A simplified approach to stem cell mobilization in multiple myeloma patients not previously treated with alkylating agents

被引:24
作者
Lerro, KA
Medoff, E
Wu, Y
Seropian, SE
Snyder, E
Krause, D
Cooper, DL
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Sect Med Oncol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Lab Med, New Haven, CT 06520 USA
关键词
multiple myeloma; hematopoietic stem cell mobilization; autologous;
D O I
10.1038/sj.bmt.1704286
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
High-dose chemotherapy and autologous stem cell rescue is considered a standard part of initial therapy for patients with multiple myeloma. Therefore, potential transplant candidates are generally treated with dexamethasone-based programs rather than alkylating agents to avoid stem cell toxicity. The optimal mobilizing regimen for patients with multiple myeloma has not been defined. However, aggressive chemotherapy may result in excessive morbidity and cost in this older, immunocompromised population. We retrospectively examined our experience with a well-tolerated regimen of 1.5 g/m(2) cyclophosphamide on day -10 followed by 10 mug/kg G-CSF beginning on day -7 in 50 consecutive patients with multiple myeloma and no prior alkylating agent therapy. Median stem cell collection was 4.88 x 10(6) CD34+ cells/kg per apheresis and 44 patients collected >5 x 10(6) CD34+ cells/kg within 2 days. In 36 patients, more than 10 x 10(6) CD34+ cells/kg were collected including 33 patients who required 1-2 days of collection. One patient required hospitalization for fever/neutropenia and two required weekend apheresis. We conclude that 1.5 g/m(2) cyclophosphamide plus 10 mug/kg G-CSF is a safe, effective, highly predictable mobilizing program that uniformly provided enough stem cells for one transplant and enough stem cells for two transplants.
引用
收藏
页码:1113 / 1117
页数:5
相关论文
共 29 条
[1]   A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Stoppa, AM ;
Sotto, JJ ;
Fuzibet, JG ;
Rossi, JF ;
Casassus, P ;
Maisonneuve, H ;
Facon, T ;
Ifrah, N ;
Payen, C ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) :91-97
[2]  
ATTAL M, 2002, AM SOC HEMATOL, V100, pA5
[3]   Negative selection of peripheral blood stem cells to support a tandem autologous transplantation programme in multiple myeloma [J].
Barbui, AM ;
Galli, M ;
Dotti, G ;
Belli, N ;
Borleri, G ;
Gritti, G ;
Bellavita, P ;
Viero, P ;
Comotti, B ;
Barbui, T ;
Rambaldi, A .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 116 (01) :202-210
[4]   Total therapy with tandem transplants for newly diagnosed multiple myeloma [J].
Barlogie, B ;
Jagannath, S ;
Desikan, KR ;
Mattox, S ;
Vesole, D ;
Siegel, D ;
Tricot, G ;
Munshi, N ;
Fassas, A ;
Singhal, S ;
Mehta, J ;
Anaissie, E ;
Dhodapkar, D ;
Naucke, S ;
Cromer, J ;
Sawyer, J ;
Epstein, J ;
Spoon, D ;
Ayers, D ;
Cheson, B ;
Crowley, J .
BLOOD, 1999, 93 (01) :55-65
[5]  
Boccadoro M, 2002, HAEMATOLOGICA, V87, P846
[6]  
Corso A, 2002, HAEMATOLOGICA, V87, P1041
[7]   A quantitative PCR assay for the detection of low amounts of malignant cells In multiple myeloma [J].
Cremer, FW ;
Kiel, K ;
Wallmeier, M ;
Goldschmidt, H ;
Moos, M .
ANNALS OF ONCOLOGY, 1997, 8 (07) :633-636
[8]  
Cremer FW, 1998, EXP HEMATOL, V26, P969
[9]   The administration of 10 μg/kg granulocyte colony-stimulating factor (G-CSF) alone results in a successful peripheral blood stem cell collection when previous mobilization with chemotherapy and hematopoietic growth factor failed [J].
D'Hondt, L ;
Emmons, RVB ;
André, M ;
Guillaume, T ;
Feyens, AM ;
Canon, JL ;
Humblet, Y ;
Longueville, J ;
Symann, M .
LEUKEMIA & LYMPHOMA, 1999, 34 (1-2) :105-109
[10]   Comparable engraftment kinetics following peripheral-blood stem-cell infusion mobilized with granulocyte colony-stimulating factor with or without cyclophosphamide in multiple myeloma [J].
Desikan, KR ;
Barlogie, B ;
Jagannath, S ;
Vesole, DH ;
Siegel, D ;
Fassas, A ;
Munshi, N ;
Singhal, S ;
Mehta, J ;
Tindle, S ;
Nelson, J ;
Bracy, D ;
Mattox, S ;
Tricot, G .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) :1547-1553