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Report:
Costs push hepatitis therapy out of reach
Investigators: Francis Andre and Ching Lung Lai
Monday Mar 11th, 2002
by Julie Clayton
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Transmission electron micrograph
of hepatitis B virions,
CDC/Dr. Erskine Palmer.
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Around 400 million people carrying
hepatitis B virus could benefit from long-term treatment with
lamivudine. But the drug's cost and a campaign by its
manufacturer, GlaxoSmithKline, to "find and treat early," provoked
complaints at a pre-congress symposium this afternoon.
The grim statistics are familiar to those who attended the
symposium sponsored by GlaxoSmithKline (GSK): hepatitis B virus (HBV)
kills between 1 and 2.5 million people a year and, overall, 15 to
25% of HBV carriers will die from chronic hepatitis, cirrhosis or
hepatocellular carcinoma.
In some parts of the world, particularly south east Asia,
carriers also face a high risk of an additional infection with the
hepatitis A virus (HAV), leading to more rapid and severe disease.
According to Francis Andre, of GSK Belgium, the response should
be a strategy already being piloted in Malaysia. Use rapid
diagnostic kits to identify HBV carriers who have not yet
developed any symptoms of disease, he said, and offer them a
combination of treatment with either lamivudine or interferon,
plus vaccination against HAV.
"We now have the total package of weapons to deal with
hepatitis B," he noted. "The earlier you treat, probably the
better the result will be."
On cost effectiveness, Andre said that a recent economic
benefit study looked promising. But pharmaceutical companies would
not survive if they gave into persistent demands to reduce costs,
he insisted.
"You mustn't always ask us to come to the help of poor
countries," he said. "There must be other mechanisms," he added,
referring to private initiatives such as the
Global Alliance for
Vaccines and Immunization (Gavi).
Presenting the latest results of lamivudine therapy, Ching Lung
Lai, of Queen Mary Hospital at the University of Hong Kong,
stressed the drug's safety and effectiveness over at least 5 years
for individuals with liver disease.
But other investigators, such as Betty Young, of the Pamela
Youde Eastern Hospital in Hong Kong, remain concerned over the
cost and long-term complications for treating all chronic
carriers, including the appearance of drug-resistant mutants.
"I think this area has to be researched further," she told
BioMedNet News.
According to Lai, however, viral mutants did not appear to
worsen the outlook for patients, as they were "less competent and
less aggressive" than the wild-type virus. Furthermore, new
nucleoside analogue agents may soon be available to counteract the
mutants, he proposed.
He warned, however, that the wild type virus becomes active
again as soon as lamivudine therapy stops. In places where the
cost of the drug means that continued therapy cannot be
guaranteed, the treatment should be avoided altogether, Lai told a
participant from Poland.
Furthermore, while lamivudine treatment appears effective at
blocking viral replication, it does not eliminate the virus
altogether, which reduces its appeal as a therapy for HBV
carriers, according to
John Tam of the Chinese University of Hong Kong.
"For the general public at the moment we really don't see a
very big advantage from lamivudine treatment," Tam told
BioMedNet News. "You don't see complete clearance," he said.
In addition, as a nucleoside analogue, lamividine poses the
theoretical risks of causing DNA damage, creating risks if
patients become pregnant while on treatment. The need to use
long-term contraception then becomes a big issue, Tam warned.
Delegates agreed on the potential benefits of vaccinating
chronic HBV carriers against the hepatitis A virus. For low-income
countries, however, the lack of infrastructure presents a
substantial obstacle to locating those in need.
"Introducing hep A vaccination for all chronic hep B carriers
is a great idea," noted Jacob John, pediatrician and former
president of the Indian Academy of Pediatrics, and advisor to the
Indian Government. "But in countries like India you need to have
the ability to test and find people who are hep B positive ...
these issues are where we fall down," he said. "There's no good
health system catching these people in India."
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