Current partner codePEPTIDESDE

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

Status

Recruiting

Phase

Phase 2 / Phase 3

Enrollment

493

Locations

9

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

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.

Full detailed description

Approximately 360 evaluable patients determined to have high-risk localized or locally advanced PCa, with PSMA positive non-localized disease or a Decipher high score (\> 0.6) will be enrolled to the Phase 3 trial. Subjects with PSMA positive non-localized disease for which a Decipher result cannot be obtained, will also be enrolled to the Phase 3 study. All Phase 3 subjects will be randomly assigned in a 1:1 ratio to receive darolutamide plus Luteinizing hormone releasing hormone (ant)-agonists (LHRHA), or darolutamide matched placebo plus LHRHA, for up to 96 weeks (24 months). All Phase 3 subjects will also receive primary standard of care (SOC) radiation therapy (RT). Subjects in Phase 3 should be commenced on an LHRHA and darolutamide or placebo within 14 days after randomization (unless started earlier) plus SOC RT. Only patients with a PSMA PET-CT showing more than 5 M1 lesions are allowed to receive docetaxel in both arms of the Phase 3 trial. Docetaxel should be started within 4 weeks from randomization. Randomization of Phase 3 subjects will be stratified by 1 versus \> 1 high-risk features, N1 versus M1 PSMA positive versus PSMA negative disease, Decipher low/ intermediate versus high versus unknown score and clinical trial site. Approximately 133 evaluable patients determined to have localized PCa by PSMA PET/ CT (PSMA negative) with a low/ intermediate Decipher test score (≤ 0.85) will enter the non-randomized, Phase 2, single treatment arm, de-intensification study. Subjects with localized PCa by PSMA PET/ CT who return a high Decipher score (\> 0.85) will be enrolled and randomized into the Phase 3 study. Subjects with localized PCa by PSMA PET/ CT for which a Decipher result cannot be obtained, will be deemed ineligible for study participation. All Phase 2 study subjects will receive darolutamide for the study duration for up to 96 weeks (24 months) and primary SOC RT.

Interventions

Treatment arms and agents.

DRUG

Darolutamide

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

DRUG

Darolutamide matched placebo

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

RADIATION

Radiotherapy

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

DRUG

Zoladex 3.6Mg Implant

3.6 mg, subcutaneous use

DRUG

Zoladex LA

10.8 mg, subcutaneous use

DRUG

Decapeptyl sustained release 22.5 mg

22.5 mg, intramusculair injection

DRUG

Decapeptyl sustained release 11.25 mg

11.25 mg, intramusculair injection

DRUG

Depo-Eligard 45 mg

45 mg, subcutaneous use

DRUG

Depo-Eligard 22.5 mg

22.5 mg, subcutaneous use

DRUG

Depo-Eligard 7.5 mg

7.5 mg, subcutaneous use

DRUG

Firmagon 120 MG Injection

120 mg, subcutaneous use

DRUG

Firmagon 80 MG Injection

80 mg, subcutaneous use

Timeline

From registration to results.

  1. First posted

    Feb 28, 2024

  2. Study start

    Dec 13, 2023

  3. Primary completion

    Jul 31, 2030

  4. Study completion

    Dec 31, 2030

  5. Results posted

    Not reported

  6. Registry updated

    Mar 19, 2026

Outcomes

What the study measures.

Primary outcomes

Phase 3: PSMA PET metastasis free survival (ppMFS)

Time frame · Time from randomization to the date of at least 1 new PSMA-PET positive distant lesion as compared to baseline or date of death from any cause, assessed up to 42 months

Improvement in PSMA PET metastasis free survival (ppMFS)

Phase 2: quality of life (sexual subdomain)

Time frame · At 12 months

EPIC mean changes in sexual subdomain scores over time will be compared, both for change from baseline and absolute scores

Phase 2: quality of life (hormonal subdomain)

Time frame · At 12 months

EPIC mean changes in hormonal subdomain scores over time will be compared, both for change from baseline and absolute scores

