A Diagnostic Prediction Model for Prostate Cancer in Patients With PI-RADS Score 3

NCT ID: NCT06507462

Last Updated: 2025-02-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

460 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-01-01

Study Completion Date

2024-10-31

Brief Summary

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The goal of this observational study is to construct a predictive model for improving the diagnostic accuracy in patients with PI-RADS score of 3. The main aims of this study are:

* Construct a diagnostic model of patients with PI-RADS of score.
* Internal and external validation of the model.
* Decision curve analysis. The data of participants was collected retrospectively.

Detailed Description

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For patients with a PI-RADS score of 3, the diagnosis of prostate cancer is still use prostate biopsy, but the detection rates of prostate cancer and clinically significant prostate cancer are approximately 30% and 15%. It can be seen that most patients with PI-RADS 3 undergo unnecessary prostate biopsy and bear the risk of complications such as urinary tract infection. This makes most patients with PI-RADS 3 choose to refuse invasive prostate biopsy. Although researchers are committed to exploring biomarkers with high sensitivity and specificity, the application of biomarkers alone often cannot achieve the expected results. At present, the guidelines have recommended the use of diagnostic prediction models to assess patients' prostate cancer risk. Doctors and patients use diagnostic models to assess the risk of prostate cancer before prostate biopsy. For patients with a low probability of cancer, biopsy can be temporarily avoided, which to a certain extent reduces the phenomenon of prostate cancer overdiagnosis. This study plans to work with multiple medical centers to conduct statistical analysis based on existing prostate cancer screening markers combined with patients' clinical data such as prostate volume, prostate-specific antigen density, apparent diffusion coefficient, PI-RADS score and postoperative Gleason score, and then construct a prostate cancer diagnostic model to improve the diagnostic accuracy of prostate cancer for patients with PI-RADS score of 3. This will be of great significance for improving the early diagnosis of patients with PI-RADS 3 and reducing unnecessary prostate puncture biopsies.

Conditions

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Prostate Cancer

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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Patients with clinical suspicion of prostate cancer and have PI-RADS score of 3

Patients with clinical suspicion of prostate cancer (see inclusion criteria) and have PI-RADS score (results of mpMRI) of 3.

prostate biopsy

Intervention Type PROCEDURE

All patients were required to underwent transperineal prostate biopsy and have corresponding pathological diagnosis results.

Interventions

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prostate biopsy

All patients were required to underwent transperineal prostate biopsy and have corresponding pathological diagnosis results.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Patients with clinically suspected prostate cancer (abnormal PSA level or DRE);
2. All patients have undergone mpMRI and have complete imaging data;
3. The PI-RADS score of patients was 3;
4. Prostate biopsy was performed and has clear pathological results.

Exclusion Criteria

1. The patient's serum tPSA is \<4ng/ml or \>100ng/ml;
2. Repeated prostate biopsy;
3. The patient's clinical, imaging, or pathological data are incomplete.
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Anhui Provincial Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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XiaoJun

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jun Xiao, Pro.

Role: PRINCIPAL_INVESTIGATOR

The First Affiliated Hospital of USTC

Locations

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Department of Urology, The First Affiliated Hospital of Bengbu Medical University

Bengbu, Anhui, China

Site Status

Department of Urology, The First Affiliated Hospital of USTC

Hefei, Anhui, China

Site Status

Department of Urology, The First Affiliated Hospital of Wannan Medical College

Wuhu, Anhui, China

Site Status

Countries

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China

Other Identifiers

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2024-ky312

Identifier Type: -

Identifier Source: org_study_id

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