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
[1]  
BENSINGER W, 1993, BLOOD, V81, P3158
[2]   HEMATOPOIETIC RESCUE AFTER HIGH-DOSE CHEMOTHERAPY USING AUTOLOGOUS PERIPHERAL-BLOOD PROGENITOR CELLS OR BONE-MARROW - A RANDOMIZED COMPARISON [J].
BEYER, J ;
SCHWELLA, N ;
ZINGSEM, J ;
STROHSCHEER, I ;
SCHWANER, I ;
OETTLE, H ;
SERKE, S ;
HUHN, D ;
SIEGERT, W .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (06) :1328-1335
[3]  
CHAO NJ, 1993, BLOOD, V81, P2031
[4]  
CIAVARELLA D, 1991, BIOTECHNOLOGY BLOOD, P317
[5]  
Damiani D, 1997, BLOOD, V90, P36
[6]  
DEMUYNCK H, 1995, ANN HEMATOL, V71, P29, DOI 10.1007/BF01696229
[7]  
Dicke KA, 1997, EXP HEMATOL, V25, P34
[8]  
FAUCHER C, 1994, BONE MARROW TRANSPL, V14, P895
[9]  
HANSEN PB, 1995, BONE MARROW TRANSPL, V16, P373
[10]   Peripheral blood stem cell and bone marrow transplantation for solid tumors and lymphomas: Hematologic recovery and costs - A randomized, controlled trial [J].
Hartmann, O ;
LeCorroller, AG ;
Blaise, D ;
Michon, J ;
Philip, I ;
Norol, F ;
Janvier, M ;
Pico, JL ;
Baranzelli, MC ;
Rubie, H ;
Coze, C ;
Pinna, A ;
Meresse, V ;
Benhamou, E .
ANNALS OF INTERNAL MEDICINE, 1997, 126 (08) :600-+