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Performance of multiparametric prostate magnetic resonance imaging validated by targeted and systematic transperineal biopsies.
Hsi, Richard A; Dinh, Tru-Khang; Greer, Matthew; Bensen, Carleen; Mitchell, Marc A; Li, Amy Y; Stamm, Andrew; Henne, Manfred.
Afiliación
  • Hsi RA; Seattle Cancer Care Alliance Peninsula Poulsbo Washington USA.
  • Dinh TK; University of Washington Seattle Washington USA.
  • Greer M; University of Washington Seattle Washington USA.
  • Bensen C; Olympic Medical Center Port Angeles Washington USA.
  • Mitchell MA; The Doctors Clinic Silverdale Washington USA.
  • Li AY; The Doctors Clinic Silverdale Washington USA.
  • Stamm A; The Doctors Clinic Silverdale Washington USA.
  • Henne M; Rayus Imaging Poulsbo Washington USA.
BJUI Compass ; 4(1): 96-103, 2023 Jan.
Article en En | MEDLINE | ID: mdl-36569501
ABSTRACT

Objective:

To measure the performance of multiparametric (mp) magnetic resonance imaging (MRI) to identify intraprostatic tumour deposits using a systematic and targeted MR-guided transperineal prostate biopsy technique. Materials and

Methods:

Patients underwent a combined systematic and targeted MR-guided transperineal biopsy procedure in the dorsal lithotomy position under general anaesthesia. Systematic biopsies were spaced 10 mm or less apart and additional biopsies targeted any Prostate Imaging-Reporting and Data System (PI-RADS) 3, 4 or 5 lesions identified on mpMRI. Cancer detection rates were calculated on a per patient and per lesion basis.

Results:

A total of 125 patients underwent the biopsy procedure. The positive predictive value (PPV) of mpMRI per patient was 59% for any cancer and 49% for Gleason score (GS) ≥ 7 cancer. The negative predictive value (NPV) of mpMRI per patient was 67% for any cancer and 88% for GS ≥ 7 cancer. On a per lesion basis, the PPV of PI-RADS 3 lesions for any and GS ≥ 7 cancer was 24% and 10%. For PI-RADS 4 lesions it was 42% and 32%. For PI-RADS 5 lesions, it was 76% and 70%. MpMRI failed to identify GS ≥ 7 cancer found on systematic biopsy in 22% of patients.

Conclusion:

Based on a combination of systematic and targeted transperineal prostate biopsies, mpMRI showed a high NPV and low PPV for GS ≥ 7 cancer on a per patient basis. The PPV of mpMRI on a per lesion basis increased with increasing PI-RADS score. However, there were a significant number of both false positive as well as false negative (mpMRI invisible) areas within the prostate that contained GS ≥ 7 cancer. Therefore, pathologic confirmation using both targeted and systematic mapping biopsy is necessary to accurately identify all intraprostatic tumour deposits.
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Texto completo: 1 Colección: 01-internacional Tipo de estudio: Prognostic_studies Idioma: En Revista: BJUI Compass Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Prognostic_studies Idioma: En Revista: BJUI Compass Año: 2023 Tipo del documento: Article