|
Many liver cancers can be prevented by public health measures
that reduce exposure to known risk factors for this disease.
Avoiding and treating hepatitis infections
Worldwide, the most significant risk factor for liver cancer
is chronic infection with hepatitis B virus (HBV) and hepatitis C virus
(HCV).
A vaccine to help prevent hepatitis B infection has been
available since the early 1980s. The Centers for Disease Control and
Prevention (CDC) recommends that all children, as well as adults at
risk (health care workers, those whose behaviors may put them at risk,
etc.) get this vaccine to reduce the risk of hepatitis and liver
cancer.
There is no vaccine for hepatitis C. Preventing HCV infection,
as well as HBV infection in people who have not been immunized, is
based on understanding how these infections occur. These viruses can be
spread through sharing contaminated needles (such as in drug use),
unprotected sex, and through childbirth.
Blood transfusions were once a major source of infection as
well, but this has become extremely rare. Blood banks in the United
States test donated blood to look for these viruses. All infected blood
is discarded. Because of screening, the risk of getting a hepatitis
infection from a blood transfusion in the United States is extremely
low.
People at high risk for hepatitis B or C should be tested for
these infections so they can be watched for liver disease and treated
if needed. Several drugs can be used to treat hepatitis B and C.
Two drugs, interferon alfa and ribavirin, are often used to
treat chronic hepatitis C. Interferon can be given alone or along with
ribavirin. Combined treatment using a newer form of interferon (called peg-interferon) and
ribavirin seems to be the most effective treatment at this time.
Treatment usually lasts for 6 months to a year and can eliminate the
hepatitis C virus in many people. One of the problems with this
treatment is that it can cause severe side effects, including flu-like
symptoms, fatigue, depression, and low blood counts, which can make it
hard to take.
A number of drugs can be used to treat chronic hepatitis B,
including interferon (and peg-interferon), lamivudine (Epivir-HBV),
adefovir (Hepsera), entecavir (Baraclude), telbivudine (Tyzeka), and
tenofovir (Viread). These drugs have been shown to reduce the number of
viruses in the blood and lessen liver damage. Although they do not cure
the disease, they lower the risk of cirrhosis and may lower the risk of
liver cancer, as well.
Limiting alcohol and tobacco use
In the United States, alcohol abuse remains a major cause of
the cirrhosis that can lead to liver cancer. Prevention of liver
cancers linked with alcohol abuse remains a challenge. Quitting smoking
may also slightly lower the risk of liver cancer, as well as lowering
the risk for many other life-threatening diseases.
Limiting exposure to cancer-causing
chemicals
Changing the way certain grains are stored in tropical and
subtropical countries could reduce exposure to cancer-causing
substances such as aflatoxins. Many developed countries already have
regulations to prevent and monitor grain contamination.
Most developed countries also have regulations to protect
consumers and workers from known cancer-causing chemicals. These
regulations have essentially eliminated certain chemicals as a cause of
liver cancer. The U. S. Environmental Protection Agency (EPA) recently
lowered the allowable level of arsenic in drinking water in the United
States. But this may continue to be a problem in areas of the world
where naturally occurring arsenic commonly gets into drinking water.
Treating diseases that increase liver cancer
risk
Certain inherited diseases can cause cirrhosis of the liver,
increasing the risk for liver cancer. Finding and treating these
diseases early in life could lower this risk. For example, all children
in families with hemochromatosis should be screened for the disease and
treated if they have it. Treatment lowers their iron intake and removes
small amounts of blood to use up the body's excess stores of iron.
Last Medical Review: 11/05/2009 Last Revised: 11/05/2009
|