Secondary outcomes

Overall survival

Time frame · Time interval between randomization and time of death, assessed up to 42 months

Overall survival

Prostate-cancer specific survival

Time frame · Time interval between randomization and prostate cancer death, assessed up to 42 months

Prostate-cancer specific survival

Biochemical progression-free survival

Time frame · Measured from the date of randomization to the date event, or death or censored at the last known follow-up date, assessed up to 42 months

Increase in PSA of \>2 ng/ml above the nadir PSA level

Time to next systemic therapy

Time frame · Measured from date of randomization to time of death, or censored at the last known follow-up date, assessed up to 42 months

Time to next systemic therapy

Frequency and severity of adverse events

Time frame · From signing ICF until 30 days after the last dose of study treatment.

Frequency and severity of adverse events

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
MALE
Healthy volunteers
No

Inclusion Criteria: 1. Histopathology-proven PCa 2. High-risk locally advanced disease is defined as any of the following factors: PSA \> 20 ng/mL OR T-stage 3 or 4 OR Gleason score 8-10 OR cN1. Note: documentation of the clinical T-stage may be obtained from any clinical assessment acceptable for clinical T staging including physical exam (DRE), transrectal ultrasound, CT or MRI. Documentation for the N1 stage can be defined on CT or MRI. 3. An Eastern Cooperative Oncology Group (ECOG) Performance Status grade of 0 or 1. 4. Willingness to undergo a PSMA PET/ CT with or without contrast. 1. Subjects who are PSMA PET/ CT positive for at least one regional or distant (extra-pelvic) lesion at screening (PSMA PET scans will be assessed as described in the study imaging manual), will be eligible to be randomized to either arm of the Phase 3 study. A lesion is considered positive if it has a E-PMSA score of 4 or 5. 2. Pending confirmation of their Decipher score, subjects who are PSMA PET/ CTnegative for regional or distant lesions at screening (PSMA PET scans will be assessed as described in the study imaging manual), will be eligible for inclusion in either the Phase 3 study (if a high \[\> 0.85\] Decipher score is confirmed) or the non-randomized Phase 2 study (if a low/ intermediate \[≤ 0.85\] Decipher score is confirmed). 5. Willingness to have their primary tumor sequenced for determination of Decipher score 1. Subjects who have a negative PSMA PET/ CT and a tumor with a low/ intermediate Decipher score (≤ 0.85) will be eligible to enter the non-randomized Phase 2 study. 2. Subjects who have a negative PSMA PET/ CT and a tumor with a high Decipher score (\> 0.85) will be eligible to be randomized to either arm of the Phase 3 study. 3. In subjects with positive PSMA PET/ CT, the Decipher score will not determine the treatment allocation. 6. Willingness to undergo SOC RT and long-term ADT (treatment with darolutamide and/ or LHRHA) 7. Subject is able and willing to provide written informed consent, which includes compliance with and ability to undergo all study procedures and attend the scheduled follow-up visit/s per protocol. 8. Subject must be over 18 years of age. 9. Subject able to swallow whole study drug tablets. 10. To avoid risk of drug exposure through the ejaculate (even men with vasectomies), subjects must use a condom during sexual activity while on study drug and for 3 months after the last administration of study treatment. Donation of sperm is not allowed during the treatment phase and for 3 months after the last administration of study treatment. 11. Adequate organ function determined by the following local laboratory values: 1. Adequate bone marrow function: Hemoglobin ≥ 100 g/L, white cell count (WCC) ≥ 4.0 x 109/L, absolute neutrophil count (ANC) ≥ 1.5 x 109/L and platelets \> 100 x 109/L 2. Adequate renal function: calculated creatinine clearance \> 30 mL/min (Cockroft-Gault) 3. Adequate liver function: ALT \< 2 x upper limit of normal (ULN) and total bilirubin \< 1.5 x ULN, (or if total bilirubin is between 1.5 to 2 x ULN, they must have a normal conjugated bilirubin) 4. Testosterone levels \> 50 ng/dL Exclusion Criteria: 1. Definitive radiologic evidence of metastatic disease outside of the pelvic nodes (M1a, M1b or M1c) on conventional imaging (i.e., bone scan, CT scan, MRI) 2. PCa with predominant non-adenocarcinoma features (sarcomatoid or spindle or neuroendocrine small cell or squamous cell components or other non-adenocarcinoma) 3. Prior pelvic radiotherapy 4. Contraindications for pelvic radiotherapy 5. Contraindications for ADT (treatment with darolutamide and/ or LHRHA) 6. Contraindications or known allergy to PSMA PET/ CT tracers. 