The PRIMARY Scoring System on PSMA PET for Clinically Significant Prostate Cancer Detection: A Systematic Review and Meta-Analysis.
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TL;DR
Ion channels and extrachromosomal DNA have emerged as key drivers of such adaptive processes by influencing signaling, metabolism, and immune interactions.
OpenAlex 토픽 ·
Prostate Cancer Diagnosis and Treatment
Prostate Cancer Treatment and Research
Medical Imaging Techniques and Applications
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Ion channels and extrachromosomal DNA have emerged as key drivers of such adaptive processes by influencing signaling, metabolism, and immune interactions.
- 표본수 (n) 1974
- Sensitivity 89%
- Specificity 90%
- 연구 설계 meta-analysis
APA
Felipe Alves Mourato, Luiza G. Schmitt, et al. (2026). The PRIMARY Scoring System on PSMA PET for Clinically Significant Prostate Cancer Detection: A Systematic Review and Meta-Analysis.. Clinical nuclear medicine, 51(5), 406-415. https://doi.org/10.1097/RLU.0000000000006309
MLA
Felipe Alves Mourato, et al.. "The PRIMARY Scoring System on PSMA PET for Clinically Significant Prostate Cancer Detection: A Systematic Review and Meta-Analysis.." Clinical nuclear medicine, vol. 51, no. 5, 2026, pp. 406-415.
PMID
41631935 ↗
Abstract 한글 요약
[PURPOSE OF THE REPORT] The PRIMARY score standardizes interpretation of PSMA PET for intraprostatic assessment of clinically significant prostate cancer (csPCa). Although early studies are promising, no meta-analysis has systematically evaluated its accuracy. We aimed to assess the diagnostic performance of PRIMARY and compare it with PI-RADS.
[MATERIAL AND METHODS] A systematic review and meta-analysis were performed according to PRISMA-DTA guidelines. Studies assessing the PRIMARY score on PSMA PET/CT or PET/MRI for csPCa detection were included. The primary analysis focused on biopsy-naïve patients; secondary analyses incorporated all studies irrespective of prior histology, evaluated thresholds (≥3 vs. ≥4), compared PRIMARY with PI-RADS, and examined combined performance. Pooled sensitivity and specificity were estimated with a bivariate random-effects model.
[RESULTS] Thirteen studies (n=1974) were included. In biopsy-naïve cohorts (6 studies), PRIMARY ≥3 achieved pooled sensitivity/specificity of 90% (95% CI: 86%-93%) and 63% (95% CI: 57%-69%). In an expanded analysis of 9 studies regardless of prior biopsy, values were 87% (82%-90%) and 56% (46%-65%). Across 5 studies directly comparing thresholds, raising the cutoff from ≥3 to ≥4 reduced sensitivity from 89% to 81% but increased specificity from 53% to 72%. Three head-to-head studies showed comparable accuracy between PRIMARY and PI-RADS.
[CONCLUSIONS] PRIMARY demonstrates high sensitivity and moderate specificity for csPCa, comparable to PI-RADS. In biopsy-naïve men it shows robust performance, and combination with mpMRI further improves sensitivity. Threshold selection should reflect clinical intent, supporting PRIMARY as a tool for pre-biopsy risk stratification and integrated diagnostic workflows.
[MATERIAL AND METHODS] A systematic review and meta-analysis were performed according to PRISMA-DTA guidelines. Studies assessing the PRIMARY score on PSMA PET/CT or PET/MRI for csPCa detection were included. The primary analysis focused on biopsy-naïve patients; secondary analyses incorporated all studies irrespective of prior histology, evaluated thresholds (≥3 vs. ≥4), compared PRIMARY with PI-RADS, and examined combined performance. Pooled sensitivity and specificity were estimated with a bivariate random-effects model.
[RESULTS] Thirteen studies (n=1974) were included. In biopsy-naïve cohorts (6 studies), PRIMARY ≥3 achieved pooled sensitivity/specificity of 90% (95% CI: 86%-93%) and 63% (95% CI: 57%-69%). In an expanded analysis of 9 studies regardless of prior biopsy, values were 87% (82%-90%) and 56% (46%-65%). Across 5 studies directly comparing thresholds, raising the cutoff from ≥3 to ≥4 reduced sensitivity from 89% to 81% but increased specificity from 53% to 72%. Three head-to-head studies showed comparable accuracy between PRIMARY and PI-RADS.
[CONCLUSIONS] PRIMARY demonstrates high sensitivity and moderate specificity for csPCa, comparable to PI-RADS. In biopsy-naïve men it shows robust performance, and combination with mpMRI further improves sensitivity. Threshold selection should reflect clinical intent, supporting PRIMARY as a tool for pre-biopsy risk stratification and integrated diagnostic workflows.
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