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Not Yet Recruiting NCT05670691

a Study of Combined mpMRI and PSMA PET/CT for Highly Suspicious Patients Performing Radical Prostatectomy Without Biopsy

Conditions: Prostatic Neoplasms, Prostatectomy, Prostate Biopsy

Sex: Male
Ages: 18 Years – N/A
Enrollment: 71
Sponsor: Fudan University

Summary

This is an observational, open, single-arm, prospective, staged entry(based on Fleming's Group-Sequential Design) clinical studyThe Goal is to evaluate the feasibility and clinical value of direct robot assisted laparoscopic radical prostatectomy without prostate biopsy in patients with high clinical suspicion of prostate cancer based on a prostate MRI PI-RADS score of ≥4 and the PSMA PET/CT positive criteria.The Primary endpoint is positive pathological diagnosis of prostate cancer after direct radical prostatectomy without prostate biopsy.The question addressed is whether the feasibility of biopsy-free radical prostatectomy could be scientifically and rationally derived based on Fleming's Group-Sequential design.

Eligibility Criteria

Inclusion Criteria:age ≥ 18 years.consent and ability to complete a multiparametric MRI of the prostate.consent and ability to complete PSMA PET/CT.multiparametric MRI of the prostate with a PI-RADS score of 4 or 5 for suspicious lesions.Positive PSMA PET/CT. Its positive is defined as a suspicious lesion score of 2 or 3 (see remarks for specific scoring criteria).good physical condition with an ECOG score of 0 or 1.no history of radiotherapy or other surgery to the pelvisthe presence of pelvic lymph node enlargement (>2 cm) or metastasis is allowed; ≤5 bone and lymph node metastases are allowedthe patient has good cardiac, pulmonary, hepatic and renal function and is able to tolerate local treatment (surgery or external radiotherapy) of the primary site and metastases, and the treatment will not cause serious complications for the patient.the patient participates voluntarily and has signed an informed consent formthe patient is able to receive treatment and subsequent follow-upthe expected survival time is greater than 1 year.Exclusion Criteria:unwillingness or inability to perform multiparametric MRI of the prostate; or PI-RADS score of 0-3request for prostate puncture biopsy.unwillingness or inability to perform PSMA PET/CT; or PSMA PET/CT score of 0 or 1refusing radical prostate cancer surgery, or choosing other primary lesion treatment modalities other than radical prostate cancer surgerypoor physical condition that prevents them from tolerating radical prostate cancer surgeryMore than 5 bone and lymph node metastases, visceral metastaseshistory of combined other malignant tumors (except basal cell carcinoma of the skin or other tumors that have been cured for more than 5 years)other serious medical conditions, such as: unstable heart disease after treatment, myocardial infarction within 6 months prior to treatment, cardiac function class 3-4 (NYHA); uncontrolled hypertension (>150/90 mmHg, severe neurological or psychological disorders including dementia or epilepsy) with medical treatment; uncontrolled active infection; acute gastric ulcer; hypercalcemia; chronic obstructive lung disease.have participated in other clinical studies prior to enrollment.Note: Positive PSMA PET/CT, defined as based on the miPSMA score scale suggested by the PROMISE Institute (score 0 - below the depth of blood contrast; score 1 - equal to or above the blood contrast and below the liver contrast; score 2 - equal to or above the liver contrast and below the parotid contrast; score 3 - equal to or above the liver parotid contrast.)

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05670691). StuddyBuddy aggregates publicly available trial information.