溃疡性结肠炎相关性结直肠癌的危险因素分析

Risk factors analysis of ulcerative colitis associated colorectal cancer

  • 摘要: 目的:探讨溃疡性结肠炎相关性结直肠癌(UC-CRC)的危险因素。
    方法:采用回顾性病例对照研究方法。收集2004年3月至2015年6月河南省肿瘤医院收治的536例溃疡性结肠炎(UC)患者的临床病理资料。观察指标:(1)随访结果:获得随访例数、随访时间、UC-CRC发病例数、发病年龄、UC-CRC病理学类型。(2)影响UC-CRC发生的危险因素分析:性别、发病年龄、病程、病情严重程度、疾病分型、病变范围、吸烟史、结直肠癌家族史、贫血、低蛋白血症、体质量下降、肠外表现、结肠息肉、倒灌性回肠炎、不典型增生、焦虑或抑郁状态、治疗方法、定期内镜复查。采用门诊和电话方式进行随访,了解患者病情转归情况。UC确诊后3年内,每6个月行1次肠镜检查,3年后每年行1次肠镜检查。随访时间截至2017年4月。偏态分布的计量资料采用M(范围)表示,单因素分析采用x2检验和Fisher确切概率法,多因素分析采用Logistic回归模型。
    结果:(1)随访结果:536例患者中,450例获得随访,随访时间为26.0~120.0个月,中位随访时间为76.4个月。536例患者中,随访期间16例并发UC-CRC,其中男9例,女7例;结直肠癌发病年龄为14~78岁,平均发病年龄44岁;病理学类型:右半结肠高分化腺癌5例,左半结肠高中分化腺癌3例,左半结肠印戒细胞癌2例,直肠中分化管状腺癌3例,直肠高分化乳头状腺癌2例,恶性淋巴瘤1例。(2)影响UC-CRC发生的危险因素分析:单因素分析结果显示:患者病程、病变范围、结肠息肉、不典型增生是影响UC-CRC发生的危险因素(x2=14.848,18.885,10.554,P<0.05)。多因素分析结果显示:病程>10年、病变范围累及全结肠、结肠息肉、不典型增生是影响UC-CRC发生的独立危险因素(OR=12.893,17.847,7.326,19.742,95%可信区间:1.726~74.337,1.445~89.793,1.263~43.128,3.625~96.524,P<0.05)。
    结论:病程>10年、病变范围累及全结肠、伴有不典型增生的结肠息肉是UC进展为UC-CRC的独立危险因素。

     

    Abstract: Objective:To explore the risk factors of ulcerative colitisassociated colorectal cancer (UC-CRC).
    Methods:The retrospective casecontrol study was conducted. The clinicopathological data of 536 patients with ulcerative colitis (UC) who were admitted to the Henan Tumor Hospital from March 2004 to June 2015 were collected. Observation indicators: (1) followup results: cases with followup, followup time, cases of UC-CRC, age of onset, pathological type of UC-CRC; (2) risk factors analysis affecting occurrence of UC-CRC: gender, age of onset, course of disease, severity of disease, disease classification, extent of lesion, smoking history, family history of colorectal cancer, anemia, hypoproteinemia, body weight loss, extraintestinal manifestations, colonic polyps, backwash ileitis, atypical hyperplasia, anxiety or depression, treatment method and regular endoscopy reexamination. Followup using outpatient examination and telephone interview was performed to detect prognosis of patients up to April 2017. Patients underwent colonoscopy once every 6 months within 3 years after diagnosis and once every 1 year after 3 years. Measurement data with skewed distribution were described as M (range). The univariate analysis was done using the chisquare test and Fisher exact probability. The multivariate analysis was done using the Logistic regression model.
    Results:(1) Followup results: of 536 patients, 450 were followed up for 26.0-120.0 months, with a median time of 76.4 months. During the followup, 16 patients were complicated with UC-CRC, including 9 males and 7 females. Age of onset of colorectal cancer was 14-78 years,with an average age of onset of 44 years. Pathological type: highdifferentiated right colon adenocarcinoma was detected in 5 patients, highand moderatedifferentiated left colon adenocarcinoma in 3 patients, left colon signetring cell carcinoma in 2 patients, moderatedifferentiated rectal tubular adenocarcinoma in 3 patients, highdifferentiated rectal papillary adenocarcinoma in 2 patients and malignant lymphoma in 1 patient. (2) Risk factors analysis affecting occurrence of UC-CRC: the results of univariate analysis showed that course of disease, extent of lesion, colonic polyps and atypical hyperplasia were risk factors affecting occurrence of UC-CRC (x2=14.848, 18.885, 10.554, P<0.05). The results of multivariate analysis showed that course of disease >10 years, lesion involving the whole colon, colonic polyps and atypical hyperplasia were independent risk factors affecting occurrence of UC-CRC (OR=12.893, 17.847, 7.326, 19.742, 95% confidence interval: 1.726-74.337, 1.445-89.793, 1.263-43.128, 3.625-96.524, P<0.05).
    Conclusion:The course of disease >10 years, lesion involving the whole colon, atypical hyperplasia and colonic polyps are independent risk factors affecting occurrence of UC-CRC.

     

/

返回文章
返回