Hereditary Diffuse Gastric CancerLast Updated: July 01, 2009 This section has been reviewed and approved by the Cancer.Net Editorial Board, 06/09 Overview
What is hereditary diffuse gastric cancer? Hereditary diffuse gastric cancer (HDGC) is an inherited condition associated with an increased risk of gastric (stomach) cancer. The stomach is the area between the esophagus (swallowing tube) and the start of the intestine. It is a reservoir for food, and the chemicals that help to digest food are made there. Some people commonly refer to the stomach as the entire abdomen. However, doctors make a distinction between the stomach, which is an organ, and the abdomen, which is the area of the body between the chest and pelvic bones that holds many organs. Diffuse gastric cancer is a specific type of stomach cancer that tends to affect much of the stomach rather than staying in one area of the stomach. The average age for someone with HDGC to be diagnosed with stomach cancer is 38; gastric cancers not associated with this syndrome tend to occur in individuals older than 60. Women with HDGC also have an increased risk of lobular breast cancer. People with HDGC may also have some increased risk of colorectal cancer. What causes HDGC? HDGC is a genetic condition. This means that the cancer risk and other features of HDGC can be passed from generation to generation in a family. The gene associated with HDGC is called CHD1. A mutation (alteration) in the CHD1 gene gives a person an increased risk of developing gastric cancer and other cancers associated with HDGC. Researchers believe that other genes may be associated with HDGC, and studies are ongoing to learn more about this condition. How is HDGC inherited? Normally, every cell has two copies of each gene: one inherited from the mother and one inherited from the father. HDGC follows an autosomal dominant inheritance pattern, in which a mutation happens in only one copy of the gene. This means that a parent with a gene mutation may pass along a copy of their normal gene or a copy of the gene with the mutation. Therefore, a child who has a parent with a mutation has a 50% chance of inheriting that mutation. A brother, sister, or parent of a person who has a mutation also has a 50% chance of having the same mutation. How common is HDGC? The specific number of families with HDGC is unknown. The overall incidence of gastric cancer varies in different parts of the world. In the United States, it is estimated that less than 1% of the population will develop stomach cancer. The highest rate of gastric cancer is found in China, Japan, and other countries in Southeast Asia, as well as in Central and South America. How is HDGC diagnosed? Guidelines for the diagnosis of HDGC syndrome have been proposed, but may change over time as more is learned about this condition. Currently, the diagnosis of HDGC is suspected if a person or family meets any of the criteria listed below:
Genetic testing for mutations in the CDH1 gene is available. However, only about 30% of families that appear to have HDGC will have a mutation found in the CDH1 gene. Therefore, both clinical and genetic aspects must be considered in counseling individuals about the potential for their family to have HDGC, and talking with a genetic counselor or geneticist (a doctor with training in genetic diseases and conditions) that is familiar with the syndrome is recommended. What are the estimated cancer risks associated with HDGC? Not everyone who inherits a gene mutation for HDGC will develop cancer. In people who have this gene mutation, the risk for diffuse gastric cancer is estimated to be about 65% for men and 80% for women. Women with HDGC also have about a 40% risk of lobular breast cancer. The risk of colorectal cancer in people with HDGC has not been estimated. What are the screening options for HDGC? Screening for stomach cancer is suggested for people known to be at risk for HDGC. However, the effectiveness of current screening techniques for the early diagnosis of stomach cancer is not proven. Screening recommendations may also change over time as new technologies are developed and more is learned about HDGC. It is important to talk with your doctor about appropriate screening tests. Current Options for Screening
Additional Screening for Women Women at risk for HDGC should be considered at high risk for breast cancer and talk with their doctor about breast cancer screening options at the age of 35, or ten years before the age of the youngest affected relative. Screening options include:
Other Screening Colonoscopy, which is endoscopy of the colon, every one to two years, should be considered in families where both gastric cancer and colorectal cancer have been diagnosed. Colorectal cancer screening should begin five to 10 years earlier than the earliest diagnosis of colorectal cancer in the family or by age 50, whichever is sooner. Learn more about what to expect when having common tests, procedures, and scans. Questions to ask the doctor If you are concerned about your risk of cancer, talk with your doctor. Consider asking the following questions of your doctor:
If you are concerned about your family history and think you or other family members may have HDGC, consider asking the following questions:
Additional resources What to Expect When You Meet With a Genetic Counselor National Cancer Institute American Cancer Society CancerCare To find a genetic counselor in your area, ask your doctor or visit these websites: National Society of Genetic Counselors National Cancer Institute: |
