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NCT07782112Not yet recruiting

Best Salvage Treatment for High-risk Relapsing Prostate Cancer (PEACE-9 - ESCALATE-RT)

Summary

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.

Inclusion criteria

• 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

Exclusion criteria

• More than 5 distant PSMA positive metastases and/or brain or leptomeningeal metastases. • 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 • Contraindications to pelvic RT and/or MDT • Prior evidence of distant metastatic disease • Contraindications to ADT • 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

Contacts

The trial team's contact details are shown on request.

See the official trial record
Status
Not yet recruiting
Phase
Phase 3
Study type
Interventional
Countries
Switzerland, France, Belgium
Sponsor
Ente Ospedaliero Cantonale, Bellinzona(Other)
Protocol no.
PEACE-9 - ESCALATE-RT
Conditions
Prostatic Neoplasms, Biochemical Recurrence, Oligometastatic Prostate Cancer
Interventions
Radiation, Drug

Treatments studied

  • Radiotherapy for MDT ± WPRT
  • Androgen Deprivation Therapy (ADT)
  • Enzalutamide

Collaborators

Clinical Trial Unit Ente Ospedaliero Cantonale

Locations · 19

  • Aarau, SwitzerlandKSANot yet recruiting at this site
  • Bellinzona, SwitzerlandIOSI-EOCNot yet recruiting at this site
  • Bern, SwitzerlandInselspitalNot yet recruiting at this site
  • Chur, SwitzerlandKSGRNot yet recruiting at this site
  • Münsterlingen, SwitzerlandSpital ThurgauNot yet recruiting at this site
  • Winterthur, SwitzerlandKSWNot yet recruiting at this site
  • Zurich, SwitzerlandUSZNot yet recruiting at this site
  • Bordeaux, FranceInstitut BergoniéNot yet recruiting at this site
  • Lille, FranceCentre Oscar LambretNot yet recruiting at this site
  • Saint-Etienne, FranceCHU de Saint-EtienneNot yet recruiting at this site
  • Saint-Herblain, FranceInstitut de Cancérologie de l'OuestNot yet recruiting at this site
  • Villejuif, FranceInstitut Gustave RoussyNot yet recruiting at this site
  • Aalst, BelgiumAZorg AalstNot yet recruiting at this site
  • Antwerp, BelgiumIridium NetwerkNot yet recruiting at this site
  • Bruges, BelgiumAZ Sint-JanNot yet recruiting at this site
  • Brussels, BelgiumInstitut Bordet - HUB BrusselNot yet recruiting at this site
  • Hasselt, BelgiumJessa ziekenhuisNot yet recruiting at this site
  • Kortrijk, BelgiumAZ GroeningeNot yet recruiting at this site
  • Mechelen, BelgiumAZ Sint-Maarten MechelenNot yet recruiting at this site

In total, worldwide, all 19 sites listed in the registry are planned; recruitment has not opened yet.

Site status per the ClinicalTrials.gov registry (last update posted: August 24, 2026).

This status may have changed and says nothing about your eligibility: before taking any step, check with your oncologist or the site.

See also

Other versions

These results are indicative and do not replace medical advice — discuss them with your doctor.