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
[1]   Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases [J].
Allard, WJ ;
Matera, J ;
Miller, MC ;
Repollet, M ;
Connelly, MC ;
Rao, C ;
Tibbe, AGJ ;
Uhr, JW ;
Terstappen, LWMM .
CLINICAL CANCER RESEARCH, 2004, 10 (20) :6897-6904
[2]  
[Anonymous], CANCER
[3]  
[Anonymous], INVEST NEW DRUGS
[4]  
[Anonymous], INVEST NEW DRUGS
[5]   About tyrosine kinase inhibitors (TKIs) in prostate cancer: where do we go from here? [J].
Aragon-Ching, J. B. ;
Dahut, W. L. .
ANNALS OF ONCOLOGY, 2010, 21 (01) :183-184
[6]   Final analysis of a phase II trial using sorafenib for metastatic castration-resistant prostate cancer [J].
Aragon-Ching, Jeanny B. ;
Jain, Lokesh ;
Gulley, James L. ;
Arlen, Philip M. ;
Wright, John J. ;
Steinberg, Seth M. ;
Draper, David ;
Venitz, Juergen ;
Jones, Elizabeth ;
Chen, Clara C. ;
Figg, William D. ;
Dahut, William L. .
BJU INTERNATIONAL, 2009, 103 (12) :1636-1640
[7]  
Araujo J, 2009, J CLIN ONCOL, V27
[8]   Tumorigenesis and the angiogenic switch [J].
Bergers, G ;
Benjamin, LE .
NATURE REVIEWS CANCER, 2003, 3 (06) :401-410
[9]   A phase II clinical trial of sorafenib in androgen-independent prostate cancer [J].
Dahut, William L. ;
Scripture, Charity ;
Posadas, Edwin ;
Jain, Lokesh ;
Gulley, James L. ;
Arlen, Philip M. ;
Wright, John J. ;
Yu, Yunkai ;
Cao, Liang ;
Steinberg, Seth M. ;
Aragon-Ching, Jeanny B. ;
Venitz, Juergen ;
Jones, Elizabeth ;
Chen, Clara C. ;
Figg, William D. .
CLINICAL CANCER RESEARCH, 2008, 14 (01) :209-214
[10]   Phase I clinical trial of oral 2-methoxyestradiol, an antiangiogenic and apoptotic agent, in patients with solid tumors [J].
Dahut, WL ;
Lakhani, NJ ;
Gulley, JL ;
Arlen, PM ;
Kohn, EC ;
Kotz, H ;
McNally, D ;
Parr, A ;
Nguyen, D ;
Yang, SX ;
Steinberg, SM ;
Venitz, J ;
Sparreboom, A ;
Figg, WD .
CANCER BIOLOGY & THERAPY, 2006, 5 (01) :22-27