A New Therapy Paradigm for Prostate Cancer Founded on Clinical Observations

被引:30
作者
Efstathiou, Eleni [2 ,3 ]
Logothetis, Christopher J. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Stanford Alexander Tissue Derivat Lab, Houston, TX 77030 USA
[2] Univ Athens, David H Koch Ctr Appl Res Genitourinary Canc, Athens, Greece
[3] Univ Athens, Dept Genitourinary Med Oncol, Athens, Greece
关键词
PHASE-II TRIAL; UROGENITAL SINUS MESENCHYME; RADICAL PROSTATECTOMY; TUMOR MICROENVIRONMENT; NEOADJUVANT DOCETAXEL; ANDROGEN RECEPTOR; BIOCHEMICAL RELAPSE; IMATINIB MESYLATE; BONE METASTASES; CHEMOTHERAPY;
D O I
10.1158/1078-0432.CCR-09-1215
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Efficacy equivalent to that reported in other common adult solid tumors considered to be chemotherapy-sensitive has been reported with Docetaxel in patients with castrate-resistant prostate cancer. However, in contrast to other cancers, the expected increase in efficacy with the use of chemotherapy in earlier disease states has not been reported to date in prostate cancer. On the basis of these observations, we speculated that the therapy development paradigm used successfully in other cancers may not apply to the majority of prostate cancers. Several lines of supporting clinical and experimental observations implicate the tumor microenvironment in prostate carcinogenesis and resistance to therapy. We conclude that a foundation to guide the development of therapy for prostate cancer is required. The therapy paradigm we propose accounts for the central role of the tumor microenvironment in bone and, if correct, will lead to microenvironment-targeted therapy. Clin Cancer Res; 16(4); 1100-7. (C) 2010 AACR.
引用
收藏
页码:1100 / 1107
页数:8
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