机构地区:[1]中国医学科学院北京协和医学院、北京协和医院基本外科结直肠专业组,北京100730 [2]中国医学科学院北京协和医学院、北京协和医院病理科,北京100730
出 处:《中华胃肠外科杂志》2024年第6期591-599,共9页Chinese Journal of Gastrointestinal Surgery
基 金:中国医学科学院医学与健康科技创新工程项目(2022⁃I2M⁃C&T⁃A⁃001,2023⁃I2M⁃C&T⁃B⁃026)。
摘 要:目的分析非转移性结肠癌不同肿瘤位置(左半结肠或右半结肠)患者的临床病理特征及生存的差异,探讨肿瘤位置和错配修复状态(MMR)对生存的影响。方法采用回顾性队列研究的方法。检索北京协和医院结直肠外科结肠癌前瞻性登记数据库2016年1月至2020年8月期间,接受根治性切除、且病理检查证实为非转移性结肠腺癌患者的病例资料和随访信息。将起源于中肠,位于回盲部、升结肠和横结肠近2/3的肿瘤定义为右半结肠癌;而将起源于后肠,位于横结肠远1/3、降结肠和乙状结肠的肿瘤定义为左半结肠癌。使用χ^(2)检验或Mann⁃Whitney U检验比较两组患者临床病理特征的差异,使用Kaplan⁃Meier曲线和Log⁃rank检验进行两组患者的生存分析并比较组间的无病生存率(DFS)和总体生存率(OS)。使用Cox回归分析生存的影响因素,使用倾向性评分匹配以调整混杂后再进行生存分析。结果共纳入856例结肠癌患者,其中肿瘤TNM分期Ⅰ期129例(15.1%),Ⅱ期391例(45.7%),Ⅲ期336例(39.3%);错配修复缺陷(dMMR)139例(16.2%)。左半结肠癌442例(51.6%,左半结肠癌组),右半结肠癌414例(48.4%,右半结肠癌组)。相比右半结肠癌,左半结肠癌患者的男性比例高[62.0%(274/442)比54.1%(224/414),χ^(2)=5.462,P=0.019],中位体质指数也高[24.2(21.9,26.6)kg/m2比23.2(21.3,25.5)kg/m2,U=78789.0,P<0.001],高、中分化腺癌比例[93.2%(412/442)比83.1%(344/414),χ^(2)=22.266,P<0.001]更高;dMMR状态[9.0%(40/442)比23.9%(99/414),χ^(2)=34.721,P<0.001]和合并脉管侵犯[24.0%(106/442)比30.2%(125/414),χ^(2)=4.186,P=0.041]比例更低。所有患者中位随访时间48(33,59)个月。Log⁃rank检验结果显示,左半结肠癌组患者与右半结肠癌组患者的DFS(P=0.668)和OS(P=0.828)差异无统计学意义。多因素Cox回归分析发现,dMMR是结肠癌患者DFS的独立保护因素(HR=0.419,95%CI:0.204~0.862,P=0.018);T3~4(HR=2.178,95%CI:1.089~4.359,P=0.028)、N+(HR=2.1Objective To analyze the differences in clinicopathological features of colon cancers and survival between patients with right-versus left-sided colon cancers.Methods This was a retrospective cohort study.Information on patients with colon cancer from January 2016 to August 2020 was collected from the prospective registry database at Peking Union Medical College Hospital.Primary tumors located in the cecum,ascending colon,and proximal two‐thirds of the transverse colon were defined as right-sided colon cancers(RCCs),whereas primary tumors located in the distal third of the transverse colon,descending colon,or sigmoid colon were defined as left‐sided colon cancers(LCCs).Clinicopathological features were compared using theχ^(2)test or Mann‐Whitney U test.Survival was estimated by Kaplan‐Meier curves and the log‐rank test.Factors that differed significantly between the two groups were identified by multivariate survival analyses performed with the Cox proportional hazards function.One propensity score matching was performed to eliminate the effects of confounding factors.Results The study cohort comprised 856 patients,with TNM Stage I disease,391(45.7%)with Stage II,and 336(39.3%)with Stage III,including 442(51.6%)with LCC and 414(48.4%)with RCC and 129(15.1%).Defective mismatch repair(dMMR)was identified in 139 patients(16.2%).Compared with RCC,the proportion of men(274/442[62.0%]vs.224/414[54.1%],χ^(2)=5.462,P=0.019),body mass index(24.2[21.9,26.6]kg/m2 vs.23.2[21.3,25.5]kg/m2,U=78,789.0,P<0.001),and well/moderately differentiated cancer(412/442[93.2%]vs.344/414[83.1%],χ^(2)=22.266,P<0.001)were higher in the LCC than the RCC group.In contrast,the proportion of dMMR(40/442[9.0%]vs.99/414[23.9%],χ^(2)=34.721,P<0.001)and combined vascular invasion(106/442[24.0%]vs.125/414[30.2%],χ^(2)=4.186,P=0.041)were lower in the LCC than RCC group.The median follow‐up time for all patients was 48(range 33,59)months.The log‐rank test revealed no significant differences in disease-free survival(DFS)(P=0.668)or ov
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