A randomized multicenter comparison of bone marrow and peripheral blood in recipients of matched sibling allogeneic transplants for myeloid malignancies

被引:235
作者
Couban, S
Simpson, DR
Barnett, MJ
Bredeson, C
Hubesch, L
Kang, HL
Shore, TB
Walker, IR
Browett, P
Messner, HA
Panzarella, T
Lipton, JH
机构
[1] Queen Elizabeth 2 Hlth Sci Ctr, Halifax, NS B3H 2Y9, Canada
[2] Dalhousie Univ, Dept Med, Halifax, NS, Canada
[3] N Shore Hosp, Auckland, New Zealand
[4] Vancouver Hosp & Hlth Sci Ctr, Vancouver, BC V5Z 1M9, Canada
[5] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
[6] Med Coll Wisconsin, Stat Ctr, Int Bone Marrow Transplant Registry, Hlth Policy Inst, Milwaukee, WI 53226 USA
[7] Ottawa Hosp, Dept Med, Ottawa, ON, Canada
[8] Univ Ottawa, Ottawa, ON K1N 6N5, Canada
[9] London Hlth Sci Ctr, Dept Med, London, ON, Canada
[10] London Hlth Sci Ctr, Dept Oncol, London, ON, Canada
[11] Univ Western Ontario, London Reg Canc Ctr, London, ON N6A 3K7, Canada
[12] Cornell Univ, New York Presbyterian Hosp, Weill Med Coll, New York, NY USA
[13] McMaster Univ, Dept Med, Hamilton, ON L8S 4L8, Canada
[14] Univ Auckland, Fac Med & Hlth Sci, Auckland, New Zealand
[15] Princess Margaret Hosp, Dept Med Oncol, Toronto, ON M4X 1K9, Canada
[16] Princess Margaret Hosp, Dept Biostat, Toronto, ON M4X 1K9, Canada
[17] Univ Toronto, Toronto, ON, Canada
关键词
D O I
10.1182/blood-2002-01-0048
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytokine-mobilized peripheral blood it increasingly used instead of bone marrow as the source of cells for allogenelc transplantation. Although cells lead to faster hematologic recovery, their effects on graft-versus-host disease, relapse, and survival are less certain. Between January 1996 and February 2000, 228 patients With chronic myeloid leukemia, acute myeloid leukemia, or myelodysplasia were randomized to receive either bone marrow or peripheral blood allografts from HLA-matched siblings. All patients received busulfan and cyclophosphamide as conditioning chemotherapy and cyclosporine and methotrexate as graft-versus-host disease prophylaxis. We compared the times to neutrophil and platelet recovery, acute and chronic graft-versus-host disease, relapse, and overall survival between the groups. The median times to neutrophil recovery were 19 days and 23 days and the times to platelet recovery were 16 days and 22 days in the peripheral blood and bone marrow groups, respectively (P < .0001 for both comparisons). The cumulative incidence of grades II to IV acute graft-versus-host disease 100 days after transplantation was 44% in both groups (hazard ratio, 0.99; 95% confidence interval, 0.66-1.49; P > .9), and the incidence of extensive chronic graft-versus-host disease at 30 months after transplantation was 40% with peripheral blood and 30% with bone marrow (hazard ratio, 1.23; 95% confidence interval, 0.78-1.96; P = .37). There was no statistically significant difference in the probability of relapse of the underlying disease between the groups. The probabilities of survival at 30 months after transplantation were 68% and 60% in the peripheral blood and bone marrow groups, respectively (hazard ratio, 0.62; 95% confidence interval, 0.39-0.97; P = .04). In patients with chronic myeloid leukemia, acute myelold leukemia, and myelodysplasia undergoing allogeneic transplantation from matched siblings, the use of peripheral blood instead of bone marrow leads to faster hematologic recovery, similar risk of graft-versus-host disease, and improved survival. (C) 2002 by The American Society of Hematology.
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页码:1525 / 1531
页数:7
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