远端或近端早期胃癌组织病理学特征差异及黏膜下层浸润的危险因素分析
Analysis of histopathological features and risk factors of submucosal invasion in distal or proximal early gastric cancer
投稿时间:2025-03-04  修订日期:2025-05-13
DOI:
中文关键词:  近端位置  早期胃癌  黏膜下层浸润  危险因素
英文关键词:proximal location  early gastric cancer  submucosal invasion  risk factor
基金项目:湖北省卫生健康委员会科研项目(WJ2021M070)
作者单位邮编
赵建红* 长江大学附属黄冈市中心医院 438000
岑红兵 长江大学附属黄冈市中心医院 
杨志勇 长江大学附属黄冈市中心医院 
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中文摘要:
      目的 探讨远端或近端早期胃癌(EGC)组织病理学特征差异及黏膜下层浸润的危险因素。方法回顾性队列包括2020年3月至2024年5月在本院接受手术或内镜黏膜下剥离术(ESD)的EGC患者,按照肿瘤位置1:1匹配,近端组和远端组各69例。主要结局为黏膜下层浸润,并构建列线图预测模型;次要结局为近端和远端组织病理学特征差异。结果 近端组GC患者弥漫型、黏膜下层浸润和外科手术患者比例显著高于远端组(P<0.05)。与黏膜层浸润组相比,黏膜下层浸润组肿瘤直径以及近端位置、凹陷型、未分化、弥漫型和脉管侵犯患者比例显著升高(P<0.05)。经LASSO回归筛选和多变量Logistic回归模型分析,结果显示近端位置、肿瘤直径≥20mm、脉管侵犯是黏膜下层浸润的独立危险因素(P<0.05)。通过绘制列线图对4个危险因素的重要性进行排序,结果显示,EGC患者黏膜下层浸润的危险因素依次为脉管侵犯、近端GC、肿瘤直径≥20mm和凹陷型GC。ROC曲线分析,列线图模型预测黏膜下层浸润的AUC为0.77(95%CI:0.70~0.85),同时Hosmer-Lemeshow拟合优度检验显示该模型拟合良好(χ2=4.862,P=0.433)。经临床决策曲线分析,当高风险阈值为0.05~0.9时,列线图模型预测黏膜下层浸润具有较好的净临床收益。结论 与远端EGC相比,近端EGC患者弥漫型以及黏膜下层浸润的比例更高。近端位置、凹陷型、肿瘤直径和脉管侵犯是EGC黏膜下层浸润的危险因素。因此,近端EGC因其较高的黏膜下层浸润风险,需要慎重的治疗决策。
英文摘要:
      ObjGCtive To investigate the histopathological features and risk factors of submucosal invasionin distal or proximal early gastric cancer (EGC). Methods The retrospective cohort includes EGC patients who underwent surgery or endoscopic submucosal dissection (ESD) at our hospital from March 2020 to May 2024, matched 1:1 according to tumor location, with 69 patients in the proximal group and 69 patients in the distal group. The main outcome was submucosal infiltration, and a column chart prediction model was constructed; The secondary outcome was the difference in histopathological features between proximal and distal tissues. Results The proportion of GC patients with diffuse, submucosal invasionand surgical operation in proximal group was significantly higher than that in distal group (P<0.05). Compared with the mucosa invasion group, the tumor diameter and proximal location, the proportion of patients with sunken, undifferentiated, diffuse and vascular invasion were significantly increased in the submucosa invasion group (P<0.05). LASSO regression screening and multivariate Logistic regression model analysis showed that proximal location, tumor diameter ≥20mm and vascular invasion were independent risk factors for submucosal invasion (P<0.05). The results showed that the risk factors for submucosal invasion in EGC patients were vascular invasion, proximal GC, tumor diameter ≥20mm, and sunken GC. ROC curve analysis showed that the AUC of submucosal invasionpredicted by the nomogram model was 0.77 (95%CI: 0.70-0.85), and the Hosmer-Lemeshow goodness of fit test showed that the model was well fitted (χ2=4.862, P=0.433). According to clinical decision curve analysis, when the high risk threshold was 0.05 ~ 0.9, the nematic model predicted that the submucosal invasionhad a good net clinical benefit. Conclusion Compared with distal EGC, patients with proximal EGC have a higher proportion of diffuse and submucosal infiltration. Proximal location, concave type, tumor diameter and vascular invasion were risk factors for EGC submucosal invasion. Therefore, proximal EGC requires careful treatment decisions due to its higher risk of submucosal invasion.
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