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克罗恩病相关结直肠癌:一项斯堪的纳维亚基于人群的队列研究。

Colorectal cancer in Crohn's disease: a Scandinavian population-based cohort study.

机构信息

Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden; Department of Clinical Science and Education Södersjukhuset, Karolinska Institutet, Stockholm, Sweden; Sachs' Children and Youth Hospital, Stockholm South General Hospital, Stockholm, Sweden.

Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark; Department of Surgery, Randers Regional Hospital, Randers, Denmark.

出版信息

Lancet Gastroenterol Hepatol. 2020 May;5(5):475-484. doi: 10.1016/S2468-1253(20)30005-4. Epub 2020 Feb 14.

Abstract

BACKGROUND

Crohn's disease is a risk factor for colorectal cancer (CRC). However, available studies reflect older treatment and surveillance strategies, and most have assessed risks for incident CRC without taking surveillance and lead-time bias into account. Such biases can be accounted for by assessing CRC incidence by tumour stage and CRC mortality by tumour stage. We aimed to assess rates of incident CRC and CRC mortality among patients with Crohn's disease compared with the general population.

METHODS

For this nationwide register-based cohort study, we used International Classification of Disease codes in national patient registers and pathology reports to identify incident cases of Crohn's disease. In Denmark we searched for incident cases between January, 1977, and December, 2011, and in Sweden between January, 1969, and December, 2017. For each patient with Crohn's disease, we identified up to ten reference individuals in national population registers and matched them by sex, age, calendar year, and place of residence. Matched reference individuals had to be alive and free of inflammatory bowel disease at the start of follow-up of index patients with Crohn's disease, and stopped contributing to reference person-years if they were diagnosed with inflammatory bowel disease. Our main outcome was death from CRC (main or contributory cause of death) as captured in the cause-of-death registers. Our secondary outcome was incident CRC, as defined by the cancer registers. We used Cox regression to estimate hazard ratios (HRs) for incident CRC and CRC mortality, taking tumour stage into account. We used a series of Cox models to estimate cause-specific HRs of the different competing outcomes (CRC diagnosis, CRC death, and other causes of death) and adjusted for tumour stage at CRC diagnosis.

FINDINGS

During the 1969-2017 study period, we identified 47 035 patients with incident Crohn's disease (13 056 in Denmark and 33 979 in Sweden) and 463 187 matched reference individuals. During follow-up, 296 (0·47 per 1000 person-years) CRC deaths occurred among individuals with Crohn's disease compared with 1968 (0·31 per 1000 person-years) in reference individuals, corresponding to an overall adjusted HR of 1·74 (1·54-1·96). 499 (0·82 per 1000 person-years) cases of incident CRC were diagnosed in patients with Crohn's disease compared with 4084 (0·64 per 1000 person-years) cases in reference individuals, corresponding to an overall adjusted HR of 1·40 (95% CI 1·27-1·53). Patients with Crohn's disease who were diagnosed with CRC were at increased risk of CRC mortality compared with reference individuals also diagnosed with CRC (HR 1·42 [1·16-1·75] when adjusted for tumour stage), and tumour stage at CRC diagnosis did not differ between groups (p=0·27). Patients with Crohn's disease who had follow-up of 8 years or longer or who were diagnosed with primary sclerosing cholangitis (PSC) and hence were potentially eligible for CRC surveillance had an increased overall risk of CRC death (HR 1·40 [1·16-1·68]) or CRC diagnosis (HR 1·12 [0·98-1·28]). However, in patients potentially eligible for CRC surveillance we only found significantly increased risks in patients diagnosed with Crohn's disease before the age of 40 years, patients with disease activity in the colon only, or patients with PSC.

INTERPRETATION

Patients with Crohn's disease are at increased risk of CRC diagnosis and CRC death. Patients with Crohn's disease who have CRC have a higher mortality than patients without Crohn's disease who are also diagnosed with CRC. CRC surveillance should likely be focused on patients diagnosed with Crohn's disease before the age of 40 years, on patients with colon inflammation, and on those who have PSC.

