Hepatitis C Update

LIVER RESEARCH ISSN 2379-4038 Editorial * Open Journal http://dx.doi.org/10.17140/LROJ-2-e003 Hepatitis C Update Corresponding author Omar Massoud, MD, PhD Director of Clinical Liver Research Division of Gastroenterology and Herpetology UAB Liver Center Department of Medicine University of Alabama at Birmingham 365 Boshell Diabetes Building 1808 7th Ave South Birmingham AL 35294, USA E-mail: omassoud@uab.edu Volume 2 : Issue 1 Article Ref. #: 1000LROJ2e003 Article History Received: September 17th, 2015 Accepted: September 18th, 2015 Published: September 22nd, 2015 Citation Massoud O. Hepatitis C update. Liver Res Open J. 2015; 2(1): e1-e2. doi: 10.17140/LROJ-2-e003 Omar Massoud, MD, PhD* Director of Clinical Liver Research, Division of Gastroenterology and Herpetology, UAB Liver Center, Department of Medicine, University of Alabama at Birmingham, 365 Boshell Diabetes Building, 1808 7th Ave South Birmingham, AL 35294, USA The pace of Hepatitis C Virus (HCV) drug development in recent years has accelerated dramatically. But, for patients to benefit from these impressive advances, practitioners (i.e. “us”) need to know the most recent and accurate data on the diagnosis and treatment. In 2013, The American Association for Study of Liver Disease (AASLD) and the Infectious Disease Society of America (IDSA), put together web-based guidelines, which are frequently updated: www.hcvguidelines.org and www.aasld.org/practice-guidelines.1 The size of the problem: In the USA, the prevalence is 1.8% (4.1 million), 80% of them are viremic. It is the principal cause of death from liver disease. It is the leading indication for liver transplantation in the USA. Although, HCV is a curable disease, it is under-diagnosed and under-treated.2 Three quarters of individuals with HCV are unaware they are infected. 66-87% of patients diagnosed with HCV have not received antiviral treatment. Screening and diagnosis: 65-69% of anti-HCV positive patients were born between 1945 and 1964. Persons born between 1945 and 1964 had a 4.6 times higher prevalence of HCV than persons born prior to 1945 or after 1964 (3.7% vs. 0.73%).3 Treatment: Before treatment, you need to know: genotype and viral load, previous treatment, and presence of absence of cirrhosis.4 Generally speaking, 4 regimens are currently available. Ledipasvir/sofosbuvir × 12 weeks (8 weeks at discretion of practitioner), Paritaprevir/ritonavir/ombitasvir+dasabuvir + RBV × 12 weeks, Daclatasvir/sofosbuvir × 12 weeks and Sofusbuvir +Simeprevir±RBV × 12 weeks.5 HCV Genotype 1A • Daily (400 mg) daclatasvir (60 mg) and sofosbuvirfor 12 weeks (no cirrhosis) or 24 weeks with or without weight-based RBV (cirrhosis). • Daily fixed-dose combination of ledipasvir (90 mg)/sofosbuvir (400 mg) for 12 weeks. • Daily fixed-dose combination of paritaprevir (150 mg)/ritonavir (100 mg)/ombitasvir (25 mg) plus twice-daily dosed dasabuvir (250 mg) and weight-based RBV for 12 weeks (no cirrhosis) or 24 weeks (cirrhosis). • Daily simeprevir (150 mg) and sofosbuvir (400 mg) for 12 weeks (no cirrhosis) or 24 weeks (cirrhosis without the Q80K polymorphism) with or without weight-based RBV. HCV Genotype 1B Copyright ©2015 Massoud O. This is an open access article distributed under the Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Liver Res Open J • Daily (400 mg) daclatasvir (60 mg) and sofosbuvirfor 12 weeks (no cirrhosis) or 24 weeks with or without weight-based RBV (cirrhosis). • Daily fixed-dose combination of ledipasvir (90 mg)/sofosbuvir (400 mg) for 12 weeks. • Daily fixed-dose combination of paritaprevir (150 mg)/ritonavir (100 mg)/ombitasvir (25 mg) plus twice-daily dosed dasabuvir (250 mg) and weight-based RBV for 12 weeks. • Daily simeprevir (150 mg) and sofosbuvir (400 mg) for 12 weeks (no cirrhosis) or 24 weeks (cirrhosis) with or without weight-based RBV. HCV Genotype 2 • Daily sofosbuvir (400 mg) and weight-based RBV for 12 weeks. Page e1 LIVER RESEARCH ISSN 2379-4038 Open Journal http://dx.doi.org/10.17140/LROJ-2-e003 HCV Genotype 4 • Daily fixed-dose combination of ledipasvir (90 mg)/sofosbuvir (400 mg) for 12 weeks. • Daily fixed-dose combination of paritaprevir (150 mg)/ritonavir (100 mg)/ombitasvir (25 mg) and weight-based RBV for 12 weeks. • Daily sofosbuvir (400 mg) and weight-based RBV for 24 weeks. HCV Genotype 5&6 • Daily fixed-dose combination of ledipasvir (90 mg)/sofosbuvir (400 mg) for 12 weeks. Whom to Initiate HCV Therapy? Treatment is recommended for all patients with chronic HCV infection, except those with short life expectancies owing to comorbid conditions. Immediate treatment is assigned the highest priority for those patients with advanced fibrosis (Metavir stage F3), those with compensated cirrhosis (Metavir stage F4), liver transplant recipients, and patients with severe extrahepatic hepatitis C. REFERENCES 1. AASLD/IDSA/IAS–USA. Recommendations for testing, managing, and treating hepatitis C. Available at: http://www.hcvguidelines.org 2011; Accessed September 1, 2015. 2. Ghany MG, Strader DB, Thomas DL, Seeff LB. Diagnosis, management, and treatment of hepatitis C. Hepatology. 2009; 49: 1335-1374. 3. Armstrong GL, Wasley A, Simard EP, et al. The prevalence of hepatitis C virus infection in the United States, 1999 through 2002. Ann Intern Med. 2006; 144(10): 705-714. doi: 10.7326/0003-4819-144-10-200605160-00004 4. Soriano V, Perelson AS, Zoulim F. Why are there different dynamics in the selection of drug resistance in HIV and hepatitis B and C viruses? Antimicrob Chemother. 2008; 62(1): 1-4. doi: 10.1093/jac/dkn175 5. Rousseau CM, Ioannou GN, Todd-Stenberg JA, et al. Racial differences in the evaluation and treatment of hepatitis C among veterans: a retrospective cohort study. Am J Public Health. 2008; 98(5): 846-882. doi: 10.2105/AJPH.2007.113225 Liver Res Open J Page e2