Patel Nicolas, Benipal Bikramjit
Internal Medicine, New York University School of Medicine, New York, USA.
Internal Medicine, Temple University, Philadelphia, USA.
Cureus. 2019 Jan 25;11(1):e3962. doi: 10.7759/cureus.3962.
Introduction Cholangiocarcinoma is an aggressive and rare cancer of the bile duct with a very poor prognosis. It accounts for approximately three percent of gastrointestinal cancers but nearly 20 percent of deaths are from hepatobiliary cancers. Cholangiocarcinoma is also a clinically silent disease that presents at advanced stages. In this study, we wanted to identify subpopulations at the greatest risk of developing cholangiocarcinoma such that we can improve diagnosis and ultimately reduce the cancer mortality rate. Methods The United States Cancer Registry (USCS) was used to obtain data for cholangiocarcinoma from 2001 to 2015. Incidence analysis was done for sex, race, stage, primary location (intrahepatic bile duct or extrahepatic bile duct), and US regional location. Results The overall incidence of cholangiocarcinoma from 2001 to 2015 was 1.26 per 100,000 people per year. The overall incidence rates were greatest for each stratification in males, Asian and Pacific Islanders (API), distant disease, intrahepatic bile duct cholangiocarcinoma (ICC), and in the Northeast. Incidence rates were increasing between 2001 and 2015 in all subpopulations. Compared to extrahepatic bile duct cholangiocarcinoma (ECC), ICC increased significantly between 2001 and 2015. From 2001 to 2007, the annual percent change (APC) for ICC was 2.79, from 2007 to 2010 the APC was 17.02, and from 2010 to 2015 the APC was 9.67. Moreover, the incidence of distant disease also increased significantly with an APC of 9.22. Conclusion In our study, we analyzed the incidence of cholangiocarcinoma in all 50 states in the USA. We found that the incidence is increasing in all subpopulations and specifically at a dramatic rate for ICC and those with distant disease at the time of diagnosis. Ultimately, our findings identified at-risk populations who need closer monitoring for cholangiocarcinoma.
引言
胆管癌是一种侵袭性强且罕见的胆管癌,预后很差。它约占胃肠道癌症的3%,但近20%的死亡是由肝胆癌导致的。胆管癌也是一种在晚期才出现临床症状的疾病。在本研究中,我们希望确定发生胆管癌风险最高的亚人群,以便改善诊断并最终降低癌症死亡率。
方法
利用美国癌症登记处(USCS)获取2001年至2015年胆管癌的数据。对性别、种族、分期、原发部位(肝内胆管或肝外胆管)和美国地区位置进行发病率分析。
结果
2001年至2015年胆管癌的总体发病率为每年每10万人中有1.26例。在男性、亚裔和太平洋岛民(API)、远处疾病、肝内胆管癌(ICC)以及东北部地区,各分层的总体发病率最高。2001年至2015年期间,所有亚人群的发病率都在上升。与肝外胆管癌(ECC)相比,2001年至2015年期间ICC显著增加。2001年至2007年,ICC的年变化百分比(APC)为2.79,2007年至2010年为17.02,2010年至2015年为9.67。此外,远处疾病的发病率也显著增加,APC为9.22。
结论
在我们的研究中,我们分析了美国所有50个州胆管癌的发病率。我们发现所有亚人群的发病率都在上升,特别是ICC以及诊断时患有远处疾病的人群发病率上升幅度显著。最终,我们的研究结果确定了需要对胆管癌进行密切监测的高危人群。