Novel Voxel-Based MRI Risk Score LADCT <sub>2</sub> as a Tool for Prediction of Prostate Cancer: A Proof of Concept With Retrospective Study

IntroductionBiparametric magnetic resonance imaging (MRI) preserves enough information to enable the prediction of prostate cancer (PCa). This fast, cost-effective, and non-invasive modality includes acquisition of T2-weighted images, and accelerated diffusion-weighted imaging (DWI) sequences with corresponding apparent diffusion coefficient (ADC) maps. In this proof-of-concept study, we aimed to assess the prediction of PCa using a tumor location-(L) dependent risk score (LADCT<sub>2</sub>) generated from an ADC and T2 images - based model.MethodsThe single-center institutional retrospective cohort study used 113 patients who underwent multiparametric MRI (mpMRI) for the diagnosis and management of PCa. A discovery cohort (n = 58) and an evaluation cohort (n = 55) were identified from a prospectively maintained institutional cancer registry. The discovery cohort consisted of patients who underwent MRI-guided TRUS biopsies, whereas the evaluation cohort consisted of patients who received only standard TRUS biopsy. Among the discovery cohort, we developed a predictive risk score (LADCT<sub>2</sub>) using a multivariable logistic regression model that incorporated tumor location (L) with normalized mean signal differences of T2-and ADC- tumor region of interest. The primary outcome assessed the predictive accuracy of the LADCT<sub>2</sub> risk score in predicting PCa.ResultsOur results demonstrated that the LADCT<sub>2</sub> score exhibited excellent predictive accuracy for PCa among both the evaluation (AUC = 0.84, OR = 2.80 [95% CI, 1.04-7.52]; <i>P</i> = .04), and discovery (AUC = 0.77, OR = 2.71 [95% CI, 1.38-5.35]; <i>P</i> = .003) cohorts. Additionally, it also predicted for clinically significant PCa among both the discovery (AUC = 0.71, OR = 2.11 [95% CI, 1.16-3.84]; <i>P</i> = .01), and evaluation (AUC = 0.65, OR = 1.94 [95% CI, 1.02-3.69]; <i>P</i> = .04) cohorts.ConclusionThe novel LADCT<sub>2</sub> risk score may function as an effective risk stratification tool to support clinical decision-making in the management of PCa.

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Journal
Cancer Control
Published
2026-03-01
DOI
https://doi.org/10.1177/10732748261433288
Primary Topic
Prostate Cancer Diagnosis and Treatment
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article
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article

Novel Voxel-Based MRI Risk Score LADCT 2 as a Tool for Prediction of Prostate Cancer: A Proof of Concept With Retrospective Study

María L. Sandoval, Arthur A. Parsee, K. Latifi, Asmaa El-Kenawi et al.
Cancer Control
Prostate Cancer Diagnosis and Treatment
article

Novel Voxel-Based MRI Risk Score LADCT 2 as a Tool for Prediction of Prostate Cancer: A Proof of Concept With Retrospective Study

María L. Sandoval, Arthur A. Parsee, K. Latifi, Asmaa El-Kenawi, Esther N. Katende, Kosj Yamoah, M. Echevarria, Shivanshu Awasthi, Purvish Trivedi, N. Parikh, Timothy R. Rebbeck, Jasreman Dhillon, Kenneth Gage, Jong Y. Park
article en

Abstract

IntroductionBiparametric magnetic resonance imaging (MRI) preserves enough information to enable the prediction of prostate cancer (PCa). This fast, cost-effective, and non-invasive modality includes acquisition of T2-weighted images, and accelerated diffusion-weighted imaging (DWI) sequences with corresponding apparent diffusion coefficient (ADC) maps. In this proof-of-concept study, we aimed to assess the prediction of PCa using a tumor location-(L) dependent risk score (LADCT<sub>2</sub>) generated from an ADC and T2 images - based model.MethodsThe single-center institutional retrospective cohort study used 113 patients who underwent multiparametric MRI (mpMRI) for the diagnosis and management of PCa. A discovery cohort (n = 58) and an evaluation cohort (n = 55) were identified from a prospectively maintained institutional cancer registry. The discovery cohort consisted of patients who underwent MRI-guided TRUS biopsies, whereas the evaluation cohort consisted of patients who received only standard TRUS biopsy. Among the discovery cohort, we developed a predictive risk score (LADCT<sub>2</sub>) using a multivariable logistic regression model that incorporated tumor location (L) with normalized mean signal differences of T2-and ADC- tumor region of interest. The primary outcome assessed the predictive accuracy of the LADCT<sub>2</sub> risk score in predicting PCa.ResultsOur results demonstrated that the LADCT<sub>2</sub> score exhibited excellent predictive accuracy for PCa among both the evaluation (AUC = 0.84, OR = 2.80 [95% CI, 1.04-7.52]; <i>P</i> = .04), and discovery (AUC = 0.77, OR = 2.71 [95% CI, 1.38-5.35]; <i>P</i> = .003) cohorts. Additionally, it also predicted for clinically significant PCa among both the discovery (AUC = 0.71, OR = 2.11 [95% CI, 1.16-3.84]; <i>P</i> = .01), and evaluation (AUC = 0.65, OR = 1.94 [95% CI, 1.02-3.69]; <i>P</i> = .04) cohorts.ConclusionThe novel LADCT<sub>2</sub> risk score may function as an effective risk stratification tool to support clinical decision-making in the management of PCa.

Cancer ControlVol. 33
Moffitt Cancer Center (US), Dana-Farber Cancer Institute (US), Dana-Farber/Harvard Cancer Center (US), University School (US), Indiana University School of Medicine, Indiana University (US)
Openalex Percentile: Top 5%
Prostate Cancer Diagnosis and Treatment
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