BRCA Testing for Ovarian Cancer Risk: Unlocking Your Genetic Blueprint

June 22, 2025

BRCA Testing for Ovarian Cancer Risk: Unlocking Your Genetic Blueprint

BRCA testing for ovarian cancer is like having a conversation with your DNA about your future health risks. It’s a powerful tool that can reveal crucial information about your likelihood of developing this often-silent disease. But let’s be honest: navigating genetic testing can feel overwhelming, with complex medical terms and statistics that seem designed to confuse rather than clarify.

At Not These Ovaries, we believe knowledge empowers action — especially when it comes to ovarian cancer. That’s why we’re breaking down BRCA testing in plain terms, helping you understand what it means for your health and your family’s future.

Understanding BRCA Genes and Their Role in Ovarian Cancer

BRCA1 and BRCA2 genes function as your body’s DNA repair crew, working around the clock to fix damaged genetic material and prevent cells from growing out of control. When these genes operate normally, they serve as powerful tumor suppressors, keeping cancer at bay.

But sometimes these genes carry mutations — genetic changes that compromise their protective abilities. When BRCA genes can’t do their job properly, your risk of developing certain cancers, including ovarian cancer, increases significantly.

Here’s what the numbers tell us: While approximately 1.3% of women in the general population will develop ovarian cancer during their lifetime, this risk jumps dramatically for women with BRCA mutations:

  • BRCA1 mutations: 39-46% lifetime risk by age 70
  • BRCA2 mutations: 10-27% lifetime risk by age 70

These aren’t small increases—they represent a fundamental shift in cancer risk that can influence major life decisions.

However, carrying a BRCA mutation doesn’t guarantee you’ll develop ovarian cancer. Think of it as having a warning system that alerts you to take extra precautions and maintain heightened awareness of your health.

Who Should Consider BRCA Testing for Ovarian Cancer?

BRCA testing isn’t recommended for everyone, but certain factors make it particularly valuable. You might benefit from BRCA testing if you have:

Personal Health History:

Family History Red Flags:

  • Multiple relatives with ovarian cancer or breast cancer
  • Breast cancer in family members under age 50
  • Male relatives with breast cancer
  • Known BRCA mutations in your family

Ethnic Background:

  • Ashkenazi Jewish ancestry (higher prevalence of BRCA mutations)
  • Other populations with known BRCA founder mutations

Remember, genetic counselors evaluate many factors beyond this list. If you’re concerned about your ovarian cancer risk factors, discussing your family history with a healthcare provider can help determine if BRCA testing makes sense for your situation.

Does BRCA Test for Ovarian Cancer Specifically?

Here’s where things get important to understand: BRCA testing doesn’t actually detect ovarian cancer itself. Instead, it identifies mutations in the BRCA1 and BRCA2 genes that are associated with an increased risk of developing ovarian cancer.

Think of it this way: BRCA testing reveals your genetic predisposition, not your current cancer status. A positive result means you carry genetic changes that increase your lifetime risk of developing ovarian cancer, but it’s not a cancer diagnosis. You could have a BRCA mutation and never develop cancer, or you could develop cancer without having any known genetic mutations.

Conversely, a negative BRCA test result doesn’t provide immunity against ovarian cancer. Most ovarian cancers actually occur in women who don’t carry BRCA mutations.

BRCA testing is fundamentally about understanding your genetic risk landscape, which then guides decisions about prevention strategies, screening protocols, and treatment options if cancer does develop.

How BRCA Gene Testing for Ovarian Cancer Works

Getting BRCA tested isn’t as intimidating as it might sound, and exciting developments are making it even more accessible.

Initial genetic counseling: Your journey begins with a genetic counselor who specializes in hereditary cancer syndromes. They’ll create a detailed family tree, review your medical history, and explain what BRCA testing can and cannot tell you about your health.

Sample collection: The actual testing process is straightforward — either a blood draw or saliva sample. Your genetic material goes to a specialized laboratory where technicians examine your BRCA1 and BRCA2 genes for known disease-causing mutations.

Results review: Within 2 to 4 weeks, you’ll meet again with your genetic counselor to discuss your results and plan next steps based on your specific situation.

Breakthrough in testing technology: Exciting developments are making BRCA testing more accessible. Researchers at Dana-Farber Cancer Institute have developed a novel approach that identifies specific microRNA patterns in blood samples — similar to how COVID-19 tests work. In preliminary studies, this method correctly identified BRCA mutations 94% of the time.

While still in development, this innovation could eventually make BRCA testing as routine as checking cholesterol levels during annual physical exams, potentially expanding access to genetic risk information for millions more people.

The whole process, whether traditional or using future innovations like this new method, is designed to be as stress-free as possible. And remember — knowledge is power. Whatever the results, you’ll be better equipped to make informed decisions about your health.

