The Prostate Health Index aids multi-parametric MRI in diagnosing significant prostate cancer

To evaluate the performance of the Prostate Health Index (PHI) in magnetic resonance imaging-transrectal ultrasound (MRI-TRUS) fusion prostate biopsy for the detection of clinically significant prostate cancer (csPCa). We prospectively enrolled 164 patients with at least one Prostate Imaging Reporti...

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Published in:Scientific reports Vol. 11; no. 1; p. 1286
Main Authors: Fan, Yu-Hua, Pan, Po-Hsun, Cheng, Wei-Ming, Wang, Hsin-Kai, Shen, Shu-Huei, Liu, Hsian-Tzu, Cheng, Hao-Min, Chen, Wei-Ren, Huang, Tzu-Hao, Wei, Tzu-Chun, Huang, I-Shen, Lin, Chih-Chieh, Huang, Eric Y. H., Chung, Hsiao-Jen, Huang, William J. S., Lin, Tzu-Ping
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 05-03-2021
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Summary:To evaluate the performance of the Prostate Health Index (PHI) in magnetic resonance imaging-transrectal ultrasound (MRI-TRUS) fusion prostate biopsy for the detection of clinically significant prostate cancer (csPCa). We prospectively enrolled 164 patients with at least one Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) ≥ 3 lesions who underwent MRI-TRUS fusion prostate biopsy. Of the PSA-derived biomarkers, the PHI had the best performance in predicting csPCa (AUC 0.792, CI 0.707–0.877) in patients with PI-RADS 4/5 lesions. Furthermore, the predictive power of PHI was even higher in the patients with PI-RADS 3 lesions (AUC 0.884, CI 0.792–0.976). To minimize missing csPCa, we used a PHI cutoff of 27 and 7.4% of patients with PI-RADS 4/5 lesions could have avoided a biopsy. At this level, 2.0% of cases with csPCa would have been missed, with sensitivity and NPV rates of 98.0% and 87.5%, respectively. However, the subgroup of PI-RADS 3 was too small to define the optimal PHI cutoff. PHI was the best PSA-derived biomarker to predict csPCa in MRI-TRUS fusion prostate biopsies in men with PI-RADS ≥ 3 lesions, especially for the patients with PI-RADS 3 lesions who gained the most value.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-020-78428-6