- Not Yet Recruiting
- Treatment
- Interventional
- Randomized
- Drug
- PHASE4
- Brazilian Clinical Research Institute
- 18 Years -
Study Purpose
A Randomized Trial of Neoadjuvant Leuprorelin, Darolutamide or Both Prior to Radical Prostatectomy for Intermediate or High-risk Prostate Cancer. Prospective, randomized, parallel group, open-label with blinded endpoint adjudication multicenter clinical trial.To assess, among patients with unfavorable intermediate to high-risk prostate cancer, whether a neoadjuvant combined treatment with leuprorelin (Leuprorelin) and darolutamide is superior to monotherapy in terms of complete or almost complete pathological response.A total of 144 patients with unfavorable intermediate to high-risk prostate cancer scheduled for radical prostatectomy with extended pelvic lymph node dissection will be randomized 1:1:1 to oral darolutamide, SC leuprorelin (Leuprorelin) or both (48 patients per arm) for 24 weeks.
Intervention
Drug : Darolutamide Oral Tablet
Drug : leuprorelin
Eligibility Requirements
Men ≥18 years of age;
Histologically confirmed unfavorable intermediate or high/very high risk non metastatic (by conventional imaging) prostate adenocarcinoma intended for surgery without neuroendocrine differentiation or small cell features;
Unfavorable intermediate-risk:
* ISUP grade 3, and/or \> 50% positive biopsy cores and/or at least two intermediate-risk factors. Intermediate-risk factors:
* Clinical tumor stage T2b or T2c (MRI based);
* ISUP grade 2 or 3;
* Prostate-specific antigen (PSA) level of 10-20 ng/mL.
High-risk or very high-risk:
* ≥cT3a (MRI based) or ISUP 4-5 or PSA\>20 ng/mL;
* cN1.
ECOG 0-1;
Baseline testosterone \> 230 ng/dL;
No prior prostate cancer treatment;
Sexually active male subjects must agree to use condoms as an effective barrier method and refrain from sperm donation, and/or their female partners of reproductive potential to use a method of effective birth control, during the treatment with darolutamide and for 1 week after the end of treatment with darolutamide to prevent pregnancy;
Written informed consent.
Unresectable prostate cancer;
Histology of small cell carcinoma prostate cancer or adenocarcinoma with neuroendocrine features;
Any prior prostate cancer treatment;
Any active infection requiring IV antibiotics;
Known additional malignancy that has a life-expectancy \< 2 years;
Had any of the following within 6 months before randomization: stroke, myocardial infarction, severe/unstable angina pectoris, coronary/peripheral artery bypass graft, heart failure with New York Heart Association Class Functional III or IV;
Uncontrolled severe hypertension as indicated by a resting systolic BP ≥ 180 mmHg or diastolic BP ≥ 110 mmHg despite medical management;
A gastrointestinal (GI) disorder or procedure which is expected to interfere significantly with absorption of darolutamide;
Inability to swallow oral medications;
Receipt of medications (e.g. finasteride, dutasteride) or agents that are likely to alter serum PSA levels within \<= 42 days or 5 half-lives prior to registration, whichever is shorter.
Recruiting status
Not Yet Recruiting
Estimated enrollment
144
Study start date
Oct 31, 2024
Study end date
Sep 30, 2026
Last updated
Mar 22, 2025
Primary purpose
Treatment
Design
Interventional
Intervention
Drug
Study phase
PHASE4
Allocation
Randomized
Sponsor:
Brazilian Clinical Research Institute
Collaborator:
Bayer
Investigator:
Fernando C Maluf, MD
Publications
N/A
Websites
N/A
NCT06627530
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