FUNDING

Swedish Medical Society, Karolinska Institutet, Regional Agreement on Medical Training and Clinical Research between Stockholm County Council and Karolinska Institutet (ALF), Forte Foundation, Swedish Cancer Foundation, and Independent Research Fund Denmark.

摘要

背景

克罗恩病是结直肠癌(CRC)的一个风险因素。然而,现有研究反映了较旧的治疗和监测策略,并且大多数研究都是在没有考虑到监测和领先时间偏倚的情况下评估CRC 发病风险的。通过按肿瘤阶段评估 CRC 发病和 CRC 死亡率,可以考虑到这些偏差。我们的目的是评估与一般人群相比,克罗恩病患者的 CRC 发病和 CRC 死亡率。

方法

本研究为全国基于登记的队列研究,我们使用国家患者登记和病理报告中的国际疾病分类代码来确定克罗恩病的新发病例。在丹麦,我们于 1977 年 1 月至 2011 年 12 月期间进行了病例搜索,在瑞典,我们于 1969 年 1 月至 2017 年 12 月期间进行了病例搜索。对于每一例克罗恩病患者,我们在国家人群登记册中确定了多达 10 名参照个体,并按性别、年龄、日历年份和居住地进行了匹配。匹配的参照个体必须在克罗恩病患者的随访开始时存活且没有炎症性肠病,并且如果他们被诊断为炎症性肠病,则停止为参照人年做出贡献。我们的主要结局是结直肠癌死亡(主要或辅助死因),由死因登记册记录。我们的次要结局是癌症登记册定义的 CRC 发病。我们使用 Cox 回归来估计发病风险比(HR)和 CRC 死亡率,考虑到肿瘤分期。我们使用一系列 Cox 模型来估计不同竞争结果(CRC 诊断、CRC 死亡和其他死亡原因)的特定原因 HR,并按 CRC 诊断时的肿瘤分期进行调整。

结果

在 1969 年至 2017 年的研究期间,我们确定了 47356 例新发病例的克罗恩病患者(丹麦 13056 例,瑞典 33979 例)和 463187 名匹配的参照个体。在随访期间,476 例(每 1000 人年 0.47 例)患有克罗恩病的患者发生 CRC 死亡,而参照个体中 1968 例(每 1000 人年 0.31 例),总调整 HR 为 1.74(1.54-1.96)。在克罗恩病患者中,499 例(每 1000 人年 0.82 例)诊断为 CRC,而参照个体中 4084 例(每 1000 人年 0.64 例),总调整 HR 为 1.40(95%CI 1.27-1.53)。与参照个体中同样诊断为 CRC 的患者相比,诊断为 CRC 的克罗恩病患者发生 CRC 死亡的风险更高(调整肿瘤分期后 HR 为 1.42 [1.16-1.75]),且两组的肿瘤分期无差异(p=0.27)。对于随访时间为 8 年或更长时间的患者,或被诊断为原发性硬化性胆管炎(PSC)且因此可能有资格进行 CRC 监测的患者,CRC 死亡或 CRC 诊断的总体风险增加(HR 1.40 [1.16-1.68])。然而,在有资格进行 CRC 监测的患者中,我们仅发现年龄在 40 岁以下、结肠炎症仅在结肠中、或患有 PSC 的患者发生 CRC 发病和 CRC 死亡的风险显著增加。

解释

克罗恩病患者发生 CRC 诊断和 CRC 死亡的风险增加。患有 CRC 的克罗恩病患者的死亡率高于没有患有 CRC 的患者。CRC 监测可能需要集中在年龄在 40 岁以下、结肠炎症、以及患有 PSC 的患者。

资金

瑞典医学协会、卡罗林斯卡学院、斯德哥尔摩县议会与卡罗林斯卡学院之间的医疗培训和临床研究区域协议(ALF)、Forte 基金会、瑞典癌症基金会和丹麦独立研究基金会。

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