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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">transmed</journal-id><journal-title-group><journal-title xml:lang="ru">Трансляционная медицина</journal-title><trans-title-group xml:lang="en"><trans-title>Translational Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2311-4495</issn><issn pub-type="epub">2410-5155</issn><publisher><publisher-name>Almazov National Medical Research Centre, Saint Petersburg, Russia</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18705/2311-4495-2024-11-1-65-76</article-id><article-id custom-type="edn" pub-id-type="custom">DLBDVT</article-id><article-id custom-type="elpub" pub-id-type="custom">transmed-832</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОНКОЛОГИЧЕСКИЕ ЗАБОЛЕВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CANCER</subject></subj-group></article-categories><title-group><article-title>Интегральный нейроонкологический диагноз как основа персонализированного лечения опухолей головного мозга (на примере глиом у детей</article-title><trans-title-group xml:lang="en"><trans-title>Integral neuro-oncological diagnosis As the basis for personalized treatment Of brain tumors (on the example of gliomas In children)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6165-9544</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Назаралиева</surname><given-names>Э. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Nazaralieva</surname><given-names>E. T.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Элеонора Тууганбаевна Назаралиева, к. м. н., старший научный сотрудник</p><p>НИЛ нейрохирургии детского возраста</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Eleonora T. Nazaralieva, Candidate of Medical Sciences, Senior Researcher</p><p>Research Laboratory of Pediatric Neurosurgery</p><p>Saint Petersburg</p></bio><email xlink:type="simple">neleonora@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6206-2133</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Забродская</surname><given-names>Ю. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Zabrodskaya</surname><given-names>Yu. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Юлия Михайловна Забродская, д. м. н., заведующая НИЛ</p><p>НИЛ патоморфологии нервной системы</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Yulia M. Zabrodskaya, Doctor of Medical Sciences, Head of the Laboratory</p><p>Research Laboratory of Pathomorphology of the Nervous System</p><p>Saint Petersburg</p></bio><email xlink:type="simple">zabrjulia@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9787-8132</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Герасимов</surname><given-names>А. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Gerasimov</surname><given-names>A. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Александр Павлович Герасимов, старший научный сотрудник</p><p>НИЛ нейрохирургии детского возраста </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Aleksandr P. Gerasimov, Senior Researcher</p><p>Research Laboratory of Pediatric Neurosurgery</p><p>Saint Petersburg</p></bio><email xlink:type="simple">apgerasimow@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8539-2239</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шевцов</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shevtsov</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Максим Алексеевич Шевцов, д. б. н., ведущий научный сотрудник, заведующий НИО</p><p>НИО трансляционной онкологии</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Maksim A. Shevtsov, Doctor of Biological Sciences, Leading Researcher, Head of Center</p><p>Research Center for Translational Oncology</p><p>Saint Petersburg</p></bio><email xlink:type="simple">shevtsov-max@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0955-9180</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Назаралиева</surname><given-names>Э. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Nazaralieva</surname><given-names>E. T.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Эльнура Тууганбаевна Назаралиева, врач-патологоанатом, ассистент</p><p>кафедра патологической анатомии</p><p>Бишкек</p></bio><bio xml:lang="en"><p>Elnura T. Nazaralieva, Pathologist, Assistent</p><p>Department of Pathological Anatomy</p><p>Bishkek</p></bio><email xlink:type="simple">amazanit@yandex.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6219-7270</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ким</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kim</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Александр Вонгиевич Ким, д. м. н., заведующий ДНХО, доцент</p><p>ДНХО № 7; кафедра нейрохирургии</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Aleksandr V. Kim, Doctor of Medical Sciences, Head ofthe Department, Associate Professor</p><p>Children’s Neurosurgical Department No. 7; Department of Neurosurgery</p><p>Saint Petersburg</p></bio><email xlink:type="simple">kimoza@mail.ru</email><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Джаналиев</surname><given-names>Б. