Are Radiomic Spleen Features Useful for Assessing the Response to Infliximab in Patients With Crohn's Disease? A Multicenter Study.

IF 3 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinical and Translational Gastroenterology Pub Date : 2024-05-01 DOI:10.14309/ctg.0000000000000693
Chao-Tao Tang, Fang Yin, Yitian Yin, Zide Liu, Shunhua Long, Chun-Yan Zeng, Yong Chen, You-Xiang Chen
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Abstract

Introduction: To develop and validate a radiomics nomogram for assessing the response of patients with Crohn's disease (CD) to infliximab.

Methods: Radiomics features of the spleen were extracted from computed tomography enterography images of each patient's arterial phase. The feature selection process was performed using the least absolute shrinkage and selection operator algorithm, and a radiomics score was calculated based on the radiomics signature formula. Subsequently, the radiomic model and the clinical risk factor model were separately established based on the radiomics score and clinically significant features, respectively. The performance of both models was evaluated using receiver operating characteristic curves, decision curve analysis curves, and clinical impact curves.

Results: Among the 175 patients with CD, 105 exhibited a clinical response, and 60 exhibited clinical remission after receiving infliximab treatment. Our radiomic model, comprising 20 relevant features, demonstrated excellent predictive performance. The radiomic nomogram for predicting clinical response showed good calibration and discrimination in the training cohort (area under the curve [AUC] 0.909, 95% confidence interval [CI] 0.840-0.978), the validation cohort (AUC 0.954, 95% CI 0.889-1), and the external cohort (AUC = 0.902, 95% CI 0.83-0.974). Accordingly, the nomogram was also suitable for predicting clinical remission. Decision curve analysis and clinical impact curves highlighted the clinical utility of our nomogram.

Discussion: Our radiomics nomogram is a noninvasive predictive tool constructed from radiomic features of the spleen. It also demonstrated good predictive accuracy in evaluating CD patients' response to infliximab treatment. Multicenter validation provided high-level evidence for its clinical application.

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放射学脾脏特征是否有助于评估克罗恩病患者对英夫利西单抗的反应?一项多中心研究。
目的开发并验证用于评估克罗恩病(CD)患者对英夫利西单抗反应的放射组学提名图:方法:从每位患者动脉期的计算机断层扫描肠造影(CTE)图像中提取脾脏的放射组学特征。采用最小绝对收缩和选择算子(LASSO)算法进行特征选择,并根据放射组学特征公式计算放射组学得分(Rad-score)。随后,根据辐射组学得分和临床重要特征分别建立了辐射组学模型和临床风险因素模型。使用接收者操作特征曲线(ROC)、决策曲线分析(DCA)曲线和临床影响曲线(CIC)对两种模型的性能进行了评估:结果:在175名CD患者中,有105人在接受英夫利西单抗(IFX)治疗后出现临床反应,60人出现临床缓解。我们的放射学模型由20个相关特征组成,具有出色的预测性能。用于预测临床反应的放射学提名图在训练队列(AUC=0.909,95% CI=0.840-0.978)、验证队列(AUC=0.954,95% CI=0.889-1)和外部队列(AUC=0.902,95% CI=0.83-0.974)中显示出良好的校准性和区分度。因此,提名图也适用于预测临床缓解。决策曲线分析和临床影响曲线凸显了我们的提名图的临床实用性:我们的放射组学提名图是一种根据脾脏放射组学特征构建的非侵入性预测工具。结论:我们的放射组学提名图是根据脾脏的放射组学特征构建的非侵入性预测工具,在评估 CD 患者对英夫利西单抗治疗的反应方面也表现出良好的预测准确性。多中心验证为其临床应用提供了高水平的证据。
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来源期刊
Clinical and Translational Gastroenterology
Clinical and Translational Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
7.00
自引率
0.00%
发文量
114
审稿时长
16 weeks
期刊介绍: Clinical and Translational Gastroenterology (CTG), published on behalf of the American College of Gastroenterology (ACG), is a peer-reviewed open access online journal dedicated to innovative clinical work in the field of gastroenterology and hepatology. CTG hopes to fulfill an unmet need for clinicians and scientists by welcoming novel cohort studies, early-phase clinical trials, qualitative and quantitative epidemiologic research, hypothesis-generating research, studies of novel mechanisms and methodologies including public health interventions, and integration of approaches across organs and disciplines. CTG also welcomes hypothesis-generating small studies, methods papers, and translational research with clear applications to human physiology or disease. Colon and small bowel Endoscopy and novel diagnostics Esophagus Functional GI disorders Immunology of the GI tract Microbiology of the GI tract Inflammatory bowel disease Pancreas and biliary tract Liver Pathology Pediatrics Preventative medicine Nutrition/obesity Stomach.
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