Related Experiment Video
Updated: Jun 8, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
The impact of progression-directed therapy on survival in metastatic castration-refractory prostate cancer: MEDCARE
Kato Rans1, Karolien Goffin2,3, Steven Joniau4,5
1Department of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.
Background:
Metastatic castration-refractory prostate cancer (mCRPC) presents a therapeutic challenge despite advancements in treatment. Once mCRPC is attained, patients face limited survival prospects. Next-line systemic treatment (NEST) is the standard of care for progressive mCRPC, encompassing various therapeutic options with associated toxicity and costs. In patients with oligoprogressive mCRPC, data suggest that progression-directed therapy (PDT), such as metastasectomy or stereotactic body radiotherapy, delays the initiation of NEST.
Methods And Design:
The MEDCARE phase III trial aims to assess the impact of PDT on overall survival (OS) in oligoprogressive mCRPC. In this multicentric, randomised, prospective trial, we aim to randomise 246 patients in 1:1 allocation ratio between the standard-of-care therapy (surveillance or NEST) or PDT while continuing the current systemic treatment. Patients will be stratified based on number of progressive lesions (one vs ≥one), location of progressive lesions (local recurrence, N or M1a vs M1b or M1c) and previous systemic therapy (palliative androgen-deprivation therapy [pADT] vs pADT + androgen receptor-targeted agent or patients who received docetaxel in the past). The primary endpoint is OS, and the secondary endpoints include quality of life, radiographic progression-free survival (PFS), modified PFS, prostate cancer-specific survival and PDT-induced toxicity.
Discussion:
This is the first randomised phase 3 trial in the setting of PDT in patients with oligoprogressive mCRPC with OS as the primary endpoint.
Insights
Progression-directed therapy (PDT) may delay the need for next-line systemic treatment (NEST) in patients with oligoprogressive metastatic castration-refractory prostate cancer (mCRPC). This phase 3 trial investigates PDT
Area of Science:
- Oncology
- Prostate Cancer Research
- Clinical Trials
Background:
- Metastatic castration-refractory prostate cancer (mCRPC) poses significant therapeutic challenges with limited survival options.
- Next-line systemic treatment (NEST) is standard for progressive mCRPC but involves toxicity and cost.
- Progression-directed therapy (PDT) may delay NEST initiation in oligoprogressive mCRPC.
Purpose of the Study:
- To evaluate the impact of progression-directed therapy (PDT) on overall survival (OS) in patients with oligoprogressive metastatic castration-refractory prostate cancer (mCRPC).
- To compare PDT against standard-of-care therapy (surveillance or NEST) in this patient population.
Main Methods:
- The MEDCARE phase III trial is a multicentric, randomized, prospective study.
- 246 patients with oligoprogressive mCRPC will be randomized 1:1 to receive either standard-of-care or PDT while continuing current systemic treatment.
- Stratification will be based on lesion number/location and prior therapies; primary endpoint is OS.
Main Results:
- This section is not yet available as the trial is ongoing.
- Secondary endpoints include quality of life, progression-free survival, and treatment toxicity.
Conclusions:
- This is the first randomized phase 3 trial to investigate progression-directed therapy (PDT) in patients with oligoprogressive metastatic castration-refractory prostate cancer (mCRPC), using overall survival (OS) as the primary endpoint.
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