Thalidomide in hematologic malignancies: Future directions

被引:6
作者
Alexanian, R
Anderson, KC
Barlogie, B
Stirling, DI
Thomas, DA
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Univ Arkansas Med Sci, Little Rock, AR 72205 USA
[4] Celgene Corp, Warren, NJ USA
关键词
D O I
10.1016/S0037-1963(00)90081-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Alternatives to traditional cytotoxic agents are needed to target the biologic processes associated with progression of multiple myeloma. Recent studies suggest that angiogenesis is sustained when patients with multiple myeloma achieve remission and may contribute to disease relapse and poor patient survival. Antiangiogenic therapy has been proposed as a strategy for reducing the risk of disease recurrence in patients with multiple myeloma. Accumulating evidence suggests that the combination of cytotoxic chemotherapy and antiangiogenic therapy has increased antitumor effects compared with either strategy alone. Preliminary findings of phase II studies suggest that thalidomide, an agent with antiangiogenic properties, has major activity in patients with refractory multiple myeloma. Based on this promising activity, a number of clinical trials are ongoing or planned to further assess the therapeutic potential of thalidomide as a single agent and in combination with chemotherapy in multiple myeloma and other hematologic malignancies. Copyright (C) 2000 by W.B. Saunders Company.
引用
收藏
页码:35 / 39
页数:5
相关论文
共 43 条
[1]  
ALEXANIAN R, 1994, NEW ENGL J MED, V330, P484
[2]  
Anderson KC, 1999, SEMIN HEMATOL, V36, P14
[3]  
Anderson KC, 1999, SEMIN HEMATOL, V36, P3
[4]   Thalidomide: lack of mutagenic activity across phyla and genetic endpoints [J].
Ashby, J ;
Tinwell, H ;
Callander, RD ;
Kimber, I ;
Clay, P ;
Galloway, SM ;
Hill, RB ;
Greenwood, SK ;
Gaulden, ME ;
Ferguson, MJ ;
Vogel, E ;
Nivard, M ;
Parry, JM ;
Williamson, J .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1997, 396 (1-2) :45-64
[5]  
Barlogie B, 1997, CLIN CANCER RES, V3, P2605
[6]   Superiority of tandem autologous transplantation over standard therapy for previously untreated multiple myeloma [J].
Barlogie, B ;
Jagannath, S ;
Vesole, DH ;
Naucke, S ;
Cheson, B ;
Mattox, S ;
Bracy, D ;
Salmon, S ;
Jacobson, J ;
Crowley, J ;
Tricot, G .
BLOOD, 1997, 89 (03) :789-793
[7]   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
[8]  
BARLOGIE B, 1999, P AN M AM SOC CLIN, V18, pA5
[9]  
Barlow S.M., 1992, Journal of Human Muscle Performance, V1, P1
[10]   CHEMOTHERAPY OF PLASMA-CELL MYELOMA AND THE INCIDENCE OF ACUTE-LEUKEMIA [J].
BERGSAGEL, DE ;
BAILEY, AJ ;
LANGLEY, GR ;
MACDONALD, RN ;
WHITE, DF ;
MILLER, AB .
NEW ENGLAND JOURNAL OF MEDICINE, 1979, 301 (14) :743-748