Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06575257

Neoadjuvant Therapy of Darolutamide Plus ADT for High Risk Prostate Cancer

The purpose of this study is to determine if treatment with Darolutamide plus androgen deprivation therapy (ADT) before radical prostatectomy (RP) with pelvic lymph node dissection (pLND) in participants with high-risk localized or locally advanced prostate cancer results in an improvement in pathological complete response (pCR) rate and pathological tumor volume with minimal residual disease (MRD)) as compared to ADT.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–75 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

The First Affillated Hospital, the Air Force Medical University

Xi’an, Shanxi, 710032, China

Location status: Recruiting

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients must be ≥ 18 and ≤75 years of age.
  • All patients must have a histologically or cytologically diagnosis of prostate cancer and must be eligible for radical prostatectomy.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status score ≤1.
  • All patients must complete mpMRI or 68Ga-PSMA PET / CT before and after neoadjuvant treatment.
  • All patients must undergo thorough tumor staging and meet one of the following criteria: 1. multi-parameter MRI or PSMA PET / CT shows clinical staging of primary tumor ≥ cT2c or cN+or locally advanced, 2. Gleason score of primary tumor ≥ 8, 3. prostate specific antigen (PSA) ≥20 ng/ml.
  • Patients must have adequate organ function as defined by the following criteria(within 28 days prior to registration):

white blood cell (WBC) ≥ 4.0 × 109 / L platelets≥ 100 × 109 / L hemoglobin ≥ 9 g / dL international normalized ratio (INR) < 1.5. total bilirubin (TBIL)≤1.5 x upper limit of normal (ULN) SGOT (AST) and SGPT (ALT) ≤ 2.5 x ULN serum creatinine ≤2×ULN

  • Patients must participate voluntarily and sign an informed consent form (ICF), indicating that they understand the purpose and required procedures of the study, and are willing to participate in. Patients must be willing to obey the prohibitions and restrictions specified in the research protocol.

Exclusion criteria

  • clinical or radiological evidence of regional or extra-regional lymph node metastases or bone metastases or visceral metastases.
  • Prior androgen deprivation therapy (medical or surgical) or focal treatment of prostate cancer or prostate cancer radiotherapy or prostate cancer chemotherapy.
  • severe or uncontrolled concurrent infections.
  • New York Heart Association Class III or IV congestive heart failure at the time of screening.
  • uncontrolled severe hypertension, persistent uncontrolled diabetes, oxygen-dependent lung disease, chronic liver disease, or HIV infection.
  • Patients with mental illness, mental disability or inability to give informed consent are not eligible.
  • Patients have had other malignancies other than prostate cancer in the past 5 years, but cured basal cell or squamous cell skin cancers can be enrolled.

Treatment and study plan

Darolutamide

Drug

600 mg orally twice daily for 12 weeks before radical prostatectomy

Goserelin 3.6 MG

Drug

3.6 mg goserelin hypodermic once per 4 weeks

Primary outcomes

  1. Pathologic Complete Response Rate

    Time frame: After 12 weeks of neoadjuvant therapy + RP + PLND

    The proportion of subjects with no morphologically recognizable cancer cell in tumor specimens after radical prostatectomy

  2. Proportion of Subjects With Minimal Residual Disease

    Time frame: After 12 weeks of neoadjuvant therapy + RP + PLND

    The proportion of subjects that have residual tumors with maximum diameter of 5 mm or less after radical prostatectomy

Secondary outcomes

  1. Rate of Stage Degradation

    Time frame: After 12 weeks of neoadjuvant therapy + RP + PLND

    Clinical or pathological stage degradation after neoadjuvant therapy

  2. Rate of Positive Surgical Margins

    Time frame: After 12 weeks of neoadjuvant therapy + RP + PLND

    The proportion of subjects with positive surgical margins after radical prostatectomy

  3. Rate of Complete Serum Remission

    Time frame: After 12 weeks of neoadjuvant therapy

    The proportion of subjects whose PSA is less than or equal to 0.2 ng/ml after 3 months of treatment

  4. Proportion of subjects without PSA progression

    Time frame: 2 years after RP

    The proportion of subjects whose PSA has never gone below 1 ng/ml or who receive any radiotherapy or systemic treatment after radical prostatectomy

  5. Imaging Response Rate

    Time frame: After 12 weeks of neoadjuvant therapy

    The proportion of subjects whose primary tumor is in complete remission on imaging or residual tumor's maximum diameter is less than 0.5cm

  6. Recovery time of urinary continence (day)

    Time frame: 1 years after RP

    The recovery time of urinary continence (day) after radical prostatectomy, defined as 0 pad/day.

  7. biochemical recurrence-free survival (bRFS)

    Time frame: 3 years after RP

    biochemical recurrence-free survival (bRFS) defined as time to PSA ≥ 0.2 ng/ml after radical prostatectomy.

  8. metastasis-free survival (MFS)

    Time frame: 5 years after RP

    time from date of randomization to date of evidence of systemic disease on bone scan or cross-sectional imaging.

Study contacts

Contact information is provided by the study sponsor or research team.

Jingliang Zhang, MD

CONTACT

[email protected]

Weijun Qin, MD

CONTACT

[email protected]

029-84771579

Sponsors and collaborators

Lead sponsor

Xijing Hospital

Other

Registry information

Official study title

Neoadjuvant ADT +/- Darolutamide Followed by Radical Prostatectomy for High-risk Prostate Cancer: a Randomized, Open Label Trial

Important dates

Study start
2024
Primary completion
2026
Study completion
2029
First posted
Aug 28, 2024
Registry last updated
Aug 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.