Fact CheckerSign in

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
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

Full criteria on ClinicalTrials.gov

Sites (19)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
AZorg Aalst
Coordinator of this site? Confirm its status
AalstBelgiumUnknown status
Iridium Netwerk
Coordinator of this site? Confirm its status
AntwerpBelgiumUnknown status
AZ Sint Jan
Coordinator of this site? Confirm its status
BrugesBelgiumUnknown status
Institut Bordet - HUB Brussel
Coordinator of this site? Confirm its status
BrusselsBelgiumUnknown status
JESSA Ziekenhuis
Coordinator of this site? Confirm its status
HasseltBelgiumUnknown status
AZ Groeninge
Coordinator of this site? Confirm its status
KortrijkBelgiumUnknown status
AZ Sint Maarten Mechelen
Coordinator of this site? Confirm its status
MechelenBelgiumUnknown status
KSA
Coordinator of this site? Confirm its status
AarauSwitzerlandUnknown status
IOSI-EOC
Coordinator of this site? Confirm its status
BellinzonaSwitzerlandUnknown status
Inselspital
Coordinator of this site? Confirm its status
BernSwitzerlandUnknown status
KSGR
Coordinator of this site? Confirm its status
ChurSwitzerlandUnknown status
Spital Thurgau
Coordinator of this site? Confirm its status
MünsterlingenSwitzerlandUnknown status
KSW
Coordinator of this site? Confirm its status
WinterthurSwitzerlandUnknown status
USZ
Coordinator of this site? Confirm its status
ZurichSwitzerlandUnknown status
Institut Bergonie
Coordinator of this site? Confirm its status
BordeauxFranceUnknown status
Centre Oscar Lambret
Coordinator of this site? Confirm its status
LilleFranceUnknown status
Chu de Saint Etienne
Coordinator of this site? Confirm its status
Saint-EtienneFranceUnknown status
Institut de Cancérologie de l'Ouest
Coordinator of this site? Confirm its status
Saint-HerblainFranceUnknown status
Institut Gustave Roussy
Coordinator of this site? Confirm its status
VillejuifFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.