Hepatitis C treatment failure is associated with increased risk of hepatocellular carcinoma

被引:29
|
作者
Lu, Mei [1 ]
Li, Jia [1 ]
Rupp, Loralee B. [2 ]
Holmberg, Scott D. [3 ]
Moorman, Anne C. [3 ]
Spradling, Philip R. [3 ]
Teshale, Eyasu H. [3 ]
Zhou, Yueren [1 ]
Boscarino, Joseph A. [4 ]
Schmidt, Mark A. [5 ]
Lamerato, Lois E. [1 ]
Trinacty, Connie [6 ]
Trudeau, Sheri [1 ]
Gordon, Stuart C. [7 ]
机构
[1] Henry Ford Hlth Syst, Dept Publ Hlth Sci, Detroit, MI USA
[2] Henry Ford Hlth Syst, Ctr Hlth Policy & Hlth Serv Res, Detroit, MI USA
[3] Ctr Dis Control & Prevent, Div Viral Hepatitis, Natl Ctr HIV AIDS Viral Hepatitis STD & TB Preven, Atlanta, GA USA
[4] Geisinger Hlth Syst, Ctr Hlth Res, Danville, PA USA
[5] Kaiser Permanente Northwest, Ctr Hlth Res, Portland, OR USA
[6] Kaiser Permanente Hawaii, Ctr Hlth Res, Waipahu, HI USA
[7] Henry Ford Hlth Syst, Div Gastroenterol & Hepatol, Detroit, MI USA
关键词
antiviral treatment; sustained virological response; treatment failure; SUSTAINED VIROLOGICAL RESPONSE; INTERFERON THERAPY; CIRRHOSIS; MORTALITY; INFECTION; FIBROSIS; CARE; EPIDEMIOLOGY; PROGRESSION; SOFOSBUVIR;
D O I
10.1111/jvh.12538
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Sustained virological response (SVR) to antiviral therapy for hepatitis C (HCV) reduces risk of hepatocellular carcinoma (HCC), but there is little information regarding how treatment failure (TF) compares to lack of treatment. We evaluated the impact of treatment status on risk of HCC using data from the Chronic Hepatitis Cohort Study (CHeCS-an observational study based in four large US health systems, with up to 7 years of follow-up on patients). Multivariable analyses were used to adjust for bias in treatment selection, as well as other covariates, followed by sensitivity analyses. Among 10 091 HCV patients, 3681 (36%) received treatment, 2099 (57%) experienced treatment failure (TF), and 1582 (43%) of these achieved sustained virological response (SVR). TF patients demonstrated almost twice the risk of HCC than untreated patients [adjusted hazard ratio (aHR) = 1.95, 95% confidence interval (CI) 1.50-2.53]; this risk persisted across all stages of fibrosis. Several sensitivity analyses validated these results. Although African Americans were at increased risk of treatment failure, they were at lower risk for HCC and all-cause mortality compared to White patients. SVR patients had lower risk of HCC than TF patients (aHR = 0.48, CI 0.31-0.73), whereas treatment - regardless of outcome - reduced all-cause mortality (aHR = 0.45, CI 0.34-0.60 for SVR patients; aHR = 0.78, CI 0.65-0.93 for TF patients).
