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Peer-reviewedCC BY-NC-NDBMC cancer

Comparative diagnostic accuracy of PSMA-PET versus conventional imaging for Initial T/N/M staging of intermediate- to high-risk prostate cancer: a patient-level paired bivariate meta-analysis.

  1. 1Department of Urology, West China Hospital, Sichuan University, Chengdu, China.
  2. 2Department of Urology, West China Hospital, Sichuan University, Chengdu, China. [email protected].

Abstract

Purpose

To compare the patient-level diagnostic accuracy of PSMA-PET with multiparametric magnetic resonance imaging (mpMRI), computed tomography (CT), and bone scintigraphy (BS) for initial T, N, and M staging of newly diagnosed intermediate- to high-risk prostate cancer using paired studies.Methods

We searched PubMed, Embase, Web of Science, and Scopus from inception to December 1, 2025, for paired studies in which the same patients underwent PSMA-PET and conventional imaging, with histopathology or predefined composite criteria as the reference standard. Risk of bias was assessed with QUADAS-2 and QUADAS-C. Pooled sensitivity and specificity with 95% confidence intervals (CIs) were estimated using bivariate composite-likelihood models. Modality effects were tested by meta-regression and likelihood ratio tests, and absolute between-modality differences with 95% CIs were estimated using the delta method.Results

Forty-three studies including 4,023 patients were analyzed. For local T staging, PSMA-PET did not show uniform superiority over mpMRI. For extraprostatic extension, PSMA-PET/CT did not differ significantly from mpMRI in sensitivity (absolute difference, -7.6 percentage points; 95% CI, -16.1 to 0.9; p = 0.08) or specificity (-7.0 percentage points; 95% CI, -14.7 to 0.8; p = 0.08); no significant differences were observed for seminal vesicle invasion. In an exploratory six-study comparison, PSMA-PET/MRI had higher sensitivity than mpMRI for extraprostatic extension (+ 12.1 percentage points; 95% CI, 1.9 to 22.2; p = 0.02). For regional lymph node staging, PSMA-PET/CT sensitivity was 69.3% (95% CI, 56.6-79.7) versus 45.3% (95% CI, 33.0-58.3) for mpMRI (difference, + 24.1 percentage points; 95% CI, 6.0-40.3; p = 0.009), whereas specificity did not differ (difference, + 3.2 percentage points; 95% CI, -4.6 to 11.8; p = 0.41). For bone metastasis staging, PSMA-PET had greater sensitivity than BS (95.8% [95% CI, 92.8-98.7] versus 76.2% [95% CI, 68.7-83.8]) and greater specificity (92.8% [95% CI, 89.9-95.7] versus 77.4% [95% CI, 71.3-83.5]; both p < 0.001).Conclusions

PSMA-PET/CT was more sensitive than mpMRI for regional lymph node staging, while specificity was comparable. PSMA-PET had greater sensitivity and specificity than bone scintigraphy for bone metastasis staging. For local T staging, PSMA-PET did not show uniform superiority over mpMRI.

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BibTeX
@article{wu2026comparative,
  title = {{Comparative diagnostic accuracy of PSMA-PET versus conventional imaging for Initial T/N/M staging of intermediate- to high-risk prostate cancer: a patient-level paired bivariate meta-analysis.}},
  author = {Haowen Wu and Wei Zhang and Luchen Yang and Xin Yan and Pan Song and Qiang Dong},
  journal = {BMC cancer},
  year = {2026},
  month = jul,
  doi = {10.1186/s12885-026-16639-2},
  url = {https://europepmc.org/article/MED/42928137},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Comparative diagnostic accuracy of PSMA-PET versus conventional imaging for Initial T/N/M staging of intermediate- to high-risk prostate cancer: a patient-level paired bivariate meta-analysis.
AU  - Haowen Wu
AU  - Wei Zhang
AU  - Luchen Yang
AU  - Xin Yan
AU  - Pan Song
AU  - Qiang Dong
PY  - 2026
DA  - 2026/07/28
JO  - BMC cancer
DO  - 10.1186/s12885-026-16639-2
UR  - https://europepmc.org/article/MED/42928137
AB  - Purpose  To compare the patient-level diagnostic accuracy of PSMA-PET with multiparametric magnetic resonance imaging (mpMRI), computed tomography (CT), and bone scintigraphy (BS) for initial T, N, and M staging of newly diagnosed intermediate- to high-risk prostate cancer using paired studies.Methods  We searched PubMed, Embase, Web of Science, and Scopus from inception to December 1, 2025, for paired studies in which the same patients underwent PSMA-PET and conventional imaging, with histopathology or predefined composite criteria as the reference standard. Risk of bias was assessed with QUADAS-2 and QUADAS-C. Pooled sensitivity and specificity with 95% confidence intervals (CIs) were estimated using bivariate composite-likelihood models. Modality effects were tested by meta-regression and likelihood ratio tests, and absolute between-modality differences with 95% CIs were estimated using the delta method.Results  Forty-three studies including 4,023 patients were analyzed. For local T staging, PSMA-PET did not show uniform superiority over mpMRI. For extraprostatic extension, PSMA-PET/CT did not differ significantly from mpMRI in sensitivity (absolute difference, -7.6 percentage points; 95% CI, -16.1 to 0.9; p = 0.08) or specificity (-7.0 percentage points; 95% CI, -14.7 to 0.8; p = 0.08); no significant differences were observed for seminal vesicle invasion. In an exploratory six-study comparison, PSMA-PET/MRI had higher sensitivity than mpMRI for extraprostatic extension (+ 12.1 percentage points; 95% CI, 1.9 to 22.2; p = 0.02). For regional lymph node staging, PSMA-PET/CT sensitivity was 69.3% (95% CI, 56.6-79.7) versus 45.3% (95% CI, 33.0-58.3) for mpMRI (difference, + 24.1 percentage points; 95% CI, 6.0-40.3; p = 0.009), whereas specificity did not differ (difference, + 3.2 percentage points; 95% CI, -4.6 to 11.8; p = 0.41). For bone metastasis staging, PSMA-PET had greater sensitivity than BS (95.8% [95% CI, 92.8-98.7] versus 76.2% [95% CI, 68.7-83.8]) and greater specificity (92.8% [95% CI, 89.9-95.7] versus 77.4% [95% CI, 71.3-83.5]; both p < 0.001).Conclusions  PSMA-PET/CT was more sensitive than mpMRI for regional lymph node staging, while specificity was comparable. PSMA-PET had greater sensitivity and specificity than bone scintigraphy for bone metastasis staging. For local T staging, PSMA-PET did not show uniform superiority over mpMRI.
SN  - 1471-2407
ER  -