Castration-resistant Prostate Cancer: From New Pathophysiology to New Treatment Targets

被引:132
作者
Chi, Kim N. [1 ]
Bjartell, Anders [2 ]
Dearnaley, David [3 ,4 ]
Saad, Fred [5 ]
Schroeder, Fritz H. [6 ]
Sternberg, Cora [7 ]
Tombal, Bertrand [8 ]
Visakorpi, Tapio [9 ]
机构
[1] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
[2] Malmo Univ Hosp, Malmo, Sweden
[3] Royal Marsden NHS Trust, Sutton, Surrey, England
[4] Inst Canc Res, Sutton, Surrey, England
[5] Univ Montreal, Montreal, PQ, Canada
[6] Erasmus Univ, Rotterdam, Netherlands
[7] San Camillo & Forlanini Hosp, Rome, Italy
[8] Clin Univ St Luc, B-1200 Brussels, Belgium
[9] Univ Tampere, FIN-33101 Tampere, Finland
基金
英国医学研究理事会;
关键词
Prostate cancer; Androgens; Androgen receptor; Vascular endothelial growth factor; Immunotherapy; Apoptosis; Chaperone proteins; Clusterin; Insulin-like growth factor-1; Receptor activator of nuclear factor kappa B; Endothelin; Src kinase; MITOXANTRONE PLUS PREDNISONE; IGF BINDING PROTEIN-3; PHASE-II TRIAL; ANTISENSE OLIGONUCLEOTIDE; EUROPEAN ORGANIZATION; RECEPTOR EXPRESSION; RANDOMIZED-TRIAL; CLINICAL-TRIALS; HORMONE; GROWTH;
D O I
10.1016/j.eururo.2009.06.027
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Context: Castration-resistant prostate cancer (CRPC) refers to patients who no longer respond to surgical or medical castration. Standard treatment options are limited. Objective: To review the concepts and rationale behind targeted agents currently in late-stage clinical testing for patients with CRPC. Evidence acquisition: Novel targeted therapies in clinical trials were identified from registries. The MEDLINE database was searched for all relevant reports published from 1996 to October 2009. Bibliographies of the retrieved articles and major international meeting abstracts were hand-searched to identify additional studies. Evidence synthesis: Advances in our understanding of the molecular mechanisms underlying prostate cancer (PCa) progression has translated into a variety of treatment approaches. Agents targeting androgen receptor (AR) activation and local steroidogenesis, angiogenesis, immunotherapy, apoptosis, chaperone proteins, the insulin-like growth factor (IGF) pathway, RANK-ligand, endothelin receptors, and the Src family kinases are entering or have recently completed accrual to phase 3 trials for patients with CRPC. Conclusions: A number of new agents targeting mechanisms of PCa progression with early promising results are in clinical trials and have the potential to provide novel treatment options for CRPC in the near future. (C) 2009 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:594 / 605
页数:12
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