引用
收藏
页码:718 / 729
页数:12
相关论文
共 50 条
  • [41] Clinical Efficacy and Post-Treatment Seromarkers Associated with the Risk of Hepatocellular Carcinoma among Chronic Hepatitis C Patients
    Mei-Hsuan Lee
    Chung-Feng Huang
    Hsueh-Chou Lai
    Chun-Yen Lin
    Chia-Yen Dai
    Chun-Jen Liu
    Jing-Houng Wang
    Jee-Fu Huang
    Wen-Pang Su
    Hung-Chih Yang
    Kwong-Ming Kee
    Ming-Lun Yeh
    Po-Heng Chuang
    Shih-Jer Hsu
    Ching-I Huang
    Jung-Ta Kao
    Chieh-Chang Chen
    Sheng-Hung Chen
    Wen-Juei Jeng
    Hwai-I Yang
    Yong Yuan
    Sheng-Nan Lu
    I-Shyan Sheen
    Chen-Hua Liu
    Cheng-Yuan Peng
    Jia-Horng Kao
    Ming-Lung Yu
    Wan-Long Chuang
    Chien-Jen Chen
    Scientific Reports, 7
  • [42] Clinical Efficacy and Post-Treatment Seromarkers Associated with the Risk of Hepatocellular Carcinoma among Chronic Hepatitis C Patients
    Lee, Mei-Hsuan
    Huang, Chung-Feng
    Lai, Hsueh-Chou
    Lin, Chun-Yen
    Dai, Chia-Yen
    Liu, Chun-Jen
    Wang, Jing-Houng
    Huang, Jee-Fu
    Su, Wen-Pang
    Yang, Hung-Chih
    Kee, Kwong-Ming
    Yeh, Ming-Lun
    Chuang, Po-Heng
    Hsu, Shih-Jer
    Huang, Ching-I
    Kao, Jung-Ta
    Chen, Chieh-Chang
    Chen, Sheng-Hung
    Jeng, Wen-Juei
    Yang, Hwai-I
    Yuan, Yong
    Lu, Sheng-Nan
    Sheen, I-Shyan
    Liu, Chen-Hua
    Peng, Cheng-Yuan
    Kao, Jia-Horng
    Yu, Ming-Lung
    Chuang, Wan-Long
    Chen, Chien-Jen
    SCIENTIFIC REPORTS, 2017, 7
  • [43] Increased risk of hepatocellular carcinoma in viral hepatitis associated end-stage liver disease (ESLD).
    Perez, RG
    Zein, NN
    Steers, JL
    Wiesner, RH
    HEPATOLOGY, 1997, 26 (04) : 109 - 109
  • [44] Comment on "Diabetic MAFLD is associated with increased risk of hepatocellular carcinoma and mortality in chronic viral hepatitis patients"
    Zhao, Gang
    Shi, Xiaobao
    Zhang, Lingyun
    Liang, Hongyuan
    INTERNATIONAL JOURNAL OF CANCER, 2024, 154 (07) : 1324 - 1325
  • [45] High viral load and hepatitis B virus subgenotype Ce are associated with increased risk of hepatocellular carcinoma
    Chan, Henry Lik-Yuen
    Tse, Chi-Hang
    Mo, Frankie
    Koh, Jane
    Wong, Vincent Wai-Sun
    Wong, Grace Lai-Hung
    Chan, Stephen Lam
    Yeo, Winnie
    Sung, Joseph Jao-Yiu
    Mok, Tony Shu-Kam
    JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (02) : 177 - 182
  • [46] UGT1A7 haplotype is associated with an increased risk of hepatocellular carcinoma in hepatitis B carriers
    Kong, Sun-Young
    Ki, Chang-Seok
    Yoo, Byung Chul
    Kim, Jong-Won
    CANCER SCIENCE, 2008, 99 (02) : 340 - 344
  • [47] Low level of hepatitis B viremia is associated with increased risk of hepatocellular carcinoma in compensated cirrhotic patients
    Lin, Wei-Chun
    Lin, Ke
    Li, Ming-Kai
    Liu, Xiao
    Huang, Yi-Fei
    Wang, Xing
    Wu, Bin
    WORLD JOURNAL OF HEPATOLOGY, 2024, 16 (11)
  • [48] Association Between Hepatocellular Carcinoma and Hepatitis C Direct-Acting Antiviral Treatment Failure
    Le Roux, Michelle
    Civan, Jesse
    Fenkel, Jonathan M.
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2018, 113 : S1581 - S1582
  • [49] Hepatic steatosis is associated with increased frequency of hepatocellular carcinoma in patients with hepatitis C-related cirrhosis
    Pekow, Joel
    Bhan, Atul K.
    Hui, Zheng
    Chung, Raymond T.
    GASTROENTEROLOGY, 2006, 130 (04) : A775 - A775
  • [50] Is direct acting antiviral therapy for hepatitis c viral infection associated with increased risk of hepatocellular carcinoma before or after liver transplantation?
    Jain, Ashokkumar
    Miller, Danielle
    Kadry, Zakiyah
    HEPATOBILIARY SURGERY AND NUTRITION, 2019, 8 (05) : 563 - 565