Integral neuro-oncological diagnosis As the basis for personalized treatment Of brain tumors (on the example of gliomas In children)

Author:

Nazaralieva E. T.1ORCID,Zabrodskaya Yu. M.1ORCID,Gerasimov A. P.1ORCID,Shevtsov M. A.2ORCID,Nazaralieva E. T.3ORCID,Kim A. V.4ORCID,Djanaliev B. R.3,Samochernykh K. A.1ORCID

Affiliation:

1. Polenov Russian Scientific Research Institute of Neurosurgery — branch Almazov National Medical Research Centre

2. Institute of Cytology of the Russian Academy of Sciences; Almazov National Medical Research Centre, World-Class Research Centre for Personalized Medicine

3. I. K. Akhunbaev Kyrgyz State Medical Academy

4. Almazov National Medical Research Centre, World-Class Research Centre for Personalized Medicine

Abstract

   Brain tumors are the most common group of neoplasms in children, which is in the top-3 causes of infant mortality from oncopathology.   The aim of the study is to make a literature review of modern approaches to the personalization of treatment of CNS tumors in children based on the study of molecular genetics, immunohistochemical and imagingт characteristics.   The article provides a description of the most common types of neoplasms of the nervous system — low grade gliomas (LGG), high grade gliomas (HGG), mixed glioneural tumors, etc. The molecular genetics, immunohistochemical, visualization characteristics of each type of gliomas are described. Modern information on prognosis and treatment of tumors is also given in the publication. The prognosis of the course of LGG/GNT in children depends more often on the patient’s age, histology, and location of the tumor, as well as its molecular profile. Older patients have a more favorable prognosis than younger children. Well-visualized tumors located superficially have a better outcome than diffuse gliomas, as well as deeply located tumors. Detection of BRAF mutations and FGFR rearrangements may indicate a better prognosis than in the presence of SNV. Local mutations of BRAF with concomitant deletion of CDKN2A, as well as mutations with H3.3 pK27 are the most dangerous.

Publisher

Arterialnaya Gipertenziya

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