RecruitingPhase 2Phase 3NCT06282588

Treatment of High-Risk Prostate Cancer Guided by Novel Diagnostic Radio- and Molecular Tracers

Treatment of High-Risk Prostate Cancer Guided by Novel Diagnostic Radio- and Molecular Tracers (THUNDER): A Two-part Phase 2/ 3 Trial


Sponsor

Cancer Research Antwerp

Enrollment

493 participants

Start Date

Dec 13, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This Investigator-initiated, Treatment of High-Risk Prostate Cancer Guided by Novel Diagnostic Radio- and Molecular Tracers (THUNDER) study will be conducted in subjects with high-risk localized or locally advanced prostate cancer (PCa). The study contains both a randomized Phase 3 treatment intensification study, as well as a treatment de-intensification non-randomized Phase 2 study. The aim of the THUNDER study is to improve the outcome of high-risk PCa by improved risk stratification. Novel radiotracers and a genomic classifier (Decipher) will be used to guide treatment decisions, instead of standard imaging which is limited by lower sensitivity and specificity. The hypothesis for the study is that treatment intensification based on a positive PSMA PET/ CT scan or Decipher high score (\> 0.85) improves time to new metastases detected on PSMA PET/ CT in high-risk PCa. In patients who are PSMA PET/ CT negative with a low/ intermediate Decipher score (≤ 0.85), it is hypothesized that treatment de-intensification will improve patient quality of life while maintaining a good oncological outcome. The study will be conducted at multiple centers across Europe. Participation in the study will comprise a screening period, where the screening assessments must be completed before subjects are enrolled and randomized (only for Phase 3 subjects). Eligible, consenting subjects will then undergo treatment according to their assigned study phase and treatment group, to occur over up to 96 weeks (24 months) with a post-treatment follow-up period to monitor safety and efficacy. The study will be closed when 96 events have been registered for the primary endpoint, which is expected to be at 7-8 years from the time of randomization of the first subject.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying whether using advanced diagnostic tools — specifically PSMA PET/CT imaging (a specialized scan that detects prostate cancer cells) and genomic testing (Decipher score) — can help guide better treatment decisions for men with high-risk prostate cancer. **You may be eligible if...** - You have been diagnosed with prostate cancer confirmed by biopsy - Your cancer is high-risk, defined by a PSA level over 20, clinical stage T3/T4, Gleason score 8–10, or lymph node involvement (N1) - You are in good physical condition (ECOG 0-1) - You are willing to undergo a PSMA PET/CT scan **You may NOT be eligible if...** - You have already received treatment for prostate cancer (surgery, radiation, or hormone therapy) - You have evidence of distant spread on initial imaging - You have significant other health conditions making treatment unsafe Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDarolutamide

2x300 mg tablets twice daily, for up to 96 weeks

DRUGDarolutamide matched placebo

2x300 mg tablets twice daily, for up to 96 weeks

RADIATIONRadiotherapy

Preferred regimens: 60 to 62 Gy delivered in 20 fractions of 3.0 to 3.1Gy per fraction; 36.25 Gy delivered in 5 fractions of 7.25 Gy per fraction, 2-3 fractions per week

DRUGZoladex 3.6Mg Implant

3.6 mg, subcutaneous use

DRUGZoladex LA

10.8 mg, subcutaneous use

DRUGDecapeptyl sustained release 22.5 mg

22.5 mg, intramusculair injection

DRUGDecapeptyl sustained release 11.25 mg

11.25 mg, intramusculair injection

DRUGDepo-Eligard 45 mg

45 mg, subcutaneous use

DRUGDepo-Eligard 22.5 mg

22.5 mg, subcutaneous use

DRUGDepo-Eligard 7.5 mg

7.5 mg, subcutaneous use

DRUGFirmagon 120 MG Injection

120 mg, subcutaneous use

DRUGFirmagon 80 MG Injection

80 mg, subcutaneous use

DRUGDocetaxel

75 mg per square m, IV infusion


Locations(9)

ZAS Sint-Augustinus

Wilrijk, Antwerp, Belgium

AZORG

Aalst, Belgium

AZ Sint-Jan

Bruges, Belgium

Saint Luc

Brussels, Belgium

UZ Gent

Ghent, Belgium

AZ Groeninge

Kortrijk, Belgium

CHU Liège

Liège, Belgium

AZ Delta

Roeselare, Belgium

VITAZ

Sint-Niklaas, Belgium

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NCT06282588


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