Genuine- and induced-oligometastatic castration-resistant prostate cancer: clinical features and clinical outcomes after progressive site-directed therapy

Springer Science and Business Media LLC - Tập 53 - Trang 1119-1125 - 2021
Soichiro Yoshida1, Taro Takahara2,3, Yuki Arita4, Kazuma Toda5, Ichiro Yamada6, Hajime Tanaka1, Minato Yokoyama, Yoh Matsuoka1, Ryoichi Yoshimura5, Yasuhisa Fujii1
1Department of Urology, Tokyo Medical and Dental University, Graduate School, Tokyo, Japan
2Department of Biomedical Engineering, Tokai University School of Engineering, Kanagawa, Japan
3Department of Radiology, Advanced Imaging Center, Yaesu Clinic, Tokyo, Japan
4Departments of Diagnostic Radiology, Keio University, School of Medicine, Tokyo, Japan
5Department of Radiation Therapeutics and Oncology, Tokyo Medical and Dental University, Tokyo, Japan
6Department of Diagnostic Radiology and Nuclear Medicine, Tokyo Medical and Dental University, Tokyo, Japan

Tóm tắt

To evaluate the clinical characteristics of genuine- and induced-oligometastatic castration-resistant prostate cancer (OM-CRPC) and assess the therapeutic effect of progressive-site directed therapy (PSDT). We performed a retrospective analysis of 45 patients with OM-CRPC. Whole-body diffusion-weighted MRI (WB-DWI) was used to diagnose oligo-progressive disease. Based on the clinical and radiological findings, the OM-CRPCs were classified as genuine or induced. PSDT was performed with the intent to ablate all the progressive sites detected on WB-DWI with radiotherapy. Systemic therapy remained unchanged during and after PSDT. A total of 31 (69%) and 14 (31%) patients were diagnosed with genuine- and induced-OM-CRPC, respectively. The genuine-OM-CRPC group had significantly fewer patients treated with taxane-based chemotherapy and new hormonal drugs than the induced-OM-CRPC group. Of these, 26 OM-CRPC patients were treated with PSDT, and a 50% PSA decline was observed in 14 (93%) of 15 patients with genuine-OM-CRPC and 4 (36%) of 11 patients with induced-OM-CRPC (P = 0.033). Further, the duration of PSA-progression-free survival was significantly longer in the genuine-OM-CRPC group than in the induced-OM-CRPC group (8.7 vs. 5.8 months, P = 0.040). PSDT can be a promising treatment option for genuine-OM-CRPC. The procedure might also be considered effective for induced-OM-CRPC, although there was less therapeutic benefit of PSDT in patients with induced-OM-CRPC than in patients with genuine-OM-CRPC.

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