Emerging drugs for prostate cancer

被引:5
作者
Siddiqui, Kashif [1 ]
Klotz, Laurence H. [1 ]
机构
[1] Univ Toronto, Sunnybrook Hlth Sci Ctr, Div Urol, Toronto, ON M4N 3M5, Canada
关键词
castration resistant prostate cancer; new drugs; pipeline drugs; prostate cancer; RANDOMIZED PHASE-II; ANDROGEN DEPRIVATION THERAPY; HUMAN GLANDULAR KALLIKREIN; COLONY-STIMULATING FACTOR; ORAL PLATINUM ANALOG; HIGH-DOSE CALCITRIOL; MONOCLONAL-ANTIBODY; CONTROLLED-TRIAL; CELLULAR IMMUNOTHERAPY; 2ND-LINE CHEMOTHERAPY;
D O I
10.1517/14728210903142147
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Prostate cancer mortality usually occurs as a result of castrate resistant disease. Many approaches are currently being evaluated to improve the treatment of this condition. These include drugs that induce androgen deprivation, that is, LHRH antagonists; more active or less toxic chemotherapy agents; immunologic approaches, including passive and active immunization; drugs that target the androgen receptor and/or androgen synthesis; drugs that target specific pathways, including tyrosine kinase inhibitors, angiogenesis inhibitors, endothelin antagonists and matrix metalloproteinase inhibitors; and antioxidants and cell cycle inhibitors. Many of these agents seem promising. The rationale, biologic activity and therapeutic results of these emerging drugs are reviewed.
引用
收藏
页码:455 / 470
页数:16
相关论文
共 143 条
[1]  
Alpha-Tocopherol Beta Carotene Cancer Prevention Study Group, 1994, N Engl J Med, V330, P1029, DOI 10.1056/NEJM199404143301501
[2]  
*AM CANC SOC, 2007, CANC STAT
[3]  
*AM CANC SOC, 2005, CANC STAT
[4]   Chemoprevention of prostate cancer in men at high risk: Rationale and design of the reduction by dutasteride of prostate cancer events (reduce) trial [J].
Andriole, G ;
Bostwick, D ;
Brawley, O ;
Gomella, L ;
Tindall, D ;
Breed, S ;
Somerville, M ;
Rittmaster, R .
JOURNAL OF UROLOGY, 2004, 172 (04) :1314-1317
[5]   Effect of the dual 5α-reductase inhibitor dutasteride on markers of tumor regression in prostate cancer [J].
Andriole, GL ;
Humphrey, P ;
Ray, P ;
Gleave, ME ;
Trachtenberg, J ;
Thomas, LN ;
Lazier, CB ;
Rittmaster, RS .
JOURNAL OF UROLOGY, 2004, 172 (03) :915-919
[6]   A randomized phase II study of concurrent docetaxel plus vaccine versus vaccine alone in metastatic androgen-independent prostate cancer [J].
Arlen, PM ;
Gulley, JL ;
Parker, C ;
Skarupa, L ;
Pazdur, M ;
Panicali, D ;
Beetham, P ;
Tsang, KY ;
Grosenbach, DW ;
Feldman, J ;
Steinberg, SM ;
Jones, E ;
Chen, C ;
Marte, J ;
Schlom, J ;
Dahut, W .
CLINICAL CANCER RESEARCH, 2006, 12 (04) :1260-1269
[7]   Antiandrogen, vaccine and combination therapy in patients with nonmetastatic hormone refractory prostate cancer [J].
Arlen, PM ;
Gulley, JL ;
Todd, N ;
Lieberman, R ;
Steinberg, SM ;
Morin, S ;
Bastian, A ;
Marte, J ;
Tsang, KY ;
Beetham, P ;
Grosenbach, DW ;
Schlom, J ;
Dahut, W .
JOURNAL OF UROLOGY, 2005, 174 (02) :539-546
[8]   New drugs in prostate cancer [J].
Armstrong, Andrew J. ;
Carducci, Michael A. .
CURRENT OPINION IN UROLOGY, 2006, 16 (03) :138-145
[9]   Phase I clinical trial of a selective inhibitor of CYP17, abiraterone acetate, confirms that castration-resistant prostate cancer commonly remains hormone driven [J].
Attard, Gerhardt ;
Reid, Alison H. M. ;
Yap, Timothy A. ;
Raynaud, Florence ;
Dowsett, Mitch ;
Settatree, Sarah ;
Barrett, Mary ;
Parker, Christopher ;
Martins, Vanessa ;
Folkerd, Elizabeth ;
Clark, Jeremy ;
Cooper, Colin S. ;
Kaye, Stan B. ;
Dearnaley, David ;
Lee, Gloria ;
de Bono, Johann S. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (28) :4563-4571
[10]   High levels of phosphorylated form of Akt-1 in prostate cancer and non-neoplastic prostate tissues are strong predictors of biochemical recurrence [J].
Ayala, G ;
Thompson, T ;
Yang, G ;
Frolov, A ;
Li, RL ;
Scardino, P ;
Ohori, M ;
Wheeler, T ;
Harper, W .
CLINICAL CANCER RESEARCH, 2004, 10 (19) :6572-6578