drugset / Trial / NCT06282588

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

NCT06282588

RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2023-12-13
Primary completion
2030-07-31
Completion
2030-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Darolutamide Other / unclassified 600 mg Oral
Background Decapeptyl Unknown 11.25 mg Intramuscular
Background Decapeptyl Unknown 22.5 mg Intramuscular
Background Degarelix Other / unclassified 80 mg Subcutaneous
Background Degarelix Other / unclassified 120 mg Subcutaneous
Background Docetaxel Small molecule 75 mg/m2 Intravenous
Background Goserelin Other / unclassified 3.6 mg Subcutaneous
Background Goserelin Other / unclassified 10.8 mg Subcutaneous
Background Leuprolide Other / unclassified 7.5 mg Subcutaneous
Background Leuprolide Other / unclassified 22.5 mg Subcutaneous
Background Leuprolide Other / unclassified 45 mg Subcutaneous

Indications