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Updated: Jun 7, 2025

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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
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Combined Fixed-duration Systemic Treatment and Metastasis-directed Radiotherapy for Oligometastatic Hormone-sensitive
Praful Ravi1, Caiwei Zhong1, Wanling Xie1
1Dana-Farber Cancer Institute, Boston, MA, USA.
European Urology Oncology
|November 15, 2024
Summary
Nearly half of men with oligometastatic hormone-sensitive prostate cancer achieved long-term remission after "total therapy." This treatment strategy shows promise for durable outcomes in select patients with advanced prostate cancer.
Area of Science:
- Oncology
- Urology
- Medical Imaging
Background:
- Oligometastatic hormone-sensitive prostate cancer (omHSPC) presents a challenge in achieving long-term remission.
- The efficacy of
- total therapy
- (androgen deprivation therapy [ADT] with or without androgen receptor pathway inhibitors [ARPI], metastasis-directed therapy, and local therapy) in omHSPC is not well-defined.
Purpose of the Study:
- To evaluate the outcomes of
- total therapy
- in patients with omHSPC after treatment completion.
- To assess clinical progression-free survival (cPFS), eugonadal progression-free survival (PFS), and time to restart of ADT (TTrADT).
Main Methods:
- Retrospective analysis of 89 consecutive omHSPC patients treated with
- total therapy
- at a single institution.
- Utilized Kaplan-Meier and Cox regression models to analyze outcomes.
- Included patients with prostate-specific antigen ≤0.1 ng/ml post-systemic therapy.
Main Results:
- At a median follow-up of 37 months, 45% of patients remained progression-free at 3 years (3-yr cPFS rate).
- The median time to restart ADT (TTrADT) was 47 months, with 60% not restarting ADT by 3 years.
- Longer duration of systemic therapy (≥12 months) was the sole significant predictor of improved outcomes.
Conclusions:
- Total therapy
- can lead to long-term durable remission in a subset of omHSPC patients.
- Approximately 45% of patients remained progression-free at 3 years post-therapy.
- Prospective trials are warranted to further validate this therapeutic approach.

