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
[71]   Apoptotic signaling induced by immunomodulatory thalidomide analogs in human multiple myeloma cells: therapeutic implications [J].
Mitsiades, N ;
Mitsiades, CS ;
Poulaki, V ;
Chauhan, D ;
Richardson, PG ;
Hideshima, T ;
Munshi, NC ;
Treon, SP ;
Anderson, KC .
BLOOD, 2002, 99 (12) :4525-4530
[72]   Molecular sequelae of histone deacetylase inhibition in human malignant B cells [J].
Mitsiades, N ;
Mitsiades, CS ;
Richardson, PG ;
McMullan, C ;
Poulaki, V ;
Fanourakis, G ;
Schlossman, R ;
Chauhan, D ;
Munshi, NC ;
Hideshima, T ;
Richon, VM ;
Marks, PA ;
Anderson, KC .
BLOOD, 2003, 101 (10) :4055-4062
[73]   Molecular sequelae of proteasome inhibition in human multiple myeloma cells [J].
Mitsiades, N ;
Mitsiades, CS ;
Poulaki, V ;
Chauhan, D ;
Fanourakis, G ;
Gu, XS ;
Bailey, C ;
Joseph, M ;
Libermann, TA ;
Treon, SP ;
Munshi, NC ;
Richardson, PG ;
Hideshima, T ;
Anderson, KC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (22) :14374-14379
[74]   The proteasome inhibitor PS-341 potentiates sensitivity of multiple myeloma cells to conventional chemotherapeutic agents: therapeutic applications [J].
Mitsiades, N ;
Mitsiades, CS ;
Richardson, PG ;
Poulaki, V ;
Tai, YT ;
Chauhan, D ;
Fanourakis, G ;
Gu, XS ;
Bailey, C ;
Joseph, M ;
Libermann, TA ;
Schlossman, R ;
Munshi, NC ;
Hideshima, T ;
Anderson, KC .
BLOOD, 2003, 101 (06) :2377-2380
[75]   Mechanism of action of 2-methoxyestradiol: new developments [J].
Mooberry, SL .
DRUG RESISTANCE UPDATES, 2003, 6 (06) :355-361
[76]   Comparison of 200 mg/m2 melphalan and 8 Gy total body irradiation plus 140 mg/m2 melphalan as conditioning regimens for peripheral blood stem cell transplantation in patients with newly diagnosed multiple myeloma:: final analysis of the Intergroupe Francophone du Myelome 9502 randomized trial [J].
Moreau, P ;
Facon, T ;
Attal, M ;
Hulin, C ;
Michallet, M ;
Maloisel, F ;
Sotto, JJ ;
Guilhot, F ;
Marit, G ;
Doyen, C ;
Jaubert, A ;
Fuzibet, JG ;
François, S ;
Benboubker, L ;
Monconduit, M ;
Voillat, L ;
Macro, M ;
Berthou, C ;
Dorvaux, V ;
Pignon, B ;
Rio, B ;
Matthes, T ;
Casassus, P ;
Caillot, D ;
Najman, N ;
Grosbois, B ;
Bataille, R ;
Harousseau, JL .
BLOOD, 2002, 99 (03) :731-735
[77]  
MORRIS T, 2003, HEMATOL J, V4
[78]   Clinical activity of arsenic trioxide for the treatment of multiple myeloma [J].
Munshi, NC ;
Tricot, G ;
Desikan, R ;
Badros, A ;
Zangari, M ;
Toor, A ;
Morris, C ;
Anaissie, E ;
Barlogie, B .
LEUKEMIA, 2002, 16 (09) :1835-1837
[79]  
NILSSON P, 1994, ONCOGENE, V9, P3043
[80]  
Nimmanapalli R, 2003, CANCER RES, V63, P5126