Evidence map›Paper›PMID 42273125›Full record

ArticleQuantitative imaging in medicine and surgery2026

Evaluation of MRI-based risk models versus PI-RADS version 2.1 and arterial spin labeling perfusion imaging strategy for clinically significant prostate cancer.

Wanwan Wang, Xin Zheng, Jing Wang, Nian Liu, Shengxian Cai, Yunjun Xu

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Article in Quantitative imaging in medicine and surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Wanwan Wang *Division of Life Sciences and Medicine, The First Affiliated Hospital of the University of Science and Technology of China, University of Science and Technology of China, Hefei, China.
Xin Zheng *Department of Imaging, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Jing WangDivision of Life Sciences and Medicine, The First Affiliated Hospital of the University of Science and Technology of China, University of Science and Technology of China, Hefei, China.
Nian LiuDivision of Life Sciences and Medicine, The First Affiliated Hospital of the University of Science and Technology of China, University of Science and Technology of China, Hefei, China.
Shengxian CaiDepartment of Imaging, Dangshan County People's Hospital, Suzhou, China.
Yunjun XuDivision of Life Sciences and Medicine, The First Affiliated Hospital of the University of Science and Technology of China, University of Science and Technology of China, Hefei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Arterial spin labeling (ASL) is a non-invasive magnetic resonance imaging (MRI) technique that enables quantitative assessment of prostate blood flow (PBF). Although the Prostate Imaging Reporting and Data System (PI-RADS) v2.1 is widely used for risk stratification of clinically significant prostate cancer (csPCa), whether combining ASL with the PI-RADS system can improve diagnostic accuracy remains to be explored. This study aimed to evaluate the risk of csPCa by integrating non-invasive ASL-derived PBF measurements with PI-RADS v2.1 scores in a clinical-imaging model. Methods: Of 233 patients with suspected prostate cancer (PCa) who underwent biparametric magnetic resonance imaging (bp-MRI) and ASL, 133 had pathologically confirmed benign or malignant lesions. The analysis included PBF measurements, PI-RADS v2.1 scores, and relevant clinical data from this cohort. This study employed both univariable and multivariable logistic regression to sequentially identify prognostic features. The diagnostic performance of PBF, PI-RADS v2.1 scores, and their combination in detecting csPCa was assessed using receiver operating characteristic (ROC) analysis. Bootstrap resampling was used for internal validation to ensure model stability. A nomogram was constructed to visualize the predictive model for csPCa risk, and decision curve analysis (DCA) was performed to evaluate its clinical utility. Results: Independent risk factors for csPCa included maximum prostate blood flow (PBF-max), PI-RADS v2.1 score, total prostate-specific antigen (tPSA), and prostate volume (PV). The diagnostic performance for csPCa, measured by the area under the curve (AUC), was 0.872 for PBF-max alone and 0.916 for the PI-RADS v2.1 score alone. Their combination significantly improved accuracy, yielding an AUC of 0.965. Furthermore, PI-RADS v2.1 scores demonstrated a strong positive correlation with PBF-max (r=0.62). Conclusions: The non-invasive quantification of PBF via ASL enhances the diagnostic capability of PI-RADS v2.1 scores for the detection of csPCa.

Indexed as

arterial spin labeling perfusion imaging (ASL perfusion imaging)clinical-imaging modelClinically significant prostate cancer (csPCa)Prostate Imaging Reporting and Data System score (PI-RADS score)

Identifiers

PMID42273125
PMCPMC13247904

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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.