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

U

University of Science and Technology of China (USTC)

Status

Completed

Conditions

Prostate Cancer

Treatments

Procedure: prostate biopsy

Study type

Observational

Funder types

Other

Identifiers

NCT06507462
2024-ky312

Details and patient eligibility

About

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.

Full description

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.

Enrollment

460 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

460 participants in 1 patient group

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

Trial contacts and locations

3

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Central trial contact

Changming Wang, M.D.

Data sourced from clinicaltrials.gov

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