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OncoRisk Complete test

OncoRisk Complete is the most extensive, comprehensive oncogenetics panel that covers the analysis of 88 genes to determine the hereditary risks of the most common cancers based on the patient's DNA analysis.

The OncoRisk Complete test examines genetic mutations that can increase the likelihood of developing cancer and provides information about individual risks.

Who can use the OncoRisk Complete test?

First of all, patients who are planning to become parents should pay special attention to the OncoRisk Complete test, as the service will allow them to assess the potential risks of developing cancer in future parents and thus make informed decisions about family planning.
The test is especially recommended for couples planning IVF treatment. OncoRisk Complete makes it possible to avoid unpredictable genetic consequences and take advantage of the possibility of preimplantation genetic diagnosis of embryos if one of the future parents has a mutation in a gene that is associated with the possibility of developing cancer.
Patients who have an increased risk of cancer (for example, relatives with a history of breast, ovarian, colon, or other types of cancer);
Patients with an increased need for cancer prevention, as well as families with hereditary cancer.

Переваги:

The OncoRisk Complete test will provide accurate and detailed information about the predisposition to various types of cancer, which will allow early detection of the disease and recommend personalized tests for patients who need treatment with assisted reproductive technologies.

If mutations in genes are detected by the OncoRisk Complete test, a geneticist at IVMED will help you find out important information during a personal consultation at your request.

OncoRisk Complete is an important mechanism for:

early detection of potential risks of developing cancer,
providing personalized recommendations to reduce the likelihood of developing cancer,
identifying which mutation is present and in which gene, for further effective planning of preventive measures,
Obtaining recommendations for personalized research in the treatment of patients with reproductive problems.

Preparation and/or course of the procedure

For the OncoRisk Complete extended panel of hereditary cancers (88 genes), the material is venous blood or buccal epithelium.

The term for this analysis is 20 working days from the date of receipt of the samples for testing by the laboratory.

Features and interesting facts

Hereditary forms of cancer account for a significant percentage of all cancer cases.

These types of cancer are clearly associated with the inheritance of a gene with a "breakdown" - a pathogenic mutation. Altered genes with mutations are passed down from generation to generation and significantly increase the risk of developing diseases. Each patient carrying a hereditary oncogenic mutation has a several (and sometimes hundreds) times higher chance of contracting a specific cancer.

It is well known that a person inherits 50% of the genes in the germ cells (gametes) from the father and 50% from the mother, meaning that a damaged gene with mutations can be inherited from either parent. The probability of inheriting such a gene is 50%. The same probability of inheriting a mutation exists in the brothers and sisters of a patient who carries mutations in genes. For more distant relatives, the possibility of inheriting mutations decreases in proportion to the degree of kinship.

The following markers indicate a possible hereditary mutation:

family accumulation and hereditary transmission of the disease;
early age of onset of the disease;
bilateral or multifocal lesions;
specific tumor associations;
several forms of cancer in the patient or one of his relatives;
the presence of a pathogenic hereditary mutation in a close relative.

If you have a history of cancer in your family, you should find out if you and your family are at risk of developing hereditary forms of cancer.

All procedures

Women:

Diseases:

Men:

Pregnancy management and preimplantation diagnostics

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Why choose IVMED?

A team of experienced professionals

Clinical practice of leading specialists for over 20 years. We have helped more than 10,000 couples become parents. We have experience in solving the most difficult cases of infertility.

Individual programs for everyone

Diagnostic tests, the choice of treatment, medications, programs - everything is adapted to your individual indicators and circumstances.

Legality and complete confidentiality

The clinic operates in compliance with all applicable laws. We guarantee anonymity and medical confidentiality.

Modern genetic laboratory

Cytogenetic and molecular genetic studies from a single gene to the whole genome. Preimplantation genetic diagnosis of 24 embryo chromosomes by NGS (Next Generation Sequencing) with an accuracy of 99.99%.