A. Oakhill et al., UNRELATED DONOR BONE-MARROW TRANSPLANTATION FOR CHILDREN WITH RELAPSED ACUTE LYMPHOBLASTIC-LEUKEMIA IN SECOND COMPLETE REMISSION, British Journal of Haematology, 94(3), 1996, pp. 574-578
Allogeneic sibling bone marrow transplantation (BMT) is the recommende
d treatment for relapsed childhood acute lymphoblastic leukaemia (ALL)
, but appropriate donors are only available in 30% of cases. Unfortuna
tely, BMT from unrelated donors (UD) has been associated with high rat
es of severe graft-versus-host disease (GvHD) and transplant-related m
ortality (TRM). In an attempt to improve outcome in UD-BMT we have ass
essed the impact of T-cell depletion using CAMPATH-1 (anti-CD52) monoc
lonal antibodies in 50 consecutively referred patients with relapsed A
LL in second remission. All were previously treated according to MRC p
rotocols UKALL X and XI, and then given chemotherapy on MRC R1 from re
lapse until UD-BMT. 19 patients had relapsed on and 31 off therapy. Pa
tients and donors were fully matched at HLA-A. -B, -DR and -DQ loci in
29 cases and mismatched in 21 (four mismatched for more than one anti
gen). Pre-transplant conditioning comprised CAMPATH-1G, cyclophosphami
de and total body irradiation. Bone marrow was T-cell depleted in vitr
o using CAMPATH-1 antibodies. Additional GvHD prophylaxis consisted of
cyclosporin A (42 cases), cyclosporin plus methotrexate (four) or non
e (four). 47 patients engrafted. The incidence of acute GvHD was very
low: two patients with grade II disease in the matched group, four wit
h grade II-IV in the mismatched group. Only four chronic GVHD. The act
uarial event-free have (EFS) at 2 years is 53%, with no significant di
fference between the matched and mismatched group. Further leukaemic r
elapse was the most important cause of failure. These results are simi
lar to the most favourable published reports for HLA-matched sibling B
MT in relapsed ALL.