Hep C Edition.pdf | Page 3

Chronic Hepatitis C Optimizing Care In A Rapidly Changing Landscape Sandy Hickey, RPh Ryan Nolan, PharmD, MBA, CSP Diplomat Specialty Pharmacy The authors report no financial conflicts with any products discussed in this paper. In only a few decades drug therapy for chronic hepatitis C has evolved tremendously from interferononly monotherapy to the anticipated interferon-free oral regimens that are expected to come to market in 2014. Over time we have also seen incredible improvements in drug effectiveness, ease of administration, and side effect profiles. Today, with over 20 oral therapies in phase II and III trials, we are anticipating significant changes in the approach to hepatitis C drug therapy.1 The treatment of hepatitis C has never been simple. Specialty pharmacies and their high-touch models of care help alleviate the complexities of treatment through patient education, side effect management, laboratory reminders, and response-guided therapy. In order to continue providing innovative, high-quality care, specialty pharmacies must prepare and educate their organizations on what’s coming. In this article we will discuss the history of hepatitis C drug therapy, current treatment strategies, the drug development pipeline, and the care needed to support patients on their treatment journey. Introduction The hepatitis C virus (HCV) is the most common blood borne pathogen in the United States (U.S.) affecting approximately 3-4 million people.2 There are six genotypes associated with HCV; genotype 1 is the most prevalent in the U.S. and has historically been the most difficult to treat.3 Of those infected, 45% to 85% of patients are not aware that they have the virus because of its insidiously slow and silent spread.4 Those that are exposed to the virus are commonly asymptomatic or the symptoms they develop are mild and can be confused with other ailments that include abdominal pain, fatigue, fever, loss of appetite, and nausea.3 HCV infection is most prevalent among those born between the years of 1945-1965.4 Injection drug use is considered the single largest risk factor for infection.5 Other risk factors associated with transmission include the receipt of blood, blood products, or organs donated prior to 1992, use of clotting factors prior to 1987, needlestick injuries in a professional setting, tattoos, or vertical transmission from an infected mother to her child during birth.5 Approximately 85% of patients infected with HCV will go on to develop chronic HCV.3 If left untreated the chronic inflammation of the liver can lead to fibrosis, cirrhosis, and hepatocellular carcinoma.3 The goal of treating HCV is to eradicate the infection.3 Therapy is considered successful when patients achieve sustained virologic response (SVR).3 Sustained virologic response is defined as undetectable viral levels measured 12-24 weeks after the completion of therapy.3 While many factors can influence the ability to achieve SVR, adherence to therapy is one of the most significant. In one study it was found that patients were much more likely to achieve SVR when they were at least 80% adherent to their therapy regimen.6 3