AN UNDERUSED TOOL FOR DETECTING CANCER VULNERABILITY: GENETIC TESTS
“Everyone has some risk of developing cancer, and in most cases the disease develops by chance. However, some people are genetically predisposed to developing certain types of cancer.”
Dr. Niloy Jewel Samadder, gastroenterologist and hepatologist
PHOENIX
Genetic testing can uncover inherited genetic mutations, and it is an underused tool that could individualize cancer therapies and improve survival, scientists say.
In a new study published in JAMA Oncology, scientists with Mayo Clinic’s Center for Individualized Medicine conducted genetic testing in more than 3,000 patients who were diagnosed with cancer at Mayo Clinic Cancer Center locations in Arizona, Florida and Minnesota. In all, the scientists found that 1 in 8 patients with cancer had an inherited cancerrelated gene mutation.
This mutation would not have been detected in half of these patients using a standard guideline-based approach.
“We found that 13.5 percent of patients had an inherited mutation in a gene associated with the development of their cancer,” said Niloy Jewel Samadder, M.D., a Mayo Clinic gastroenterologist and hepatologist, who is the study’s author. “Everyone has some risk of developing cancer, and in most cases the disease develops by chance. However, some people are genetically predisposed to developing certain types of cancer, such as breast or colon cancers.”
A genetic mutation can cause a gene to malfunction and lead to a cell becoming cancerous. Although many mutations that cause cancer happen by chance in a single cell, the study confirms that nearly 10 to 25 percent are inherited mutations that set off a cycle of events that can lead to cancer.
Samadder said that uncovering these hidden inherited genetic mutations could help families manage cancer care and lead to targeted cancer therapies that can save lives.
In the two-year Interrogating Cancer Etiology Using Proactive Genetic Testing (INTERCEPT) study, Mayo Clinic provided free genetic testing and counseling to 3,084 Mayo Clinic patients as part of their standard cancer care. The project, representing the largest known multicenter study of universal testing of patients with cancer, included a broad mix of cancer stages and types, including breast, colorectal, lung, ovarian, pancreatic, bladder, prostate and endometrial cancers.
The researchers were surprised to find that the standard guidelines physicians relied on to determine which patients with cancer should undergo genetic testing were only able to identify 48 percent of the patients with an inherited genetic mutation.
“More than half of the patients who developed cancer due to inherited mutations were being missed, and that has major implications for family members,” said Samadder, who presented his study at the American Society of Human Genetics on Oct. 30.
During the study, the researchers found that one-third of the patients with the highest-risk cancer genes had a change in their medical management after their genetic mutation was discovered, including the type of surgery or chemotherapy they received.
“This targeted treatment would have been lost if the patients had not received genetic testing,” Samadder said.
“Genetic testing is underutilized in cancer care, both for patients and for their families, often due to outdated guidelines that restrict testing to a narrow group of high-risk patients,” said Robert Nussbaum, M.D., chief medical officer of Invitae Corp., which performed the genetic sequencing and analysis for the project. “All cancer patients should have access to complete genetic information that can guide their care and inform their families’ health.” Nussbaum was a contributing author on the study.
Sharing genetic risks with family members
Just as important as a patient discovering an inherited cancer mutation is the fact that they can then share the heritable cause of their disease with relatives, Samadder said, so family members can pursue care in hopes of detecting disease sooner and managing cancer.
“We can help prevent cancer in their loved ones because it is genetic, and they share these cancercausing genetic changes with their children, siblings and others in their families,” Samadder explained. “We can target prevention strategies for those high-risk individuals and hopefully prevent cancer altogether in future generations of their family.”
All blood-related family members of patients found to have a genetic mutation were offered free genetic testing. Overall, 1 in 5 of these family members underwent testing. The next steps will be to incorporate the study findings into the care of all patients with cancer at Mayo Clinic.
“Steps are being taken to ensure all patients are offered genomic sequencing to better understand the genes that led to the development of their cancer, and how to precisely target treatment and improve survival,” Samadder said.
“Genetic testing is underutilized in cancer care, both for patients and for their families, often due to outdated guidelines that restrict testing to a narrow group of high-risk patients.”
Dr. Robert Nussbaum