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基于LASSO-Cox回归构建肿瘤相关髓系细胞浸润特征模型预测胃癌患者术后总生存期

Construction of a tumor-associated myeloid cell infiltration signature model based on LASSO-Cox regression for predicting postoperative overall survival in patients with gastric cancer

  • 摘要:
    目的 探讨肿瘤相关髓系细胞浸润特征对胃癌患者术后总生存期(overall survival, OS)的影响。
    方法 回顾性纳入2005年1月至2019年12月在复旦大学附属中山医院行胃癌根治术的患者,按1∶1的比例将患者随机分为训练组(n=167)和内部验证组(n=168)。选择同期在复旦大学附属中山医院厦门医院诊治的147例胃癌患者作为外部验证组(n=147)。通过免疫组织化学技术评估所有患者胃癌肿瘤组织(primary tumor, PT)、侵袭边界(invasive margin, IM)和正常组织(normal tissue, NT)18种免疫标志物的分布特征,包括11种髓系细胞标志物(CD11b、CD33、CD11c、CD14、CD15、CD16、CD68、CD86、CD163、CD206和CD66b)和7种免疫检查点分子(CD73、IDO、LAG3、PD-1、SIGLEC9、SIRPA和TIM3)。采用LASSO回归和Cox比例风险模型筛选训练组中影响胃癌患者术后OS的免疫标志物,建立术后1、3、5年OS的预测模型,将内部和外部验证组数据代入预测模型进行验证。绘制受试者工作特征(receiver operating characteristic, ROC)曲线并计算曲线下面积(area under the curve, AUC)以评价模型区分度。
    结果 在训练组中,LASSO回归和Cox比例风险模型共提取4个免疫标志物特征(CD14_PT、CD15_PT、CD206_PT和SIGLEC9_PT)构建预测模型。ROC曲线显示,模型预测胃癌患者术后1、3、5年OS的AUC分别为 0.74、0.75、0.84。内部验证组和外部验证组中模型预测胃癌患者术后1、3、5年OS的AUC分别为0.74、0.72、0.72和0.72、0.71、0.74。Cox多因素回归分析显示,风险评分为胃癌患者术后OS的独立危险因素。
    结论 基于LASSO-Cox回归构建的模型预测性能较好,能有效预测胃癌患者术后OS,可用于术后高风险胃癌患者的强化治疗依据。

     

    Abstract:
    Objective To explore the impact of tumor-associated myeloid cell infiltration signatures on postoperative overall survival (OS) in patients with gastric cancer.
    Methods A retrospective analysis was performed on patients who underwent radical gastrectomy at Zhongshan Hospital, Fudan University from January 2005 to December 2019. Patients were randomly divided into a training set (n=167) and an internal validation set (n=168) at a 1:1 ratio. Meanwhile, 147 patients with gastric cancer treated at Zhongshan Hospital (Xiamen), Fudan University during the same period were enrolled as the external validation set (n=147). Immunohistochemistry was used in all patients to evaluate the distribution characteristics of 18 immune markers in three regions of gastric cancer tissues, namely primary tumor (PT), invasive margin (IM), and normal tissue (NT). These markers include 11 myeloid cell markers (CD11b, CD33, CD11c, CD14, CD15, CD16, CD68, CD86, CD163, CD206, and CD66b) and 7 immune checkpoints (CD73, IDO, LAG3, PD-1, SIGLEC9, SIRPA, and TIM3). LASSO regression and Cox proportional hazards model were applied to screen immune markers associated with postoperative OS in gastric cancer patients, and a predictive model for 1-, 3-, and 5-year postoperative OS was established. Data from the internal and external validation set were used for internal and external verification of the predictive model. Receiver operating characteristic (ROC) curves were plotted and the area under the curve (AUC) was calculated to assess the discriminative ability of the model.
    Results In the training set, LASSO regression and Cox proportional hazards model identified 4 immune marker signatures (CD14_PT, CD15_PT, CD206_PT, and SIGLEC9_PT) to construct the predictive model. ROC curve analysis showed that the AUCs of the model for predicting 1-, 3-, and 5-year postoperative OS were 0.74, 0.75, and 0.84, respectively. When the model was applied to the internal and external validation sets, the AUCs for 1-, 3-, and 5-year postoperative OS were 0.74, 0.72, 0.72 (internal validation set) and 0.72, 0.71, 0.74 (external validation set), respectively. Cox multivariate regression analysis showed that the risk score was an independent risk factor for postoperative OS in patients with gastric cancer.
    Conclusion The model constructed based on LASSO-Cox regression exhibits good predictive performance and can effectively predict postoperative OS in gastric cancer patients, which may serve as a basis for intensive treatment of high-risk patients after surgery.

     

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