They achieve:
Circulating cancer cells (CCCs) are cells that are detached from the primary tumor and are drift by blood or lymph flow. It is these cells that will create the metastases, where they will find suitable conditions. Their quantity levels in blood are very small, but these are the cells that will determine the future of the patient. Detection and isolation is a priority for most personalized oncology centers in the Western world. In Greece, the technology of the specialized research group RGCC, which has developed the innovative method of abstract cell selection, is used for these tests. This technology provides 86.6% sensitivity and 83.3% specificity in identifying and matching CCCs.
From the patient's blood sample, all non-cancerous cells (red and white blood cells, platelets) are sequentially removed, leaving only the CCC at the end. The high success rates are due precisely to the fact that CCCs have not undergone any treatment with identifying antibodies, filters and other isolation methods. So they retain all their vitality and qualities. At the end the CCCs are then cultivated in appropriate nutrients.
There is growing interest in personalized cancer treatments around the world. Determination of the appropriate treatment for each case can be done only with the chemosensitivity test of the cultivated tumor cells. The concept is the same as the antibiotic susceptibility test of microbial cultures. In contrast, conventional oncology is primarily based on the statistical analysis of groups of patients who have been treated comparatively with different drugs.
The scientific value of these statistical studies is great, but it does not concern any particular patient. It concerns the response of a whole set of patients, in purely statistical terms. In contrast, the chemosensitivity test performed by RGCC relates exclusively to the cancer cells of a particular patient. It determines which specific drugs and other natural substances give the best therapeutic response for this unique patient.
These tests are performed on the patient's blood, except in cases of brain tumors, where biopsy material from the tumor itself is usually needed.
Cancer cells from the sample are isolated, identified and cultivated for the following analyzes:
It has been documented in the literature that the overall response rate of patients to empirical chemotherapy (protocols) is disappointingly low: Specifically, the contribution of empirical chemotherapy to 5-year survival of patients has been determined at the level of 2.1 - 2.3% !!! (https://www.ncbi.nlm.nih.gov/pubmed/15630849).
This frustratingly low efficiency is justified: Cancer is caused by serious and multiple damage to genetic material, which in addition is accompanied by accidental evolving genetic instability. Thus, each malignancy behaves differently in each patient than in others, but also changes in the course of the disease in the same patient. Patients are all different and their diseases are not only different but also variable!
The tumor consists of several subpopulations of cells, which have different characteristics. One of these subpopulations is of crucial importance, because it virtually drives the disease progression, resistance to treatment and the tendency to relapse. This subpopulation is cancer stem cells like cells, or tumor initiating cells.
When tumor cells are destroyed during any cancerkilling treatment, and then the test finds no residue, the cancer cells may in fact have a population of 109 έως 1012 cells. The resolution of standard diagnostic tests cannot "see" cells of this size, that is, about 0.5 cm, nor of the circulating cancer cells, of course. This diagnostic limit determines when conventional oncology considers the patient to be disease free. But this is clearly not the case.
This remnant cell population, consisting essentially of cancer stem cells, will give a relapse. At this stage, only cancer stem cells can survive, precisely because the "successfuly" chemotherapy does not affect them, as their metabolism and reproduction rate is extremely slow. If the treatment was more or less successful, it is understood that many more cells remain, except for the stem cells. These will then colonize distant parts of the body and create metastases (if not created earlier, before treatment).
For these reasons we need to detect the CCCs and their sensitivities early, in order to achieve the maximum result. Also, during the recession phase, it is important to detect the new properties that have been found in stem cells, and therefore the test is repeated in follow-up.
In conclusion, the biological and genetic analysis of cancer cells is the decisive test at every step, precisely because it will allow the medical team to adapt the treatment to the specificity and variability of the disease at each stage.
With personalization in oncology we are able to revive the patient's hope.
While we do not despise the therapeutic means of conventional oncology, on the contrary, we enrich the treatment....
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