Genetic testing can provide information to individualize treatment plans and optimize outcomes
Germline (inherited) testing should be conducted at initial diagnosis of prostate cancer in certain populations to understand if genetic mutations are present, as these are associated with high-risk cancer. Germline testing could also be conducted at the time of disease progression to metastatic disease, if not done previously. Knowing mutation status can also help determine the best treatment approach. This test can be done through saliva, blood, or tissue samples.1
Somatic (acquired) testing should be performed in patients once they receive a diagnosis of metastatic disease. If the patient still has his prostate, this test can be completed with a prostate biopsy of the cancer tissue to determine if any gene mutations are present.1,2
| Up to 15% of men with metastatic prostate cancer have mutations in1: |
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| Homologous recombination repair (HRR) genes, such as BRCA2, BRCA1, ATM, CHEK2, PALB2 |
| Mismatch repair (MMR) genes such as MLH1, MSH2, PMS2, and MSH6 |
| Pathogenic variant HOXB13 |
Many different tests can be done to target specific genes or by conducting a prespecified or large gene panel. Genetic counselors are available to help guide which test is appropriate for your patient and help interpret results. Some companies that offer genetic testing can help find a genetic counselor in your area.