1. Understand the Terms
What is a biomarker?
A biomarker is a gene, protein, or other substance that is in your blood, bodily fluids, or cells.
What is biomarker testing?
Biomarker testing is a way to look for those biomarkers that can provide information about your cancer. Biomarker
testing can be called different names, including:
- Genomic testing or profiling
- Tumor testing or subtyping
- Tumor genetic testing
- Somatic testing
- Companion diagnostic testing (when paired with a specific treatment)
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Some biomarker tests can test a solid tumor, and some can test your blood and other fluids (i.e., liquid biopsies).
Why is biomarker testing useful?
Biomarkers may affect how certain cancer treatments will work and understanding your biomarkers can help you
and your health care team make treatment decisions that are best for you. This is often called personalized or
precision medicine. Biomarker testing is a key part of getting access to precision medicine. For example, some
targeted treatments may only work if you have certain biomarkers.
Is biomarker testing different from genetic testing?
Genetic testing is not the same as biomarker testing. Genetic testing is a test to find out if you have an inherited
genetic mutation. You inherit your genes, and sometimes genetic mutations, from your parents. Genetic mutations
may make it more likely that you will develop a specific type of cancer. For example, if you have the BRCA1 or
BRCA2 mutations, you have a higher chance of getting breast, ovarian, and other cancers. For more information
about genetic testing, visit: cdc.gov/genomics-and-health/counseling-testing/genetic-testing.html.