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Combined Prostate-specific Membrane Antigen Positron Emission Tomography and Multiparametric Magnetic Resonance Imaging for the Diagnosis of Clinically Significant Prostate Cancer.

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European urology oncology 2025 Vol.8(5) p. 1393-1405
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PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
2153 patients) that referenced combined imaging against histopathology were included.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Synchronous reading of PSMA-PET/computed tomography (CT) with mpMRI was significantly more sensitive but less specific than PSMA-PET/MRI. [CONCLUSIONS AND CLINICAL IMPLICATIONS] Combined imaging improves the diagnostic accuracy of csPCa and may help better select patients for a prostate biopsy.

Chow KM, Lee A, Peh D, Tan YG, Tay KJ, Ho H, Cheng C, Lam W, Thang SP, Tuan J, Mee LY, Ngo T, Khor LY, Yuen J, Eapen R, Lawrentschuk N, Hofman M, Murphy D, Chen K

📝 환자 설명용 한 줄

[BACKGROUND AND OBJECTIVE] More than half of men who undergo a prostate biopsy based on positive multiparametric magnetic resonance imaging (mpMRI) findings do not have clinically significant prostate

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 연구 설계 systematic review

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BibTeX ↓ RIS ↓
APA Chow KM, Lee A, et al. (2025). Combined Prostate-specific Membrane Antigen Positron Emission Tomography and Multiparametric Magnetic Resonance Imaging for the Diagnosis of Clinically Significant Prostate Cancer.. European urology oncology, 8(5), 1393-1405. https://doi.org/10.1016/j.euo.2025.04.017
MLA Chow KM, et al.. "Combined Prostate-specific Membrane Antigen Positron Emission Tomography and Multiparametric Magnetic Resonance Imaging for the Diagnosis of Clinically Significant Prostate Cancer.." European urology oncology, vol. 8, no. 5, 2025, pp. 1393-1405.
PMID 40506357

Abstract

[BACKGROUND AND OBJECTIVE] More than half of men who undergo a prostate biopsy based on positive multiparametric magnetic resonance imaging (mpMRI) findings do not have clinically significant prostate cancer (csPCa). Prostate-specific membrane antigen (PSMA) positron emission tomography (PET) may complement mpMRI to better triage men with suspected prostate cancer (PCa) and reduce the number of unnecessary biopsies performed. A diagnostic test accuracy systematic review and meta-analysis was performed to determine the diagnostic accuracy of combined imaging for csPCa detection with pairwise comparisons with mpMRI and PSMA-PET alone. A decision curve analysis (DCA) compared the strategies of performing an upfront biopsy versus combined imaging for suspected PCa patients, across varying thresholds for accepting the risk of missing a csPCa diagnosis.

[METHODS] A search of the PubMed, Embase, Central, and Scopus databases, from inception to January 2024, was conducted. Twenty studies (2153 patients) that referenced combined imaging against histopathology were included. Bivariate meta-analyses and metaregression were performed to determine the diagnostic parameters and assess the differences between imaging modalities.

[KEY FINDINGS AND LIMITATIONS] Combined imaging had sensitivity, specificity, positive predictive value (PPV), and negative predictive value of, respectively, 92% (95% confidence interval [CI] 87, 95), 64% (95% CI 48, 77), 80% (95% CI 68, 92), and 82% (95% CI 68, 97) at patient-level, and 82% (95% CI 77, 94), 85% (95% CI 77, 94), 79% (95% CI 52, 97), and 81% (95% CI 74, 98) at lesion-level analyses. Head-to-head comparisons showed significantly higher specificity and PPV than mpMRI at patient- and lesion-level analyses. On the DCA, combined imaging outperforms upfront biopsy at risk thresholds of 8% onwards. Synchronous reading of PSMA-PET/computed tomography (CT) with mpMRI was significantly more sensitive but less specific than PSMA-PET/MRI.

[CONCLUSIONS AND CLINICAL IMPLICATIONS] Combined imaging improves the diagnostic accuracy of csPCa and may help better select patients for a prostate biopsy.

MeSH Terms

Humans; Prostatic Neoplasms; Male; Multiparametric Magnetic Resonance Imaging; Positron-Emission Tomography; Glutamate Carboxypeptidase II; Antigens, Surface

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