基于计算机断层扫描的放射组学分析结合肺癌血清肿瘤标记物在肺鳞癌和肺腺癌鉴别中的应用。

Journal of cancer research and therapeutics Pub Date : 2024-08-01 Epub Date: 2024-08-29 DOI:10.4103/jcrt.jcrt_79_24
Tongrui Zhang, Jun Li, Guangli Wang, Huafeng Li, Gesheng Song, Kai Deng
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引用次数: 0

摘要

目的通过计算机断层扫描(CT)放射组学与肺癌血清肿瘤标志物(STM)建立肺癌分类预测模型:研究对象为 200 名 NSCLC 患者。收集了包括年龄、性别和 STM(鳞状细胞癌 [SCC]、神经元特异性烯醇化酶 [NSE]、癌胚抗原 [CEA]、促胃泌素释放肽 [PRO-GRP] 和细胞角蛋白 19 片段 [cYFRA21-1])在内的临床数据。使用最小绝对收缩和选择算子(LASSO)算法从训练集中生成放射组学特征。利用多变量逻辑回归分析确定了风险因素,并根据放射组学特征和临床特征构建了放射组学提名图。利用训练集评估了提名图的能力,并利用验证集进行了验证。使用校正曲线和 Hosmer-Lemeshow 检验来评估放射组学模型对训练集和测试集的预测性能:结果:从 1234 个放射组学参数中筛选出 29 个参数作为建立放射组学模型的重要因素。训练集(曲线下面积 [AUC] = 0.925; 95% 置信区间 [CI]:训练集(曲线下面积 [AUC] = 0.925;95% 置信区间 [CI]:0.885-0.966)和验证集(曲线下面积 [AUC] = 0.921;95% 置信区间 [CI]:0.854-0.989)显示,结合 STM 的 CT 放射组学特征能准确预测肺鳞癌和肺腺癌。此外,根据 Hosmer-Lemeshow 检验,逻辑回归模型在训练集(P = 0.954)和测试集(P = 0.340)中表现出良好的性能。良好的校准曲线一致性也表明了提名图的良好性能:结论:CT放射组学特征与肺癌STM的结合在NSCLC的病理分类中表现良好。与放射组学特征法相比,基于放射组学特征和临床因素的提名图在NSCLC的鉴别诊断中表现更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of computed tomography-based radiomics analysis combined with lung cancer serum tumor markers in the identification of lung squamous cell carcinoma and lung adenocarcinoma.

Objective: To establish a prediction model of lung cancer classification by computed tomography (CT) radiomics with the serum tumor markers (STM) of lung cancer.

Materials and methods: Two-hundred NSCLC patients were enrolled in our study. Clinical data including age, sex, and STM (squamous cell carcinoma [SCC], neuron-specific enolase [NSE], carcinoembryonic antigen [CEA], pro-gastrin-releasing peptide [PRO-GRP], and cytokeratin 19 fragment [cYFRA21-1]) were collected. A radiomics signature was generated from the training set using the least absolute shrinkage and selection operator (LASSO) algorithm. The risk factors were identified using multivariate logistic regression analysis, and a radiomics nomogram based on the radiomics signature and clinical features was constructed. The capability of the nomogram was evaluated using the training set and validated using the validation set. A correction curve and the Hosmer-Lemeshow test were used to evaluate the predictive performance of the radiomics model for the training and test sets.

Results: Twenty-nine of 1234 radiomics parameters were screened as important factors for establishing the radiomics model. The training (area under the curve [AUC] = 0.925; 95% confidence interval [CI]: 0.885-0.966) and validation sets (AUC = 0.921; 95% CI: 0.854-0.989) showed that the CT radiomics signature, combined with STM, accurately predicted lung squamous cell carcinoma and lung adenocarcinoma. Moreover, the logistic regression model showed good performance based on the Hosmer-Lemeshow test in the training (P = 0.954) and test sets (P = 0.340). Good calibration curve consistency also indicated the good performance of the nomogram.

Conclusion: The combination of the CT radiomics signature and lung cancer STM performed well for the pathological classification of NSCLC. Compared with the radiomics signature method, the nomogram based on the radiomics signature and clinical factors had better performance for the differential diagnosis of NSCLC.

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