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Djanaliev</surname><given-names>B. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Болот Рахманович Джаналиев, д. м. н., профессор</p><p>кафедра патологической анатомии</p><p>Бишкек</p></bio><bio xml:lang="en"><p>Bolot R. Djanaliev, Doctor of Medical Sciences, Professor</p><p>Department of Pathological Anatomy</p><p>Bishkek</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0350-0249</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Самочерных</surname><given-names>К. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Samochernykh</surname><given-names>K. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Константин Александрович Самочерных, д. м. н., профессор РАН, директор РНХИ, заведующий центром</p><p>НЦМУ «Центр персонализированной медицины»; научно-исследовательский центр персонализированной онкологии </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Konstantin A. Samochernykh, Doctor of Medical Sciences, professor of the Russian Academy of Sciences, director of the Institute, Head of the Center</p><p>World-Class Research Centre for Personalized Medicine; Research Center for Personalized Oncology</p><p>Saint Petersburg</p></bio><email xlink:type="simple">neurobaby12@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Российский научно-исследовательский нейрохирургический институт имени профессора А. Л. Поленова — филиал Федерального государственного бюджетного учреждения «Национальный медицинский исследовательский центр имени В. А. Алмазова»&#13;
Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Polenov Russian Scientific Research Institute of Neurosurgery — branch Almazov National Medical Research Centre</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение науки «Институт цитологии Российской академии наук»; Федеральное государственное бюджетное учреждение&#13;
«Национальный медицинский исследовательский центр имени В. А. Алмазова» Министерства здравоохранения Российской Федерации, Научный центр мирового уровня «Центр персонализированной медицины»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Cytology of the Russian Academy of Sciences; Almazov National Medical Research Centre, World-Class Research Centre for Personalized Medicine</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Кыргызская государственная медицинская академия имени И. К. Ахунбаева</institution><country>Кыргызстан</country></aff><aff xml:lang="en"><institution>I. K. Akhunbaev Kyrgyz State Medical Academy</institution><country>Kyrgyzstan</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение&#13;
«Национальный медицинский исследовательский центр имени В. А. Алмазова» Министерства здравоохранения Российской Федерации, Научный центр мирового уровня «Центр персонализированной медицины»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Almazov National Medical Research Centre, World-Class Research Centre for Personalized Medicine</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>13</day><month>03</month><year>2024</year></pub-date><volume>11</volume><issue>1</issue><fpage>65</fpage><lpage>76</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Назаралиева Э.Т., Забродская Ю.М., Герасимов А.П., Шевцов М.А., Назаралиева Э.Т., Ким А.В., Джаналиев Б.Р., Самочерных К.А., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Назаралиева Э.Т., Забродская Ю.М., Герасимов А.П., Шевцов М.А., Назаралиева Э.Т., Ким А.В., Джаналиев Б.Р., Самочерных К.А.</copyright-holder><copyright-holder xml:lang="en">Nazaralieva E.T., Zabrodskaya Y.M., Gerasimov A.P., Shevtsov M.A., Nazaralieva E.T., Kim A.V., Djanaliev B.R., Samochernykh K.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://transmed.almazovcentre.ru/jour/article/view/832">https://transmed.almazovcentre.ru/jour/article/view/832</self-uri><abstract><p>   Опухоли головного мозга представляют собой наиболее распространенную группу новообразований у детей, входящую в топ-3 причин детской смертности от онкопатологии.</p><p>   Целью работы был анализ литературных данных о современных подходах к персонализации лечения опухолей ЦНС у детей на основании изучения молекулярно-генетических, иммуногистохимических, визуализационных характеристик.