Perspectives for combination therapy to overcome drug-resistant multiple myeloma

被引:35
作者
Catley, L [1 ]
Tai, YT [1 ]
Chauhan, D [1 ]
Anderson, KC [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
关键词
multiple myeloma; bortezomib; thalidomide; rapamycin; HDAC inhibitors; proteasome inhibitors; drug resistance;
D O I
10.1016/j.drup.2005.06.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The introduction of melphalan and prednisone 40 years ago was a significant advance in the treatment of multiple myeloma (MM). In the following decades, significant advances were few, but included landmarks, such as the introduction of VAD and autologous transplantation during the 1980s and bisphosphonates in the 1990s. Although response rates to therapy were increased, overall survival was not significantly improved. In 1999, the treatment of myeloma was revolutionized by the introduction of thalidomide. Subsequently, the development of the immunomodulatory thalidomide analogues and the proteasome inhibitor bortezomib have impacted on response rates to therapy in relapsed and refractory myeloma and are currently being evaluated as primary therapy for myeloma. Early results suggest activity in combination with standard therapy to overcome drug resistance in patients with early stage disease and are changing treatment strategies in multiple myeloma. As an increasing number of other novel therapeutics is identified and mechanisms of resistance are elucidated, combinations of these drugs will be developed to optimize new therapeutic regimens. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:205 / 218
页数:14
相关论文
共 136 条
[41]   Long-term results of the R-CHOP study in the treatment of elderly patients with diffuse large B-cell lymphoma:: A study by the groupe d'Etude des lymphomes de l'adulte [J].
Feugier, P ;
Van Hoof, A ;
Sebban, C ;
Solal-Celigny, P ;
Bouabdallah, R ;
Fermé, C ;
Christian, B ;
Lepage, E ;
Tilly, H ;
Morschhauser, F ;
Gaulard, P ;
Salles, G ;
Bosly, A ;
Gisselbrecht, C ;
Reyes, F ;
Coiffier, B .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (18) :4117-4126
[42]  
Fuino L, 2003, MOL CANCER THER, V2, P971
[43]   Apoptosis pathways: turned on their heads? [J].
Fulda, S ;
Debatin, KM .
DRUG RESISTANCE UPDATES, 2003, 6 (01) :1-3
[44]   Insulin-like growth factor I is a growth and survival factor in human multiple myeloma cell lines [J].
GeorgiiHemming, P ;
Wiklund, HJ ;
Ljunggren, O ;
Nilsson, K .
BLOOD, 1996, 88 (06) :2250-2258
[45]   Ascorbic acid enhances arsenic trioxide-induced cytotoxicity in multiple myeloma cells [J].
Grad, JM ;
Bahlis, NJ ;
Reis, I ;
Oshiro, MM ;
Dalton, WS ;
Boise, LH .
BLOOD, 2001, 98 (03) :805-813
[46]   Adherence of multiple myeloma cells to bone marrow stromal cells upregulates vascular endothelial growth factor secretion: therapeutic applications [J].
Gupta, D ;
Treon, SP ;
Shima, Y ;
Hideshima, T ;
Podar, K ;
Tai, YT ;
Lin, B ;
Lentzsch, S ;
Davies, FE ;
Chauhan, D ;
Schlossman, RL ;
Richardson, P ;
Ralph, P ;
Wu, L ;
Payvandi, F ;
Muller, G ;
Stirling, DI ;
Anderson, KC .
LEUKEMIA, 2001, 15 (12) :1950-1961
[47]  
HAROUSSEAU J, 2005, P AM SOC CLIN ONCOL
[48]   Recombinant humanized anti-CD40 monoclonal antibody triggers autologous antibody-dependent cell-mediated cytotoxicity against multiple myeloma cells [J].
Hayashi, T ;
Treon, SP ;
Hideshima, T ;
Tai, YT ;
Akiyama, M ;
Richardson, P ;
Chauhan, D ;
Grewal, IS ;
Anderson, KC .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 121 (04) :592-596
[49]   Apoptotic pathways activated by histone deacetylase inhibitors: implications for the drug-resistant phenotype [J].
Henderson, C ;
Brancolini, C .
DRUG RESISTANCE UPDATES, 2003, 6 (05) :247-256
[50]  
Hideshima T, 2001, CANCER RES, V61, P3071