Negative Predictive Value of Biparametric Prostate Magnetic Resonance Imaging in Excluding Significant Prostate Cancer: A Pooled Data Analysis Based on Clinical Data from Four Prospective, Registered Studies
| Autor: | Tapio Pahikkala, Ileana Montoya Perez, Hannu J. Aronen, Juha Knaapila, Tarja Lamminen, Pekka Taimen, Kari T. Syvänen, Aida Kiviniemi, Ivan Jambor, Janne Verho, Jani Saunavaara, Harri Merisaari, Peter J. Boström, Otto Ettala |
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| Rok vydání: | 2020 |
| Předmět: |
Data Analysis
Male medicine.medical_specialty Urology 030232 urology & nephrology Subgroup analysis 03 medical and health sciences Prostate cancer 0302 clinical medicine Prostate Predictive Value of Tests Biopsy Medicine Humans Prospective Studies medicine.diagnostic_test business.industry Cancer Prostatic Neoplasms Magnetic resonance imaging Gold standard (test) Middle Aged medicine.disease Magnetic Resonance Imaging Clinical trial medicine.anatomical_structure 030220 oncology & carcinogenesis Radiology business |
| Zdroj: | European urology focus. 7(3) |
| ISSN: | 2405-4569 |
| Popis: | Background Multiparametric prostate magnetic resonance imaging (mpMRI) can be considered the gold standard in prostate magnetic resonance imaging (MRI). Biparametric prostate MRI (bpMRI) is faster and could be a feasible alternative to mpMRI. Objective To determine the negative predictive value (NPV) of Improved Prostate Cancer Diagnosis (IMPROD) bpMRI as a whole and in clinical subgroups in primary diagnostics of clinically significant prostate cancer (CSPCa). Design, setting, and participants This is a pooled data analysis of four prospective, registered clinical trials investigating prebiopsy IMPROD bpMRI. Men with a clinical suspicion of prostate cancer (PCa) were included. Intervention Prebiopsy IMPROD bpMRI was performed, and an IMPROD bpMRI Likert scoring system was used. If suspicious lesions (IMPROD bpMRI Likert score 3–5) were visible, targeted biopsies in addition to systematic biopsies were taken. Outcome measurements and statistical analysis Performance measures of IMPROD bpMRI in CSPCa diagnostics were evaluated. NPV was also evaluated in clinical subgroups. Gleason grade ≥3 + 4 in any biopsy core taken was defined as CSPCa. Results and limitations A total of 639 men were included in the analysis. The mean age was 64 yr, mean prostate-specific antigen level was 8.9 ng/ml, and CSPCa prevalence was 48%. NPVs of IMPROD bpMRI Likert scores 3–5 and 4–5 for CSPCa were 0.932 and 0.909, respectively, and the corresponding positive predictive values were 0.589 and 0.720. Only nine of 132 (7%) men with IMPROD bpMRI Likert score 1–2 had CSPCa and none with Gleason score >7. Thus, 132 of 639 (21%) study patients could have avoided biopsies without missing a single Gleason >7 cancer in the study biopsies. In the subgroup analysis, no clear outlier was present. The limitation is uncertainty of the true CSPCa prevalence. Conclusions IMPROD bpMRI demonstrated a high NPV to rule out CSPCa. IMPROD bpMRI Likert score 1–2 excludes Gleason >7 PCa in the study biopsies. Patient summary We investigated the feasibility of prostate magnetic resonance imaging (MRI) with the Improved Prostate Cancer Diagnosis (IMPROD) biparametric MRI (bpMRI) protocol in excluding significant prostate cancer. In this study, highly aggressive prostate cancer was excluded using the publicly available IMPROD bpMRI protocol ( http://petiv.utu.fi/multiimprod/ ). |
| Databáze: | OpenAIRE |
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