</p><p>   В статье дана полная и детальная характеристика часто встречающихся видов новообразований нервной системы — глиом низкой степени злокачественности (LGG), глиом высокой степени злокачественности (HGG), смешанных глионевральных опухолей и др. Описаны молекулярно-генетические, иммуногистохимические, визуализационные характеристики каждого вида глиом. Также представлены современные сведения о прогнозе и лечении новообразований. Установлено, например, что прогноз течения LGG/GNT у детей чаще зависит от возраста ребенка, гистологии и локализации опухоли, а также ее молекулярного профиля. У более старших пациентов прогноз более благоприятный, чем у младших детей. Хорошо визуализирующиеся опухоли, расположенные поверхностно (полушарные или мозжечковые), чаще характеризуются лучшим исходом, чем диффузные глиомы, а также глубоко расположенные опухоли. BRAF-мутации и перегруппировки FGFR могут свидетельствовать о лучшем прогнозе, чем при наличии SNV. В то же время точечные мутации BRAF с сопутствующей делецией CDKN2A, а также мутации с H3.3 pK27 являются наиболее опасными.</p></abstract><trans-abstract xml:lang="en"><p>   Brain tumors are the most common group of neoplasms in children, which is in the top-3 causes of infant mortality from oncopathology.</p><p>   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.</p><p>   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.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>глиома высокой степени злокачественности</kwd><kwd>глиома низкой степени злокачественности</kwd><kwd>опухоль</kwd><kwd>ЦНС</kwd><kwd>HGG</kwd><kwd>LGG</kwd></kwd-group><kwd-group xml:lang="en"><kwd>CNS</kwd><kwd>high grade glioma</kwd><kwd>HGG</kwd><kwd>LGG</kwd><kwd>low grade glioma</kwd><kwd>tumor</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена в рамках Госзадания: Разработка новой технологии лечения больных вторичными новообразованиями головного мозга и рецидивирующими менингиомами. № ЕГИСУ 123021000128-4</funding-statement><funding-statement xml:lang="en">The work was carried out within the framework of the State Task: Development of a new technology for the treatment of patients with secondary brain tumors and recurrent meningiomas. No. EGISU 123021000128-4</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Ostrom QT, Cioffi G, Waite K, et al. CBTRUS Statistical Report: Primary brain and other central nervous system tumors diagnosed in the United States in 2014-2018. Neuro-Oncology. 2021; 23: 101–105. DOI: 10.1093/neuonc/noz150.</mixed-citation><mixed-citation xml:lang="en">Ostrom QT, Cioffi G, Waite K, et al. CBTRUS Statistical Report: Primary brain and other central nervous system tumors diagnosed in the United States in 2014-2018. Neuro-Oncology. 2021; 23: 101–105. DOI: 10.1093/neuonc/noz150.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Alleman K, Knecht E, Huang J, et al. Multimodal Deep Learning-Based Prognostication in Glioma Patients : A Systematic Review. Cancers (Basel). 2023; 15 (2): 545. DOI: 10.3390/cancers15020545.</mixed-citation><mixed-citation xml:lang="en">Alleman K, Knecht E, Huang J, et al. Multimodal Deep Learning-Based Prognostication in Glioma Patients : A Systematic Review. Cancers (Basel). 2023; 15 (2): 545. DOI: 10.3390/cancers15020545.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Grigore FN, Yang SJ, Chen CC, Koga T. Pioneering models of pediatric brain tumors. Neoplasia. 2023; 36: 100859. DOI: 10.1016/j.neo.2022.100859.</mixed-citation><mixed-citation xml:lang="en">Grigore FN, Yang SJ, Chen CC, Koga T. Pioneering models of pediatric brain tumors. Neoplasia. 2023; 36: 100859. DOI: 10.1016/j.neo.2022.100859.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Louis DN, Perry A, Wesseling P, et al. The 2021 WHO Classification of tumors of the central nervous system: A summary. Neuro Oncol. 2021; 23:1231–1251. DOI: 10.1093/neuonc/noab106.</mixed-citation><mixed-citation xml:lang="en">Louis DN, Perry A, Wesseling P, et al. The 2021 WHO Classification of tumors of the central nervous system: A summary. Neuro Oncol. 2021; 23:1231–1251. DOI: 10.1093/neuonc/noab106.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Johnson KJ, Bauchet L, Francis SS, et al. Pediatric brain tumors: Origins, epidemiology, and classification — The 2022 Brain Tumor Epidemiology Consortium meeting report. Clin Neuropathol. 2023; Jan 12. DOI: 10.5414/NP301520.</mixed-citation><mixed-citation xml:lang="en">Johnson KJ, Bauchet L, Francis SS, et al. Pediatric brain tumors: Origins, epidemiology, and classification — The 2022 Brain Tumor Epidemiology Consortium meeting report. Clin Neuropathol. 2023; Jan 12. DOI: 10.5414/NP301520.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Ehret F, Kaul D, Clusmann H, et al. Machine learning-based radiomics in neuro-oncology. Acta Neurochir Suppl. 2022; 134:139–151. DOI: 10.1007/978-3-030-85292-4_18.</mixed-citation><mixed-citation xml:lang="en">Ehret F, Kaul D, Clusmann H, et al. Machine learning-based radiomics in neuro-oncology. Acta Neurochir Suppl. 2022; 134:139–151. DOI: 10.1007/978-3-030-85292-4_18.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Dastmalchi F, Deleyrolle LP, Karachi A, et al. Metabolomics Monitoring of Treatment Response to Brain Tumor Immunotherapy. Front Oncol. 2021; Jun 3;11:691246. DOI: 10.3389/fonc.2021.691246.