July 05, 2016
2 min read

HCV increases risk for head and neck cancers

You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

Hepatitis C virus infection appeared associated with an increased risk for certain nonoropharyngeal cancers and human papillomavirus-positive oropharyngeal cancer, according to results of a case–control study.

In 2009, The University of Texas MD Anderson Cancer Center opened the first clinic in the United States to manage HCV infection in patients with cancer.

“To our surprise, we saw a number of head and neck cancer patients who tested positive for the hepatitis C virus,” Harrys A. Torres, MD, associate professor of infectious disease, infection control and employee health at MD Anderson, said in a press release. “Obviously, a hepatitis C infection could impact how patients respond to their cancer therapy. We also realized that many of our hepatitis patients were excluded from clinical trials. Now that many with hepatitis C can be cured, it is important we first address and potentially cure the virus, so that they can have access to necessary cancer therapy."

Torres and colleagues reviewed the medical records of 34,545 patients with cancer tested for HCV antibodies to identify any association between HCV and head and neck cancers. Researchers also reviewed human papillomavirus (HPV) test results from biopsy reports of patients with oropharyngeal cancer.

From the overall cohort, researchers included data from 409 patients with oropharyngeal (n = 164) or nonoropharyngeal (n = 245) cancer, as well as from a control group of 694 patients with smoking-associated cancers — specifically, cancers of the lung (n = 378), esophagus (n = 168) and bladder (n = 148).

Of these 1,103 patients (median age at diagnosis, 62 years), 79.2% were white and 72.4% were men.

The prevalence of HCV seropositivity was higher in patients with oropharyngeal cancer (14%; 95% CI, 8.7-19.4) — especially among those who were HPV–positive (16.9%; 95% CI, 8.7-24.9) — and in patients with nonoropharyngeal head and neck cancer (20%; 95% CI, 14.9-25) than in the control group (6.5%; 95% CI, 4.6-8.3).

Models adjusted for factors, such as age at cancer diagnosis, sex, smoking history and alcohol consumption, showed HCV seropositivity was significantly associated with nonoropharyngeal head and neck cancer (OR = 2.85, 95% CI, 1.38-5.88) and HPV–positive oropharyngeal cancers (OR = 2.97, 95% CI, 1.31-6.76).

However, results showed that nasopharyngeal cancer was an exception to this association (OR = 1.3, 95% CI, 0.22-7.64).

Researchers acknowledged limitations to these results, including that the control group consisted of patients with cancer rather than being a cancer-free population. Torres and colleagues also noted the possibility of Berkson's bias — or different exposure rates in the control group and general population — because the HCV infection prevalence in the control group was 6% compared with 1.5% in the general population.

Although HCV has long been associated with liver cancer and non-Hodgkin lymphoma, these data are the first to show HCV also is associated with certain head and neck cancers.

“Our results add to the growing body of epidemiological evidence that HCV infection has extra-hepatic manifestations and may be associated with non–liver-related cancers,” Torres and colleagues wrote.

“What we are trying to make all understand is that this an infection that has consequences — and it's an infection we can cure,” Torres said. by Nick Andrews

Disclosure: Torres reports consultant roles with Astellas, Genentech, Gilead Science, Janssen Pharmaceuticals, Merck, Novartis, Pfizer, Theravance Biopharma and Vertex Pharmaceuticals. Please see the full study for a list of all other researchers’ relevant financial disclosures.