Updating Hepatocellular Carcinoma Trends
September 7, 2010
New data
demonstrate that hepatocellular carcinoma (HCC) incidence rates have
increased dramatically since the 1970s, but survival rates in HCC are
improving. Better surveillance of high-risk patients is critical.
The incidence of hepatocellular
carcinoma (HCC) in the United States has historically been lower than
that of other countries, but studies have shown that rates of the
disease have increased substantially in recent decades. In addition,
primary liver cancer mortality rates have increased faster than
mortality rates for any other leading cause of cancer. “It’s important
for clinicians to learn about the changing epidemiology of malignancies
because this information directly impacts patient care,” says Jennifer
C. Obel, MD.
Several treatment options are available for
patients with early-stage HCC, including resection, transplantation, and
liver-directed therapies like chemoembolization (in well-selected
patients with localized HCC). However, many patients who are diagnosed
with HCC have advanced disease and are only candidates for palliative
therapies. “Most HCC is thought to be associated with either chronic
hepatitis C virus (HCV) or hepatitis B virus (HBV) infection,” Dr. Obel
says. “In the U.S., more than 3 million people are chronically infected
with HCV. Chronic infection with HBV is less common overall, but more
common among certain ethnic groups.” HCC typically develops in patients
with underlying cirrhosis. Commonly reported risk factors for cirrhosis
include alcohol-induced liver disease, HCV and HBV infection, obesity,
and type 2 diabetes.
Assessing Incidence & Survival
In the March 2009 issue of the Journal of Clinical Oncology,
researchers at the National Cancer Institute examined trends in HCC
from 1975 to 2005. The report found that the incidence of HCC tripled in
the United States during this time period. Between 2000 and 2005, liver
cancer rates increased significantly among African-American, Hispanic,
and Caucasian men between the ages of 50 and 59 (Table 1).
The researchers suggest that increases in this age group may be
partially due to an epidemic of hepatitis C infection that occurred in
the 1960s when they were young adults.
“Despite the rising incidence of HCC,” says Dr. Obel, “the 2- to 4-year survival rates doubled from 1975 to 2005 [Table 2].
This improvement may be attributed to the fact that more patients were
diagnosed with early-stage HCC when the disease can be cured by surgery.
When detected early, there are significantly more treatment options for
HCC.” Dr. Obel added that this finding is significant because it is
important not only to diagnose cancer, but these early diagnoses must
improve outcomes to have the desired effect.
Dr. Obel notes that aggressive treatments
appear to be improving long-term survival in HCC patients.
“Transplantation and resection have improved in recent years,” she says.
“Also, the advent of targeted chemotherapies holds promise for patients
with regional and advanced-stage HCC.”
Surveillance Important for High-Risk Patients
According to Dr. Obel, it is important for
clinicians to monitor patients at increased risk of HCC. “Around the
U.S.,” she says, “patients at increased risk for developing HCC are
being entered into surveillance programs in which they are followed by
serum alpha-fetoprotein testing, abdominal ultrasound, and diagnostic
imaging approximately every 6 months. Active surveillance has the
potential to diagnose patients when the disease is asymptomatic. An
early diagnosis is our most formidable way to cure liver cancer.”
In addition to surveillance, Dr. Obel says
that aggressive treatments appear to be improving long-term survival in
HCC patients with localized-stage tumors. “In addition to improvements
in transplantation and resection, there have also been advances in the
development of targeted HCC therapies. These agents hold some promise
for further improvements in prognoses, especially among patients with
regional and distant-stage HCC. The key is to ensure that clinicians
assess the risk of HCC in those patients with underlying conditions that
place them at increased risk. After that, patients can subsequently be
enrolled into screening programs for HCC, similar to how patients with
substantial risk factors for colon cancer are screened more aggressively
with colonoscopy.”
Coordinated Efforts Required
Dr. Obel notes that prevention efforts need to be coordinated. “The Journal of Clinical Oncology
study indicated that despite better HCC survival rates, improvements
are still needed,” she says. “The 1-year cause-specific survival rate
remained lower than 50%. Primary HCC prevention measures should include
hepatitis B vaccination programs, screening of the blood supply for
hepatitis viruses, and campaigns to discourage IV drug abuse. Other
prevention measures should focus on detecting asymptomatic HCC. This can
be accomplished by periodically screening high-risk patients and then
conducting follow-up tests when suspicious lesions are detected. The
data reported in the study give us hope that greater awareness of liver
cancer and its risk factors may help lessen the burden of HCC.”
Additional Resources:
Altekruse SF, McGlynn KA, Reichman ME. Hepatocellular carcinoma incidence, mortality, and survival trends in the United States from 1975 to 2005. J Clin Onc. 2009 Feb 17 [Epub ahead of print]. Available at: http://jco.ascopubs.org/cgi/content/abstract/JCO.2008.20.7753v1.
El-Serag HB, Davila JA, Petersen NJ, et al. The continuing increase in the incidence of hepatocellular carcinoma in the United States: an update. Ann Intern Med. 2003;139:817-823.
Schwarz RE, Smith DD: Trends in local therapy for hepatocellular carcinoma and survival outcomes in the US population. Am J Surg. 2008;195:829-836.
El-Serag HB, Marrero JA, Rudolph L, et al. Diagnosis and treatment of hepatocellular carcinoma. Gastroenterology. 2008;134:1752-1763.
Davila JA, Morgan RO, Shaib Y, et al. Hepatitis C infection and the increasing incidence of hepatocellular carcinoma: a population-based study. Gastroenterology. 2004;127:1372-1380.
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