The First Affillated Hospital, the Air Force Medical University
Xi’an, Shanxi, 710032, China
Location status: Recruiting
NCT Number: NCT06575257
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.
Interested in participating?
Request Info18 year–75 year
Male
Interventional
Phase 2
Xi’an, Shanxi, 710032, China
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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
Exclusion criteria
600 mg orally twice daily for 12 weeks before radical prostatectomy
3.6 mg goserelin hypodermic once per 4 weeks
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
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
Time frame: After 12 weeks of neoadjuvant therapy + RP + PLND
Clinical or pathological stage degradation after neoadjuvant therapy
Time frame: After 12 weeks of neoadjuvant therapy + RP + PLND
The proportion of subjects with positive surgical margins after radical prostatectomy
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
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
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
Time frame: 1 years after RP
The recovery time of urinary continence (day) after radical prostatectomy, defined as 0 pad/day.
Time frame: 3 years after RP
biochemical recurrence-free survival (bRFS) defined as time to PSA ≥ 0.2 ng/ml after radical prostatectomy.
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.
Contact information is provided by the study sponsor or research team.
Xijing Hospital
Other
Neoadjuvant ADT +/- Darolutamide Followed by Radical Prostatectomy for High-risk Prostate Cancer: a Randomized, Open Label Trial
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.
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