Outcomes of autologous stem cell transplantation in patients with multiple myeloma who received dexamethasone-based nonmyelosuppressive induction therapy

被引:13
作者
Anagnostopoulos, A
Aleman, A
Yang, Y
Donato, M
Weber, D
Champlin, R
Smith, T
Alexanian, R
Giralt, S
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Blood & Marrow Transplantat, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Lymphoma Myeloma, Houston, TX 77030 USA
关键词
multiple myeloma; autologous stem cell transplant; nonmyelosuppressive induction; dexamethasone;
D O I
10.1038/sj.bmt.1704398
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
High-dose chemotherapy (HDC) followed by autologous stem cell transplantation (ASCT) imp roves survival in myeloma (MM). The role of induction therapy on outcomes of ASCT in MM has not been systematically studied. Nonmyelosuppressive (NMS) steroid-based induction can be used in MM, with the potential of reducing neutropenias and other toxic effects prior to ASCT. NMS induction however could be associated with poorer outcomes if disease control or stem cell collection were inadequate. We studied outcomes of 136 MM patients who underwent HDC and ASCT as part of their initial therapy between March 1998 and December 2000. Of these, 46 received HDC and ASCT without any exposure to myelosuppressive agents, 39 received myelosuppressive therapy for disease control and/or stem cell collection, and 51 received alkylating agent-based initial treatment. We compared OS and EFS rates, stem cell collectability, and contamination of the grafts with monoclonal plasma cells. After a median of 33 months, response rates, EFS and OS rates were comparable in the three groups of patients. Adequacy of stem cell collection and plasma cell contamination were similar. Our data support the hypothesis that NMS induction for patients with MM is safe and effective and does not compromise the results of HDC.
引用
收藏
页码:623 / 628
页数:6
相关论文
共 20 条
[1]  
ALEXANIAN R, 1995, SEMIN HEMATOL, V32, P20
[2]  
ALEXANIAN R, 1992, BLOOD, V80, P887
[3]   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
[4]  
Blade Joan, 1998, British Journal of Haematology, V102, P1115, DOI 10.1046/j.1365-2141.1998.00930.x
[5]  
Crowly J, 2001, SEMIN HEMATOL, V38, P203
[6]  
Dimopoulos MA, 1996, AM J HEMATOL, V52, P77, DOI 10.1002/(SICI)1096-8652(199606)52:2<77::AID-AJH2>3.3.CO
[7]  
2-T
[8]  
DONATO M, 2000, ASH
[9]  
GIRALT S, 2001, 8 INT MYEL WORKSH BA
[10]  
GOLDMAN JM, 1993, BLOOD, V82, P2235