Magnetic Resonance Imaging/Ultrasound-Fusion Biopsy Significantly Upgrades Prostate Cancer Versus Systematic 12-core Transrectal Ultrasound Biopsy
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文摘

Background

Gleason scores from standard, 12-core prostate biopsies are upgraded historically in 25?33 % of patients. Multiparametric prostate magnetic resonance imaging (MP-MRI) with ultrasound (US)-targeted fusion biopsy may better sample the true gland pathology.

Objective

The rate of Gleason score upgrading from an MRI/US-fusion-guided prostate-biopsy platform is compared with a standard 12-core biopsy regimen alone.

Design, setting, and participants

There were 582 subjects enrolled from August 2007 through August 2012 in a prospective trial comparing systematic, extended 12-core transrectal ultrasound biopsies to targeted MRI/US-fusion-guided prostate biopsies performed during the same biopsy session.

Outcome measurements and statistical analysis

The highest Gleason score from each biopsy method was compared.

Interventions

An MRI/US-fusion-guided platform with electromagnetic tracking was used for the performance of the fusion-guided biopsies.

Results and limitations

A diagnosis of prostate cancer (PCa) was made in 315 (54 % ) of the patients. Addition of targeted biopsy led to Gleason upgrading in 81 (32 % ) cases. Targeted biopsy detected 67 % more Gleason ¡Ý4 + 3 tumors than 12-core biopsy alone and missed 36 % of Gleason ¡Ü3 + 4 tumors, thus mitigating the detection of lower-grade disease. Conversely, 12-core biopsy led to upgrading in 67 (26 % ) cases over targeted biopsy alone but only detected 8 % more Gleason ¡Ý4 + 3 tumors. On multivariate analysis, MP-MRI suspicion was associated with Gleason score upgrading in the targeted lesions (p < 0.001). The main limitation of this study was that definitive pathology from radical prostatectomy was not available.

Conclusions

MRI/US-fusion-guided biopsy upgrades and detects PCa of higher Gleason score in 32 % of patients compared with traditional 12-core biopsy alone. Targeted biopsy technique preferentially detects higher-grade PCa while missing lower-grade tumors.

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