Angiogenesis Inhibitors in Prostate Cancer Therapy

被引:0
作者
Yu, Eun-Mi [1 ]
Jain, Maneesh [1 ]
Aragon-Ching, Jeanny B. [1 ]
机构
[1] George Washington Univ, Med Ctr, Dept Med, Div Hematol & Oncol, Washington, DC 20037 USA
关键词
ENDOTHELIAL GROWTH-FACTOR; PHASE-II TRIAL; TYROSINE KINASE; CLINICAL-TRIAL; BEVACIZUMAB; THALIDOMIDE; EXPRESSION; SORAFENIB;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Limited treatment options exist for metastatic castrate-resistant prostate cancer (mCRPC). The concept of targeting tumors via anti-angiogenic mechanisms has been studied over the last decade, giving rise to a new class of anti-cancer drugs. Currently, the use of angiogenesis inhibition in prostate cancer is the focus of many ongoing clinical trials, with tumor progression and overall survival established as outcome measures. Several anti-angiogenic agents are currently under investigation with varying mechanisms by which they exert activity against prostate tumors. We describe the significant findings and outcomes of clinical trials involving the use of these drugs in mCRPC patients, along with how these results will translate to their use in the clinical setting. Open interventional trials that are currently recruiting participants are also mentioned. While the use of angiogenesis inhibition holds promise in the treatment of prostate cancer, several challenges still exist. The foreseeable clinical implications and limitations of anti-angiogenic therapy and the potential use of biomarkers are hereby discussed. [Discovery Medicine 10(55):521-530, december 2010]
引用
收藏
页码:521 / 530
页数:10
相关论文
共 39 条
[11]   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
[12]   Circulating Tumor Cells Predict Survival Benefit from Treatment in Metastatic Castration-Resistant Prostate Cancer [J].
de Bono, Johann S. ;
Scher, Howard I. ;
Montgomery, R. Bruce ;
Parker, Christopher ;
Miller, M. Craig ;
Tissing, Henk ;
Doyle, Gerald V. ;
Terstappen, Leon W. W. M. ;
Pienta, Kenneth J. ;
Raghavan, Derek .
CLINICAL CANCER RESEARCH, 2008, 14 (19) :6302-6309
[13]   Down-regulation of vascular endothelial growth factor in a human colon carcinoma cell line transfected with an antisense expression vector specific for c-src [J].
Ellis, LM ;
Staley, CA ;
Liu, WB ;
Fleming, RYD ;
Parikh, NU ;
Bucana, CD ;
Gallick, GE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (02) :1052-1057
[14]   Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer [J].
Ferrara, N ;
Hillan, KJ ;
Gerber, HP ;
Novotny, W .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (05) :391-400
[15]  
FOLKMAN J, 1971, NEW ENGL J MED, V285, P1182
[16]  
Gansler T, 2010, CA-CANCER J CLIN, V60, P1, DOI [10.3322/caac.20073, 10.3322/caac.20049]
[17]  
Isambert N, 2008, J CLIN ONCOL, V26
[18]   Effects of sustained antiangiogenic therapy in multistage prostate cancer in TRAMP model [J].
Isayeva, Tatyana ;
Chanda, Diptiman ;
Kallman, Lisa ;
Eltoum, Isam-Eldin A. ;
Ponnazhagan, Selvarangan .
CANCER RESEARCH, 2007, 67 (12) :5789-5797
[19]   Tumoristatic Effects of Endostatin in Prostate Cancer Is Dependent on Androgen Receptor Status [J].
Isayeva, Tatyana ;
Moore, Lakisha D. ;
Chanda, Diptiman ;
Chen, Dongquan ;
Ponnazhagan, Selvarangan .
PROSTATE, 2009, 69 (10) :1055-1066
[20]  
Karakunnel JJ, 2009, J CLIN ONCOL, V27