Docrates Cancer Center makes use of the knowledge of both the human genome and the cancer genome in its treatments. Docrates uses several different genetic and other kinds of tests aimed at better understanding – through the careful profiling of a tumor – which drugs should be used (e.g. targeted drugs) and which drugs should be avoided due to the fact that they are likely to be ineffective. The tests can also help to determine the primary site of the cancer in situations where a metastatic cancer is diagnosed without an obvious primary tumor. The tests may also provide further information when making a prognosis for the cancer.
The tests are done using tissue, blood or saliva samples.
Examples of tests used by Docrates:
Biocept is a very sensitive method for detecting the most common genetic mutations from a blood sample. Furthermore, the test can be used to analyse the biomarkers of circulating tumor cells in the bloodstream of a person with metastatic cancer. The test can be useful in situations where a tissue sample cannot be obtained. (http://biocept.com/patients/)
At Docrates, an individual’s genetic predisposition to cancer can be assessed using a gene test. A saliva sample is taken, and the sample is used to analyse the most common genes known to be associated with an increased risk of cancer. The test can be done in situations such as when there has been an unusually large number of cancers in an individual’s immediate family, or the individual otherwise suspects that they may carry genetic defects that could be associated with a higher risk of cancer. (http://www.genomill.com/products/color)
During a Guardant 360 test, a large number (73) of cancer genes are analysed using a liquid biopsy. The test is very sensitive (the detection threshold is 0.04% and the accuracy is 99.9%). The test can be useful is situations where it is difficult to obtain a tissue sample of the primary tumor or its metastasis, and the aim is to find out, through genetic testing, which treatments (e.g. targeted drugs) would be suitable for the patient. (www.guardanthealth.com/guardant360)
CMI (Caris MI Profile)
The CMI test specifies a large number of factors, both genes and structures found on the surface of cancer cells or in cancer tissue, i.e. biomarkers, using a sample taken from a tumor. The test result can be helpful in choosing the drug therapy in situations where there is no obvious research-based treatment option. (www.carismolecularintelligence.com)
OncoDEEP & TRACE
The OncoDEEP & TRACE test is carried out in two phases. The OncoDEEP test specifies a large number of factors, both genes and structures found on the surface of cancer cells or in cancer tissue, i.e. biomarkers, using a sample taken from a tumor. The test result can be helpful in choosing the drug therapy in situations where there is no obvious research-based treatment option. For the OncoTRACE test, a blood sample is taken and used to analyse genes based on the findings of the OncoDNA test. The OncoTRACE test provides information on all metastases – not only the one the tissue sample was taken from. If the tissue sample was taken during an earlier phase of the illness, the test also provides information about the changes that have taken place in the expression of genetic defects in the intervening period. The OncoTRACE test can, when repeated during the treatment or when a new treatment is being planned, be used to detect changes in the genetic defect profile, which can provide more information for planning the new treatment. (www.oncodna.com/distributors)
The Oncotype DX test is used when planning the adjuvant drug therapy for breast cancer, in situations where it is judged that chemotherapy could be discontinued without it worsening the prognosis. The test is done using a tissue sample taken from the breast tumor. (breast-cancer.oncotypedx.com/en-GB/Patient-Invasive)
The FoundationOne analysis is used to analyse 315 genes associated with cancer in the tumor. The analysis is very comprehensive because, unlike many other tests, FoundationOne surveys the whole of the genes that are being analysed and detects all types of mutations, even the rare ones.
FoundationACT is a liquid biopsy analysis where a blood sample is used to analyse 62 genes of a tumor’s DNA found in the bloodstream. The liquid biopsy method is particularly useful if it is not possible to obtain a normal tissue sample from the tumor or when the aim is to monitor the patient’s response to targeted drug therapy.
A report is produced for the physician’s use based on the detected mutations. This report details which approved targeted drugs or clinical drug trials could be suitable for the patient. (www.foundationmedicine.fi)
A comprehensive test report by the laboratory is prepared in connection with all the tests. It is important to carefully go through the test results with your treating physician. For the Colour test, the results are examined together with a clinical geneticist. This ensures that the interpretation of the test results is correct and the measures taken after the test results are appropriate.
To find out more about genetic profiling and testing, please call our booking on tel. +358 10 773 2000.