Wan Jian, Wang Xuan, Zhang Yujie, Chen Min, Wang Min, Wu Kaichun, Liang Jie
State Key Laboratory of Cancer Biology, National Clinical Research Center for Digestive Diseases and Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, China.
Department of Neurology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Aliment Pharmacol Ther. 2022 Mar;55(6):632-644. doi: 10.1111/apt.16789. Epub 2022 Feb 15.
Due to limited research on the natural history of indefinite for dysplasia (IND) and low-grade dysplasia (LGD) in inflammatory bowel disease (IBD), the management of these patients is controversial.
This systematic review and meta-analysis aimed to estimate the incidence and identify the risk factors for advanced neoplasia in IBD patients with IND and LGD.
PubMed, Embase and Cochrane Central Register of Controlled Trials were searched until 24 December, 2021, to identify studies that reported pathological results of follow-up colonoscopy or surgery in IBD patients with IND and LGD. The main outcomes were the incidence and risk factors for advanced neoplasia in IBD patients with IND and LGD.
Based on the analysis of 38 studies, the pooled incidences of advanced neoplasia in IBD patients with IND and LGD were 9.9% (95% CI 4.4%-15.4%) and 10.7% (95% CI 7.0%-14.4%) respectively. The risk factors for advanced neoplasia in IND patients were primary sclerosing cholangitis (PSC) and aneuploidy. The risk factors for advanced neoplasia in LGD patients included male, PSC, previous IND, colonic stricture, index lesion ≥1 cm, distal location, multifocal lesions, distal and flat lesions, nonpolypoid/flat lesions and invisible lesions.
The incidence of advanced neoplasia was similar between IND and LGD in IBD patients, as high as one in ten, so more rigorous surveillance is also suggested in IND patients. Since the effects of most factors were derived from the pooled results of only two to three studies, further research was needed to confirm our results.
由于对炎症性肠病(IBD)中不典型增生不确定(IND)和低级别不典型增生(LGD)的自然史研究有限,这些患者的管理存在争议。
本系统评价和荟萃分析旨在估计IBD患者中IND和LGD发生高级别肿瘤的发生率,并确定相关危险因素。
检索PubMed、Embase和Cochrane对照试验中央注册库至2021年12月24日,以确定报告IBD患者中IND和LGD的随访结肠镜检查或手术病理结果的研究。主要结局是IBD患者中IND和LGD发生高级别肿瘤的发生率和危险因素。
基于38项研究的分析,IBD患者中IND和LGD发生高级别肿瘤的合并发生率分别为9.9%(95%CI 4.4%-15.4%)和10.7%(95%CI 7.0%-14.4%)。IND患者发生高级别肿瘤的危险因素是原发性硬化性胆管炎(PSC)和非整倍体。LGD患者发生高级别肿瘤的危险因素包括男性、PSC、既往IND、结肠狭窄、指数病变≥1 cm、远端部位、多灶性病变、远端扁平病变、非息肉样/扁平病变和不可见病变。
IBD患者中IND和LGD发生高级别肿瘤的发生率相似,高达十分之一,因此也建议对IND患者进行更严格的监测。由于大多数因素的影响仅来自两到三项研究的汇总结果,需要进一步研究来证实我们的结果。