Evidence map›Paper›PMID 41896841›Full record

ArticleBMC urology2026

Added value of systematic biopsy in patients with positive MRI-US fusion targeted biopsy for clinically significant prostate cancer: a single-center retrospective study.

Jingwen Zhang, Jiatao Chen, Jingyi Jin, Jiangang Chen, Bing Zheng

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In one paragraph

Article in BMC urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jingwen ZhangDepartment of Urology, Nantong First People's Hospital, Nantong, China.
Jiatao ChenDepartment of Urology, Nantong First People's Hospital, Nantong, China.
Jingyi JinDepartment of Urology, Nantong First People's Hospital, Nantong, China.
Jiangang ChenDepartment of Urology, Nantong First People's Hospital, Nantong, China. urologistcjg@163.com.
Bing ZhengDepartment of Urology, Nantong First People's Hospital, Nantong, China. ntzb2008@163.com.

Funding

Medical Research Project of Nantong Health Commission MS2024032Natural Science Foundation of Nantong Municipality JC2025081
6 · The paper itself

Abstract

purposeTo evaluate the added value of systematic biopsy (SB) in patients with positive targeted biopsy (TB) in the context of transperineal MRI-US fusion prostate biopsy, specifically focusing on clinically significant prostate cancer (csPCa), and to identify characteristics of patients who may benefit from a TB-only strategy.

methodsWe retrospectively enrolled 260 patients who underwent transperineal MRI-US fusion biopsy (4-core TB plus 12-core SB) at Nantong First People’s Hospital between May 2024 and November 2025. All patients had positive TB results for prostate cancer. SB zero-benefit for csPCa was defined as TB detecting csPCa (Grade Group ≥ 2) while SB detecting no csPCa (either negative or only Grade Group 1). Multivariate logistic regression was used to analyze predictors of SB zero-benefit. A predictive model was constructed and validated using Bootstrap (2000 resamples). Model performance was assessed using ROC curves, calibration plots, and decision curve analysis (DCA).

resultsAmong 260 patients with TB-detected csPCa, 25 (9.6%) exhibited SB zero-benefit for csPCa. Compared with the SB-positive group (n = 235), the SB zero-benefit group exhibited significantly larger prostate volume, lower PSAD, smaller lesion size, and a distribution toward lower-risk PI-RADS scores. Multivariate analysis revealed that lesion size (OR = 0.802, 95%CI: 0.657–0.978, P = 0.030) and PI-RADS score (4 vs. 3: OR = 0.022, P < 0.001; 5 vs. 3: OR = 0.027, P = 0.013) were independent predictors of SB zero-benefit. The predictive model demonstrated excellent discrimination (AUC = 0.910, 95%CI: 0.851–0.968; bootstrap-corrected AUC = 0.892) with acceptable calibration (Hosmer-Lemeshow P = 0.503). At the optimal cutoff (predicted probability = 0.122), sensitivity of 84.0%, specificity of 87.2%, and negative predictive value (NPV) of 98.1%. If SB had been omitted, 25 patients (9.6%) with csPCa detected only by SB would have been missed, while TB alone detected 100% of csPCa in this cohort. DCA showed higher net benefit across threshold probabilities of 0.1–0.9 compared to the “biopsy-all” strategy.

conclusionsApproximately 10% of patients with TB-detected csPCa exhibited SB zero-benefit, characterized by small lesions (≤ 11 mm) and low PI-RADS scores (3–4). The predictive model based on lesion size and PI-RADS effectively identified patients with low SB value (NPV 98.1%) in this internal validation. However, given the single-center retrospective design, small event number (n = 25), lack of external validation, and the 9.6% miss rate if SB were omitted, this model requires prospective multicenter validation before clinical implementation. For patients at initial diagnosis, a transperineal TB-only strategy may warrant further prospective validation in selected patients with PI-RADS 3–4 lesions ≤ 11 mm, whereas PI-RADS 5 lesions should undergo combined biopsy given the risk of false-positive MRI findings and the need for maximal cancer characterization. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Image-Guided BiopsyMagnetic Resonance Imaging, InterventionalProstateProstatic NeoplasmsUltrasonography, InterventionalAgedClinical RelevanceHumansMagnetic Resonance ImagingMaleMiddle AgedRetrospective StudiesMRI-US fusionProstate cancerRisk stratificationSystematic biopsyTargeted biopsy

Identifiers

PMID41896841
PMCPMC13147857

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.