By Nicole Brudos Ferrara
Colorectal cancer begins when healthy cells in the colon or rectum develop mutations, or changes, in their DNA. These damaged cells then become cancerous, grow and divide uncontrollably, and form a tumor. Genetic factors play a role in this process.
Some gene mutations passed through generations of your family can increase your risk of colorectal cancer significantly. The most common inherited syndromes that increase colorectal cancer risk are familial adenomatous polyposis and Lynch syndrome, also known as hereditary nonpolyposis colorectal cancer. But you don't need a family history of colorectal cancer to have a genetic mutation that could cause the disease.
"Someone can have developed a mutation in their germ line and be the first person in the family to have colorectal cancer," says Lisa Boardman, M.D., a gastroenterologist and hepatologist at Mayo Clinic. "Family history is not the end of the story."
Here's what experts at Mayo Clinic want you to know about genetics and colorectal cancer, the third leading cause of cancer-related deaths in the U.S., according to the National Cancer Institute:
Niloy Jewel Samadder, M.D., a gastroenterologist and hepatologist at Mayo Clinic, and researchers in Mayo Clinic's Center for Individualized Medicine, recently found 1 in 6 patients with colorectal cancer had an inherited cancer-related gene mutation that likely predisposed them to the disease. In addition, the researchers discovered that 60% of these colorectal cancer cases would not have been detected using a standard guideline-based approach.
According to Dr. Samadder, these findings are important for three reasons:
"When we looked specifically at patients with colorectal cancer in this study, we found 15% had a genetic predisposition to colorectal cancer. And about 30% of the time, we saw modifications in their treatment plan occur because of genetic testing, whether it was surgery or the use of different treatment options," says Dr. Samadder. "The guidelines we use to identify who should undergo genetic tests performed terribly. Had we relied solely on the guidelines, only 50% of patients who had a genetic mutation identified would have been captured."
"Anybody with a colorectal cancer diagnosis should speak to their primary care physician, oncologist or surgeon about the importance of genetic testing to identify if there was a mutated gene that predisposes them to cancer," says Dr. Samadder. "Knowing this could potentially change the management of their cancer to improve survival — and help prevent cancer in their loved ones."
"Anyone who has colorectal cancer should get genetic screening," agrees Dr. Boardman. "Even if you have no family history of colorectal cancer, we still recommend it."
Genetic testing for Lynch syndrome is particularly important. Lynch syndrome is an inherited condition that increases your risk of colon and endometrial cancers, and several other cancers. Families that have Lynch syndrome usually have more instances of colon cancer or endometrial cancer than is typically expected. Lynch syndrome also causes cancers to occur at an earlier age than they might in the general population.
"The importance of Lynch syndrome is you're not just at risk of colorectal cancer, but you could be at risk of small bowel, stomach, uterine, skin and even brain cancers," says Dr. Samadder. "In the individual with the gene mutation for Lynch syndrome, surveillance can be broadened beyond colorectal cancer screening."
If you have Lynch syndrome, your children have a 50% chance of having it as well, as do other first-degree relatives.
Researchers also have learned that colorectal cancer in people with Lynch syndrome responds well to immunotherapy, says Dr. Samadder. Recent studies also have suggested that aspirin can reduce the risk of cancer in people with Lynch syndrome.
If you've been diagnosed with colorectal cancer, Dr. Samadder recommends three steps:
"Anyone who has a first-degree relative with colon cancer is at high risk for colorectal cancer, but it's not necessarily related to an underlying genetic condition," says Dr. Boardman. "Knowing your family history is important."
You should know your family medical history for all cancer types, as diagnosis for one cancer could indicate that you're at higher risk for other cancers. It's also important to be aware of any relatives who may have been diagnosed with multiple cancers, or those who were diagnosed at a young age. Even knowing if a first-degree relative has had a polyp removed during colorectal cancer screening can be important. All these factors can play a role in your risk for colorectal and other cancers.
Knowing your family's cancer history means you can take a proactive approach to cancer prevention. "We recommend patients who have a first-degree family history of colorectal cancer start screening with colonoscopy 10 years earlier than the youngest age of colorectal cancer diagnosis in the family, or at age 40, whichever is younger, and repeat every five years," says Dr. Samadder.
If you have multiple family members with colorectal cancer or have a first-degree relative who developed colorectal cancer at an age younger than 60, Dr. Samadder recommends you consider genetic testing in addition to screening.
For tips on how to talk to your family about their medical history, read this.
Research conducted by physician-scientists like Drs. Samadder and Boardman has led to improvements in prevention and treatment, and the survival of more people diagnosed with colorectal cancer. The five-year survival rate in the U.S. is now 64.7%, and death rates have been falling on average 2% each year from 2010 to 2019, according to the National Cancer Institute.
Recognize Colorectal Cancer Awareness Month this March by following the advice of Drs. Samadder and Boardman to get the best possible preventive screening and treatment for colorectal cancer — and share this information with others.
This article originally appeared on the Mayo Clinic Cancer Center blog.
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Tags: cancer, center for individualized medicine, colon cancer, DNA Testing, Dr. Niloy "Jewel" Samadder, gene sequencing, Genetics, genomic medicine, genomic medicine, hereditary colon cancer, Lynch syndrome, Precision Medicine