If you or a loved one has recently been diagnosed with cancer, one of the first things you’ll likely want to do is learn as much as possible about your disease. This includes understanding the genetic makeup of your tumor. Genomic cancer testing can provide valuable information about the specific genes that are mutated in your tumor. In this blog post, we will discuss what genomic cancer testing is, and how it can help you and your doctor make informed decisions about your treatment.

What is genomic cancer testing and why is it important for cancer patients and their families?

Genomic cancer testing is a type of DNA testing that looks for specific mutations in the genes of a person’s tumor. This information can be used to help design more targeted and personalized treatment plans. Additionally, genomic cancer testing can also provide important insights into a person’s risk of developing certain types of cancers.

How does genomic cancer testing work?

Genomic cancer testing usually begins with a biopsy, in which a small sample of tissue is taken from the tumor. This sample is then analyzed for specific mutations in the genes.

One of the benefits of genomic cancer testing is that it can provide more information about the specific genes that are mutated in your tumor. Additionally, genomic cancer testing is often more accurate than traditional tests, such as pathology and genetic sequencing. This means that genomic cancer testing can help your doctor design a more targeted and personalized treatment plan for you.

Another benefit of genomic cancer testing is that it can also provide important insights into your risk of developing certain types of cancers. This information can help you and your doctor make informed decisions about your cancer prevention and screening.

What happens after a patient completes genomic cancer testing?

After a patient completes genomic cancer testing, the results of the test will be analyzed by a team of specialists. This team will use the results of the test to develop a personalized treatment plan for the patient.

In some cases, the results of genomic cancer testing may show that a patient is at high risk for developing certain types of cancers. In these cases, the patient may be advised to undergo additional cancer screenings or take preventive measures.

How will genomic cancer testing impact future treatment options for patients with cancer?

As more and more patients undergo genomic cancer testing, the results of these tests will help to improve our understanding of how cancer develops and grows. This information will be used to develop new and improved treatments for patients with cancer.

Additionally, genomic cancer testing may help doctors to identify which patients are most likely to respond to certain types of treatment. This information can be used to tailor treatment plans specifically for each patient, which may improve the effectiveness of cancer treatment.

Genomic cancer testing is a rapidly evolving field, and the impact that it will have on future treatment options for patients with cancer is still unknown. However, as more and more patients undergo this type of testing, we will gain a better understanding of how to use this information to improve cancer treatment.

If you have been diagnosed with cancer, genomic testing may be an option for you. Be sure to discuss all of the risks and benefits of this type of testing with your doctor before making a decision.

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