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miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
Association Between Tumor Multifocality on Multi-parametric MRI and Detection of Clinically-Significant Prostate
Kamyar Ghabili1, Matthew Swallow1, Rachael L Sherrer2
1Department of Urology, Yale University School of Medicine, New Haven, CT.
Objective:
To investigate whether presence of multifocality on multi-parametric magnetic resonance imaging would increase the likelihood of detecting clinically-significant prostate cancer in a PI-RADS 4 lesion.
Methods:
We identified patients with at least 1 PI-RADS 4 lesion who underwent multi-parametric magnetic resonance imaging-ultrasound fusion prostate biopsy. Patients were grouped into 1 of 4 cohorts-cohort 1 (a PI-RADS 4 index lesion and an additional PI-RADS 2 or 3 lesion), cohort 2 (single lesion with PI-RADS 4), cohort 3 (2 or more PI-RADS 4 lesions), or cohort 4 (a PI-RADS 4 lesion and an index lesion with PI-RADS 5). We compared the rate of grade group (GG) ≥ 2 pathology on targeted biopsy of PI-RADS 4 lesions between cohorts and evaluated clinical and radiological factors associated with cancer detection.
Results:
The overall rate of GG ≥ 2 pathology in the PI-RADS 4 lesions was 35.2%. The rate of GG ≥ 2 pathology in the cohorts 1, 2, 3, and 4 was 21.7%, 36.3%, 49.1%, and 42.7%, respectively (P< .001). On multivariable analysis, age (OR1.06, P < .001), clinical stage T2 (OR1.59, P= .03), prostate-specific antigen density (OR1.43, P < .001), peripheral zone lesion (OR1.62, P = .04), and study cohort (cohort 2 vs 1, OR1.93, P = .006; and cohort 3 vs 1, OR3.28, P < .001) were significantly associated with the risk of GG ≥ 2 in the PI-RADS 4 lesion.
Conclusion:
On targeted biopsy of the PI-RADS 4 lesions, the proportion of GG ≥ 2 pathology is approximately 35%. Rate of GG ≥ 2 detection in PI-RADS 4 lesions might differ based on their location, multifocality, and PI-RADS classifications of other lesions identified.
Insights
The presence of multifocality in prostate MRI scans may increase the detection of clinically significant prostate cancer within PI-RADS 4 lesions. This finding highlights the importance of considering lesion characteristics for accurate cancer diagnosis.
Area of Science:
- Urology
- Radiology
- Oncology
Background:
- Prostate cancer detection relies on accurate interpretation of multi-parametric magnetic resonance imaging (mpMRI).
- Prostate Imaging-Reporting and Data System (PI-RADS) 4 lesions require careful evaluation due to their intermediate suspicion for malignancy.
- Understanding factors influencing cancer detection in PI-RADS 4 lesions is crucial for biopsy decisions.
Purpose of the Study:
- To determine if multifocality on mpMRI influences the detection rate of clinically significant prostate cancer (Grade Group [GG] ≥ 2) in PI-RADS 4 lesions.
- To compare cancer detection rates across different configurations of PI-RADS 4 lesions and other identified lesions.
Main Methods:
- Retrospective analysis of patients with at least one PI-RADS 4 lesion undergoing mpMRI-ultrasound fusion prostate biopsy.
- Patients were categorized into four cohorts based on the presence and characteristics of PI-RADS 4 lesions and other lesions (PI-RADS 2, 3, or 5).
- Comparison of GG ≥ 2 pathology detection rates in PI-RADS 4 lesions between cohorts, with evaluation of associated clinical and radiological factors.
Main Results:
- The overall detection rate of GG ≥ 2 pathology in PI-RADS 4 lesions was 35.2%.
- Detection rates varied significantly by cohort: 21.7% (cohort 1), 36.3% (cohort 2), 49.1% (cohort 3), and 42.7% (cohort 4).
- Multivariable analysis identified age, clinical stage T2, prostate-specific antigen density, peripheral zone location, and specific study cohorts as significant predictors of GG ≥ 2 detection.
Conclusions:
- Approximately 35% of PI-RADS 4 lesions yield Grade Group ≥ 2 pathology upon targeted biopsy.
- The likelihood of detecting significant prostate cancer in PI-RADS 4 lesions is influenced by lesion location, multifocality, and the PI-RADS classification of co-existing lesions.
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