Article

Hepatitis C Antiviral Drugs Reduce Liver Cancer Risk

Chronic infection with hepatitis C virus is the leading cause of hepatocellular carcinoma.

The single leading cause of hepatocellular carcinoma (HCC) around the world is chronic infection with hepatitis C virus (HCV).

Other risk factors associated with an increased incidence of HCC include liver fibrosis, cirrhosis, increased age, male sex, diabetes, obesity, smoking, excessive alcohol intake, hepatitis B virus (HBV) co-infection, and HCV genotype 3 infection.

Prior to the recent availability of direct-acting antivirals (DAAs) for the treatment of HCV, interferons were a mainstay of therapy. Evidence suggests that interferon-based therapy to achieve sustained virologic response (SVR) in patients with chronic HCV dramatically reduces the risk of HCC, although it may take many years to fully realize that risk reduction.

Recent studies have reached disparate conclusions regarding the impact of DAAs on the risk of HCC among patients with HCV who have achieved SVR. As a result, Gilead Sciences, Inc., a biopharmaceutical company responsible for bringing a number of DAAs to the market, funded an investigation to further elucidate the relationship between DAAs and the risk of HCC.

Amanda Singer, PhD, MPH, researcher at Gilead and lead study author, and colleagues explained the rationale for their investigation, “The seriousness of HCC as a potential treatment-related outcome, contrasted with the serious implications of withholding HCV treatment from sick patients due to a potentially unfounded concern of an increased risk of HCC development after DAA therapy, warrants further investigation.”

Click here to continue reading on MD Magazine.

Related Videos
Anthony Perissinotti, PharmD, BCOP, discusses unmet needs and trends in managing chronic lymphocytic leukemia (CLL), with an emphasis on the pivotal role pharmacists play in supporting medication adherence and treatment decisions.
Image Credit: © alenamozhjer - stock.adobe.com
pharmacogenetics testing, adverse drug events, personalized medicine, FDA collaboration, USP partnership, health equity, clinical decision support, laboratory challenges, study design, education, precision medicine, stakeholder perspectives, public comment, Texas Medical Center, DNA double helix
pharmacogenetics challenges, inter-organizational collaboration, dpyd genotype, NCCN guidelines, meta census platform, evidence submission, consensus statements, clinical implementation, pharmacotherapy improvement, collaborative research, pharmacist role, pharmacokinetics focus, clinical topics, genotype-guided therapy, critical thought
Image Credit: © Andrey Popov - stock.adobe.com
Image Credit: © peopleimages.com - stock.adobe.com
TRUST-I and TRUST-II Trials Show Promising Results for Taletrectinib in ROS1+ NSCLC
World Standards Week 2024: US Pharmacopeia’s Achievements and Future Focus in Pharmacy Standards