COMMENTARY

Can't Afford a Cure: How Cost Keeps HCV Care Out of Reach

John W. Ward, MD

Disclosures

March 07, 2016

Editorial Collaboration

Medscape &

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Up to 3.5 million people are living with hepatitis C virus (HCV) in the United States, and an estimated 150 million people are chronically infected worldwide.[1,2] Globally, more than 700,000 HCV-infected people die each year from cirrhosis or primary liver cancer.[1] New cases of HCV infection are also a concern. In the United States, the rate of acute infection has increased by an alarming 150% during recent years, primarily fueled by increases in injection-drug use.[1]

Recent clinical trials have demonstrated that new, simple-to-use treatment regimens for persons living with HCV infection are safe and highly effective, leading to cure in the vast majority of patients—the public health implications of which could be profound. The effectiveness of a combination of sofosbuvir and velpatasvir in patients who have failed to respond to previous treatment and in those with decompensated cirrhosis, a contraindication for earlier HCV treatment regimens, is also very promising, with high rates of cure regardless of HCV genotype.[3]

Given the benefits of safe, easy-to-use, and curative HCV therapy, why be concerned about the impact of HCV on individuals and the public as a whole? The answer is simple: Patients do not benefit from a drug that they cannot afford. Although studies by the Centers for Disease Control and Prevention have shown that treating all people currently infected with HCV is cost-effective from a societal perspective,[4] the price of currently licensed medications, at $83,000-$153,000 per course of treatment, is an insurmountable barrier for many.

Despite US recommendations that all people currently infected with HCV should receive treatment,[5] health plans and payers have responded to the high cost of HCV medications by instituting restrictive reimbursement policies. In most state Medicaid programs, only patients in whom the infection has progressed to severe liver disease qualify for HCV treatment.[6] Drug expenditures for the treatment of HCV infection have declined as a result of mandated 23% rebates for Medicaid and privately negotiated prices by health plans, but inequities in patient access to such therapies persist.

To respond to current cost-related barriers to HCV cure and promote health equity, on November 5, 2015, the Centers for Medicare & Medicaid Services (CMS) notified state programs that limitations on drug coverage should not deny access to clinically appropriate antiviral therapy for beneficiaries with HCV infection. CMS also requested that manufacturers disclose value-based pricing agreements so that states can participate in such arrangements.[1]

Beyond affordable drug pricing, benefits of curative therapy can be realized only for persons who have been tested for HCV, know they are infected with HCV, and linked to care. In the United States, at least half of all people living with HCV infection remain undiagnosed.[7] A combination of testing strategies is recommended to identify people with ongoing transmission risks, especially those who inject drugs. Testing is also recommended for people born during 1945-1965 (baby boomers), a population with a disproportionately high rate of chronic HCV. People infected in the distant past are at highest risk of dying from HCV infection. In the United States, even a modest increase in implementation of the CDC recommendation for HCV testing of all people who were born from 1945 through 1965 could avert more than 320,000 deaths when that testing is linked to care and curative treatment.[4]

The care cascade—the progressive steps needed to identify HCV-infected patients, provide them with care and treatment, and elicit cure—is lacking in the United States and in most other countries.[6,7] A limiting factor with currently licensed therapies is the requirement that HCV-infected persons undergo genotyping and disease staging before the initiation of therapy, complicating and delaying the treatment process. Most HCV-infected people do not receive this level of care. The new sofosbuvir–velpatasvir regimen could simplify HCV management by reducing the need for these steps, paving the way for simple "test and cure" strategies appropriate for primary care and other settings, such as addiction-treatment programs. Educating providers about HCV testing, care, and treatment and creating innovative models for the delivery of care can also increase the robustness of the current care cascade.[1,7]

The availability of simple, safe, and curative regimens creates opportunities for improving the health of the millions of patients living with HCV infection. At a population level, the effect of HCV medications will be determined by affordability and equitable access to HCV testing, care, and treatment. Only through these improvements can our focus be directed to what matters most: reducing the morbidity and mortality associated with HCV infection, stopping HCV transmission, and ultimately eliminating HCV as a public health threat in the United States and worldwide.

Web Resources

Hepatitis C Professional Resources

John W. Ward, MD, is director of the Division of Viral Hepatitis at the Centers for Disease Control and Prevention (CDC). He is responsible for research, surveillance, policies, and programs to prevent viral hepatitis transmission and disease. Dr Ward's previous work includes early studies of HIV transmission, natural history, and leading US HIV/AIDS surveillance. Dr Ward has authored over 150 scientific publications; served as editor of MMWR, CDC's health bulletin; and was the editor of Silent Victories, a history of public health in the 20th century, published by Oxford University Press. Dr Ward received his MD from the University of Alabama School of Medicine in Birmingham and completed his internal medicine training at the University of Alabama Hospitals. He is a faculty member of the Department of Medicine, Emory University, Atlanta, Georgia.

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