A randomised study of allogeneic transplantation with stem cells from blood or bone marrow

被引:94
作者
Heldal, D
Tjonnfjord, G
Brinch, L
Albrechtsen, D
Egeland, T
Steen, R
Solheim, BG
Evensen, SA
机构
[1] Univ Oslo, Natl Hosp, Dept Med, Oslo, Norway
[2] Univ Oslo, Natl Hosp, Dept Surg B, Oslo, Norway
[3] Univ Oslo, Natl Hosp, Inst Immunol, Oslo, Norway
关键词
blood progenitor cells; allogeneic bone marrow transplantation; G-CSF;
D O I
10.1038/sj.bmt.1702422
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Sixty-one consecutive adult patients with leukaemia, primary myelofibrosis or myelodysplastic syndrome with an HLA-identical or one antigen mismatched family donor were randomised to allogeneic transplantation with PBPC or BM. Progenitor cells were mobilised into the blood by giving the donors 10 mu g/kg/day G-CSF subcutaneously for 5-7 days. G-CSF was not given to patients after transplantation. The time to neutrophil counts >0.5 x 10(9)/l was 17 days (95% CI 15.2-18.8 days) in the PBPC group compared to 23 (95 % CI 20.3-25.7 days) in the BM group (P = 0.0005). The time to platelet counts >20 x 10(9)/l was 13 days (95% CI 11.7-14.3 days) in the PBPC group and 21 days (95% CI 18.7-23.3 days) in the BM group (P = 0.0005), Acute GVHD of grades II-IV developed in six patients transplanted with PBPC and three patients transplanted. with BM. The numbers of patients with chronic GVHD were 15 and 8, respectively. Transplant-related mortality and leukaemia-free survival showed no significant differences. Transplantation with PBPC appears preferable for the recipient due to faster neutrophil and platelet recovery. However, the final conclusion can not be drawn before long-term results on chronic GVHD and relapse incidence in longer randomised trials are available.
引用
收藏
页码:1129 / 1136
页数:8
相关论文
共 42 条
[11]  
DREGER P, 1993, BLOOD, V81, P1404
[12]   The risk of residual molecular and cytogenetic disease in patients with Philadelphia-chromosome positive first chronic phase chronic myelogenous leukemia is reduced after transplantation of allogeneic peripheral blood stem cells compared with bone marrow [J].
Elmaagacli, AH ;
Beelen, DW ;
Opalka, B ;
Seeber, S ;
Schaefer, UW .
BLOOD, 1999, 94 (02) :384-389
[13]   Allogeneic peripheral blood progenitor cell transplantation in a murine model: Evidence for an improved graft-versus-leukemia effect [J].
Glass, B ;
Uharek, L ;
Zeis, M ;
Dreger, P ;
Loffler, H ;
Steinmann, J ;
Schmitz, N .
BLOOD, 1997, 90 (04) :1694-1700
[14]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304
[15]   PERIPHERAL-BLOOD STEM-CELLS FOR ALLOGRAFTING [J].
GOLDMAN, J .
BLOOD, 1995, 85 (06) :1413-1415
[16]   Blood and marrow transplantation activity in Europe 1996 [J].
Gratwohl, A ;
Passweg, J ;
Baldomero, H ;
Hermans, J .
BONE MARROW TRANSPLANTATION, 1998, 22 (03) :227-240
[17]   Blood and marrow transplantation activity in Europe 1995 [J].
Gratwohl, A ;
Hermans, J ;
Baldomero, H .
BONE MARROW TRANSPLANTATION, 1997, 19 (05) :407-419
[18]  
HELDAL D, 1997, BONE MARROW TRANS S1, V19, P73
[19]   From vice to disease? The concepts of dipsomania and inebriety, 1860-1908 [J].
Johnstone, G .
SOCIAL & LEGAL STUDIES, 1996, 5 (01) :37-+
[20]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481