“We are witnessing a revolution in the treatment of hepatitis C virus…. There is no
question that these treatments that can save millions of lives must be made universally
available at an affordable price.” – Francois Barre-Sinoussi, President of the International
AIDS Society [1]
Globally, approximately 184 million people are chronically infected with the Hepatitis
C virus (HCV), the majority of whom reside in low- and middle-income countries [2].
HCV is a very common co-infection of HIV with an estimated four to five million people
affected [3]. While HCV is a global epidemic it has a disproportionate effect on marginalised
groups, in particular people who inject drugs (PWID). The global prevalence of HCV
among PWID was estimated at 67% in 2010, with more than 10 million PWID living with
the virus [4]. Moreover, among PWID who are living with HIV, approximately 75% are
co-infected with HCV [5]. While the burden of HCV falls disproportionately upon people
who inject drugs, treatment coverage among this group remains extremely low, estimated
at just 2%-4% of those eligible for treatment [6]. This is similar to the 4% coverage
of antiretroviral therapy among PWID who are living with HIV [7].
A treatment revolution?
While both HIV and Hepatitis C are bloodborne viruses, Hepatitis C is curable. Until
recently, the standard of care was pegylated interferon (PEG-IFN) and ribavirin (RBV),
but this regimen has significant drawbacks, including the requirement of a long treatment
duration (24 to 48 weeks or longer) and frequent and sometimes severe side effects
from both drugs [8]. Moreover, cure rates are low, at around 50% in low- and middle-income
countries [9]. Recent developments in direct-acting antivirals (DAAs) to treat HCV
have been hailed as revolutionary [10], and adding a first-generation DAA to PEG-IFN/RBV
increased cure rates in genotype 1 patients to 75% [11]. (Genotype 1 is the most prevalent
HCV genotype globally, and traditionally the most difficult to cure.) Newer-generation
DAAs have brought cure rates up to 90% or higher and are easier to take [12]. Within
the next couple of years, it is expected that all-oral DAA combinations with few side
effects, taken for 8 to 12 weeks, will cure most people with HCV including those considered
“hard to treat [13].” Many pharmaceutical companies are producing HCV DAAs and there
are dozens of additional treatment candidates in the drug development pipeline. Several
products, including Gilead’s sofosbuvir and Janssen’s simeprevir, have recently been
approved in the United States and Europe [14].
Profits before patients?
A substantial body of literature suggests that HCV is treatable among PWID and that,
with the right support, adherence levels among PWID are equal to those of their non-drug-using
peers [15]. Many of the barriers that exclude this group from treatment are structural
or are based on stigma and discrimination [6]. However another significant barrier
for all people with HCV, particularly in relation to new medications, is cost. Eighty-five
percent of Hepatitis C patients reside in low- and middle-income countries, many of
which have meagre health budgets, and patients in these countries generally are expected
to pay for medications out-of-pocket [16]. Pegylated interferon, at around US$ 20,000
per course of treatment, has proven to be too expensive for people in many countries
[16]. Sofosbuvir, which is expected to be the mainstay of HCV therapy for the near
future, has the potential to benefit many more patients when combined with other medications,
but its cost of US$ 84,000 per 12-week course (with comparable prices in Europe) will
keep it out of reach for the majority of hepatitis C patients for the foreseeable
future [16,17].
Given that the market for sofosbuvir will have an estimated worth of around US$ 9
billion by 2017 [18], civil society organisations and treatment advocates have called
for a reduction in the price of new medications to US$ 500 per course [19].
Some progress has already been made through advocacy: in Egypt, which has the highest
HCV prevalence in the world at 14% in the general population [20], the production
of generic medications to rival brand-name competitors has allowed the government
to secure prices of just US$ 2,000 per course of PEG-IFN [16]. Most recently the government
negotiated a 99% discount on the US price of sofosbuvir, bringing it down to just
US $900 per 12-week course [21].
