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Magnetic Resonance Imaging in Prostate Cancer Screening

Tamás FazekasCentre for Translational Medicine, Semmelweis University, Budapest, HungarySung Ryul ShimDepartment of Biomedical Informatics, College of Medicine, Konyang University, Daejeon, Republic of KoreaGiuseppe BasileUnit of Urology, Urological Research Institute, Division of Oncology, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, ItalyMichaël BaboudjianDepartment of Urology, Assistance Publique des Hôpitaux de Marseille, North Academic Hospital, Marseille, FranceTamás KóiCentre for Translational Medicine, Semmelweis University, Budapest, HungaryMikołaj PrzydaczDepartment of Urology, Jagiellonian University Medical College, Krakow, PolandMohammad AbufarajDivision of Urology, Department of Special Surgery, Jordan University Hospital, The University of Jordan, Amman, JordanGuillaume PloussardDepartment of Urology, La Croix du Sud Hospital, Quint Fonsegrives, FranceVeeru KasivisvanathanDivision of Surgery and Interventional Science, University College London, London, EnglandJuan Gómez RivasDepartment of Urology, Hospital Universitario La Paz, Madrid, SpainGiorgio GandagliaUnit of Urology, Urological Research Institute, Division of Oncology, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, ItalyTibor SzarvasDepartment of Urology, Semmelweis University, Budapest, HungaryIvo G. SchootsDepartment of Radiology and Nuclear Medicine, Erasmus MC Cancer Institute, University Medical Centre, Rotterdam, the NetherlandsRoderick C.N. van den BerghDepartment of Urology, Erasmus MC, Rotterdam, the NetherlandsMichael LeapmanDepartment of Urology, Yale School of Medicine, New Haven, ConnecticutPéter NyírádyCentre for Translational Medicine, Semmelweis University, Budapest, HungaryShahrokh F. ShariatComprehensive Cancer Center, Department of Urology, Medical University of Vienna, Vienna, AustriaPaweł RajwaComprehensive Cancer Center, Department of Urology, Medical University of Vienna, Vienna, Austria
2024en
ABI

Аннотация

Importance: Prostate magnetic resonance imaging (MRI) is increasingly integrated within the prostate cancer (PCa) early detection pathway. Objective: To systematically evaluate the existing evidence regarding screening pathways incorporating MRI with targeted biopsy and assess their diagnostic value compared with prostate-specific antigen (PSA)-based screening with systematic biopsy strategies. Data Sources: PubMed/MEDLINE, Embase, Cochrane/Central, Scopus, and Web of Science (through May 2023). Study Selection: Randomized clinical trials and prospective cohort studies were eligible if they reported data on the diagnostic utility of prostate MRI in the setting of PCa screening. Data Extraction: Number of screened individuals, biopsy indications, biopsies performed, clinically significant PCa (csPCa) defined as International Society of Urological Pathology (ISUP) grade 2 or higher, and insignificant (ISUP1) PCas detected were extracted. Main Outcomes and Measures: The primary outcome was csPCa detection rate. Secondary outcomes included clinical insignificant PCa detection rate, biopsy indication rates, and the positive predictive value for the detection of csPCa. Data Synthesis: The generalized mixed-effect approach with pooled odds ratios (ORs) and random-effect models was used to compare the MRI-based and PSA-only screening strategies. Separate analyses were performed based on the timing of MRI (primary/sequential after a PSA test) and cutoff (Prostate Imaging Reporting and Data System [PI-RADS] score ≥3 or ≥4) for biopsy indication. Results: Data were synthesized from 80 114 men from 12 studies. Compared with standard PSA-based screening, the MRI pathway (sequential screening, PI-RADS score ≥3 cutoff for biopsy) was associated with higher odds of csPCa when tests results were positive (OR, 4.15; 95% CI, 2.93-5.88; P ≤ .001), decreased odds of biopsies (OR, 0.28; 95% CI, 0.22-0.36; P ≤ .001), and insignificant cancers detected (OR, 0.34; 95% CI, 0.23-0.49; P = .002) without significant differences in the detection of csPCa (OR, 1.02; 95% CI, 0.75-1.37; P = .86). Implementing a PI-RADS score of 4 or greater threshold for biopsy selection was associated with a further reduction in the odds of detecting insignificant PCa (OR, 0.23; 95% CI, 0.05-0.97; P = .048) and biopsies performed (OR, 0.19; 95% CI, 0.09-0.38; P = .01) without differences in csPCa detection (OR, 0.85; 95% CI, 0.49-1.45; P = .22). Conclusion and relevance: The results of this systematic review and meta-analysis suggest that integrating MRI in PCa screening pathways is associated with a reduced number of unnecessary biopsies and overdiagnosis of insignificant PCa while maintaining csPCa detection as compared with PSA-only screening.

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