Nebbia Martina, Yassin Nuha A, Spinelli Antonino
Colon and Rectal Surgery Division, Humanitas Clinical and Research Center IRCCS, Rozzano, Milano, Italy.
Deparment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milano, Italy.
Clin Colon Rectal Surg. 2020 Sep;33(5):305-317. doi: 10.1055/s-0040-1713748. Epub 2020 Jun 30.
Patients with inflammatory bowel disease (IBD) are at an increased risk for developing colorectal cancer (CRC). However, the incidence has declined over the past 30 years, which is probably attributed to raise awareness, successful CRC surveillance programs and improved control of mucosal inflammation through chemoprevention. The risk factors for IBD-related CRC include more severe disease (as reflected by the extent of disease and the duration of poorly controlled disease), family history of CRC, pseudo polyps, primary sclerosing cholangitis, and male sex. The molecular pathogenesis of inflammatory epithelium might play a critical role in the development of CRC. IBD-related CRC is characterized by fewer rectal tumors, more synchronous and poorly differentiated tumors compared with sporadic cancers. There is no significant difference in sex distribution, stage at presentation, or survival. Surveillance is vital for the detection and subsequently management of dysplasia. Most guidelines recommend initiation of surveillance colonoscopy at 8 to 10 years after IBD diagnosis, followed by subsequent surveillance of 1 to 2 yearly intervals. Traditionally, surveillance colonoscopies with random colonic biopsies were used. However, recent data suggest that high definition and chromoendoscopy are better methods of surveillance by improving sensitivity to previously "invisible" flat dysplastic lesions. Management of dysplasia, timing of surveillance, chemoprevention, and the surgical approaches are all areas that stimulate various discussions. The aim of this review is to provide an up-to-date focus on CRC in IBD, from laboratory to bedside.
炎症性肠病(IBD)患者患结直肠癌(CRC)的风险增加。然而,在过去30年中,其发病率有所下降,这可能归因于意识提高、成功的CRC监测计划以及通过化学预防改善了黏膜炎症的控制。IBD相关CRC的危险因素包括病情更严重(以疾病范围和控制不佳的疾病持续时间为反映)、CRC家族史、假性息肉、原发性硬化性胆管炎和男性。炎症上皮的分子发病机制可能在CRC的发生中起关键作用。与散发性癌症相比,IBD相关CRC的特征是直肠肿瘤较少、同时性肿瘤更多且分化较差。在性别分布、就诊时的分期或生存率方面没有显著差异。监测对于发育异常的检测及后续管理至关重要。大多数指南建议在IBD诊断后8至10年开始进行监测结肠镜检查,随后每年间隔1至2年进行后续监测。传统上,采用随机结肠活检的监测结肠镜检查。然而,最近的数据表明,高清和色素内镜检查通过提高对先前“不可见”扁平发育异常病变的敏感性,是更好的监测方法。发育异常的管理、监测时机、化学预防和手术方法都是引发各种讨论的领域。本综述的目的是提供从实验室到临床对IBD中CRC的最新关注。