Li Jian, Jiang Tao, Ren Zeng-Ci, Wang Zhen-Lei, Zhang Peng-Jun, Xiang Guo-An
The Second School of Clinical Medicine, Southern Medical University, Guangzhou 510515, Guangdong Province, China.
Department of General Surgery, Guangdong Second Provincial General Hospital, Guangzhou 510317, Guangdong Province, China.
World J Gastrointest Surg. 2022 Aug 27;14(8):833-848. doi: 10.4240/wjgs.v14.i8.833.
Colorectal cancer (CRC) is the third most common cancer worldwide, and it is the second leading cause of death from cancer in the world, accounting for approximately 9% of all cancer deaths. Early detection of CRC is urgently needed in clinical practice.
To build a multi-parameter diagnostic model for early detection of CRC.
Total 59 colorectal polyps (CRP) groups, and 101 CRC patients (38 early-stage CRC and 63 advanced CRC) for model establishment. In addition, 30 CRP groups, and 62 CRC patients (30 early-stage CRC and 32 advanced CRC) were separately included to validate the model. 51 commonly used clinical detection indicators and the 4 extrachromosomal circular DNA markers , , and that we screened earlier. Four multi-parameter joint analysis methods: binary logistic regression analysis, discriminant analysis, classification tree and neural network to establish a multi-parameter joint diagnosis model.
Neural network included carcinoembryonic antigen (CEA), ischemia-modified albumin (IMA), sialic acid (SA), and lipoprotein a (LPa) was chosen as the optimal multi-parameter combined auxiliary diagnosis model to distinguish CRP and CRC group, when it differentiated 59 CRP and 101 CRC, its overall accuracy was 90.8%, its area under the curve (AUC) was 0.959 (0.934, 0.985), and the sensitivity and specificity were 91.5% and 82.2%, respectively. After validation, when distinguishing based on 30 CRP and 62 CRC patients, the AUC was 0.965 (0.930-1.000), and its sensitivity and specificity were 66.1% and 70.0%. When distinguishing based on 30 CRP and 32 early-stage CRC patients, the AUC was 0.960 (0.916-1.000), with a sensitivity and specificity of 87.5% and 90.0%, distinguishing based on 30 CRP and 30 advanced CRC patients, the AUC was 0.970 (0.936-1.000), with a sensitivity and specificity of 96.7% and 86.7%.
We built a multi-parameter neural network diagnostic model included CEA, IMA, SA, and LPa for early detection of CRC, compared to the conventional CEA, it showed significant improvement.
结直肠癌(CRC)是全球第三大常见癌症,也是全球癌症死亡的第二大主要原因,约占所有癌症死亡人数的9%。临床实践中迫切需要早期检测CRC。
构建用于早期检测CRC的多参数诊断模型。
共纳入59个大肠息肉(CRP)组和101例CRC患者(38例早期CRC和63例晚期CRC)用于模型建立。此外,分别纳入30个CRP组和62例CRC患者(30例早期CRC和32例晚期CRC)用于验证模型。51个常用临床检测指标以及我们先前筛选出的4个染色体外环状DNA标记物 、 、 和 。采用四种多参数联合分析方法:二元逻辑回归分析、判别分析、分类树和神经网络建立多参数联合诊断模型。
包含癌胚抗原(CEA)、缺血修饰白蛋白(IMA)、唾液酸(SA)、 和脂蛋白a(LPa)的神经网络被选为区分CRP和CRC组的最佳多参数联合辅助诊断模型,在区分59个CRP和101例CRC时,其总体准确率为90.8%,曲线下面积(AUC)为0.959(0.934,0.985),敏感性和特异性分别为91.5%和82.2%。验证后,基于30个CRP和62例CRC患者进行区分时,AUC为0.965(0.930 - 1.000),其敏感性和特异性分别为66.1%和70.0%。基于30个CRP和32例早期CRC患者进行区分时,AUC为0.960(0.916 - 1.000),敏感性和特异性分别为87.5%和90.0%,基于30个CRP和30例晚期CRC患者进行区分时,AUC为0.970(0.936 - 1.000),敏感性和特异性分别为96.7%和86.7%。
我们构建了一个包含CEA、IMA、SA、 和LPa的多参数神经网络诊断模型用于早期检测CRC,与传统的CEA相比有显著改善。