Time to Castration Resistance is Associated With Overall Survival Even After the Achievement of Castration Resistance in Metastatic Prostate Cancer
- Hiroto Kato 1,2, Yusuke Goto 1,2, Satoko Kojima 1, Yusuke Onoda 1, Ken Wakai 1,2, Kyokushin Hou 1, Kazuhiro Araki 1, Shinichi Sakamoto 2, Tomohiko Ichikawa 2, Yukio Naya 1
- Hiroto Kato 1,2, Yusuke Goto 1,2, Satoko Kojima 1
- 1Department of Urology, Teikyo University Chiba Medical Center, Chiba, Japan.
- 2Department of Urology, Chiba University Graduate School of Medicine, Chiba, Japan.
- 0Department of Urology, Teikyo University Chiba Medical Center, Chiba, Japan.
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View abstract on PubMed
Summary
This summary is machine-generated.Time to castration resistance is a key prognostic factor for metastatic prostate cancer survival, even after treatment resistance develops. This finding highlights its role as a biomarker for androgen receptor signaling activity.
Area Of Science
- Oncology
- Prostate Cancer Research
- Clinical Biomarkers
Background
- Metastatic castration-sensitive prostate cancer (mCSPC) patients show variable survival in real-world settings.
- Some mCSPC patients with low tumor burden and no visceral metastasis still experience poor outcomes.
- Androgen receptor (AR) signaling remains a critical therapeutic target, even in castration-resistant disease.
Purpose Of The Study
- To investigate novel prognostic factors for metastatic castration-sensitive prostate cancer.
- To specifically assess the prognostic value of time to castration resistance (TTR) in mCSPC.
- To evaluate TTR as a potential biomarker for AR signaling activity.
Main Methods
- Retrospective analysis of 261 patients with newly diagnosed mCSPC.
- Data collected from January 2007 to December 2023 at a single institution.
- Statistical association analysis between clinical factors and overall survival (OS).
Main Results
- Median OS was 60.7 months; median TTR was 13.1 months.
- 158 out of 261 patients developed castration-resistant prostate cancer (CRPC).
- Shorter TTR, distant lymph node metastasis, ISUP grade group 5, and older age correlated with shorter OS in CRPC patients.
- Shorter TTR independently predicted shorter OS, irrespective of tumor burden or post-CRPC status.
Conclusions
- Time to castration resistance serves as a prognostic biomarker in mCSPC.
- TTR indicates persistent androgen receptor signaling activity, even after castration resistance is achieved.
- TTR is a valuable prognostic indicator regardless of initial tumor burden.
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