Intra-Practice Urologist-Level Variation in Targeted Fusion Biopsy Outcomes - Beyond the Abstract

Fusion biopsy is an important, recent addition to the prostate cancer diagnostic pathway. It is evident that fusion modestly outperforms standard biopsy in cancer detection rates.1,2 We know that radiologist variation, imaging quality, and patient-specific factors impact fusion biopsy.3-5 It remains unclear what technical variations exist across urologists adopting this emerging practice and how these affect outcomes.

In our recent manuscript, “Intra-Practice Urologist-Level Variation in Targeted Fusion Biopsy Outcomes,” we evaluated variation in cancer detection rates for 5 fusion biopsy providers in a high-volume single center. We found no significant differences in the detection of clinically significant prostate cancer across the providers. However, there was a statistically significant difference in clinically significant prostate cancer detection across the providers when biopsying PI-RADS 4 lesions. Such differences are potentially due to variations in sampling strategies and segmentation where there is wide variation in cancer detection rates, compared to PIRADS 3 and 5 lesions where the pre-test probabilities of detecting cancer can be much lower or higher, respectively.

A limitation of our study was that we were not able to control for variability in the 13 different radiologists who interpreted prostate MRI. Nevertheless, this heterogeneity reflects real-world practice in a high-volume center.

Our work demonstrates that urologists at the same center perform similarly in overall cancer detection with fusion biopsy, but there is room for standardization and quality improvement to address subtle variations at the lesion level. Continued improvement in fusion prostate biopsy will rely on a multidisciplinary approach to address the complex interplay of variations in such a highly technical procedure.

Written by: Apoorv Dhir, MD & Arvin George, MD

Institute for Healthcare Policy and Innovation, University of Michigan, Ann Arbor, MI; Division of Health Services Research, Department of Urology, University of Michigan, Ann Arbor, MI.

References:

  1. Siddiqui MM, Rais-Bahrami S, Turkbey B, George AK, Rothwax J, Shakir N, et al. Comparison of MR/ultrasound fusion-guided biopsy with ultrasound-guided biopsy for the diagnosis of prostate cancer. JAMA - Journal of the American Medical Association [Internet]. 2015 Jan 27 [cited 2021 May 23];313(4):390–7.
  2. Ahmed HU, El-Shater Bosaily A, Brown LC, Gabe R, Kaplan R, Parmar MK, et al. Diagnostic accuracy of multi-parametric MRI and TRUS biopsy in prostate cancer (PROMIS): a paired validating confirmatory study. The Lancet [Internet]. 2017 Feb 25 [cited 2021 May 23];389(10071):815–22.
  3. Sathianathen NJ, Konety BR, Soubra A, Metzger GJ, Spilseth B, Murugan P, et al. Which scores need a core? An evaluation of MR-targeted biopsy yield by PIRADS score across different biopsy indications. Prostate Cancer Prostatic Dis [Internet]. 2018 Nov 1 [cited 2021 May 23];21(4):573–8.
  4. Sonn GA, Fan RE, Ghanouni P, Wang NN, Brooks JD, Loening AM, et al. Prostate Magnetic Resonance Imaging Interpretation Varies Substantially Across Radiologists. Eur Urol Focus [Internet]. 2019 Jul 1 [cited 2021 May 23];5(4):592–9.
  5. Shankar PR, Kaza RK, Al-Hawary MM, Masch WR, Curci NE, Mendiratta-Lala M, et al. Impact of clinical history on maximum PI-RADS version 2 score: A six-reader 120-case sham history retrospective evaluation. Radiology [Internet]. 2018 [cited 2021 May 23];288(1):158–63.
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