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[浸润性肺腺癌鉴别预测模型的临床价值]

[Clinical value of a differentiation prediction model for invasive lung adenocarcinoma].

作者信息

Shan W L, Kong D, Zhang H, Zhang J D, Duan S F, Guo L L

机构信息

Department of Radiology, the Affiliated Huai'an First People's Hospital of Nanjing Medical University, Huai'an 223300, China.

GE Healthcare China, Shanghai 210000, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2022 Jul 23;44(7):767-775. doi: 10.3760/cma.j.cn112152-20200102-00002.

DOI:10.3760/cma.j.cn112152-20200102-00002
PMID:35880343
Abstract

To investigate the value of predicting the degree of differentiation of pulmonary invasive adenocarcinoma (IAC) based on CT image radiomics model and the expression difference of immunohistochemical factors between different degrees of differentiation of lesions. The clinicopathological data of patients with pulmonary IAC confirmed by surgical pathology in the Affiliated Huai'an First People's Hospital to Nanjing Medical University from December 2017 to September 2018 were collected. High-throughput feature acquisition was performed for all outlined regions of interest, and prediction models were constructed after dimensionality reduction by the minimum absolute shrinkage operator. Receiver operating characteristic curve was used to assess the predictive efficacy of clinical characteristic model, radiomics model and individualized prediction model combined with both to identify the degree of pulmonary IAC differentiation, and immunohistochemical expressions of Ki-67, NapsinA and TTF-1 were compared between groups with different degrees of IAC differentiation using rank sum test. A total of 396 high-throughput features were extracted from all IAC lesions, and 10 features with high generalization ability and correlation with the degree of IAC differentiation were screened. The mean radiomics score of poorly differentiated IAC in the training group (1.206) was higher than that of patients with high and medium differentiation (0.969, =0.001), and the mean radiomics score of poorly differentiated IAC in the test group (1.545) was higher than that of patients with high and medium differentiation (-0.815, <0.001). The differences in gender (<0.001), pleural stretch sign (=0.005), and burr sign (=0.033) were statistically significant between patients in the well and poorly differentiated IAC groups. Multifactorial logistic regression analysis showed that gender and pleural stretch sign were related to the degree of IAC differentiation (<0.05). The clinical feature model consisted of age, gender, pleural stretch sign, burr sign, tumor vessel sign, and vacuolar sign, and the individualized prediction model consisted of gender, pleural stretch sign, and radiomic score, and was represented by a nomogram. The Akaike information standard values of the radiomics model, clinical feature model and individualized prediction model were 54.756, 82.214 and 53.282, respectively. The individualized prediction model was most effective in identifying the degree of differentiation of pulmonary IAC, and the area under the curves (AUC) of the individualized prediction model in the training group and the test group were 0.92 (95% 0.86-0.99) and 0.88 (95% 0.74-1.00, respectively). The AUCs of the radiomics group model for predicting the degree of differentiation of pulmonary IAC in the training group and the test group were 0.91 (95% 0.83-0.98) and 0.87 (95% 0.72-1.00), respectively. The AUCs of the clinical characteristics model for predicting the degree of differentiation of pulmonary IACs in the training and test groups were 0.75 (95% 0.63-0.86) and 0.76 (95% 0.59-0.94), respectively. The expression level of Ki-67 in poorly differentiated IAC was higher than that in well-differentiated IAC (<0.001). The expression levels of NapsinA, TTF-1 in poorly differentiated IAC were higher than those in well-differentiated IAC (<0.05). Individualized prediction model consisted of gender, pleural stretch sign and radiomics score can discriminate the differentiation degree of IAC with the best performance in comparison with clinical feature model and radiomics model. Ki-67, NapsinA and TTF-1 express differently in different degrees of differentiation of IAC.

摘要

探讨基于CT图像放射组学模型预测肺浸润性腺癌(IAC)分化程度的价值以及不同分化程度病变间免疫组化因子的表达差异。收集2017年12月至2018年9月在南京医科大学附属淮安第一人民医院经手术病理确诊的肺IAC患者的临床病理资料。对所有勾勒出的感兴趣区域进行高通量特征提取,经最小绝对收缩算子降维后构建预测模型。采用受试者工作特征曲线评估临床特征模型、放射组学模型以及二者结合的个体化预测模型对肺IAC分化程度的预测效能,并采用秩和检验比较不同IAC分化程度组间Ki-67、NapsinA和TTF-1的免疫组化表达情况。从所有IAC病变中共提取396个高通量特征,筛选出10个具有高泛化能力且与IAC分化程度相关的特征。训练组中低分化IAC的平均放射组学评分(1.206)高于高中分化患者(0.969,P=0.001),测试组中低分化IAC的平均放射组学评分(1.545)高于高中分化患者(-0.815,P<0.001)。高分化与低分化IAC患者在性别(P<0.001)、胸膜牵拉征(P=0.005)和毛刺征(P=0.033)方面的差异具有统计学意义。多因素logistic回归分析显示,性别和胸膜牵拉征与IAC分化程度相关(P<0.05)。临床特征模型由年龄、性别、胸膜牵拉征、毛刺征、肿瘤血管征和空泡征组成,个体化预测模型由性别、胸膜牵拉征和放射组学评分组成,并以列线图表示。放射组学模型、临床特征模型和个体化预测模型的Akaike信息准则值分别为54.756、82.214和53.282。个体化预测模型在识别肺IAC分化程度方面最有效,训练组和测试组个体化预测模型的曲线下面积(AUC)分别为0.92(95%CI 0.86-0.99)和0.88(95%CI 0.74-1.00)。放射组学模型预测肺IAC分化程度的训练组和测试组AUC分别为0.91(95%CI 0.83-0.98)和0.87(95%CI 0.72-1.00)。临床特征模型预测肺IAC分化程度的训练组和测试组AUC分别为0.75(95%CI 0.63-0.86)和0.76(95%CI 0.59-0.94)。低分化IAC中Ki-67的表达水平高于高分化IAC(P<0.001)。低分化IAC中NapsinA、TTF-1的表达水平高于高分化IAC(P<0.05)。与临床特征模型和放射组学模型相比,由性别、胸膜牵拉征和放射组学评分组成的个体化预测模型对IAC分化程度的鉴别性能最佳。Ki-67、NapsinA和TTF-1在不同分化程度的IAC中表达不同。

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