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Multiparametric MRI‐Based Radiomics for Prostate Cancer Screening With PSA in 4–10 ng/mL to Reduce Unnecessary Biopsies

无线电技术 医学 前列腺癌 逻辑回归 精确检验 放射科 有效扩散系数 磁共振成像 前列腺 前列腺特异性抗原 活检 多元统计 核医学 癌症 统计 数学 内科学
作者
Yafei Qi,Shuaitong Zhang,Jingwei Wei,Gumuyang Zhang,Jing Lei,Weigang Yan,Yu Xiao,Shuang Yan,Huadan Xue,Feng Feng,Hao Sun,Jie Tian,Zhengyu Jin
出处
期刊:Journal of Magnetic Resonance Imaging [Wiley]
卷期号:51 (6): 1890-1899 被引量:65
标识
DOI:10.1002/jmri.27008
摘要

Background Whether men with a prostate‐specific antigen (PSA) level of 4–10 ng/mL should be recommended for a biopsy is clinically challenging. Purpose To develop and validate a radiomics model based on multiparametric MRI (mp‐MRI) in patients with PSA levels of 4–10 ng/mL to predict prostate cancer (PCa) preoperatively and reduce unnecessary biopsies. Study Type Retrospective. Subjects In all, 199 patients with PSA levels of 4–10 ng/mL. Field Strength/Sequence 3T, T 2 ‐weighted, diffusion‐weighted, and dynamic contrast‐enhanced MRI. Assessment Lesion regions of interest (ROIs) from T 2 ‐weighted, diffusion‐weighted, and dynamic contrast‐enhanced MRI were annotated by two radiologists. A total of 2104 radiomic features were extracted from the ROI of each patient. A random forest classifier was used to build the radiomics model for PCa in the primary cohort. A combined model was constructed using multivariate logistic regression by incorporating the radiomics signature and clinical‐radiological risk factors. Statistical Tests For continuous variables, variance equality was assessed by Levene's test and Student's t ‐test, and Welch's t ‐test was used to assess between‐group differences. For categorical variables, Pearson's chi‐square test, Fisher's exact test, or the approximate chi‐square test was used to assess between‐group differences. P < 0.05 was considered statistically significant. Results The combined model incorporating the multi‐imaging fusion model, age, PSA density (PSAD), and the PI‐RADS v2 score yielded area under the curve (AUC) values of 0.956 and 0.933 on the primary ( n = 133) and validation ( n = 66) cohorts, respectively. Compared with the clinical‐radiological model, the combined model performed better on both the primary and validation cohorts ( P < 0.05). Furthermore, the use of the combined model to predict PCa could identify more negative PCa patients than the use of the clinical‐radiological model by 18.4%. Data Conclusion The combined model was developed and validated to provide potential preoperative prediction of PCa in men with PSA levels of 4–10 ng/mL and might aid in treatment decision‐making and reduce unnecessary biopsies. Level of Evidence: 3 Technical Efficacy Stage: 3 J. Magn. Reson. Imaging 2020;51:1890–1899.
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