NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Magnetic resonance imaging/ultrasound-fusion biopsy significantly upgrades prostate cancer versus systematic 12-core transrectal ultrasound biopsy.

Author(s): Siddiqui MM, Rais-Bahrami S, Truong H, Stamatakis L, Vourganti S, Nix J, Hoang AN, Walton-Diaz A, Shuch B, Weintraub M, Kruecker J, Amalou H, Turkbey B, Merino MJ, Choyke PL, Wood BJ, Pinto PA

Publication: Eur Urol, 2013, Vol. 64, Page 713-9

PubMed ID: 23787357 PubMed Review Paper? No

Purpose of Paper

This paper compared prostate cancer diagnosis rates among matched biopsies sampled by multiparametric prostate magnetic resonance imaging with ultrasound (MP-MRI /US) or transrectal ultrasound (TRUS) and investigated the potential relationships between clinical parameters and the incidence of Gleason score upgrading after consideration of the other biopsy.

 

Conclusion of Paper

Of the 54% of patients diagnosed with prostate cancer, 81% and 80% were diagnosed based on results of TRUS-guided and MP-MRI/US-targeted biopsies, respectively. However when discordance among sampling methods was observed, cases were upgraded to a clinically significant disease more often with MP-MRI/US-targeted biopsies than those obtained by TRUS-guidance (38 versus 7 cases). Further, Gleason scores were higher in the MP-MRI/US-targeted biopsy in 81 cases and lower in 67 cases than scores obtained with TRUS-guided biopsies. Gleason score upgrading was associated with decreased prostate volume, higher prostate specific antigen (PSA) levels, and higher MRI suspicion level.

Studies

  1. Study Purpose

    This study compared prostate cancer diagnosis rates among MP-MRI /US-targeted and TRUS-guided biopsies and determined the influence of clinical parameters on upgrading patient diagnosis after consideration of both biopsies. Case-matched MP-MRI/US-targeted (mean 5.7 biospies/patient) and TRUS -guided biopsies (12 cores/patient) were obtained from 582 patients during the same biopsy session. For each guidance method, the highest Gleason score was assigned to the case independently. Specimens were characterized as clinically significant high grade (Gleason score of ≥4 + 3), clinically insignificant low grade (Gleason score ≤3 + 4), or normal/no cancer. After determination of diagnosis for each biopsy independently, the diagnosis for the case was determined based on both biopsies.

    Summary of Findings:

    A mean of 17.7 biopsies were obtained from each patient. A prostate cancer diagnosis was assigned to 315 of the 582 patients (54%), of which 255 (81%) were diagnosed based on TRUS-guided biopsy and 253 (80%) by MP-MRI/US-targeted biopsy. Of the 57 cases diagnosed with a clinically significant disease based on TRUS-guided biopsy, an identical diagnosis was assigned in 50 cases based on results of the MP-MRI/US-targeted biopsy, while 5 were diagnosed with a clinically insignificant disease and 2 were diagnosed as normal based on results obtained from the MP-MRI/US- targeted biopsy. Conversely, diagnoses assigned using TRUS-guided biopsies were upgraded based on results of MP-MRI/US targeted biopsies from clinically insignificant to clinically significant in 21 cases, and from normal to clinically significant in 17 cases. Gleason scores were higher in the MP-MRI/US-targeted biopsy than the TRUS-guided biopsy in 81 cases (43 cases were upgraded to clinically insignificant and 38 to clinically significant); however higher Gleason scores were observed among TRUS-guided biopsies in 67 cases (60 cases upgraded to clinically insignificant and 7 to clinically significant). Specimens that displayed discordant Gleason scores among biopsy methods that resulted in a diagnosis upgrade were associated with lower prostate volume (OR=0.84, P=0.0005), higher PSA level (OR=1.03, P=0.004), more lesions (OR=1.4, P=0.004), and higher MRI suspicion level (OR=1.7, P=0.04); but the association with number of lesions was not significant (P=0.6). 

    Biospecimens
    Preservative Types
    • Formalin
    Diagnoses:
    • Normal
    • Neoplastic - Carcinoma
    Platform:
    AnalyteTechnology Platform
    Morphology H-and-E microscopy
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Preaquisition Biomarker level 9.9 ± 13.1 ng/mL PSA
    Biospecimen Acquisition Method of tissue acquisition Magnetic resonance imaging-guided biopsy
    Ultrasound-guided biopsy
    Preaquisition Prognostic factor Prostate volume of 56.4 ± 31.2
    An average of 2.6 ±1.3 lesions

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