首页|结直肠侧向发育型肿瘤切除后病理诊断升级的危险因素分析及预测模型构建

结直肠侧向发育型肿瘤切除后病理诊断升级的危险因素分析及预测模型构建

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目的 探讨结直肠侧向发育型肿瘤(LST)切除后病理诊断升级的危险因素.方法 回顾性收集2018年6月至2022年12月山西省肿瘤医院收治的256例LST患者(297个病灶)的临床资料,作为建模组;收集2023年1月至2024年1月收治的125例LST患者(129个病灶),作为外部验证组.将建模组病灶根据内镜下钳夹活体组织检查术(EFB)取样标本与LST切除后组织的病理诊断对比结果将病灶分为病理无差异组和病理升级组,比较两组患者的性别、年龄、体重指数、切除前癌胚抗原水平、饮酒史、吸烟史、结直肠癌家族史、是否合并基础疾病等临床资料,以及病灶长径、病灶表面形态特征、病灶部位等内镜下特征.统计学方法采用卡方检验,切除后病理诊断升级的危险因素分析采用多因素logistic回归模型.将独立危险因素构建列线图预测模型.绘制该模型预测建模组内部抽样和外部验证组LST病灶切除后病理诊断升级的受试者操作特征曲线(ROC),以曲线下面积评价预测模型的应用价值.结果 病理升级组中有结直肠癌家族史的患者占比高于病理无差异组[38.7%(12/31)比22.2%(50/225)],差异有统计学意义(x2=4.04,P=0.045).病理升级组与病理无差异组的LST病灶大小[长径≥2 cm者分别占63.9%(23/36)和44.4%(116/261)]、表面形态特征[扁平隆起型分别占8.3%(3/36)和22.6%(59/261),颗粒均一型分别占11.1%(4/36)和28.0%(73/261),结节混合型分别占44.4%(6/36)和 24.9%(65/261),假凹陷型分别占 36.1%(13/36)和24.5%(64/261)]、病灶部位[远端结肠分别占 22.2%(8/36)和 33.3%(87/261),近端结肠分别占 16.7%(6/36)和 28.7%(75/261),直肠分别占61.1%(22/36)和37.9%(99/261)]比较,差异均有统计学意义(x2=4.80、12.62、7.08,均P<0.05).多因素logistic回归模型分析结果显示,有结直肠癌家族史[OR=2.211,95%置信区间(95%CI)1.005~4.861,P=0.049]、病灶长径≥2 cm(OR=2.212,95%CI 1.074~4.555,P=0.031)、结节混合型(OR=4.841,95%CI 1.343~17.455,P=0.016)、假凹陷型(OR=3.995,95%CI 1.084~14.721,P=0.037)、病灶位于直肠(OR=2.417,95%CI 1.024~5.705,P=0.044)均是LST切除后病理诊断升级的独立危险因素.基于上述4个危险因素构建列线图模型,建模组内部重复抽样的ROC曲线下面积为0.833(95%CI 0.752~0.913);外部验证组的ROC曲线下面积为0.848(95%CI0.736~0.960),灵敏度为0.737,特异度为0.972,最大约登指数为0.712,总准确度为0.868.结论 有结直肠癌家族史、病灶长径≥2 cm、病灶位于直肠及LST亚型为结节混合型或假凹陷型都会干扰LST病变EFB病理的准确性,导致切除后病理诊断升级.基于该4项因素的预测模型对LST切除后病理诊断升级有较好的预测效能.
Analysis of risk factors and construction of prediction model of pathological diagnosis upgrading after resection of colorectal laterally spreading tumors
Objective To investigate the risk factors affecting pathological diagnosis upgrading after resection of colorectal laterally spreading tumor(LST).Methods From June 2018 to December 2022,the clinical data of 256 patients with LST(297 lesions)admitted to Shanxi Provincial Cancer Hospital were retrospectively included as an modeling group.From January 2023 to January 2024,125 patients with LST(129 lesions)were collected as an external validation group.The pathological diagnosis of endoscopic forceps biopsy(EFB)samples and the resected LST tissue of modeling group were compared,and the patients were divided into pathological non-difference group and pathological upgrading group.The clinical data such as gender,age,body mass index(BMI),pre-resection carcinoembryonic antigen levels,drinking history,smoking history,family history of colorectal cancer,and whether complicated with underlying diseases as well as endoscopic surface morphological features such as lesion size,morphological features,and lesion location were compared between the two groups.Chi-square test was used for statistical analysis,and multivariate logistic regression analysis was used to identify the risk factors for pathological