COACTION Trial - COmbination Androgen bloCkade in inTermediate to hIgh-risk prOstate caNcer

  • 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

info icon Men ≥18 years of age;

info icon 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;

info icon 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.

info icon High-risk or very high-risk: * ≥cT3a (MRI based) or ISUP 4-5 or PSA\>20 ng/mL; * cN1.

info icon ECOG 0-1;

info icon Baseline testosterone \> 230 ng/dL;

info icon No prior prostate cancer treatment;

info icon 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;

info icon Written informed consent.

info icon Unresectable prostate cancer;

info icon Histology of small cell carcinoma prostate cancer or adenocarcinoma with neuroendocrine features;

info icon Any prior prostate cancer treatment;

info icon Any active infection requiring IV antibiotics;

info icon Known additional malignancy that has a life-expectancy \< 2 years;

info icon 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;

info icon Uncontrolled severe hypertension as indicated by a resting systolic BP ≥ 180 mmHg or diastolic BP ≥ 110 mmHg despite medical management;

info icon A gastrointestinal (GI) disorder or procedure which is expected to interfere significantly with absorption of darolutamide;

info icon Inability to swallow oral medications;

info icon 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

NCT06627530

Clinic Location Investigator Distance RECRUITING STATUS Contact