7. Prior local therapy for PCa (e.g., radical prostatectomy, high-intensity focused ultrasound \[HIFU\], cryotherapy). Subjects with previous transurethral resection of the prostate (TURP) or Millin prostatectomy are eligible for participation 8. Prior systemic therapy for PCa, except for patients with a positive PSMA PET/ CT staging with ADT started no more than 4 weeks prior to randomization. 9. Current use of 5-alpha reductase inhibitor Note: if the alpha reductase inhibitor is stopped ≥ 2 weeks prior to enrollment, the subject is eligible. 10. Current chronic use of opioid analgesics, for ≥3 weeks for oral or ≥7 days for non-oral formulations 11. History of seizure or any condition that may predispose to seizure (including, but not limited to prior stroke, transient ischemic attack or loss of consciousness within ≤1 year prior to enrollment; brain arteriovenous malformation; or intracranial masses such as schwannomas and meningiomas that are causing edema or mass effect) 12. Any condition for which, in the opinion of the Investigator, participation would not be in the best interest of the subject 13. Major surgery within 21 days prior to enrollment. 14. History of: 1. Loss of consciousness or transient ischemic attack or stroke within 6 months prior to enrollment, or 2. Significant cardiovascular disease within 6 months prior to enrollment: including myocardial infarction, unstable angina, congestive heart failure (New York Heart Association \[NYHA\] classification Grade 2 or greater), ongoing arrhythmias of Grade \> 2 (National Cancer Institute Common Terminology Criteria for Adverse Events \[NCI-CTCAE\] v5.0), thromboembolic events (e.g., deep vein thrombosis, pulmonary embolism), coronary artery bypass graft. Chronic stable atrial fibrillation on stable anticoagulant therapy is allowed. 15. Known GI disease or GI procedure that could interfere with the oral absorption or tolerance of darolutamide, including difficulty swallowing tablets 16. History of another malignancy within 5 years prior to enrollment except for those malignancies treated with curative intent with a predicted risk of relapse of less than 10% including but not limited to non-melanoma carcinoma of the skin; or adequately treated, non-muscle-invasive urothelial carcinoma of the bladder (i.e., Tis, Ta and low grade T1 tumors). All such cases with a history of malignancy within the last 5 years are to be discussed with study team before enrollment. Melanoma in-situ and other adequately treated in-situ neoplasms are not considered malignancies for the purposes of eligibility assessment 17. Concurrent illness, including severe infection that might jeopardize the ability of the subject to undergo the procedures outlined in this protocol with reasonable safety (human immunodeficiency virus \[HIV\] infection is not an exclusion criterion if it is controlled with anti-retroviral drugs that are unaffected by concomitant darolutamide) 18. Subjects who are sexually active with women of childbearing potential and not willing/able to use medically acceptable and highly effective forms of contraception during study treatment and for at least 3 months after the last administration of study treatment. Contraception must include: Additional birth control with low failure rate (less than 1% per year) when used consistently and correctly, e.g., combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal), progestogen only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable), intrauterine device (IUD), intrauterine hormone releasing system (IUS), bilateral tubal occlusion, vasectomized partner, true sexual abstinence.

Study locations

9 registered sites.

Belgium. Showing up to 24 locations stored in the fast local snapshot.

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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