Factors influencing the collection of peripheral blood stem cells in patients with acute myeloblastic leukemia and non-myeloid malignancies

被引:39
作者
Carral, A [1 ]
de la Rubia, J [1 ]
Martín, G [1 ]
Mollá, S [1 ]
Martínez, J [1 ]
Soler, MA [1 ]
Jarque, I [1 ]
Jiménez, C [1 ]
Sanz, MA [1 ]
机构
[1] Univ Hosp La Fe, Hematol Serv, Bone Marrow Transplant Unit, Valencia 46009, Spain
关键词
mobilization; stem cells; collection; acute myeloid leukemia; non-myeloid malignancies;
D O I
10.1016/S0145-2126(02)00068-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Factors influencing the collection of autologous peripheral blood stem cells (PBSCs) were studied in 182 mobilization procedures performed on 145 consecutive patients with acute myeloblastic leukemia (AML; n = 67) and with various non-myeloid malignancies (NMM; n = 78). PBSC were collected following mobilization with chemotherapy, treatment with granulocyte colony-stimulating factor (G-CSF) or chemotherapy plus G-CSF. Fewer colony-forming unit granulocyte-macrophages (CFU-GMs) were collected from patients with AML than from patients with NMM (P < 0.0001), although there were no differences in the numbers of CD34(+) cells collected between both groups. Multiple regression analysis showed that chemotherapy alone was predictive of a low CD34(+) yield in patients with NMM (regression coefficient (RC) = -2.1; P = 0.003). In addition, the interactions "diagnosis mutliple myeloma (MM) x mobilization with chemotherapy" (RC = 2.9; P = 0.004) and "diagnosis MM x mobilization with chemotherapy plus G-CSF" (RC = 2.1; P = 0.04) also remained in the model, both showing a favorable influence. In AML, mobilization with chemotherapy plus G-CSF was associated with higher CD34(+) yields (P = 0.003). In this subgroup of patients, multiple regression analysis identified the number of cycles of previous chemotherapy (<= 2 cycles; RC = 1.3; P = 0.03) and peripheral blood counts (WBC >= 1.5 x 10(9)/l and monocytes >20%; RC = 0.8; P = 0.02) as the factors most predictive of CD34(+) cell yield. These findings emphasize the need to optimize harvesting technique to enhance safety and minimize morbidity and costs of this valuable procedure. (C) 2002 Elsevier Science Ltd. All rights reserved.
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页码:5 / 12
页数:8
相关论文
共 48 条
[11]   AUTOLOGOUS PROGENITOR-CELL TRANSPLANTATION - PRIOR EXPOSURE TO STEM CELL-TOXIC DRUGS DETERMINES YIELD AND ENGRAFTMENT OF PERIPHERAL-BLOOD PROGENITOR-CELL BUT NOT OF BONE-MARROW GRAFTS [J].
DREGER, P ;
KLOSS, M ;
PETERSEN, B ;
HAFERLACH, T ;
LOFFLER, H ;
LOEFFLER, M ;
SCHMITZ, N .
BLOOD, 1995, 86 (10) :3970-3978
[12]   Factors influencing platelet recovery after blood cell transplantation in multiple myeloma [J].
Gertz, MA ;
Lacy, MQ ;
Inwards, DJ ;
Pineda, AA ;
Chen, MG ;
Gastineau, DA ;
Tefferi, A ;
Kyle, RA ;
Litzow, MR .
BONE MARROW TRANSPLANTATION, 1997, 20 (05) :375-380
[13]   Blood and marrow transplantation activity in Europe 1997 [J].
Gratwohl, A ;
Passweg, J ;
Baldomero, H ;
Hermans, J .
BONE MARROW TRANSPLANTATION, 1999, 24 (03) :231-245
[14]  
HAAS R, 1994, BLOOD, V83, P3787
[15]   A randomized, double-blind, placebo-controlled, phase III study of filgrastim in remission induction and consolidation therapy for adults with de novo acute myeloid leukemia [J].
Heil, G ;
Hoelzer, D ;
Sanz, MA ;
Lechner, K ;
Yin, JAL ;
Papa, G ;
Noens, L ;
Szer, J ;
Ganser, A ;
OBrien, C ;
Matcham, J .
BLOOD, 1997, 90 (12) :4710-4718
[16]  
ISCOVE NN, 1971, BLOOD-J HEMATOL, V37, P1
[17]  
Jowitt SN, 1998, BRIT J HAEMATOL, V100, P688
[18]   Factors associated with successful mobilization of peripheral blood progenitor cells in 200 patients with lymphoid malignancies [J].
Ketterer, N ;
Salles, G ;
Moullet, I ;
Dumontet, C ;
ElJaafari-Corbin, A ;
Tremisi, P ;
Thieblemont, C ;
Durand, B ;
Neidhardt-Berard, EM ;
Samaha, H ;
Rigal, D ;
Coifier, B .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 103 (01) :235-242
[19]  
KOTASEK D, 1992, BONE MARROW TRANSPL, V9, P11
[20]  
Kröger N, 1998, BRIT J HAEMATOL, V102, P1101