Mr. Bishop et al., LONG-TERM SURVIVAL IN ADVANCED CHRONIC MYELOGENOUS LEUKEMIA FOLLOWINGBONE-MARROW TRANSPLANTATION FROM HAPLOIDENTICAL RELATED DONORS, Bone marrow transplantation, 18(4), 1996, pp. 747-753
From 1987 to 1991, 26 patients with CML and a median age of 31 Sears r
eceived allogeneic BMT from a partially mismatched related donor (PMRD
) who shared at least one haplotype with the recipient. Nine patients
were in accelerated phase (AP), and 11 patients were in blast crisis (
BC) at the time of BMT. Patients were mismatched either in graft-versu
s-host or host-versus-graft directions for one antigen in 3 patients,
two antigens in 14 patients, and three antigens in 9 patients. All pat
ients were prepared with a regimen consisting of total body irradiatio
n, etoposide, cytosine arabinoside, cyclophosphamide and methylprednis
olone. All marrows were treated ex vivo with T10B91 . A-31, a monoclon
al antibody directed toward the alpha beta heterodimer of the CD3 rece
ptor, and rabbit complement, Additional GVHD prophylaxis included eith
er the anti-CD5 immunoconjugate XomaZyme-H65, cyclosporine, or both in
combination with methylprednisolone. Eight patients did not have sust
ained engraftment. The 100-day survival was 42%, The incidence of grea
ter than or equal to grade II acute GVHD was 29%. The incidence of chr
onic GVHD was 50% and was limited in all cases. The median survival at
4 years for all 26 patients was 27%, Seven patients (CP 1, AP 3, BC 3
) remain in hematologic remission 1297-2241+ days after transplantatio
n. AlloBMT from a PMRD may be considered for patients with advanced CM
L who lack a matched sibling or unrelated donor.