Clinical trial · Interventional
PSMA-PET Directed Radiation Therapy for High-Risk Prostate Cancer
PSMA-PET Directed Radiation Therapy in High and Very High-Risk Prostate Cancer
NCT07291557CI-TRIAL-00099187not yet recruitingPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In this study, prostate cancer patients whose cancer has not spread to the lymph nodes will receive radiation therapy targeted to the prostate and nearby tissues with or without whole pelvis radiation therapy. PSMA imaging will be used to visualize prostate cancer prior to starting the trial.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Prostate Only Radiation Therapy (PORT) | Radiation | — | UNRESOLVED |
| Prostate + Whole Pelvis Radiation Therapy (P-WPRT) | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Prostate Only Radiation Therapy (PORT)
- description
- Radiation therapy: prostate and surrounding tissues
- interventionNames
- Radiation: Prostate Only Radiation Therapy (PORT)
- type
- EXPERIMENTAL
- label
- Prostate + Whole Pelvis Radiation Therapy (P-WPRT)
- description
- Radiation therapy: prostate and surrounding tissues + whole pelvis radiation therapy
- interventionNames
- Radiation: Prostate + Whole Pelvis Radiation Therapy (P-WPRT)
Primary outcomes (1)
- measure
- 5-year Biochemical Failure Free Survival (BFFS)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: PSMA-N0M0 patients who have a documented history of High Risk localized adenocarcinoma of the prostate are eligible to participate if they meet the following eligibility criteria: 1. Participants capable of giving written informed consent. 2. Male. 3. Age ≥18 years. 4. ECOG ≤2. 5. Patient has histologically proven adenocarcinoma of prostate gland with an assigned Gleason score and Gleason Grade Group. 6. ≥NCCN High-Risk localized disease as per standard imaging investigations including pelvic imaging (CT, MRI) and 99Tc bone scan. High Risk prostate cancer defined as any of the following: cT3-T4 disease OR PSA ≥20 ng/ml OR Gleason grade group 4 or 5. 7. No documentation of regional nodal (N1) or metastatic (M1) prostate cancer on standard imaging (CT, MRI, or 99Tc bone scan). 8. In the opinion of the treating oncologist, patient is fit to undergo radical external beam radiotherapy to the prostate. 9. Patient commits to androgen suppression treatment as per standard of care. 10. Patient is willing to complete symptom and patient reported outcome questionnaires. 11\. Patients of childbearing / reproductive potential should use highly effective birth control methods, as defined by the investigator, during the study treatment period and for a period of 6 months after the last dose of radiation therapy. A highly effective method of birth control is defined as those that result in low failure rate (i.e. less than 1% per year) when used consistently and correctly. Note: abstinence is acceptable if this is established and preferred contraception for the patient and is accepted as a local standard. Male patients should agree to not donate sperm during the study and for 6 months after completion of radiation therapy. Exclusion Criteria: 1. Inability to complete the investigational imaging examinations due to other reasons (severe claustrophobia, radiation phobia, etc.). 2. Any additional medical condition, serious inter-current illness or other extenuating circumstance that, in the opinion of the Investigator, may significantly interfere with study performance, interpretation, or compliance with radiation 3. Patients who have initiated therapy (ADT, systemic therapy, or radiation) for their prostate cancer prior to PSMA-PET imaging. 4. History of inflammatory bowel disease, anal stenosis, colorectal surgery, or repeated endoscopic examinations/interventions related to anorectal diseases. 5. History of prostatectomy or previous pelvic radiotherapy. 6. Previous malignancy within the last five years, except BCC or SCC skin or a malignancy treated curatively with no evidence of disease for ≥5 years. 7. Bilateral hip prostheses will be ineligible for study
References
Publications (0)
Data not yet available
No reference posted for this study.