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Updated: Apr 12, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Experience with androgen deprivation therapy for prostate cancer in Japan and future perspectives
Yasuhide Kitagawa, Satoru Ueno, Hiroyuki Konaka
1Department of Integrative Cancer Therapy and Urology, Graduate School of Medical Science, Kanazawa University, Takaramachi13-1, Kanazawa, Ishikawa, Japan, 920- 8640. yasukita@med.kanazawa-u.ac.jp.
Abstract:
Novel anti-androgens and androgen biosynthesis inhibitors have been developed to treat castration-resistant prostate cancer. However, knowledge of androgen deprivation therapy (ADT) has not been developed in the criticism, including information regarding the adverse effects of hormonal therapy. We hypothesize that there are ethnic differences in the efficacy and adverse effects of ADT; therefore, this review summarizes the experience of ADT, mainly in Japan. A risk stratification instrument, the Japan Cancer of the Prostate Risk Assessment (J-CAPRA) score, was developed based on the Japan Study Group of Prostate Cancer registry, which is a large, multicenter, population-based database. It revealed that clinical outcomes were substantially better for males treated with ADT in Japan compared with those in the United States. Moreover, there were small survival differences in patients with localized and locally advanced cancer who received local therapy and primary ADT in another Japanese cohort study. In terms of adverse effects, including bone loss and cardiovascular risk, ADT appears to be better tolerated in Japanese populations than in Western cohorts. An ongoing randomized controlled trial of a trimodality treatment comprising brachytherapy, external beam radiation therapy, and neoadjuvant with or without adjuvant ADT in patients with localized high-risk prostate cancer will provide novel insights regarding adjuvant ADT. As a future perspective, the optimal selection of the type of primary ADT, including combining androgen blockade and novel hormonal compounds, adjusted according to each patient's clinicopathological background, may provide better clinical outcomes in patients with advanced prostate cancer.
Insights
Androgen deprivation therapy (ADT) shows better efficacy and fewer adverse effects in Japanese prostate cancer patients compared to Western cohorts. This suggests potential ethnic differences influencing treatment outcomes and tolerance.
Area of Science:
- Oncology
- Urology
- Endocrinology
Background:
- Novel anti-androgens and androgen biosynthesis inhibitors are crucial for treating castration-resistant prostate cancer.
- Current understanding of androgen deprivation therapy (ADT) lacks comprehensive criticism, especially regarding adverse effects.
- Hypothesized ethnic differences in ADT efficacy and side effects necessitate focused research.
Purpose of the Study:
- To review the experience and outcomes of ADT, with a primary focus on Japanese patient populations.
- To investigate potential ethnic variations in the efficacy and adverse effects of ADT for prostate cancer.
Main Methods:
- Summarized existing data and clinical experiences of ADT, predominantly from Japan.
- Utilized the Japan Cancer of the Prostate Risk Assessment (J-CAPRA) score, developed from a large, multicenter, population-based registry.
- Compared clinical outcomes and adverse events between Japanese and Western cohorts.
Main Results:
- Clinical outcomes for males treated with ADT in Japan were substantially better than in the United States.
- Japanese populations appear to tolerate ADT better, with lower incidence of bone loss and cardiovascular risks.
- Small survival differences were observed in patients receiving local therapy and primary ADT for localized/locally advanced cancer.
Conclusions:
- ADT demonstrates favorable efficacy and tolerability in Japanese prostate cancer patients compared to Western cohorts.
- Ethnic background may play a significant role in ADT outcomes and adverse event profiles.
- Personalized selection of ADT, considering patient background and novel agents, may improve outcomes in advanced prostate cancer.
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