What is genomic cancer testing?

Test Your Cancer

Imagine if you could paint a more precise picture of your cancer. Genomic cancer testing allows you to do just that - identifying unique DNA alterations, or changes, within cancer cells that determine how your tumor behaves and why it grows.
This knowledge may help your doctor recommend treatments that have been approved or are in clinical trials based on the specific alteration identified.


 

What is genomic cancer testing? 

 

Genomic research has developed rapidly over the past twenty years. By studying genes, we can now pinpoint a person’s ancestry, what diseases they may be at risk of developing and, also, the genetic triggers for a number of different cancer types. 
We are used to hearing about cancer treatments in relation to a specific part of the body such as breast, lung or prostate in a one-size-fits-all approach. 


Genomic cancer testing is important to discuss with your doctor because it has the potential to:

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Your cancer is unique, watch the video to learn more.

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What happens during a genomic cancer test?
Your doctor and testing lab teams work together to choose a testing method that will be most effective in helping to understand your tumor.

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What are the common types of tests your doctor may request?

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What can these tests find?
Genomic cancer tests can identify different DNA alterations, or changes, specific to your individual tumor, regardless of its location in the body. The results of the test can lead to options that are tailored specifically for each individual's cancer.
Types of genomic alterations can include KRAS, HER2, BRAF, EGFR, ALK, ROS1, NTRK gene fusions, and many more. 


Should you have any questions regarding genomic cancer testing, please discuss with your doctor.  


For tips & conversation starters, download the ‘Patient-Doctor Discussion Guide’ here

 

 

Date of Preparation: July 2022 / COR-VIT-AU-0019-1

Bayer Australia Pty Ltd, ABN 22 000 1 38 714, 875 Pacific Highway, Pymble NSW 2073. 
Ph: (02) 9391 6000