NCT07782112Not yet recruitingPhase 3
Best Salvage Treatment for High-risk Relapsing Prostate Cancer (PEACE-9 - ESCALATE-RT)
PEACE-9 - ESCALATE-RT: A Phase III Randomized Study in Patients With High-risk PSA Relapse After Local Therapy Treated With Enzalutamide Plus Androgen Deprivation Therapy and Comparing MDT ± Pelvic Radiotherapy Versus no Further Treatment
Source: ClinicalTrials.gov · Last updated 24 Aug 2026
Brief summary (registry, in English)
The goal of this clinical trial is to learn if adding metastasis-directed radiotherapy with or without pelvic salvage radiotherapy, to intermittent prostate cancer drugs (intensified hormone therapy) can delay the need to restart these drugs in men with oligometastactic prostate cancer recurrence. In practice, this study is open to men whose PSA level (a blood marker of cancer activity) is rising as defined by biochemical recurrence, and who have 1 to 5 areas of cancer spread (1 to 5 metastases defining oligometastatic status) found on a specialized scan (PSMA PET/CT). Since intensified hormone therapy, including androgen deprivation therapy combined with a next-generation hormone therapy, represents the standard treatment strategy for these patients, researchers want to find out if adding radiation therapy can help patients to spend more time off cancer drugs while keeping their cancer under control. The main questions this trial aims to answer are: * Does adding radiation therapy to each metastases with or without pelvic area, lengthen the time before participants need to restart drug treatment? * Does adding radiation therapy increase the number of participants whose PSA drops to a very low level (0.2 ng/mL or lower)? * Does adding radiation therapy affect participants' quality of life? Researchers will randomly assign participants (chosen by chance) to receive either enzalutamide (next-generation hormone therapy) plus androgen-deprivation therapy (first-generation hormone therapy ) alone, or the same association of these drugs combined with radiation therapy aimed at each metastases with or without pelvic area. This comparison will show whether adding radiation therapy helps participants reach a deeper PSA response and go longer without needing cancer drugs. Participants will: * Take enzalutamide and androgen-deprivation therapy for 9 months * Have an equal chance of also receiving radiation therapy to each metastases with or without pelvic area * Stop drug treatment after 9 months if their PSA drops below 0.2 ng/mL, a level showing the cancer is well controlled * Restart drug treatment if their PSA rises again during the treatment-free period * Have regular blood tests and clinic visits to check their PSA, testosterone, and overall health * Complete short quality-of-life questionnaires during the study * Take part in a study conducted at several hospitals in Switzerland, Belgium, and France.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 140 (estimated)
- First submitted
- 19 Aug 2026
- Start date
- Nov 2026
- Primary completion date
- Jul 2030
- Lead sponsor
- Ente Ospedaliero Cantonale, Bellinzona
- Diseases
- Prostate cancer
- NCT number
- NCT07782112
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 140
- From Nov 2026 to the primary completion date, Jul 2030
- 19 sites in 3 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior evidence of distant metastatic disease
- Contraindication for treatment with enzalutamide
- Prior hormonal therapy (Neoadjuvant/adjuvant therapy to treat PCa ≤ 36 months in duration and ≥ 9 months before randomization is allowed)
- Previous treatment with cytotoxic agent for PCa
- Any active malignancies (i.e., progressing or requiring any treatment in the previous 36 months) other than prostate cancer (except non-muscle invasive bladder cancer; non-melanomatous skin cancer or a malignancy that is considered cured with minimal risk of recurrence
Other illness
- Prostate recurrence (positive PSMA disease) after primary prostate irradiation
- Prostate bed recurrence (positive PSMA disease) after salvage/adjuvant irradiation
- Pelvic nodal recurrence (positive PSMA disease) after primary WPRT irradiation
Other
- More than 5 distant PSMA positive metastases and/or brain or leptomeningeal metastases.
- Contraindications to pelvic RT and/or MDT
- Contraindications to ADT
Who the study is looking for
- Histologically proven initial diagnosis of adenocarcinoma of the prostate
- Rising PSA after local therapy as defined by PSA ≥ 0.2 ng/mL after RP +/- adjuvant/salvage prostate bed RT and at least 2 ng/mL above nadir for primary RT, with a PSADT ≤ 9 months
- Serum Testosterone ≥ 150 ng/dl (6.9343 nM/L)
- On PSMA PET/CT restaging presence of: 1 to 5 distant metastases that are amenable to MDT ± N1 patients (no limit in the number of nodes)
- ECOG performance status 0 - 2
- Age \> or =18 years
- Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
- Before patient registration/randomization, written informed consent must be given according to ICH/GCP, and national/local regulations
Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers
Sites (19)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| AZorg Aalst Coordinator of this site? Confirm its status | Aalst | Belgium | Unknown status |
| Iridium Netwerk Coordinator of this site? Confirm its status | Antwerp | Belgium | Unknown status |
| AZ Sint Jan Coordinator of this site? Confirm its status | Bruges | Belgium | Unknown status |
| Institut Bordet - HUB Brussel Coordinator of this site? Confirm its status | Brussels | Belgium | Unknown status |
| JESSA Ziekenhuis Coordinator of this site? Confirm its status | Hasselt | Belgium | Unknown status |
| AZ Groeninge Coordinator of this site? Confirm its status | Kortrijk | Belgium | Unknown status |
| AZ Sint Maarten Mechelen Coordinator of this site? Confirm its status | Mechelen | Belgium | Unknown status |
| KSA Coordinator of this site? Confirm its status | Aarau | Switzerland | Unknown status |
| IOSI-EOC Coordinator of this site? Confirm its status | Bellinzona | Switzerland | Unknown status |
| Inselspital Coordinator of this site? Confirm its status | Bern | Switzerland | Unknown status |
| KSGR Coordinator of this site? Confirm its status | Chur | Switzerland | Unknown status |
| Spital Thurgau Coordinator of this site? Confirm its status | Münsterlingen | Switzerland | Unknown status |
| KSW Coordinator of this site? Confirm its status | Winterthur | Switzerland | Unknown status |
| USZ Coordinator of this site? Confirm its status | Zurich | Switzerland | Unknown status |
| Institut Bergonie Coordinator of this site? Confirm its status | Bordeaux | France | Unknown status |
| Centre Oscar Lambret Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| Chu de Saint Etienne Coordinator of this site? Confirm its status | Saint-Etienne | France | Unknown status |
| Institut de Cancérologie de l'Ouest Coordinator of this site? Confirm its status | Saint-Herblain | France | Unknown status |
| Institut Gustave Roussy Coordinator of this site? Confirm its status | Villejuif | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.