Irrefutable evidence for the use of docetaxel in newly diagnosed metastatic prostate cancer: results from the STAMPEDE and CHAARTED trials

被引:0
作者
Robert J. van Soest
Ronald de Wit
机构
[1] Erasmus University Medical Center and Cancer Institute,Departments of Urology
[2] Department of Medical Oncology,undefined
[3] Erasmus University Medical Center and Cancer Institute,undefined
来源
BMC Medicine | / 13卷
关键词
Androgen deprivation therapy; Docetaxel; Metastatic castration-resistant prostate cancer; Metastatic hormone-naïve prostate cancer; Taxanes;
D O I
暂无
中图分类号
学科分类号
摘要
Androgen deprivation therapy (ADT) has been used in the treatment of metastatic prostate cancer since the first description of its hormonal dependence in 1941. In 2004, docetaxel chemotherapy became the mainstay of treatment in metastatic castration-resistant prostate cancer (mCRPC), following robust, albeit modest, survival benefit in two randomized phase 3 trials. The recently published CHAARTED trial was the first to show that combining ADT with docetaxel in men with hormone-naïve (hormone-sensitive) metastatic prostate cancer (mHSPC) yielded a remarkable overall survival benefit of 13.6 months as compared with ADT alone. In the current issue of The Lancet, James et al. report results of the STAMPEDE trial in men with high-risk locally advanced or metastatic prostate cancer initiating long-term hormone therapy. The combination of six cycles of docetaxel with ADT in men commencing long-term ADT demonstrated a similar OS benefit compared with standard of care (SOC) by a median of 10 months. Based on the consistency of the data and the firmness of the benefit provided, docetaxel in addition to ADT should be considered SOC for men with newly diagnosed mHSPC.
引用
收藏
相关论文
共 58 条
[1]  
Petrylak DP(2004)Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer N Engl J Med 351 1513-20
[2]  
Tangen CM(2004)TAX 327 Investigators. Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer N Engl J Med 351 1502-12
[3]  
Hussain MH(2008)Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer: updated survival in the TAX 327 study J Clin Oncol 26 242-5
[4]  
Lara PN(2014)The influence of prior abiraterone treatment on the clinical activity of docetaxel in men with metastatic castration-resistant prostate cancer Eur Urol 66 646-52
[5]  
Jones JA(2015)Targeting the androgen receptor confers in vivo cross-resistance between enzalutamide and docetaxel, but not cabazitaxel, in castration-resistant prostate cancer Eur Urol 67 981-5
[6]  
Taplin ME(2013)Cross-resistance between taxanes and new hormonal agents abiraterone and enzalutamide may affect drug sequence choices in metastatic castration-resistant prostate cancer Eur J Cancer 49 3821-30
[7]  
Tannock IF(2015)Chemohormonal therapy in metastatic hormone-sensitive prostate cancer N Engl J Med 373 737-46
[8]  
de Wit R(2010)Castration-dependent pharmacokinetics of docetaxel in patients with prostate cancer J Clin Oncol 28 4562-7
[9]  
Berry WR(2015)Low-dose prednisolone in first-line docetaxel for patients with metastatic castration-resistant prostate cancer: Is there a clinical benefit? Urol Oncol 33 494.e15-20
[10]  
Horti J(2015)ELM-PC 4 investigators. Orteronel plus prednisone in patients with chemotherapy-naive metastatic castration-resistant prostate cancer (ELM-PC 4): a double-blind, multicentre, phase 3, randomised, placebo-controlled trial Lancet Oncol 16 338-48