Dattoli Cancer Center

The Benefits of Genetic and Genomic Testing

At our center, we employ multiple laboratory tests for genomic and genetic makeup that allow us to determine which specific medications and treatments may be most appropriate for each patient. We utilize the Invitae Genetic Test and the Myriad myRisk® Hereditary Cancer testing. The Myriad test is a 35-gene panel that identifies elevated risk for eight hereditary cancers. A patient may have a host of genetic pathways and mutations (including BRACA 2, BRCA1, HOXB13, ATM, CHEK2, and CDK1), and they can tell us whether or not a patient is likely to respond well to a particular agent. For example, we know that a patient with positive BRCA1 and especially positive BRCA2 gene mutations will likely have a shorter effective run with the androgen-blocking drugs Xtandi® and Zytiga®.

Another lab test analyzing serum is called a “droplet digital PCR assay,” It can also help us determine which patients will best respond to those chemical agents, Xtandi® and Zytiga®. It should be noted that genetic markers are also important in light of the patient’s family history. We want to know what the family history is with regard to other cancers. We can see that a patient’s daughters may be prone to breast or ovarian cancer, and now even colon and pancreatic cancers enter the picture in the spectrum related to prostate cancer. These cancers are essentially on the same page in our genetic makeup. Melanoma is also now seen as genetically related to prostate cancer, and all of these cancers may occur at increased frequency in the patient tested.

While genetic testing is important for the patient’s siblings and children (and also for the patient on occasion), there is even greater importance in sampling the actual cancerous tissue removed from the patient to identify somatic mutations. This is known as comprehensive genomic profiling (CGP). This test can help identify which treatment may benefit the patient (e.g., AR-7 mutations suggest resistance to Xtandi®/Zytiga® while HRR gene mutations predict response to Lynparza). Checkpoint inhibitors (e.g., PD-1) suggest sensitivity to pembrolizumab. We have used FoundationOne ®CDx as the best genomic test currently available for identifying somatic mutations. This test searches 324 genes for cancer-relevant mutations in the DNA.