TABLE I.

Summary of characteristics of HSCT patients receiving transplant for sickle cell disease or thalassemiaa

Disease Age
(yrs)
Gender Blackb Hispanic Allogeneic
HSCT Type
Myeloablative
Prep
Max aGVHD
grade
through 3m
Max cGVHD
grade
through 12m
Max organ
toxicity
through 3m
SCD 6 F Yes No Related No 0 0 Good
SCD 7 M Yes No Related Yes 0 1 Good
SCD 7 M Yes No Unrelated Yes 0 0 Good
SCD 10 M No No Related Yes 0 0 Good
SCD 13 M Yes No Related Yes 0 0 Good
SCD 17 F Yes No Related No 0 0 Good
SCD 18 M Yes No Unrelated No 2 2 Good
Thal 5 M NSd No Related Yes 0 0 Good
Thal 7 F No No Related Yes 1 0 Good
Thal 7 M No No Related No 2 0 Good
Thal 8 M No No Related Yes 0 0 Good
Thal c 8 F NSd Yes Unrelated Yes 4 2;
progressive
onset
Intermediate
to poor
Thal 13 F No No Unrelated No 1 0 Good
a

SCD=sickle cell disease; Thal=thalassemia; M=male; F=female; aGVHD=acute graft versus host disease; cGVHD=chronic graft versus host disease;

b

Child race per parent report;

c

Patient died approx. 3 months after transplant;

d

Not specified