Follow-up of negative MRI-targeted prostate biopsies: when are we missing cancer?
World Journal of Urology, ISSN: 1433-8726, Vol: 37, Issue: 2, Page: 235-241
2019
- 34Citations
- 7Usage
- 59Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations34
- Citation Indexes33
- 33
- CrossRef3
- Policy Citations1
- Policy Citation1
- Usage7
- Abstract Views7
- Captures59
- Readers59
- 59
Article Description
Introduction: Multiparametric magnetic resonance imaging (mpMRI) has improved clinicians’ ability to detect clinically significant prostate cancer (csPCa). Combining or fusing these images with the real-time imaging of transrectal ultrasound (TRUS) allows urologists to better sample lesions with a targeted biopsy (Tbx) leading to the detection of greater rates of csPCa and decreased rates of low-risk PCa. In this review, we evaluate the technical aspects of the mpMRI-guided Tbx procedure to identify possible sources of error and provide clinical context to a negative Tbx. Methods: A literature search was conducted of possible reasons for false-negative TBx. This includes discussion on false-positive mpMRI findings, termed “PCa mimics,” that may incorrectly suggest high likelihood of csPCa as well as errors during Tbx resulting in inexact image fusion or biopsy needle placement. Results: Despite the strong negative predictive value associated with Tbx, concerns of missed disease often remain, especially with MR-visible lesions. This raises questions about what to do next after a negative Tbx result. Potential sources of error can arise from each step in the targeted biopsy process ranging from “PCa mimics” or technical errors during mpMRI acquisition to failure to properly register MRI and TRUS images on a fusion biopsy platform to technical or anatomic limits on needle placement accuracy. Conclusions: A better understanding of these potential pitfalls in the mpMRI-guided Tbx procedure will aid interpretation of a negative Tbx, identify areas for improving technical proficiency, and improve both physician understanding of negative Tbx and patient-management options.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85047198770&origin=inward; http://dx.doi.org/10.1007/s00345-018-2337-0; http://www.ncbi.nlm.nih.gov/pubmed/29785491; http://link.springer.com/10.1007/s00345-018-2337-0; https://hsrc.himmelfarb.gwu.edu/smhs_uro_facpubs/497; https://hsrc.himmelfarb.gwu.edu/cgi/viewcontent.cgi?article=1497&context=smhs_uro_facpubs; https://dx.doi.org/10.1007/s00345-018-2337-0; https://link.springer.com/article/10.1007/s00345-018-2337-0
Springer Science and Business Media LLC
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