Effect of Nucleos(t)ide Analogue Therapy on Risk of Intrahepatic Cholangiocarcinoma in Patients With Chronic Hepatitis B

被引:21
|
作者
Lee, Teng-Yu [1 ,2 ]
Hsu, Yao-Chun [3 ,4 ,5 ,6 ]
Yu, Shi-Hang [1 ]
Lin, Jaw-Town [7 ,8 ]
Wu, Ming-Shiang [9 ]
Wu, Chun-Ying [1 ,10 ,11 ,12 ,13 ,14 ,15 ,16 ]
机构
[1] Taichung Vet Gen Hosp, Div Gastroenterol & Hepatol, Taichung, Taiwan
[2] Chung Shan Med Univ, Dept Med, Taichung, Taiwan
[3] Fu Jen Catholic Univ, Sch Med, Big Data Res Ctr, New Taipei, Taiwan
[4] Fu Jen Catholic Univ, Div Gastroenterol, New Taipei, Taiwan
[5] China Med Univ, Grad Inst Clin Med, Taichung, Taiwan
[6] E Da Hosp, Div Gastroenterol & Hepatol, Kaohsiung, Taiwan
[7] Fu Jen Catholic Univ, Sch Med, New Taipei, Taiwan
[8] Natl Hlth Res Inst, Inst Populat Hlth Sci, Miaoli, Taiwan
[9] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[10] Natl Yang Ming Univ, Sch Med, Fac Med, Taipei, Taiwan
[11] China Med Univ, Coll Publ Hlth, Taichung, Taiwan
[12] China Med Univ, Grad Inst Clin Med Sci, Taichung, Taiwan
[13] Natl Chung Hsing Univ, Dept Life Sci, Taichung, Taiwan
[14] Natl Chung Hsing Univ, Rong Hsing Res Ctr Translat Med, Taichung, Taiwan
[15] Natl Hlth Res Inst, Natl Inst Canc Res, Miaoli, Taiwan
[16] Taipei Vet Gen Hosp, Dept Med Res, Div Translat Med, 322,Sec 2,Shipai Rd, Taipei, Taiwan
关键词
CHB; Antiviral; Biliary; Cancer; Prevention; BILIARY-TRACT CANCERS; HEPATOCELLULAR-CARCINOMA; VIRUS INFECTION; PRIMARY LIVER; PATHOGENESIS; METAANALYSIS; EXPRESSION; ASSOCIATION; EXPERIENCE; RECURRENCE;
D O I
10.1016/j.cgh.2017.09.031
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Chronic infection with hepatitis B virus (HBV) increases risk of intrahepatic cholangiocarcinoma (ICC), but it is not clear whether antiviral therapy reduces risk. We investigated the association between nucleos(t)ide analogue therapy and ICC risk. METHODS: We performed a nationwide long-term cohort study using Taiwan's National Health Insurance Research Database to obtain data on 185,843 patients with chronic HBV infection from October 1, 2003 through December 31, 2012. We excluded patients with confounding disorders such as infection with hepatitis C virus, HIV, or other hepatitis-associated viruses; liver flukes; biliary stone diseases; cholangitis; congenital biliary anomalies; biliary tract surgeries; or cancer. We identified 10,062 patients who received nucleos(t) ide analogue therapy (the treated group), and used propensity scores to match them (1:1) with patients who received hepatoprotectants (the untreated group). Cumulative incidences of and hazard ratios (HRs) for ICC development were analyzed. RESULTS:The cumulative incidence of ICC was significantly lower in the treated group after 3 years of therapy (1.28%; 95% CI, 0.56-2.01) than in the untreated group (3.14%; 95% CI, 2.02-4.27) and after 5 years of therapy (1.53%; 95% CI, 0.73-2.33 vs 4.32% in untreated group; 95% CI, 2.96-5.6869). In multivariable regression analysis, nucleos(t) ide analogue therapy was independently associated with a reduced risk of ICC (HR, 0.44; 95% CI, 0.25-0.78; P = .005). Older age (HR 1.05 per year; 95% CI, 1.03-1.07) and cirrhosis (HR, 2.80; 95% CI, 1.52-5.1415) were independently associated with an increased risk of ICC. Sensitivity analyses verified the association between nucleos(t)ide analogue therapy and a reduced ICC risk. CONCLUSION:A nationwide long-term cohort study in Taiwan showed that nucleos(t) ide analogue therapy for chronic HBV infection is significantly associated with a reduced ICC risk.
引用
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页码:947 / +
页数:12
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