Discover What DNA Reveals About Your Cancer Risk
Our Clinical Genomics Program is here to help you feel informed about your cancer risk. Those patients scheduling their annual screen appointments (at a participating site) will be provided a cancer risk assessment to complete as part of their appointment check-in process.
Those patients who complete the cancer risk assessment will be contacted by a nurse navigator who will provide them with their cancer risk profile. If you are at high-risk, you may receive:
- High-risk surveillance pathways
- Genetic testing and genetic counseling
- Cascade testing for your family
Genetics and Cancer Risk
It’s well established that having pathogenic variants in BRCA 1/2 (and other genes) puts individuals at a much higher risk of developing hereditary cancers, primarily breast and/or ovarian cancers. Likewise, it’s well established that there are several genes associated with a higher risk of developing gastrointestinal and/or colorectal cancer, including the Lynch syndrome. Those with Lynch syndrome are also at a higher risk of developing other cancers, such as uterine, stomach, liver, kidney, and brain cancers, at a young age (<50 years old).
What to Expect During My Screening?
Watch the video to learn more about how we're pairing a genetic risk assessment with your annual mammogram screening, and what you can expect.
Participating Program Sites
The Clinical Genomics Program will be enrolling potential participants who schedule at the following locations:
Imaging Center Locations |
AdventHealth Imaging Center Waterford Lakes |
Digestive Health Locations |
AdventHealth Medical Group Gastroenterology and Hepatology at Dr. Phillips |
AdventHealth Medical Group Gastroenterology and Hepatology at Orlando |
Primary Care Locations |
AdventHealth Medical Group Family Medicine at RDV |
AdventHealth Medical Group Family Medicine at East Orlando |
Women's Care Locations |
AdventHealth Women’s Center Winter Park |
Questions? Click below to complete the form and our program team will be in touch.
Cancer Resources
Whether you've received a new diagnosis or are looking for more support, we have a variety of resources available to you. Learn more about some of the services we offer through our AdventHealth Cancer Institute.
Frequently Asked Questions
- Why are we offering clinical genomic programs?
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From disease prevention to diagnosis to treatment, genomics is the future of medicine. Genomics will be an essential component of health care not just for the individual, but for our greater community as we focus on wellness and preventative care. The implications of genomics programs are significant for today’s patients, and importantly, the future of Florida’s health.
- What are we evaluating?
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AdventHealth is implementing clinical pilots within mammography appointments, colonoscopy appointments, and primary care appointments to provide the benefits of personalized and preventative care with the goal to expand the programs across AdventHealth. With any new initiative or technology, we test it in a small population and see how the community responds before expanding to the whole organization.
- Who can join the program?
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Adults (18-70) who are scheduled for a mammography appointment, colonoscopy appointment, and/or primary care appointment at one of our pilot locations/clinics within AdventHealth. Once you have an appointment at one of these locations, you will receive an email to complete a cancer risk assessment survey. This is the first step in the program.
- How do I join the program?
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You will receive an email from Volpara Health (sent on behalf of AdventHealth). You will need to enter your date of birth to access your personal cancer risk survey. Please complete your survey before your scheduled appointment (either colonoscopy or mammography). Our care navigator will reach out after your appointment with your results and potential next steps if you are at higher-than-average risk for hereditary cancer.
- What can I expect once I join?
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Once you complete your survey, our care navigator will reach out with your results. If you are at low risk, you will continue completing your screenings, as prescribed by your health care provider. If you are at higher-than-average risk, you could be referred to our genetic counselors who will discuss genetic testing and/or you could be referred for additional tests such as ultrasounds or biopsies.
- Why are you looking at cancers that may have a hereditary cause, like breast and colon cancers?
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It’s well established that having pathogenic variants in BRCA 1/2 (and other genes) puts individuals at a much higher risk of developing hereditary cancers, primarily breast and/or ovarian cancers. Likewise, it’s well established that there are several genes associated with a higher risk of developing gastrointestinal and/or colorectal cancer, including the Lynch syndrome. Those with Lynch syndrome are also at a higher risk of developing other cancers, such as uterine, stomach, liver, kidney, and brain cancers, at a young age (<50 years old).
- Why is early detection so important?
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Early detection of cancer is associated with better health outcomes and lower cost of care to the patient. Additionally, if genetic testing shows that a patient has a higher chance to develop cancer, the patient has the opportunity to alert first-degree relatives (such as parents, children, siblings) to let them know about their potential to carry the same hereditary cancer predisposition syndrome.
- If I have breast cancer or colon cancer, could I pass this on to my children?
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If you are found to have a hereditary predisposition to develop breast cancer, each of your children will have a 50 percent chance of having it.
- Will I get billed for the DNA analysis testing?
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If the DNA analysis testing is ordered by the physician(s) involved in your care, you will be billed in the same manner as you would with any other lab tests that are medically recommended and ordered by the physician(s) involved in your care.
A majority of patients typically pay $100 or less (out of pocket). If you have a high deductible or are self-pay, the genetic testing self-pay price is around $250. Most laboratories have patient assistance programs if you cannot afford this cost.
- If DNA analysis testing indicates a potential future “pre-existing condition”, will it affect my chances of obtaining insurance in the future?
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A federal law called the Genetic Information Nondiscrimination Act (GINA) makes it illegal for health insurance companies, group health plans, and most employers to discriminate against you based on your genetic information, but GINA does not apply to life insurance, long-term care insurance, or disability insurance. More information about GINA is available at http://www.genome.gov/.
There is also Florida law that prohibits your genetic information from being used to grant or deny certain insurances, employment, mortgage, loan, credit or educational opportunities. However, a diagnosis made from your DNA analysis test results may have an effect on your access to certain insurance or insurance rates. For example, a life insurance company may consider a medical diagnosis in your medical record, even if the diagnosis was based on the results of a DNA analysis. Please know that AdventHealth and your physician(s), as your health care provider, will not use your genetic information for any of these purposes. Laws against genetic discrimination may not apply to the military.
- If I have breast cancer, can my children be denied medical or insurance coverage?
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Your family is protected by the Genetic Information Nondiscrimination Act (GINA).
- Are you going to sell my DNA to other companies?
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No, we are not going sell your DNA to other companies.
Your DNA analysis test results and other health information about you may be used and shared with others as allowed by federal and state privacy laws for:
- Treatment you receive from healthcare providers.
- Payment to AdventHealth, your physician(s) and the laboratory by health plans or other payers for your treatment.
- Health care operations of AdventHealth, your physician(s) or the laboratory. For example, health care operations include reviewing what went well with your treatment and what needs to be improved, as well as creating de-identified information that may be used and shared with others as allowed by law.
Please review the AdventHealth Joint Notice of Privacy Practices for more details about how your health information may be used and shared with others and how you may request restrictions.
- How do you de-identify and use my de-identified DNA analysis test results?
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Your personal identifying information is removed from the data elements that constitute the DNA analysis test results. By aggregating large numbers of de-identified DNA analysis data elements, scientists are able to better understand how certain genes may be associated with certain medical conditions.
- If I have further questions regarding the DNA Analysis testing, who may I speak with?
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Speak with your physician or genetic counselor who is performing your procedure or ordering the DNA analysis test. If you have additional questions about the clinical program, please contact our care navigator at Call407-440-1394.