Darolutamide+ADT Post-RP w/o ePLND in hrPC: Briganti 2019

NCT ID: NCT07282197

Last Updated: 2025-12-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-01-31
• Study Completion Date: 2029-06-30

Brief Summary

The goal of this clinical trial is to evaluate whether adjuvant darolutamide plus androgen-deprivation therapy (ADT) can reduce post-operative recurrence and improve disease control in high-risk prostate cancer patients-defined by the Briganti 2019 nomogram-who have undergone radical prostatectomy (RP) without extended pelvic lymph node dissection (ePLND). The main questions it aims to answer are:

1. What proportion of participants remains biochemical-recurrence-free at 2 years, using NCCN criteria (PSA increase >0.1 ng/mL above post-treatment nadir confirmed by two tests ≥2 weeks apart)?

2. What proportion of participants is the 2-year radiographic progression-free survival (rPFS)?

Additional key outcomes include:

• PSA undetectable rates at 6, 12, and 24 months (PSA <0.01 ng/mL).
• Safety and tolerability assessed by CTCAE v5.0.
• Exploratory** patient-reported outcomes: urinary symptoms (IPSS) and quality of life (EQ-5D-3L).

Study type & design: Phase II, single-center, single-arm, prospective interventional study. Enrollment occurs within 12 weeks after RP. ADT is delivered with a GnRH agonist (physician's choice); orchiectomy is excluded. Target sample size is approximately 40 participants; the statistical plan uses a one-sample log-rank framework. Primary and secondary endpoints are assessed over 2 years.

Participants will: Provide informed consent and undergo eligibility confirmation (high-risk per Briganti 2019; post-RP without ePLND; enrollment ≤12 weeks after surgery). Receive darolutamide + ADT according to protocol (GnRH agonist; no orchiectomy). Attend scheduled visits for PSA monitoring, safety labs, and adverse-event assessments (CTCAE v5.0). Undergo radiologic evaluations as per protocol to determine rPFS (RECIST 1.1/PCWG3). Complete IPSS and EQ-5D-3L questionnaires at specified time points to assess urinary symptoms and quality of life.

Primary endpoint: 2-year biochemical-recurrence-free rate. Key secondary endpoints: 2-year rPFS; PSA <0.01 ng/mL at 6/12/24 months; treatment-emergent adverse events.

Exploratory endpoints: IPSS and EQ-5D-3L changes over 2 years.

This trial aims to balance oncologic control with quality of life in a population for whom the therapeutic value of ePLND remains uncertain, by testing whether early adjuvant darolutamide + ADT after RP can meaningfully delay recurrence and progression while maintaining acceptable tolerability.

Conditions

Prostate Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Daro+ADT

High-risk prostate cancer patients (Briganti 2019 monogram criteria) who did not undergo extended pelvic lymph node dissection (ePLND), will receive Darolutamide 600 mg bid + ADT for 12 months within 12 weeks after RP.

Group Type: EXPERIMENTAL

Darolutamide (BAY 1841788)

Intervention Type: DRUG

Darolutamide 600 mg bid + ADT x 12 months

Interventions

Darolutamide (BAY 1841788)

Darolutamide 600 mg bid + ADT x 12 months

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• The patient volunteers to participate and signs the informed consent form (ICF);
• Age 18-75 years (inclusive), male;
• Histologically or cytologically confirmed prostatic adenocarcinoma;
• No non-regional lymph-node metastasis, bone metastasis, or other distant metastasis (e.g., visceral) by conventional imaging (bone scan, CT or MRI) or by PET/CT; i.e., M0;
• High-risk per the Briganti 2019 nomogram, i.e., risk >7%;
• PSA <0.1 ng/mL at 6 weeks after radical prostatectomy (RP);
• Has undergone RP without pelvic lymph-node dissection;
• Not suitable for adjuvant/salvage radiotherapy (RT) after RP, or the patient declines RT;
• Patients with lymph-node involvement (LNI) indicated by PSMA-PET who did not undergo extended pelvic lymph-node dissection (ePLND) may be enrolled;
• Patients with negative intraoperative obturator lymph-node biopsy who did not undergo ePLND may be enrolled;
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1;
• Adequate hematologic and organ function:

• Absolute neutrophil count (ANC) ≥1.5 × 10⁹/L (1500/µL);
• Hemoglobin ≥90 g/L (9.0 g/dL);
• Platelet count ≥100 × 10⁹/L (100,000/µL) (without transfusion and/or growth factors within 3 months prior to starting study treatment);
• Serum potassium ≥3.5 mmol/L;
• Total bilirubin (TBIL) ≤2.0 × ULN (for Gilbert syndrome, TBIL >1.5 × ULN is not eligible; if indirect bilirubin ≤1.5 × ULN, enrollment is allowed);
• AST and ALT ≤2.5 × ULN;
• Serum albumin ≥30 g/L (3.0 g/dL);
• Serum creatinine <2 × ULN;
• Patients of childbearing potential must agree to use effective contraception throughout the study and for 3 months after the last dose.

Exclusion Criteria

• Histologic features of neuroendocrine differentiation or small-cell carcinoma;
• Prior prostate cancer treatments including any of the following:

• Systemic therapy, including but not limited to: >2 months of ADT; >2 months of conventional hormonal therapy (e.g., flutamide, bicalutamide); next-generation hormonal agents (e.g., darolutamide, abiraterone, apalutamide, enzalutamide, relugolix); chemotherapy (e.g., docetaxel); immunotherapy; targeted therapy;
• Local radiotherapy;
• Planned bilateral orchiectomy during the study treatment period;
• Inability to tolerate darolutamide or ADT;
• Concurrent participation in, or planned participation in, another clinical trial;
• A malignancy other than prostate cancer within the past 5 years or concurrently, except for cured basal cell carcinoma of the skin;
• Any concomitant disease or condition that, in the investigator's judgment, presents a serious risk to patient safety, may confound study results, or may interfere with completion of the study (e.g., severe cardiovascular disease, active infection, gastrointestinal disease, neurologic or psychiatric disorders, etc.);
• Any other condition deemed by the investigator to make the patient unsuitable for this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Peking University First Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kan Gong

Role: PRINCIPAL_INVESTIGATOR

Peking University First Hospital

Locations

Peking University First Hospital

Beijing, , China

Countries

China

Central Contacts

Kan Gong

Role: CONTACT

kan.gong@bjmu.edu.cn

(86)-010-83572075

Facility Contacts

Jianhui Qiu

Role: primary

16710080711@139.com

(86)-010-83572075

Other Identifiers

23096

Identifier Type: -

Identifier Source: org_study_id