Impact of changing PI-RADS cutoff on prostate cancer detection by MRI cognitive fusion biopsy in biopsy-naïve patients

Hesham Abdel-Azim El-Helaly1, Asem Abdel-Aziz Mahmoud1, Ahmed Mohamed Magdy2, Abdelwahab Hasehem3,4,5, Hamdy Mohamed Ibrahim1, Khaled Moheyelden Mohamed1, Mohamed Hamdy Ismail1
1Urology Department, Fayoum University, Fayoum, Egypt
2Radiology Department, Fayoum University, Fayoum, Egypt
3Urology Department, Urology and Nephrology Center, Mansoura, Egypt
4Urology Department, 30th June Urology and Nephrology Center, Ismailia, Egypt
5Urology Department, Shebin Elkom Teaching Hospital, Shebin Elkom, Egypt

Tóm tắt

Multi-parametric magnetic resonance imaging may improve the detection of prostate cancer. The aim of this work is to compare between PI-RADS 3–5 and PI-RADS 4–5 as a threshold for targeted prostatic biopsy. This is a prospective clinical study that included 40 biopsy-naïve patients referred for prostate biopsy. Patients underwent prebiopsy multi-parametric (mp-MRI), followed by 12-core transrectal ultrasound-guided systematic biopsy and cognitive MRI/TRUS fusion targeted biopsy from each detected lesion. The primary endpoint was to assess the diagnostic accuracy of the PI-RAD 3–4 versus PI-RADS 4–5 lesion by mpMRI for prostate cancer detection in biopsy-naive men. The overall prostate cancer detection rate and the clinically significant cancer detection rate were 42.5% and 35%, respectively. Targeted biopsies from PI-RADS 3–5 lesions showed a sensitivity of 100%, specificity of 44%, positive predictive value of 51.7%, and negative predictive value of 100%. Restricting targeted biopsies to PI-RADS 4–5 lesions resulted in a decrease in sensitivity and negative predictive value to 73.3% and 86.2%, respectively, while specificity and positive predictive value were increased to 100% for both parameters which was statistically significant (P value < 0.0001 and P value = 0.004, respectively). Limiting the TBs to PI-RADS 4–5 lesions improves the performance of mp-MRI in the detection of prostate cancer especially aggressive tumors.

Tài liệu tham khảo

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