Allegretti Jessica R, Barnes Edward L, Cameron Anna
*Department of Medicine, Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Boston, Massachusetts; and †Department of Gynecologic Oncology, University of Calgary, Tom Baker Cancer Care, Foothills Medical Center, Alberta, Canada.
Inflamm Bowel Dis. 2015 May;21(5):1089-97. doi: 10.1097/MIB.0000000000000338.
Immunosuppression is a mainstay of therapy for both induction and maintenance of remission for inflammatory bowel disease (IBD). Women who are chronically immunosuppressed have been shown to be at higher risk of developing cervical high-grade dysplasia and/or carcinoma. There is contradictory data whether immunosuppressed patients with IBD have the same risk profile for cervical cancer as patients with solid organ transplant or HIV infection.
To determine whether the risk of cervical high-grade dysplasia and/or cancer is higher in patients with IBD on immunosuppressive therapy compared with the rates in the general population.
The studies were restricted to full-text retrospective cohort studies and case controls that had a high (6-9) Newcastle-Ottawa Score.
All pooled analyses were based on a random-effects model. Five cohort studies and 3 case-control studies of patients with IBD on any immunosuppression with cervical high-grade dysplasia/cancer (n = 995) were included in the meta-analysis. The total IBD population in these studies was 77,116. Patients with IBD had an increased risk of cervical high-grade dysplasia/cancer compared with healthy controls (odds ratio = 1.34, 95% confidence interval: 1.23-1.46). Heterogeneity was detected (I = 34.23, Q = 10.64, df = 7; P = 0.15). The source was found to be the type of study, as well as the odds ratio presented (crude versus adjusted).
There is sufficient evidence to suggest an increased risk of cervical high-grade dysplasia/cancer in patients with IBD on immunosuppressive medications compared with the general population. Given this increased risk, increased screening intervals are indicated.
免疫抑制是炎症性肠病(IBD)诱导缓解和维持缓解治疗的主要手段。长期接受免疫抑制治疗的女性患宫颈高级别发育异常和/或癌的风险更高。关于IBD免疫抑制患者患宫颈癌的风险状况是否与实体器官移植患者或HIV感染者相同,存在相互矛盾的数据。
确定接受免疫抑制治疗的IBD患者发生宫颈高级别发育异常和/或癌的风险是否高于普通人群。
研究仅限于全文回顾性队列研究和纽卡斯尔-渥太华评分较高(6-9分)的病例对照研究。
所有汇总分析均基于随机效应模型。荟萃分析纳入了五项关于接受任何免疫抑制治疗的IBD患者发生宫颈高级别发育异常/癌的队列研究和三项病例对照研究(n = 995)。这些研究中的IBD患者总数为77,116例。与健康对照相比,IBD患者发生宫颈高级别发育异常/癌的风险增加(优势比 = 1.34,95%置信区间:1.23-1.46)。检测到异质性(I² = 34.23,Q = 10.64,自由度 = 7;P = 0.15)。发现异质性来源为研究类型以及所呈现的优势比(粗比值与调整后比值)。
有充分证据表明,与普通人群相比,接受免疫抑制药物治疗的IBD患者发生宫颈高级别发育异常/癌的风险增加。鉴于这种风险增加,建议缩短筛查间隔。