diagnosis upgrading after resection.Based on the independent risk factors,the prediction models were established and validated by nomogram.The receiver operating characteristic curve(ROC)of repeated samples within the modeling group and external validation growp was plotted,and the area under the curve(AUC)was used to evaluate the predictive value of the model.Results The proportion of patients with family history of colorectal cancer in the pathological upgrading group was higher than that of the pathological non-difference group(38.7%,12/31 vs.22.2%,50/225),and the difference was statistically significant(x2=4.04,P=0.045).There were statistically significant differences in lesion size(63.9%(23/36)and 44.4%(116/261)lesions with long diameter ≥2 cm,respectively),surface morphological characteristics(flat elevated type accounted for 8.3%(3/36)and 22.6%(59/261),granular uniform type accounted for 11.1%(4/36)and 28.0%(73/261),nodular mixed type accounted for 44.4%(6/36)and 24.9%(65/261),pseudo-depressed type accounted for 36.1%(13/36)and 24.5%(64/261)),and lesion location(distal colon accounted for 22.2%(8/36)and 33.3%(87/261),proximal colon accounted for 16.7%(6/36)and 28.7%(75/261),and rectum accounted for 61.1%(22/36)and 37.9%(99/261))between the pathological upgrading group and the pathological non-difference group(x2=4.80,12.62 and 7.08,all P<0.05).The results of multivariate logistic regression analysis showed that family history of colorectal cancer(OR=2.211,95%confidence interval(95%CI)1.005 to 4.861,P=0.049),lesion length ≥ 2 cm(OR=2.212,95%CI 1.074 to 4.555,P=0.031),nodular mixed subtype(OR=4.841,95%CI 1.343 to 17.455,P=0.016),pseudo-depressed subtype(OR=3.995,95%CI 1.084 to 14.721,P=0.037),and lesion in rectum(OR=2.417,95%CI 1.024 to 5.705,P=0.044)were independent risk factors for pathological diagnosis upgrading after LST resection.A nomogram was established based on these four risk factors,with a ROC AUC of 0.833(95%CI 0.752 to0.913).The external validation results demonstrated that the ROC AUC was 0.848(95%CI0.736 to 0.960),the sensitivity was 0.737,the specificity was 0.972,the maximum Youden index was 0.712,and the overall accuracy was 0.868.Conclusions Family history of colorectal cancer,lesion length≥2 cm,lesion in rectum,and nodular mixed or pseudo-depressed subtypes may affect the accuracy of pathological diagnosis of LST lesions by EFB,and leading to pathological diagnosis upgrading after resection.The prediction model based on these four factors has good predictive efficacy in pathological diagnosis upgrading after LST resection.

Colorectal laterally spreading tumorBiopsyRisk factor

李二峰、庞婧、张丽彬、张文斌、王峰、郭斌

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山西省肿瘤医院(中国医学科学院肿瘤医院山西医院 山西医科大学附属肿瘤医院)内镜中心,太原 030012

结直肠侧向发育型肿瘤 活体组织检查 危险因素

2024

中华消化杂志
中华医学会

中华消化杂志

CSTPCD北大核心
影响因子:1.726
ISSN:0254-1432
年,卷(期):2024.44(6)