早发性结直肠癌的临床病理特征

Clinical characteristics of early-onset colorectal cancer

  • 摘要:
    目的 探讨早发性结直肠癌的临床病理特征。
    方法 采用回顾性描述性研究方法。收集2010年1月1日至2019年12月31日美国监测、流行病学和最终结果(SEER)数据库59 206例结直肠癌患者的临床病理资料;男33 213例,女25 993例;年龄为(50±7)岁。观察指标:(1)结直肠癌患者人口学和肿瘤学特征。(2)早发性和晚发性结直肠癌的临床病理特征比较。正态分布的计量资料以x±s表示,组间比较采用t检验;偏态分布的计量资料以MQ1,Q3)表示,多组间比较采用Kruskal⁃Wallis H检验。计数资料以绝对数表示,多组间比较采用χ2检验。等级资料比较采用非参数H检验。对早发性结直肠癌以年龄进行分段,分类变量的缺失数据设置为未知。
    结果 (1)结直肠癌患者人口学和肿瘤学特征。59 206例患者中,早发性和晚发性结直肠癌分别为23 104例和36 102例。59 206例患者中,13~29岁1 041例,30~34岁1 740例,35~39岁3 288例,40~44岁6 050例,45~49岁10 985例,50~54岁15 303例,55~59岁20 799例。(2)早发性和晚发性结直肠癌的临床病理特征比较。①早发性和晚发性结直肠癌患者性别、肿瘤位置、肿瘤分化程度、肿瘤组织学类型、肿瘤TNM分期、肿瘤T分期、肿瘤N分期、肿瘤M分期、术前癌胚抗原、神经浸润、癌结节、肿瘤长径比较,差异均有统计学意义(P<0.01)。进一步分析结果显示:6 350例早发性右半结肠癌患者肿瘤位置位于回盲部、升结肠、结肠肝区、横结肠分别为2 329、2 139、579、1 303例;11 361例晚发性右半结肠癌患者上述指标分别为4 563、3 945、902、1 951例;两者比较,差异有统计学意义(χ²=114.27,P<0.01)。10 742例早发性左半结肠患者肿瘤位置位于结肠脾区、降结肠、乙状结肠、直肠‑乙状结肠交界分别为553、1 354、6 404、2 431例;15 941例晚发性左半结肠癌患者上述指标分别为865、1 798、9 668、3 610例;两者比较,差异有统计学意义(χ²=35.60,P<0.01)。②23 104例早发性结直肠癌患者中,年龄为13~29岁、30~34岁、35~39岁、40~44岁、45~49岁分别为1 041、1 740、3 288、6 050、10 985例。不同年龄阶段早发性结直肠癌患者的性别、肿瘤分化程度、肿瘤组织学类型、肿瘤TNM分期、肿瘤T分期、肿瘤N分期、术前癌胚抗原、神经浸润、癌结节、肿瘤长径比较,差异均有统计学意义(P<0.01)。进一步分析结果显示:6 350例早发性右半结肠癌患者中,年龄为13~29岁患者肿瘤位置位于回盲部、升结肠、结肠肝区、横结肠分别为91、117、45、69例;年龄为30~34岁,35~39岁,40~44岁,45~49岁患者上述指标分别为165、136、47、115例,304、313、93、201例,614、535、151、330例,1 155、1 038、243、588例;5者比较,差异有统计学意义(H=36.63,P<0.01)。10 742例早发性左半结肠癌患者中,年龄为13~29岁患者肿瘤位置位于结肠脾区、降结肠、乙状结肠、直肠‑乙状结肠交界分别为32、83、260、95例;年龄为30~34岁,35~39岁,40~44岁,45~49岁患者上述指标分别为53、112、452、171例,95、230、867、342例,149、337、1 702、665例,224、592、3 123、1 158例;5者比较,差异有统计学意义(H=47.84,P<0.01)。
    结论 与晚发性结直肠癌比较,早发性结直肠癌肿瘤发生位置更多位于左半结肠和直肠,肿瘤分化程度为低分化和未分化,组织学类型为黏液腺癌,肿瘤TNM分期为Ⅲ期和Ⅳ期,神经浸润及癌结节比例均更高,且肿瘤长径更大。不同年龄段早发性结直肠癌患者,肿瘤临床病理特征也存在差异。

     

