Non-metastatic castration-resistant prostate cancer: current status and future directions

被引:7
作者
Gupta, Ruby [1 ]
Sheng, Iris Y. [2 ]
Barata, Pedro C. [4 ]
Garcia, Jorge A. [3 ]
机构
[1] William Beaumont Hosp, Dept Hematol & Med Oncol, Royal Oak, MI 48072 USA
[2] Cleveland Clin, Taussig Canc Inst, Dept Hematol & Med Oncol, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Univ Hosp Seidman Canc Ctr, GU Oncol Res Program, Cleveland, OH 44106 USA
[4] Tulane Univ, Sch Med, Deming Dept Med, Sect Hematol Oncol, 1430 Tulane Ave, New Orleans, LA 70112 USA
关键词
Non-metastatic castration-resistant prostate cancer; apalutamide; enzalutamide; darolutamide; functional imaging; POSITRON-EMISSION-TOMOGRAPHY; METASTASIS-FREE SURVIVAL; CIRCULATING TUMOR-CELLS; BIOCHEMICAL RECURRENCE; C-11-CHOLINE PET/CT; MEMBRANE ANTIGEN; BONE METASTASES; RISING PSA; PHASE-3; ACID;
D O I
10.1080/14737140.2020.1772759
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction The emergence of novel hormonal therapies and the increase availability of sensitive next-generation imaging techniques has significantly changed the management of recurrent prostate cancer. Areas covered In this review, we summarize the definition, diagnosis, treatment, and ongoing clinical trials in non-metastatic castration resistant prostate cancer (M0CRPC). We have also discussed the role of newer imaging modalities in the detection of advanced prostate cancer. Expert opinion M0CRPC is a disease state in prostate cancer when serologic progression (PSA only disease) occurs despite castrated levels of testosterone and imaging shows no evidence of metastasis. With the availability of next-generation imaging, more patients are migrating from M0CRPC to mCRPC space. This stage migration impacts the treatment options currently available in clinical practice and requires the integration of novel imaging in prospective studies moving forward. Until that data become available men with M0CRPC should be considered for therapy with any of these three novel oral AR inhibitors, with a positive impact in metastasis-free and overall survival. Treatment selection should be based on Quality of Life, side effects, and drug-drug interactions.
引用
收藏
页码:513 / 522
页数:10
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