Imperial College London, Charing Cross Hospital, London, United Kingdom.
PREDICT Center for Molecular Prediction of Inflammatory Bowel Disease, Department of Clinical Medicine, Aalborg University, Copenhagen, Denmark.
Clin Transl Gastroenterol. 2022 Jul 1;13(7):e00513. doi: 10.14309/ctg.0000000000000513. Epub 2022 Jun 15.
There is increased risk of several malignancies in inflammatory bowel disease (IBD). However, evidence regarding risk of cervical cancer in IBD is conflicting. We aimed to investigate the risk of cervical cancer in IBD by undertaking a systematic review and meta-analysis of unselected, population-based studies.
MEDLINE, EMBASE, and Cochrane Library were searched using Medical Subject Heading terms, and 2 reviewers independently screened results. Pooled hazard ratios (HRs) were calculated using random effects model meta-analysis for risk of cervical cancer in IBD. Subgroup meta-analysis was undertaken to assess risk of cervical cancer by IBD subtype (Crohn's disease and ulcerative colitis), treatment exposure, and grade of lesion.
We screened 1,393 articles to identify 5 population-based studies, including 74,310 patients with IBD and 2,029,087 reference patients, across 5 different countries. Pooled random effects model meta-analysis of these studies did not show statistically significant increased risk for cervical cancer in IBD compared with reference populations (HR: 1.24; 95% confidence interval [CI]: 0.94-1.63). Meta-analysis by grade of lesion showed increased risk of low-grade cervical lesions (HR: 1.15; 95% CI: 1.04-1.28). Meta-analysis by disease subtype indicated no statistically significant increased risk in Crohn's disease (HR: 1.36; 95% CI: 0.83-2.23) or ulcerative colitis (HR: 0.95; 95% CI: 0.72-1.25) or in patients treated with antitumor necrosis factor (HR: 1.19; 95% CI: 0.64-2.21) or thiopurines (HR: 0.96; 95% CI: 0.60-1.50).
This meta-analysis of high-quality, unselected population-based studies shows no statistically significant increased risk of cervical cancer in patients with IBD. There is, however, increased risk of low-grade cervical lesions compared with the general population.
炎症性肠病(IBD)患者发生多种恶性肿瘤的风险增加。然而,关于 IBD 患者宫颈癌风险的证据存在争议。我们旨在通过对未选择的基于人群的研究进行系统评价和荟萃分析来调查 IBD 患者宫颈癌的风险。
使用医学主题词,在 MEDLINE、EMBASE 和 Cochrane 图书馆中进行检索,并由 2 位审阅者独立筛选结果。使用随机效应模型荟萃分析计算 IBD 患者宫颈癌风险的合并危险比(HR)。进行亚组荟萃分析,以评估 IBD 亚型(克罗恩病和溃疡性结肠炎)、治疗暴露和病变程度对宫颈癌风险的影响。
我们筛选了 1393 篇文章,确定了 5 项基于人群的研究,包括来自 5 个不同国家的 74310 例 IBD 患者和 2029087 例对照患者。对这些研究的合并随机效应模型荟萃分析显示,与对照人群相比,IBD 患者宫颈癌的风险没有统计学意义的增加(HR:1.24;95%置信区间[CI]:0.94-1.63)。根据病变程度的荟萃分析显示,低级别宫颈病变的风险增加(HR:1.15;95%CI:1.04-1.28)。疾病亚型的荟萃分析表明,克罗恩病(HR:1.36;95%CI:0.83-2.23)或溃疡性结肠炎(HR:0.95;95%CI:0.72-1.25)或使用抗肿瘤坏死因子(HR:1.19;95%CI:0.64-2.21)或硫唑嘌呤(HR:0.96;95%CI:0.60-1.50)治疗的患者中,风险无统计学意义的增加。
这项高质量、未选择的基于人群的研究荟萃分析显示,IBD 患者宫颈癌的风险没有统计学意义的增加。然而,与普通人群相比,低级别宫颈病变的风险增加。