Salvage therapy for multiple myeloma with thalidomide and CED chemotherapy

被引:92
作者
Moehler, TM
Neben, K
Benner, A
Egerer, G
Krasniqi, F
Ho, AD
Goldschmidt, H
机构
[1] Heidelberg Univ, Dept Hematol Oncol Rheumatol, D-69115 Heidelberg, Germany
[2] German Canc Res Ctr, Cent Unit Biostat, D-6900 Heidelberg, Germany
关键词
D O I
10.1182/blood.V98.13.3846
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The feasibility and efficacy of a combination of thalidomide, cyclophosphamide, etoposide, and dexamethasone were studied in 56 patients with poor-prognosis multiple myeloma. Of 50 patients evaluable for response, 4% achieved complete response (CR), 64% partial response (PR), 18% minimal response (MR), 6% stable disease (SD), and 8% progressive disease (PD), resulting in an objective response rate ( : MR) of 86.0% (76.7% over-all objective response rate in intent-to-treat analysis; n = 56). Subsequent to successful remission induction, 18 patients received autologous or allogeneic stem cell transplantation. The median progression-free survival in all patients was 16 months. The median overall survival time could not be calculated, since the last observed death occurred after 16 months of follow-up (median follow-up of 14 months) with a corresponding estimated survival probability of 55%. Severe adverse effects (World Health Organization III/IV) included Infectious complications (35.7%) and cardiovascular events (7.1%). The data suggest that Thai improves antitumor activity of salvage chemotherapy regimens in poor-prognosis multiple myeloma. (C) 2001 by The American Society of Hematology.
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收藏
页码:3846 / 3848
页数:3
相关论文
共 19 条
[1]  
ALEXANIAN R, 1994, NEW ENGL J MED, V330, P484
[2]   EFFECTIVE TREATMENT OF ADVANCED MULTIPLE-MYELOMA REFRACTORY TO ALKYLATING-AGENTS [J].
BARLOGIE, B ;
SMITH, L ;
ALEXANIAN, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (21) :1353-1356
[3]  
Blade Joan, 1998, British Journal of Haematology, V102, P1115, DOI 10.1046/j.1365-2141.1998.00930.x
[4]  
BONNET JD, 1984, CANCER TREAT REP, V68, P481
[5]   THALIDOMIDE IS AN INHIBITOR OF ANGIOGENESIS [J].
DAMATO, RJ ;
LOUGHNAN, MS ;
FLYNN, E ;
FOLKMAN, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :4082-4085
[6]   CYCLOPHOSPHAMIDE AND ETOPOSIDE THERAPY WITH GM-CSF FOR VAD-RESISTANT MULTIPLE-MYELOMA [J].
DIMOPOULOS, MA ;
DELASALLE, KB ;
CHAMPLIN, R ;
ALEXANIAN, R .
BRITISH JOURNAL OF HAEMATOLOGY, 1993, 83 (02) :240-244
[7]   PRIMARY THERAPY OF MULTIPLE-MYELOMA WITH PACLITAXEL (TAXOL) [J].
DIMOPOULOS, MA ;
ARBUCK, S ;
HUBER, M ;
WEBER, D ;
LUCKETT, R ;
DELASALLE, K ;
ALEXANIAN, R .
ANNALS OF ONCOLOGY, 1994, 5 (08) :757-759
[8]   High-dose therapy with peripheral blood progenitor cell transplantation in multiple myeloma [J].
Goldschmidt, H ;
Hegenbart, U ;
Wallmeier, M ;
Hohaus, S ;
Engenhart, R ;
Wannenmacher, M ;
Haas, R .
ANNALS OF ONCOLOGY, 1997, 8 (03) :243-246
[9]   Thalidomide and its analogs overcome drug resistance of human multiple myeloma cells to conventional therapy [J].
Hideshima, T ;
Chauhan, D ;
Shima, Y ;
Raje, N ;
Davies, FE ;
Tai, YT ;
Treon, SP ;
Lin, B ;
Schlossman, RL ;
Richardson, P ;
Muller, G ;
Stirling, DI ;
Anderson, KC .
BLOOD, 2000, 96 (09) :2943-2950
[10]  
JULIUSSON G, 2000, BRIT J HAEMATOL, V108, P229