Autologous bone marrow transplantation in non-Hodgkin's lymphoma patients: effect of a brief course of G-CSF on harvest and recovery

被引:2
作者
Damiani, D
Grimaz, S
Infanti, L
Sperotto, A
Silvestri, F
Geromin, A
Cerno, M
Savignano, C
Michieli, M
Skert, C
Fanin, R
Baccarani, M
机构
[1] Univ Hosp, Div Hematol, I-33100 Udine, Italy
[2] Univ Hosp, Dept Med & Morphol Res, I-33100 Udine, Italy
[3] Univ Hosp, Dept Bone Marrow Transplant, I-33100 Udine, Italy
关键词
ABMT; G-CSF; bone marrow; engraftment;
D O I
10.1038/sj.bmt.1701979
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This study compares harvest and hematological recovery data of 100 lymphoma patients who underwent BM harvest either after a short course of G-CSF (16 mu g/kg for 3 days) (n = 57) or in steady-state conditions (n = 43). G-CSF allowed the attainment of a significantly higher median number of total nucleated cells x 10(8)/kg (4.4, range 1.4-17, vs 2.1, range 0.6-4.2; P < 0.0001), mononuclear cells x 10(8)/kg (0.55, range 0.20-1.4, vs 0.41, range 0.15-0.76, P < 0.0001) and CFU-GM/ml (310, range 10-5500, vs 80, range 10-3800, P = 0.008), with lower volumes of blood collected (17.5 ml/kg, range 8-31 vs 21.0, range 15-30, P = 0.0001). Hematological recovery was faster in patients who received pre-treated BM (median time to PMN >0.5 x 10(9)/l and to platelets >20 x 10(9)/l was 12, range 10-14, and 13, range 10-18, days, respectively) than in those autotransplanted with steady-state BM (median time to PMN >0.5 x 10(9)/l and to platelets >20 x 10(9)/l 13, range 10-18 and 14, range 10-20 days, respectively, P = 0.004 and P = 0.01). Transfusional requirement was significantly different and patients of the G-CSF group needed shorter hospitalization (17 days, range 12-24, vs 20 days, range 14-32; P = 0.02). These data suggest that treating patients with G-CSF before BM harvest improves the quality of the harvest and accelerates engraftment and hematological recovery.
引用
收藏
页码:757 / 761
页数:5
相关论文
共 25 条
[21]   Efflux of CD34+ cells from bone marrow to peripheral blood is selective in steady-state hematopoiesis and during G-CSF administration [J].
Steen, R ;
Tjonnfjord, GE ;
Groseth, LAG ;
Heldal, D ;
Egeland, T .
JOURNAL OF HEMATOTHERAPY, 1997, 6 (06) :563-573
[22]   Allogeneic peripheral blood stem cell transplantation may be associated with a high risk of chronic graft-versus-host disease [J].
Storek, J ;
Gooley, T ;
Siadak, M ;
Bensinger, WI ;
Maloney, DG ;
Chauncey, TR ;
Flowers, M ;
Sullivan, KM ;
Witherspoon, RP ;
Rowley, SD ;
Hansen, JA ;
Storb, R ;
Appelbaum, FR .
BLOOD, 1997, 90 (12) :4705-4709
[23]  
Sutherland D R, 1996, J Hematother, V5, P213, DOI 10.1089/scd.1.1996.5.213
[24]   The biology and clinical uses of blood stem cells [J].
To, LB ;
Haylock, D ;
Simmons, PJ ;
Juttner, CA .
BLOOD, 1997, 89 (07) :2233-2258
[25]  
TO LB, 1990, EXP HEMATOL, V18, P442