Novel clinical risk calculator for improving cancer predictability of mpMRI fusion biopsy in prostates
- Anthony Bruccoliere 1, Vivie Tran 1, Naseem Helo 2, Abdul Awal 3, Stephanie Stroever 3, Werner T W de Riese 4
- Anthony Bruccoliere 1, Vivie Tran 1, Naseem Helo 2
- 1School of Medicine, Department of Urology, Texas Tech University Health Sciences Center, 3601-4 Street STOP 7260, Lubbock, TX, 79430-7260, USA.
- 2Department of Radiology, University Medical Center, Lubbock, TX, 79415, USA.
- 3School of Medicine, Texas Tech University Health Sciences Center, Clinical Research Institute, Lubbock, TX, 79415, USA.
- 4School of Medicine, Department of Urology, Texas Tech University Health Sciences Center, 3601-4 Street STOP 7260, Lubbock, TX, 79430-7260, USA. Werner.Deriese@ttuhsc.edu.
- 0School of Medicine, Department of Urology, Texas Tech University Health Sciences Center, 3601-4 Street STOP 7260, Lubbock, TX, 79430-7260, USA.
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View abstract on PubMed
Summary
This summary is machine-generated.New predictive models improve prostate cancer detection for PI-RADS 3 and 4 lesions. This approach helps stratify patients, potentially reducing unnecessary biopsies and associated complications.
Area Of Science
- Radiology
- Oncology
- Medical Imaging
Background
- Prostate Imaging-Reporting and Data System (PI-RADS) is used with multiparametric MRI (mpMRI) to evaluate prostate lesions.
- Improving the prediction of clinically significant prostate cancer (csPCa) for PI-RADS grades 3-5 remains an area of active research.
- Current PI-RADS classification shows limitations in accurately predicting csPCa, particularly for intermediate scores.
Purpose Of The Study
- To develop and validate an easily implementable method to enhance the predictability of csPCa using PI-RADS scores.
- To improve the stratification of patients with PI-RADS 3 and 4 lesions.
- To reduce the rate of unnecessary prostate biopsies.
Main Methods
- A cohort of 151 patients with PI-RADS 3-5 lesions on mpMRI underwent Fusion and random US Biopsy.
- Data were collected from January 2019 to December 2022.
- Two predictive models for csPCa were developed using logistic regression with readily available clinical parameters.
Main Results
- The study included patients with PI-RADS 3 (n=49), PI-RADS 4 (n=82), and PI-RADS 5 (n=20).
- csPCa was confirmed in 12/49 (PI-RADS 3), 42/82 (PI-RADS 4), and 18/20 (PI-RADS 5) patients.
- The developed predictive models achieved an Area Under the Curve (AUC) of 0.8133 and 0.8206, indicating good predictive performance.
Conclusions
- PI-RADS classification demonstrates relevant predictability issues for grades 3 and 4.
- The proposed risk calculators offer improved stratification for patients with PI-RADS 3 and 4.
- These models can serve as valuable diagnostic tools, aiding clinical decision-making and potentially sparing patients from complications associated with unnecessary biopsies.
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