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Using Prostate Imaging-Reporting and Data System (PI-RADS) Scores to Select an Optimal Prostate Biopsy Method: A Secondary Analysis of the Trio Study.
Ahdoot, Michael; Lebastchi, Amir H; Long, Lori; Wilbur, Andrew R; Gomella, Patrick T; Mehralivand, Sherif; Daneshvar, Michael A; Yerram, Nitin K; O'Connor, Luke P; Wang, Alex Z; Gurram, Sandeep; Bloom, Jonathan; Siddiqui, M Minhaj; Linehan, W Marston; Merino, Maria; Choyke, Peter L; Pinsky, Paul; Parnes, Howard; Shih, Joanna H; Turkbey, Baris; Wood, Bradford J; Pinto, Peter A.
Afiliação
  • Ahdoot M; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: michael.ahdoot@cshs.org.
  • Lebastchi AH; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Long L; Biometric Research Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, National Institute of Health, Bethesda, MD, USA.
  • Wilbur AR; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Gomella PT; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Mehralivand S; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA; Molecular Imaging Program, Center for Cancer Research, National Institute of Health, Bethesda, MD, USA.
  • Daneshvar MA; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Yerram NK; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • O'Connor LP; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Wang AZ; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Gurram S; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Bloom J; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Siddiqui MM; Division of Urology, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Linehan WM; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Merino M; Translational Surgical Pathology Section, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Choyke PL; Molecular Imaging Program, Center for Cancer Research, National Institute of Health, Bethesda, MD, USA.
  • Pinsky P; Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Parnes H; Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Shih JH; Biometric Research Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, National Institute of Health, Bethesda, MD, USA.
  • Turkbey B; Molecular Imaging Program, Center for Cancer Research, National Institute of Health, Bethesda, MD, USA.
  • Wood BJ; Center for Interventional Oncology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA; Interventional Radiology, Radiology and Imaging Sciences, National Institutes of Health Clinical Center, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Pinto PA; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Eur Urol Oncol ; 5(2): 176-186, 2022 04.
Article em En | MEDLINE | ID: mdl-33846112
ABSTRACT

BACKGROUND:

While magnetic resonance imaging (MRI)-targeted biopsy (TBx) results in better prostate cancer (PCa) detection relative to systematic biopsy (SBx), the combination of both methods increases clinically significant PCa detection relative to either Bx method alone. However, combined Bx subjects patients to higher number of Bx cores and greater detection of clinically insignificant PCa.

OBJECTIVE:

To determine if prebiopsy prostate MRI can identify men who could forgo combined Bx without a substantial risk of missing clinically significant PCa (csPC). DESIGN, SETTING, AND

PARTICIPANTS:

Men with MRI-visible prostate lesions underwent combined TBx plus SBx. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

The primary outcomes were detection rates for grade group (GG) ≥2 and GG ≥3 PCa by TBx and SBx, stratified by Prostate Imaging-Reporting and Data System (PI-RADS) score. RESULTS AND

LIMITATIONS:

Among PI-RADS 5 cases, nearly all csPCs were detected by TBx, as adding SBx resulted in detection of only 2.5% more GG ≥2 cancers. Among PI-RADS 3-4 cases, however, SBx addition resulted in detection of substantially more csPCs than TBx alone (8% vs 7.5%). Conversely, TBx added little to detection of csPC among men with PI-RADS 2 lesions (2%) relative to SBx (7.8%).

CONCLUSIONS:

While combined Bx increases the detection of csPC among men with MRI-visible prostate lesions, this benefit was largely restricted to PI-RADS 3-4 lesions. Using a strategy of TBx only for PI-RADS 5 and combined Bx only for PI-RADS 3-4 would avoid excess biopsies for men with PI-RADS 5 lesions while resulting in a low risk of missing csPC (1%). PATIENT

SUMMARY:

Our study investigated an optimized strategy to diagnose aggressive prostate cancer in men with an abnormal prostate MRI (magnetic resonance imaging) scan while minimizing the risk of excess biopsies. We used a scoring system for MRI scan images called PI-RADS. The results show that MRI-targeted biopsies alone could be used for men with a PI-RADS score of 5, while men with a PI-RADS score of 3 or 4 would benefit from a combination of MRI-targeted biopsy and systematic biopsy. This trial is registered at ClinicalTrials.gov as NCT00102544.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Próstata / Neoplasias da Próstata Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: Eur Urol Oncol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Próstata / Neoplasias da Próstata Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Revista: Eur Urol Oncol Ano de publicação: 2022 Tipo de documento: Article