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双亲患结直肠癌患者的筛查与监测结果:家族性肠癌服务机构的经验

Outcomes of screening and surveillance in people with two parents affected by colorectal cancers: experiences from the Familial Bowel Cancer Service.

作者信息

Pan Jennifer, Slattery Masha, Shea Natalie, Macrae Finlay

机构信息

1Department of Colorectal Medicine and Genetics, Royal Melbourne Hospital, Level 1 South, 300 Grattan Street, Parkville, Victoria 3050 Australia.

2Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University, School of Medicine, 3801 Miranda Ave., Suite GI-111, Palo Alto, CA 94304 USA.

出版信息

Hered Cancer Clin Pract. 2019 Aug 16;17:25. doi: 10.1186/s13053-019-0122-8. eCollection 2019.

Abstract

BACKGROUND

The Familial Bowel Cancer Service at The Royal Melbourne Hospital was started in 1980 in order to offer bowel cancer screening services to those felt to be at a higher risk of CRC due to their family history, and upon registration in this service, patients gave consent for recording of their individual and familial medical history as pertaining to colorectal cancer in the FamBIS database. Using the FamBIS database, we sought to understand whether the subpopulation of individuals in whom both parents were diagnosed with colorectal cancer carried a higher risk of colorectal cancer or neoplastic polyps and should therefore undergo more intensive screening above that of the average-risk individual.

METHODS

We conducted a single-centre retrospective cohort-study of adults (18 years of age and older) in the FamBIS database, with review of their medical histories as pertaining to CRC diagnosis, screening, and surveillance from 1980 to 2015.

RESULTS

We identified and reviewed the medical histories of 96 registrants from 62 unique families. Registrants began screening as early as 24 years of age, with the mean age of first screening being at 44.6 ± 10.7 years old. The mean duration of screening was 17.3 ± 10.1 years, and through their screening period, registrants underwent an average of 11.5 ± 9.1 FOBTs and 4.4 ± 3.1 colonoscopies or sigmoidoscopies.Over the course of screening, 41 (42.7%) registrants were found to have at least one neoplasm of any kind (including adenomas, advanced adenomas, and CRC) as their first positive colonoscopic finding. In total, 12 (12.5%) of the registrants were found to have an advanced neoplasm over the course of screening and surveillance, while only 2 patients were found to be diagnosed with CRC.

CONCLUSIONS

The prevalence rates for neoplasms, advanced neoplasms, and CRC in our current study were statistically significantly higher compared with those seen in average-risk populations. This supports the importance of more intensive screening for this subpopulation in preventing colorectal cancers, as well as pre-and early-cancerous neoplasms.

摘要

背景

皇家墨尔本医院的家族性肠癌服务始于1980年,旨在为那些因家族病史而被认为患结直肠癌风险较高的人群提供肠癌筛查服务。在该服务中登记时,患者同意在FamBIS数据库中记录其与结直肠癌相关的个人和家族病史。利用FamBIS数据库,我们试图了解父母双方均被诊断为结直肠癌的个体亚群是否患结直肠癌或肿瘤性息肉的风险更高,因此是否应接受比平均风险个体更密集的筛查。

方法

我们对FamBIS数据库中的成年人(18岁及以上)进行了单中心回顾性队列研究,回顾了他们1980年至2015年与结直肠癌诊断、筛查和监测相关的病史。

结果

我们识别并回顾了来自62个独特家庭的96名登记者的病史。登记者最早在24岁开始筛查,首次筛查的平均年龄为44.6±10.7岁。筛查的平均持续时间为17.3±10.1年,在筛查期间,登记者平均接受了11.5±9.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa0c/6697919/4a701d38699e/13053_2019_122_Fig1_HTML.jpg

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