Reuters Health Information: Hepatitis C cure may open door to more kidney transplants
Hepatitis C cure may open door to more kidney transplants
Last Updated: 2017-05-01
By Gene Emery
NEW YORK (Reuters Health) - Kidneys infected with hepatitis
C have been successfully transplanted into 10 patients and then
cleansed of the virus.
The pilot study, reported April 30 at the 2017 American
Transplant Congress in Chicago and online by the New England
Journal of Medicine, could open the door to many more
transplants, which cost far less over the long term than
dialysis.
Hepatitis C patients have been traditionally excluded from
donating organs. But that was before development of the drug
combination of elbasvir and grazoprevir, commonly known as
Zepatier, which usually eliminates the infection.
"This trial shows how the whole face of hepatitis C has
completely changed in the last few years. It used to be a
disease we dreaded and all the options were terrible," study
coauthor Dr. Peter Reese told Reuters Health by telephone.
For kidney-transplant recipients, there was concern that the
immunosuppressive drugs given after a transplant might interfere
with the ability to eliminate the hepatitis C virus and they
might have to deal with the complications of the virus for the
rest of their lives. In fact, by the third day after
transplantation, all 10 had detectable levels of the virus in
the blood.
But after the standard 12-week regimen of Zepatier, all
traces of the virus had disappeared and remained absent for an
additional 12 weeks.
"For these patients, getting off of dialysis and getting
back to their normal lives was very much worth the risk,� Dr.
Reese said.
Merck, which markets the drug combination, helped pay for
the trial.
The treatment costs about $54,600, but just as an expensive
kidney transplant saves money in the long run, adding the
hepatitis C treatment should still be cost effective, said
Reese, an assistant professor of medicine and epidemiology at
the University of Pennsylvania and chairman of the ethics
committee for the United Network of Organ Sharing.
"These drugs are expensive. But we know a lot of companies
have similar drugs in the pipeline that will have to compete
with existing ones, so I anticipate the costs will fall," he
said. "I believe using these hepatitis C treatments might still
make kidney transplantation a very financially competitive
option compared to dialysis."
With about 12,000 kidney transplants from deceased donors
done per year and 97,000 people waiting for a kidney, it's not
clear how many extra cases can be done even if follow-up tests
confirm that the hepatitis C therapy can safely increase the
donor pool.
The University of Pennsylvania authors said more than 500
high-quality kidneys are discarded each year because they are
infected.
"It's plausible that the number is higher than that because
we know a lot of organ procurement organizations don't
vigorously pursue hepatitis C-positive organs," said Dr. Reese.
"I don't want to make the claim that this will solve the organ
crisis. It will not. But 500 is probably the floor."
The therapy might also work for other transplanted organs,
he said. But for now, the researchers have approval to test it
on 10 more people waiting for a kidney transplant "to show this
can be reproduced in larger numbers in other centers with more
permissive criteria," Dr. Reese said.
The study, known as THINKER, only used donors infected with
hepatitis C genotype 1, the most common type of infection.
Elbasvir-grazoprevir treatment was begun as soon as the
recipient showed evidence of the virus. The volunteers will be
followed for one year.
SOURCE: http://bit.ly/2oVtsrj
N Eng J Med 2017.
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