Hereditary cancer refers to cancers caused by inherited genetic mutations that increase a person’s risk of developing certain types of cancer, often at younger ages. These gene mutations can be passed down through families, affecting multiple generations. Common hereditary cancers include breast, ovarian, colorectal, pancreatic, and prostate cancers.
Thanks to decades of research and advances in genetic testing, we can now identify specific gene mutations—such as BRCA1, BRCA2, and others—that contribute to increased cancer risk. This allows us to detect cancer earlier, or even prevent it altogether, through proactive strategies like enhanced screenings, medications, lifestyle changes, and, in some cases, preventive surgery.
Understanding your family history and genetic makeup empowers healthcare providers to create a personalized Cancer Prevention Plan tailored to your level of risk. This proactive approach shifts care from reactive treatment to prevention—giving individuals and families the opportunity to take control of their health and future.
Recent advancements in genetic science have uncovered a complex interplay of inherited mutations and epigenetic factors that contribute to hereditary cancer. Researchers have identified specific gene alterations—such as those in BRCA1, BRCA2, and other high-risk genes—that significantly elevate cancer risk. These breakthroughs have made it possible to predict cancer susceptibility with greater accuracy and intervene earlier than ever before. By combining advanced genetic testing with a comprehensive review of family medical history, healthcare providers can now create personalized risk profiles tailored to each individual.
This evolving field is transforming hereditary cancer care by shifting the focus from treatment to prevention. Integrating laboratory discoveries into everyday clinical practice allows for customized monitoring, proactive screening, and the use of targeted therapies when needed. These innovations empower patients with knowledge, giving them the tools to make informed decisions and take preventive steps—turning what was once a reactive approach into a proactive, potentially life-saving strategy.
Why Choose Our Hereditary Cancer Program
The field of hereditary cancer management is rapidly evolving, driven by groundbreaking research into genetic predispositions. With the rise of advanced genomic technologies, scientists are now able to pinpoint specific mutations that increase cancer risk. These discoveries have paved the way for highly accurate diagnostic tools and personalized prevention strategies that allow clinicians to identify at-risk individuals earlier and more effectively. By leveraging these insights, healthcare providers can offer interventions tailored to each patient’s unique genetic makeup.
Today’s approach to hereditary cancer is holistic, combining genetic counseling, lifestyle modifications, ongoing surveillance, and—when appropriate—targeted therapies. This integrated model of care is supported by collaboration among researchers, clinicians, and patient advocacy organizations, all working toward the common goal of improving outcomes and empowering patients. As science continues to advance, so too will the tools and strategies available—ensuring that innovation, early detection, and compassionate care remain at the forefront of cancer prevention and treatment.
To schedule any appointment, please submit a request through our website or email us directly at frontdesk@summithealth360.com. A member of our team will contact you to confirm availability and finalize your appointment. Forms are not available online but can be sent by email upon request or completed in-office before your visit.
Take a few moments to fill out a comprehensive health questionnaire covering your medical history, current fitness level, and nutrition habits. The details you provide help us create a customized plan tailored to your unique needs and goals. This also gives our specialists insight into any specific challenges, allowing them to offer guidance that is both practical and effective.
During this session, our health experts review your questionnaire responses, discuss your health objectives, and develop a roadmap for your wellness journey. This is a collaborative effort where every question is addressed, and every concern is taken into account, ensuring a comprehensive and supportive experience.
Patient Testimonials
— Lesley Nedwick.
— jan andelson.
— Julie Flattery.
What Sets Our Program Apart
Understanding hereditary cancer can feel overwhelming, but you’re not alone. This section answers common questions about genetic risks, family implications, and available preventive options. Our goal is to provide clear, accessible information—helping you make confident, informed decisions about your health.
You can start by completing a short online questionnaire that gathers key information about your personal and family health history. This helps identify whether you may be at increased risk for hereditary cancer. A link to the questionnaire is available on our website for your convenience.
If you have a family history of multiple cancers, cancers diagnosed before age 50, or rare types of cancer, you may be eligible for genetic testing. These patterns can signal an inherited risk. Our team will evaluate your history to determine if testing is appropriate.
The assessment involves a simple genetic test performed in our office, often using a saliva or blood sample. It’s quick, non-invasive, and typically covered by insurance for those who meet clinical criteria. The results help guide your personalized prevention plan.
This plan outlines tailored steps to reduce your cancer risk based on your genetic profile. It may include enhanced screening, medication, lifestyle recommendations, or preventive surgery. Our goal is to help you make proactive, informed decisions about your health.
Myriad Genetics partners with healthcare providers to deliver reliable and clinically validated genetic testing. They are also deeply committed to maintaining the privacy and security of your genetic data. Their platform enables timely, accurate results that inform your care.
Your family history helps identify patterns of inherited cancer risk that might otherwise go unnoticed. This information allows us to build a comprehensive risk profile tailored to you. The more accurate the history, the more precise your prevention and treatment strategies can be.
During your consultation, our clinicians will review your assessment, discuss relevant genetic factors, and go over your family history in depth. You’ll receive a clear explanation of your risk level and recommended next steps. The goal is to leave with a confident, personalized plan for managing your health.
Yes—knowing your genetic risk empowers you to take proactive steps that can significantly reduce your chances of developing cancer. Early detection, increased surveillance, and preventive measures can lead to better outcomes. Genetic testing turns uncertainty into actionable care.
