New Test Helps Evaluate Erbitux's Merit

KRAS RGQ PCR kit checks for the presence of a certain mutation in KRAS gene

MONDAY, July 9 (HealthDay News) -- A new genetic test to help doctors determine if the drug Erbitux would be an effective treatment for certain colorectal cancer patients has been approved by the U.S. Food and Drug Administration.

The KRAS RGQ PCR kit checks for the presence of a certain mutation in the KRAS gene. About 40 percent of people with colon cancer are thought to have the mutation, which renders Erbitux ineffective. The test is for people whose colorectal cancer has spread to other parts of the body, the FDA said in a news release.

The American Cancer Society says more than 141,000 new cases of colon cancer were diagnosed last year in the United States, and nearly 50,000 people died of the disease.

Erbitux (cetuximab), co-marketed by Bristol-Myers Squibb and Eli Lilly, was first approved as a colon cancer treatment in 2004.

The new diagnostic was developed by Qiagen Manchester Ltd., based in Manchester, England.

More information

Visit the FDA to learn more about this approval (http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm310899.htm ).

This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.