Randomised trial of filgrastim-mobilised peripheral blood progenitor cell transplantation versus autologous bone-marrow transplantation in lymphoma patients

被引:536
作者
Schmitz, N
Linch, DC
Dreger, P
Goldstone, AH
Boogaerts, MA
Ferrant, A
Demuynck, HMS
Link, H
Zander, A
Barge, A
Borkett, K
机构
[1] UCL HOSP, LONDON, ENGLAND
[2] UNIV LEUVEN, MED CTR, DEPT HAEMATOL, LOUVAIN, BELGIUM
[3] CLIN UNIV ST LUC, DEPT HAEMATOL, BRUSSELS, BELGIUM
[4] UNIV HAMBURG, BONE MARROW TRANSPLANTAT UNIT, D-20246 HAMBURG, GERMANY
[5] HANNOVER MED SCH, DEPT HAEMATOL & ONCOL, HANNOVER, GERMANY
[6] AMGEN LTD, CAMBRIDGE, ENGLAND
关键词
D O I
10.1016/S0140-6736(96)90536-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background A randomised trial comparing filgrastim-mobilised peripheral blood progenitor cell (PBPC) transplants with autologous bone marrow transplantation (ABMT) for haematopoietic stem cell support has not been done. We compared the effects of filgrastim-mobilised PBPC or autologous bone marrow reinfused to lymphoma patients after high-dose chemotherapy in a prospective randomised multicentre trial. Methods The trial was done at six centres in three European countries. After high-dose chemotherapy (carmustine, etoposide, cytarabine, and melphalan [BEAM protocol]) 58 patients with advanced Hodgkin's disease or high-grade non-Hodgkin lymphoma received either filgrastim-mobilised PBPC (n=27) or bone marrow (n=31) for haemopoietic reconstitution. Findings The median number of days with platelet transfusions after grafting was 6 in the PBPC transplantation group and 10 in the ABMT group (estimate of treatment difference 5 days, 95% CI 3-7 days). Time to platelet recovery above 20x10(9)/L was 16 days in the PBPC transplantation group and 23 days in the ABMT group (p=0.02). Time to neutrophil recovery above 0.5x10(9)/L was also reduced in the PBPC transplantation group (11 vs 14 days, p=0.005). Patients randomised to PBPC transplantation needed fewer red blood cell transfusions (two vs three, p=0.002) and spent less time in hospital (17 vs 23 days, p=0.002). Early post-transplant morbidity and mortality as well as overall survival (median follow-up 311 days) were similar in both groups. There was no notable toxicity ascribed to filgrastim administration or the leucapheresis procedures. Interpretation In patients with lymphoma treated with high-dose chemotherapy, reinfusing filgrastim-mobilised PBPC instead of autologous bone marrow significantly reduced the number of platelet transfusions, the time to platelet and neutrophil recovery, and led to earlier discharge from hospital.
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页码:353 / 357
页数:5
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