Interpreting BRCA Testing Results in Ovarian Cancer Context

Getting your BRCA test results can feel like opening a mysterious package. What’s inside? And what does it mean? Let’s break it down:

Positive result: A mutation was found in your BRCA1 or BRCA2 gene. You typically inherit one copy of each BRCA gene from each parent, and having one normal copy is usually enough to prevent cancer development. 

However, that normal copy can become damaged over your lifetime, which is why people with inherited BRCA mutations have a higher cancer risk. It doesn’t mean you have cancer or that you’ll definitely get it, but it does mean your risk is higher than average.

Negative result: No mutations were found. Good news, right? Well, mostly. It means your risk is likely lower, but it doesn’t guarantee you won’t get ovarian cancer. Remember, most ovarian cancers aren’t related to BRCA mutations.

Variant of uncertain significance (VUS): This is the genetic equivalent of a “maybe.” It means a change was found in your BRCA gene, but we’re unsure whether it increases cancer risk. Your genetic counselor can help you understand what this means for you.

It’s important to understand that BRCA test results provide information about risk, not certainty. A positive result indicates an increased likelihood of developing ovarian cancer, but it doesn’t guarantee you will get the disease. Similarly, a negative result doesn’t mean you’re immune to ovarian cancer. These results offer valuable insight into your genetic predisposition, which can guide your healthcare decisions and screening strategies, but they can’t predict the exact outcome of your future health.

Risk Management Strategies for BRCA Mutation Carriers

If you test positive for a BRCA mutation, you have several evidence-based options to manage your increased cancer risk:

Enhanced surveillance

  • More frequent clinical exams and imaging
  • Earlier and more intensive screening protocols
  • Regular consultation with specialists like gynecologic oncologists

Preventive Surgery

  • Risk-reducing salpingo-oophorectomy (removal of ovaries and fallopian tubes)
  • Can reduce ovarian cancer risk by 85 to 90% in BRCA carriers
  • Timing depends on age, family planning, and personal preferences

Chemoprevention

  • Oral contraceptives may reduce ovarian cancer risk
  • Discussion with healthcare providers about benefits and risks

Lifestyle modifications

  • Maintaining a healthy weight
  • Regular physical activity
  • Limiting alcohol consumption
  • These don’t eliminate BRCA-related risk but support overall health

Each approach involves complex trade-offs that require careful consideration with your healthcare team. There’s no universal “right” choice. The best strategy depends on your individual circumstances, values, and preferences.

BRCA Testing and Ovarian Cancer Treatment Considerations

Your BRCA mutation status influences more than prevention—it can significantly impact ovarian cancer treatment decisions:

Treatment response: BRCA-related ovarian cancers often show enhanced sensitivity to platinum-based chemotherapy for ovarian cancer, potentially leading to better initial treatment outcomes.

Targeted therapy options: PARP inhibitors have revolutionized treatment for BRCA-related ovarian cancers. These medications exploit the DNA repair deficiency in BRCA-mutated tumors, offering new hope for extended survival.

Clinical trial eligibility: Knowing your BRCA status may qualify you for cutting-edge clinical trials testing innovative treatments designed specifically for hereditary ovarian cancers.

Family implications: Your BRCA results provide valuable information for blood relatives, who may benefit from genetic counseling and testing based on your results.

BRCA Testing: Navigating the Emotional Journey

BRCA testing involves more than medical decisions — it’s an emotional process that can impact your entire family:

Processing results: Whether positive or negative, test results can trigger complex emotions, including relief, anxiety, survivor’s guilt, or uncertainty about the future.

Family communication: Your results may have implications for relatives. Consider how and when to share genetic information, respecting both your privacy and your family’s right to know about potential risks. This can create complex family dynamics that require thoughtful navigation.

Insurance and discrimination: The Genetic Information Nondiscrimination Act (GINA) provides protection against genetic discrimination in health insurance and employment, though it doesn’t cover life insurance or disability insurance.

Reproductive planning: For younger women, BRCA results might influence decisions about family planning, including preimplantation genetic diagnosis or the timing of preventive surgeries.

Empowering Decisions Through BRCA Testing in Ovarian Cancer

BRCA testing represents one powerful tool in the fight against ovarian cancer, but it’s part of a larger strategy that includes awareness, early detection, and advancing treatment options.

At Not These Ovaries, we’re committed to funding research that helps all women facing ovarian cancer — including those with BRCA mutations and those with low-grade serous ovarian cancer and borderline tumors that may not be BRCA-related. Our mission ensures 100% of donations fund research directly, accelerating progress toward better prevention, detection, and treatment.

Your genes provide important information, but they don’t determine your destiny. Understanding your BRCA status empowers you to make informed decisions about screening, prevention, and treatment that align with your values and life goals.

Whether you choose testing or not, you’re taking control of your health journey. That’s both brave and powerful. And remember — you don’t have to navigate this path alone. Support is available every step of the way.

Have questions? Ask Hope

Hope is a conversational AI that can help you answer your questions about ovarian cancer and our charity. Click Ask Hope to start a chat session.



Recommended Reading