Precision Oncology
Paring highly specific drugs with the genetic makeup of an individual's cancer have led to improved outcomes.
Precision Oncology Overview
Precision oncology is defined as targeted immunotherapies that show a high degree of effectiveness while not presenting as many side effects as traditional treatment options. For example, many cancers are triggered by genetic changes in genes like EGFR or ALK. Chemical treatments can block these genes resulting in tumor shrinkage and improve treatment responsiveness compared to historical methods.
Immunotherapies have been shown as an excellent treatment option for many cancers. Using genomic biomarker tests, pathologists can detect specific changes within an individual’s cancer. Once a cancer tests positive for a genomic biomarker, immunotherapies can be used that specifically target that change. Commonly treated biomarkers that are susceptible to immunotherapy are HER2, PD-L1, and mismatch repair deficiency, among many others. Elevated levels of biomarkers like these indicate potentially strong responsiveness from targeted immunotherapies.
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Rewriting Cancer
Kathy Wilcox is a patient at Vanderbilt-Ingram with pancreatic cancer. Her cancer was tested for immunological susceptibility through biomarker testing. Once a marker was identified, it was matched with immunotherapy that directly targeted her cancer.
Produced for the Union of International Cancer Control (UICC) by BBC StoryWorks Commercial Productions.
Frequently Asked Questions About Precision Oncology
How long has Vanderbilt been practicing precision oncology?
We have been a leader in precision oncology since genetic testing has been available. We have evolved through multiple different genetic testing platforms, starting with our home-grown “SNaPshot” panel, and now moving into the world where nearly every patient has next-generation sequencing of 600+ genes. We have performed next-generation sequencing on samples from thousands of patients.
How do Vanderbilt-Ingram Cancer Center clinics connect patient data with the right treatments?
We analyze genetic testing results carefully with a panel of experts for our own patients, those in the region, and internationally, to provide the right treatment for the right patient. We host a regional molecular tumor board to review challenging cases, and an international tumor board with cases presented from around the globe. We have precision oncology experts in every cancer to integrate testing results with cutting-edge treatment.
We work with our talented colleagues from genetics and genetic counseling to ensure that germline mutations are identified and appropriate testing and follow up is arranged for patients and families.
Why is precision oncology needed?
Cancer is not a single disease. Even cancers that start from the same organ (for example, breast cancer) and look very similar under the microscope have vastly different genetic mutations and molecular characteristics. In many cases, understanding the genetics of a cancer will identify targets for more precise treatments.
What kind of testing is done for precision oncology?
The cornerstone is usually genetic testing of the tumor and blood. In many cases, we run a 600+ gene panel that tests for mutations and other changes in many different cancer-related genes. These tests are reviewed for mutations that might benefit from a particular targeted therapy. These tests may also identify mutations present in normal cells (called germline mutations) that may predispose a patient or their family to cancer or suggest other treatments that may be helpful.
Other tests may be done that are specific to different types of cancer. For example, breast cancer will have staining for estrogen and progesterone receptors, and the HER2 protein, as well as a gene panel that might predict whether chemotherapy is necessary in some early-stage situations. Many cancers will have staining for the PD-L1 protein to see whether immunotherapy may work.
As a patient, what do I need to provide for genetic testing?
Depending on the type of testing and what the care provider is looking into for care decisions, much of this testing is done using blood samples or from material that was already taken for a biopsy or surgically removed.
What is the future for precision oncology at Vanderbilt?
Precision oncology is a rapidly changing field. New treatments are being approved almost every month that provide new options for patients where previously none existed. We can quickly identify patients and get their testing results to their physicians right away. We are working to move beyond genetic testing alone as a precision oncology tool and find new ways of using testing and other data results. This includes new markers for immunotherapy success, microbiome profiling, and artificial intelligence (AI). We have several large-scale efforts ongoing to use AI to predict response to treatments, an area that will likely continue to expand.
Genetic Medicine at Vanderbilt
Teams of researchers work to understand the unique differences among cancers to identify potential therapeutic options, and our molecular tumor boards analyze at the unique patterns of an individual's cancer to ensure the best treatment options are selected.
Additional Genetic Medicine Resources
Genomics and Clinical Informatics
Our research teams use large datasets and infrastructure to support projects investigating human genetics to identify what may predispose or protect people from getting cancer.
Genome Maintenance Research Program
A collaborative research team of scientists and clinicians seek to understand corruption in the basic functions of cells that leads to cancer development and progression.
Hereditary Cancer Clinic (opens in a new tab)
Inherited cancers occur because a genetic variant is passed down through a family. Our specialists provide evaluations, counseling, and testing for patients who may have a family history or higher risk of developing cancer.
Global Molecular Tumor Board (opens in a new tab)
Our Global Molecular Tumor Board reviews cases through the lens of molecular and genetic characteristics. Our specialists identify potential targeted therapies and strategies tailored to the individual patients. Submit a case for to present to the tumor board.
Cancer
Decoding the ancestry gap in diagnosing and treating acute myeloid leukemia
The disease is driven by complex combinations of multiple genetic mutations rather than a single defect.
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