Single-centre experience with allogeneic bone marrow transplantation for acute lymphoblastic leukaemia in childhood: similar survival after matched-related and matched-unrelated donor transplants

被引:20
作者
Al-Kasim, FA
Thornley, I
Rolland, M
Lau, W
Tsang, R
Freedman, MH
Saunders, EF
Calderwood, S
Doyle, JJ
机构
[1] Hosp Sick Children, Div Haematol Oncol, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Dept Paediat Lab Med, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Princess Margaret Hosp, Dept Radiotherapy, Toronto, ON, Canada
[4] City Hope Natl Med Ctr, Dept Bone Marrow Transplantat, Duarte, CA 91010 USA
关键词
acute lymphoblastic leukaemia; bone marrow transplantation; HLA-matched unrelated donor; HLA-matched related donor; children;
D O I
10.1046/j.0007-1048.2001.03282.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Seventy percent of children with acute lymphoblastic leukaemia (ALL) who may benefit from bone marrow transplant (BMT) lack a human leucocyte antigen (HLA)-matched related donor (MRD). For these children, BMT from a matched unrelated donor (MUD) represents a therapeutic option. We reviewed the course of 62 children with ALL who received fully matched marrow allografts at our institution between 2990 and 1998: 36 with MRDs and 26 with MUDs. Clinical characteristics were similar in the two groups. The interval from attainment of pre-BMT complete remission to transplant was significantly longer in the MUD group. Conditioning (etoposide/total body irradiation) and graft-versus-host disease (GVHD) prophylaxis regimens were the same for all patients, and all received T cell-replete bone marrow. There was no significant difference in probability of engraftment, or time to engraftment, in the two groups. MUD BMT recipients had a significantly greater incidence of grade II-IV acute GVHD (58% versus 24% in the MRD group; P = 0.02), and demonstrated a trend towards more chronic GVHD (39% versus 15%; P = 0.06). Three years post BMT, the probabilities of transplant-related mortality were 33 +/- 11% and 20 +/- 8% in MUD and MRD groups respectively (P = 0.38); the probabilities of relapse were 28 +/- 12% and 41 +/- 9% respectively (P = 0.19). Lansky or Karnofsky performance scores in event-free survivors were 90-100 in 87% of the MUD group and 83% of the MRD group. With a median follow up of 38 months (range, 3-97), 3-year event-free survival was 49 +/- 11% and 47 9% in the MUD and MRD BMT groups respectively (P = 0.71). These results suggest that MUD BMT is a valuable therapy for children with ALL in whom BMT is indicated, and underscore the importance of efforts aimed at expediting unrelated donor searches for patients lacking a MRD.
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收藏
页码:483 / 490
页数:8
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