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Page 10 of 12                                         Rutledge et al. Hepatoma Res 2019;5:31  I  http://dx.doi.org/10.20517/2394-5079.2019.19

               pre-existing risk factors for HCC development were treated with DAA. This imbalance would appear to
               explain the higher numerical incidence of de novo HCC among DAA-treated patients. Given the success
               and cost-effectiveness of DAA therapy for the treatment of HCV infection [47-49] , clinicians should not be
               dissuaded by prior studies that suggest an increased risk of precipitating HCC development, as this seems
               to largely be a product of the presence of more advanced liver disease and increased risk factors among
               DAA-treated patients. Rather, the practice of continued surveillance for HCC for those persons with
               baseline risk factors, should continue to be reinforced.


               DECLARATIONS
               Authors’ contributions
               Contributed to the final version of the manuscript: Rutledge SM, Li DK, Chung RT
               Performed the statistical analysis: Zheng H
               Supervised the project: Chung RT

               Availability of data and materials
               Not applicable.

               Financial support and sponsorship
               Raymond T. Chung received grant support (NIH grant DK078772).


               Conflicts of interest
               All authors declared that there are no conflicts of interest.

               Ethical approval and consent to participate
               Not applicable.


               Consent for publication
               Not applicable.


               Copyright
               © The Author(s) 2019.



               REFERENCES
               1.   Mittal S, El-Serag HB. Epidemiology of hepatocellular carcinoma: consider the population. J Clin Gastroenterol 2013;47:S2-6.
               2.   Lemon SM, McGivern DR. Is hepatitis C virus carcinogenic? Gastroenterology 2012;142:1274-8.
               3.   Bruix J, Sherman M. Management of hepatocellular carcinoma: an update. Hepatology 2011;53:1020-2.
               4.   Hassan MM, Hwang LY, Hatten CJ, Swaim M, Li D, et al. Risk factors for hepatocellular carcinoma: synergism of alcohol with viral
                   hepatitis and diabetes mellitus. Hepatology 2002;36:1206-13.
               5.   Sanyal AJ, Yoon SK, Lencioni R. The Etiology of Hepatocellular Carcinoma and Consequences for Treatment. Oncologist
                   2010;15:14-22.
               6.   Janjua NZ, Chong M, Kuo M, Woods R, Wong J, et al. Long-term effect of sustained virological response on hepatocellular carcinoma
                   in patients with hepatitis C in Canada. J Hepatology 2017;66:504-13.
               7.   Brown JL. Interferon therapy reduces the risk for hepatocellular carcinoma. Gut 2000;47:610-1.
               8.   Ikeda M, Fujiyama S, Tanaka M, Sata M, Ide T, et al. Risk factors for development of hepatocellular carcinoma in patients with
                   chronic hepatitis C after sustained response to interferon. J Gastroenterol 2005;40:148-56.
               9.   Singal AK, Singh A, Jaganmohan S, Guturu P, Mummadi R, et al. Antiviral Therapy Reduces Risk of Hepatocellular Carcinoma in
                   Patients With Hepatitis C Virus-Related Cirrhosis. Clin Gastroenterol H 2010;8:192-9.
               10.  Fried MW, Shiffman ML, Reddy KR, Smith C, Marinos G, et al. Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus
                   infection. N Engl J Med 2002;347:975-82.
               11.  Harris RJ, Thomas B, Griffiths J, Costella A, Chapman R, et al. Increased uptake and new therapies are needed to avert rising
                   hepatitis C-related end stage liver disease in England: Modelling the predicted impact of treatment under different scenarios. J Hepatol
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