Moreover, India’s Natco Pharma Limited has requested that the Indian patent office
deny Gilead a patent for sofosbuvir in India, arguing that the new medication is not
“innovative enough” and relies upon “old science.” If this request is approved, it
will pave the way for the generic production of the drug [22]. Most recently, the
World Health Organization issued a strong statement within new guidelines for hepatitis
C treatment recommending the use of new medications, including sofosbuvir, and urging
a reduction in price [23].
What does this mean for Europe?
While the introduction of these new drugs constitutes one of the most important medical
breakthroughs in recent years, the exorbitant cost means that even within Europe they
are unlikely to be made available to PWID. In most Eurozone countries, sofosbuvir
will be priced at EUR 50,000 to 60,000 per 12-week course [24].
A treatment gap is already evident for less costly hepatitis C treatment within the
European Union: large variations have been reported between the economically stable
countries in northern and western Europe and those greatly affected by the 2009 financial
crisis in southern and eastern Europe. It was estimated that 6.7% of hepatitis C patients
in France undertook treatment in 2010, compared to just 0.8% in Italy [25]. The treatment
rate was also very low in Poland (0.4%), Romania (1.0%) and Russia (0.3%), and it
has been suggested that the cost of treatment was a factor [25].
Even in high-income countries, the cost of new treatment is likely to have an impact
on uptake. For example, in France it has been estimated that the price charged by
Gilead is 756 times the cost of production of sofosbuvir [17]. With 127,500 chronic
HCV patients [17] within France who could benefit from sofosbuvir, the high cost virtually
guarantees that this is not a sustainable treatment option.
Twenty-one countries within Central Asia and Eastern Europe are currently classified
as having middle-income status [26]. These countries, which are excluded from licensing
agreements with Gilead, have small health budgets and will be unable to purchase these
treatments [24].
Due to the withdrawal of the Global Fund to Fight AIDS, Tuberculosis and Malaria and
other international donors, harm reduction programmes are under threat in countries
such as Bulgaria, Georgia and Moldova [27]. Not only did Global Fund support ensure
the continuation of harm reduction services in the past, but it also was a factor
in the negotiation of lower hepatitis C medication prices in countries such as Ukraine
[28].
Recommendations
Gilead should drastically reduce the price of sofosbuvir. Doing so will promote access
to this lifesaving treatment. It has also been suggested that sales would increase
and profits would stabilise [24]. Gilead should also commit to an early access programme
for European countries whose healthcare systems are unable to afford sofosbuvir [24].
Generic competition must be fostered; the recent developments in India are paving
the way for this dynamic to emerge. The success seen in price reductions for HIV medications
as a result of the introduction of generic products should provide a model upon which
HCV treatment advocates can expand.
Within those countries in the European region that are still eligible for Global Fund
support, the Global Fund should increase its attention to hepatitis C. While the Global
Fund does not have a specific strategy for increasing access to hepatitis C prevention,
treatment and care, it does have supportive guidance. In countries with “well-documented
evidence that hepatitis C treatment and funding is available to the general population,”
Global Fund monies can be used to “fill in the gap for HIV-infected individuals [29].”
The Technical Review Panel has recommended that Global Fund resources be used to amass
evidence on the need for hepatitis treatment, create awareness of the virus, increase
prevention efforts, and support advocacy for treatment access and affordability [30].
The Global Fund could draw on the experience accumulated in programmes focusing on
HIV/HCV co-infection, such as in Georgia and Ukraine, where negotiations regarding
the cost of medications have led to substantial price reductions.
European civil society should learn from how reductions in the prices of HIV medications
have been achieved and should apply similar pressure in relation to hepatitis C medications.
A coordinated effort from a variety of stakeholders in Europe should be undertaken.
Promising developments such as those seen mostly recently in Egypt and India around
generic production should be encouraged and extended.
Civil society should be closely involved in HCV policy and programme development.
In particular, the meaningful engagement of people who use drugs is key. Funding should
also be directed towards these groups as a priority.
Innovative advocacy and coordinated efforts by civil society have resulted the formation
of an HCV civil society reference group at the World Health Organization and the inclusion
of PEG-IFN on the list of essential medicines [31]. These strategies should be leveraged
within Europe to ensure that PWID there can also access new and emerging treatments.
Competing interests
The authors declare that they have no competing interests.