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Clinical Trials/NCT05179707
NCT05179707
Unknown
N/A

A Prospective, Multicenter Research for Combination of Prostate Health Index (Phi) and mpMRI PI-RADS in the Diagnosis of Prostate Cancer

Qilu Hospital of Shandong University1 site in 1 country936 target enrollmentFebruary 1, 2022
ConditionsProstate Cancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Qilu Hospital of Shandong University
Enrollment
936
Locations
1
Primary Endpoint
Prostate Health Index
Last Updated
3 years ago

Overview

Brief Summary

Before prostate puncture, the patient's serum was collected for PHI detection, and multi-parameter MRI was performed to obtain the PI-RADS score. The sensitivity and specificity of PHI combined with PI-RADS score in the diagnosis of clinically significant prostate cancer were explored.

Detailed Description

This study is a multi-center prospective study. Patients who meet the indications for prostate puncture and whose PSA is in the gray area (4.0\~10.0 ng/mL) undergo standard prostate biopsy. The patient's serum was collected for PHI detection before puncture, and multi-parameter MRI was performed before puncture. To explore the sensitivity and specificity of PHI combined with PI-RADS score in the diagnosis of clinically meaningful prostate cancer. Assess the benefit of combining PHI and mpMRI before biopsy compared with phi or mpMRI alone. Formulate clinical recommendations for PHI and mpMRI.

Registry
clinicaltrials.gov
Start Date
February 1, 2022
End Date
October 1, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with suspected prostate cancer
  • Patients can perform standardized prostate biopsy

Exclusion Criteria

  • Have a history of prostate cancer
  • Use of drugs that affect PSA before blood sampling

Outcomes

Primary Outcomes

Prostate Health Index

Time Frame: 1 year

PHI is a simple, FDA-approved blood test that helps determine the probability of detecting prostate cancer with a biopsy. This test uses an algorithm to assess total PSA, free PSA, and p2PSA,

PI-RADS score

Time Frame: 1 year

In PI-RADS, based on the comprehensive manifestations of prostate T2WI, DWI and DCE, a scoring method is given for the possibility of clinically significant prostate cancer. Specifically: 1 point: very low, extremely unlikely to exist; 2 points: low, impossible to exist; 3 points: moderate, suspicious existence; 4 points: high, may exist; 5 points: very high, extremely likely to exist.

Prostate biospy pathology

Time Frame: 1 year

The pathological results of prostate puncture are used as the gold standard for the diagnosis of prostate cancer, indicating whether the patient is really suffering from prostate cancer

Study Sites (1)

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