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Prostate cancer risk stratification using magnetic resonance imaging-ultrasound fusion vs systematic prostate biopsy.
Khajir, Ghazal; Press, Benjamin; Lokeshwar, Soum; Ghabili, Kamyar; Rahman, Syed; Gardezi, Mursal; Washington, Samuel; Cooperberg, Matthew R; Sprenkle, Preston; Leapman, Michael S.
Affiliation
  • Khajir G; Department of Urology, Yale School of Medicine, New Haven, CT, USA.
  • Press B; Department of Urology, Yale School of Medicine, New Haven, CT, USA.
  • Lokeshwar S; Department of Urology, Yale School of Medicine, New Haven, CT, USA.
  • Ghabili K; Department of Radiology, Penn State Hershey Medical Center, Hershey, PA, USA.
  • Rahman S; Department of Urology, Yale School of Medicine, New Haven, CT, USA.
  • Gardezi M; Department of Urology, Yale School of Medicine, New Haven, CT, USA.
  • Washington S; Department of Urology, University of California San Francisco, San Francisco, CA, USA.
  • Cooperberg MR; Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, USA.
  • Sprenkle P; Department of Urology, University of California San Francisco, San Francisco, CA, USA.
  • Leapman MS; Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, USA.
JNCI Cancer Spectr ; 7(6)2023 10 31.
Article in En | MEDLINE | ID: mdl-38085220
BACKGROUND: Image-guided approaches improve the diagnostic yield of prostate biopsy and frequently modify estimates of clinical risk. To better understand the impact of magnetic resonance imaging-ultrasound fusion targeted biopsy (MRF-TB) on risk assessment, we compared the distribution of National Comprehensive Cancer Network (NCCN) risk groupings, as calculated from MRF-TB vs systematic biopsy alone. METHODS: We performed a retrospective analysis of 713 patients who underwent MRF-TB from January 2017 to July 2021. The primary study objective was to compare the distribution of National Comprehensive Cancer Network risk groupings obtained using MRF-TB (systematic + targeted) vs systematic biopsy. RESULTS: Systematic biopsy alone classified 10% of samples as very low risk and 18.7% of samples as low risk, while MRF-TB classified 10.5% of samples as very low risk and 16.1% of samples as low risk. Among patients with benign findings, low-risk disease, and favorable/intermediate-risk disease on systematic biopsy alone, 4.6% of biopsies were reclassified as high risk or very high risk on MRF-TB. Of 207 patients choosing active surveillance, 64 (31%), 91 (44%), 42 (20.2%), and 10 (4.8%) patients were classified as having very low-risk, low-risk, and favorable/intermediate-risk and unfavorable/intermediate-risk criteria, respectively. When using systematic biopsy alone, 204 patients (28.7%) were classified as having either very low-risk and low-risk disease per NCCN guidelines, while 190 men (26.6%) received this classification when using MRF-TB. CONCLUSION: The addition of MRF-TB to systematic biopsy may change eligibility for active surveillance in only a small proportion of patients with prostate cancer. Our findings support the need for routine use of quantitative risk assessment over risk groupings to promote more nuanced decision making for localized cancer.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Magnetic Resonance Imaging, Interventional Limits: Humans / Male Language: En Journal: JNCI Cancer Spectr Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Magnetic Resonance Imaging, Interventional Limits: Humans / Male Language: En Journal: JNCI Cancer Spectr Year: 2023 Type: Article Affiliation country: United States