    Abstract:
    Objective To investigate the clinicopathological characteristics of early‑onset colorectal cancer.
    Methods The retrospective and descriptive study was conducted. The clincopatholo-gical data of 59 206 patients with colorectal cancer in the Surveillance, Epidemiology, and End Results Program of the United States of America From January 1,2010 to December 31,2019 were collected. There were 33 213 males, 25 993 males, aged (50±7)years. Observation indicators: (1) demographic and oncological characteristics of colorectal cancer patients; (2) comparison of clinico-pathological characteristics between early‑onset and late‑onset colorectal cancer. Measurement data with normal distribution were represented as Mean±SD, and comparison between groups was conducted using the t test. Measurement data with skewed distribution were represented as M(Q1,Q3), and comparison among groups was conducted using the Kruskal‑Wallis H test. Count data were described as absolute numbers, and comparison among groups was conducted using the chi-square test. Comparison of ordinal data was conducted using the non-parameter H test. Patients with early-onset colorectal cancer were segmented by age, and missing data for categorical variables is set as unknown.
    Results (1) Demographic and oncological characteristics of colorectal cancer patients. Of 59 206 patients, there were 23 104 cases with early‑onset colorectal cancer and 36 102 cases with late‑onset colorectal cancer, and cases aged 13-29 years, cases aged 30-34 years, cases aged 35-39 years, cases aged 40-44 years, cases aged 45-49 years, cases aged 55-59 years were 1 041, 1 740, 3 288, 6 050, 10 985, 15 303,20 799, respectively. (2) Comparison of clinicopathological charac-teristics between early‑onset and late‑onset colorectal cancer. ① There were significant differences in gender, tumor location, degree of tumor differentiation, tumor histological type, tumor TNM staging, tumor T staging, tumor N staging, tumor M staging, preoperative carcinoembryonic antigen (CEA), perineural invasion, cancer nodule, tumor diameter between patients with early‑onset and late-onset colorectal cancer (P<0.01). Results of further analysis showed that cases with tumor located in ileocecal region, ascending colon, colon liver region, transverse colon were 2 329, 2 139, 579, 1 303 in the 6 350 patients with early‑onset right colon cancer. The above indicators were 4 563, 3 945, 902, 1 951 in the 11 361 patients with late‑onset right colon cancer. There was a significant difference in the above indicators between the two groups of patients (χ²=114.27, P<0.01). Cases with tumor located in splenic region of the colon, descending colon, sigmoid colon, rectum sigmoid junction were 553, 1 354, 6 404, 2 431 in the 10 742 patients with early‑onset left colon cancer. The above indicators were 865, 1 798, 9 668, 3 610 in the 15 941 patients with late‑onset left colon cancer. There was a significant difference in the above indicators between the two groups of patients (χ²=35.60, P<0.01). ②Of 23 104 patients with early‑onset colorectal cancer, cases aged 13-29 years, cases aged 30-34 years, cases aged 35-39 years, cases aged 40-44 years, cases aged 45-49 years were 1 041, 1 740, 3 288, 6 050, 10 985, respectively. There were significant differences in gender, degree of tumor differentiation, tumor histological type, tumor TNM staging, tumor T staging, tumor N staging, pre-operative CEA, perineural invasion, cancer nodule, tumor diameter among patients of different age groups (P<0.01). Results of further analysis showed that cases with tumor located in ileocecal region, ascending colon, colon liver region, and transverse colon were 91, 117, 45, 69 in the 6 350 early-onset right colorectal cancer patients aged 13-29 years. The above indicators were 165, 136, 47, 115, 304, 313, 93,201, 614, 535, 151, 330, 1 155, 1 038, 243, 588 in early‑onset right colorectal cancer patients aged 30-34, 35-39, 40-44, 45-49 years, respectively. There was a significant difference in the above indicators among the five groups of patients (H=36.63, P<0.01). Cases with tumor located in splenic region of the colon, descending colon, sigmoid colon, rectum sigmoid junction were 32, 83, 260, 95 in the 10 742 early‑onset left colorectal cancer patients aged 13-29 years. The above indica-tors were 53, 112, 452, 171, 95, 230, 867, 342, 149, 337, 1 702, 665, 224, 592, 3 123, 1 158 in the 10 742 early‑onset left colorectal cancer patients aged 30-34, 35-39, 40-44, 45-49 years, respectively. There was a significant difference in the above indicators among the five groups of patients (H=47.84, P<0.01).
    Conclusions Compared with late‑onset colorectal cancer, early‑onset colorectal cancer are more likely to occur in the left colon and rectum, with poorly differentiated and undifferentiated tumors, histological type of mucinous adenocarcinoma, TNM staging of stage Ⅲ and Ⅳ, higher proportion of nerve infiltration and cancer nodules, and larger tumor diameter. There are significant differences in clinicopathological characteristics of tumors among patients with early-onset colorectal cancer of different age groups.

     

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