Abstract

ContextAlthough magnetic resonance imaging (MRI) is broadly implemented into active surveillance (AS) protocols, data on the reliability of serial MRI in order to help guide follow-up biopsy are inconclusive. ObjectiveTo assess the diagnostic estimates of serial prostate MRI for prostate cancer (PCa) progression during AS. Evidence acquisitionWe systematically searched PubMed, Scopus, and Web of Science databases to select studies analyzing the association between changes on serial prostate MRI and PCa progression during AS. We included studies that provided data for MRI progression, which allowed us to calculate diagnostic estimates. We compared Prostate Cancer Radiological Estimation of Change in Sequential Evaluation (PRECISE) accuracy with institution-specific definitions. Evidence synthesisWe included 15 studies with 2240 patients. Six used PRECISE criteria and nine institution-specific definitions of MRI progression. The pooled PCa progression rate, which included histological progression to Gleason grade ≥2, was 27%. The pooled sensitivity and specificity were 0.59 (95% confidence interval [CI] 0.44–0.73) and 0.75 (95% CI 0.66–0.84) respectively. There was significant heterogeneity between included studies. Depending on PCa progression prevalence, the pooled negative predictive value for serial prostate MRI ranged from 0.81 (95% CI 0.73–0.88) to 0.88 (95% CI 0.83–0.93) and the pooled positive predictive value ranged from 0.37 (95% CI 0.24–0.54) to 0.50 (95% CI 0.36–0.66). There were no significant differences in the pooled sensitivity (p = 0.37) and specificity (p = 0.74) of PRECISE and institution-specific schemes. ConclusionsSerial MRI still should not be considered a sole factor for excluding PCa progression during AS, and changes on MRI are not accurate enough to indicate PCa progression. There was a nonsignificant trend toward improved diagnostic estimates of PRECISE recommendations. These findings highlight the need to further define the optimal triggers and timing of biopsy during AS, as well as the need for optimizing the quality, interpretation, and reporting of serial prostate MRI. Patient summaryOur study suggests that serial prostate magnetic resonance imaging (MRI) alone in patients on active surveillance is not accurate enough to reliably rule out or rule in prostate cancer progression. Other clinical factors and biomarkers along with serial MRI are required to safely tailor the intensity of follow-up biopsies.

Highlights

  • Active surveillance (AS) is a safe and increasingly utilized management strategy for low-risk and selected intermediate-risk prostate cancer (PCa) patients [1,2,3]

  • We developed a hierarchical summary receiver operating curve (SROC) and calculated the area under the curve (AUC) to examine the diagnostic accuracy of Magnetic resonance imaging (MRI) progression tested overall and defined using PRECISE criteria or institutional definitions

  • We present the first systematic review and meta-analysis that analyzed the diagnostic estimates of prostate MRI progression during AS, defined using PRECISE criteria as well as other definitions

Read more

Summary

Introduction

Active surveillance (AS) is a safe and increasingly utilized management strategy for low-risk and selected intermediate-risk prostate cancer (PCa) patients [1,2,3]. Magnetic resonance imaging (MRI) of the prostate has been an extensively studied diagnostic tool for identifying significant PCa [10,11]. The diagnostic accuracy of MRI is imperfect at identifying all clinically significant, the majority of tumors identified on systematic biopsy are of low grade [12,15]. Current guidelines suggest targeted and systematic biopsies when diagnostic MRI is suspicious [1,2]. This approach, minimalizes the risk of missing MRI-invisible clinically significant PCa, continues to overdetect GG = 1 PCa, which increases the need for AS

Objectives
Methods
Findings
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call