Outcome of Chinese patients with chronic myeloid leukaemia (CML) underwentallogeneic bone-marrow transplantation (BMT)

Citation
Ck. Lee et al., Outcome of Chinese patients with chronic myeloid leukaemia (CML) underwentallogeneic bone-marrow transplantation (BMT), AM J HEMAT, 61(2), 1999, pp. 85-89
Citations number
13
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
AMERICAN JOURNAL OF HEMATOLOGY
ISSN journal
03618609 → ACNP
Volume
61
Issue
2
Year of publication
1999
Pages
85 - 89
Database
ISI
SICI code
0361-8609(199906)61:2<85:OOCPWC>2.0.ZU;2-9
Abstract
Clinical studies have shown that patients with chronic myeloid leukaemia (C ML) treated with allogeneic bone-marrow transplantation (BMT) experience no t only prolonged disease-free survival but also complete cure in some. Ther efore, we followed a cohort of 81 Chinese patients who received allogeneic BMT. Patients and Methods: The donors were either relatives (65 siblings, 1 pare nt) or unrelated volunteers (15). BMT was performed at a median interval of 11.6 months from diagnosis of CML, and the stages of disease before BMT we re: first chronic phase (60 patients), accelerated or second chronic phase in (10 patients), and blastic crisis (11 patients). Three conditioning regi mens were employed: Bu-Cy, Cy-TBI, or Bu-Cy-TBI, Standard cyclosporin and s hort methotrexate protocol were used for acute graft-versus-host disease (G VHD) prophylaxis. Results: There were five graft failures with three after related BMT. Patie nts after related or unrelated BMT had a comparable rate of neutrophil reco very (median = 22 days), but significant delay in platelet recovery occurre d after unrelated BMT (median = 34 vs. 20 days, P < 0.05). The latter also had higher incidence of acute GvHD (73% vs. 41%, P < 0.05), although the in cidence of chronic GVHD was not different between groups. At a median follo w-up of 43.5 months, patients after related BMT had a significantly better rate of disease-free survival (68% vs. 37.3%, P < 0.05) and overall surviva l (81% vs. 38.9%, P < 0.05) at 4 years. Subgroup analysis of patients after related BMT showed the outcome was better when they were transplanted at f irst chronic phase, Multivariate analysis showed that advanced disease (RR = 2.01, 95% CI = 1.48-2.73) significantly worsened the outcome of BMT, wher eas the presence of chronic GvHD had a protective effect against relapse an d survival (RR = 0.09, 95% CI = 0.02-0.38), Conclusion: Allogeneic BMT is a curative form of treatment for patients wit h CML, Treatment outcome is best for those who undergo transplants from HLA -matched siblings during the first chronic phase, Am. J. Hematol. 61:85-89, 1999. (C) 1999 Wiley-Liss, Inc.