</mixed-citation><mixed-citation xml:lang="en">Dastmalchi F, Deleyrolle LP, Karachi A, et al. Metabolomics Monitoring of Treatment Response to Brain Tumor Immunotherapy. Front Oncol. 2021; Jun 3;11:691246. DOI: 10.3389/fonc.2021.691246.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Jaju A, Yeom KW, Ryan ME. MR imaging of pediatric brain tumors. Diagnostics. 2022; 12: 961. DOI: 10.3390/diagnostics12040961.</mixed-citation><mixed-citation xml:lang="en">Jaju A, Yeom KW, Ryan ME. MR imaging of pediatric brain tumors. Diagnostics. 2022; 12: 961. DOI: 10.3390/diagnostics12040961.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Lotan E, Jain R, Razavian N, et al. State of the Art: Machine learning applications in glioma imaging. AJR Am. J. Roentgenol. 2019; 212: 26–37. DOI: 10.2214/AJR.18.20218.</mixed-citation><mixed-citation xml:lang="en">Lotan E, Jain R, Razavian N, et al. State of the Art: Machine learning applications in glioma imaging. AJR Am. J. Roentgenol. 2019; 212: 26–37. DOI: 10.2214/AJR.18.20218.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Bi J, Chowdhry S, Wu S, et al. Altered cellular metabolism in gliomas - an emerging landscape of actionable co-dependency targets. Nat Rev Cancer. 2020; 20(1): 57–70. DOI: 10.1038/s41568-019-0226-5.</mixed-citation><mixed-citation xml:lang="en">Bi J, Chowdhry S, Wu S, et al. Altered cellular metabolism in gliomas - an emerging landscape of actionable co-dependency targets. Nat Rev Cancer. 2020; 20(1): 57–70. DOI: 10.1038/s41568-019-0226-5.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Wagner MW, Hainc N, Khalvati F, et al. Radiomics of pediatric low-grade gliomas: Toward a pretherapeutic differentiation of BRAFmutated and BRAF-fused tumors. AJNR Am J Neuroradiol. 2021; 42: 759–765. DOI: 10.3174/ajnr.A6998.</mixed-citation><mixed-citation xml:lang="en">Wagner MW, Hainc N, Khalvati F, et al. Radiomics of pediatric low-grade gliomas: Toward a pretherapeutic differentiation of BRAFmutated and BRAF-fused tumors. AJNR Am J Neuroradiol. 2021; 42: 759–765. DOI: 10.3174/ajnr.A6998.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Cacciotti C, Fleming A, Ramaswamy V. Advances in the molecular classification of pediatric brain tumors: a guide to the galaxy. J Pathol. 2020; 251(3): 249–261. DOI: 10.1002/path.5457.</mixed-citation><mixed-citation xml:lang="en">Cacciotti C, Fleming A, Ramaswamy V. Advances in the molecular classification of pediatric brain tumors: a guide to the galaxy. J Pathol. 2020; 251(3): 249–261. DOI: 10.1002/path.5457.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang J, Wu G, Miller CP, et al. Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. Nat Genet.2013; 45:602. DOI: 10.1038/ng.2611.</mixed-citation><mixed-citation xml:lang="en">Zhang J, Wu G, Miller CP, et al. Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. Nat Genet.2013; 45:602. DOI: 10.1038/ng.2611.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Bowles EJ, Miglioretti DL, Kwan ML, et al. Long-term medical imaging use in children with central nervous system tumors. PLoS One. 2021; 16(4):e0248643. URL: https://www.researchgate.net/publication/351042528_Long-term_medical_imaging_use_in_children_with_central_nervous_system_tumors.</mixed-citation><mixed-citation xml:lang="en">Bowles EJ, Miglioretti DL, Kwan ML, et al. Long-term medical imaging use in children with central nervous system tumors. PLoS One. 2021; 16(4):e0248643. URL: https://www.researchgate.net/publication/351042528_Long-term_medical_imaging_use_in_children_with_central_nervous_system_tumors.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Jones DTW, Gronych J, Lichter P, et al. MAPK pathway activation in pilocytic astrocytoma. Cell Mole Life Sci. 2012; 69: 1799–1811. DOI: 10.1007/s00018-011-0898-9.</mixed-citation><mixed-citation xml:lang="en">Jones DTW, Gronych J, Lichter P, et al. MAPK pathway activation in pilocytic astrocytoma. Cell Mole Life Sci. 2012; 69: 1799–1811. DOI: 10.1007/s00018-011-0898-9.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Ryall S, Tabori U, Hawkins C. Pediatric low-grade glioma in the era of molecular diagnostics. Acta Neuropathol Commun. 2020; 8 (1): 30. DOI: 10.1186/s40478-020-00902-z.</mixed-citation><mixed-citation xml:lang="en">Ryall S, Tabori U, Hawkins C. Pediatric low-grade glioma in the era of molecular diagnostics. Acta Neuropathol Commun. 2020; 8 (1): 30. DOI: 10.1186/s40478-020-00902-z.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Alrayahi J, Zapotocky M, Ramaswamy V, et al. Pediatric brain tumor genetics: What radiologists need to know. Radiographic. 2018; 38: 2102–2122. DOI: 10.1148/rg.2018180109.</mixed-citation><mixed-citation xml:lang="en">Alrayahi J, Zapotocky M, Ramaswamy V, et al. Pediatric brain tumor genetics: What radiologists need to know. Radiographic. 2018; 38: 2102–2122. DOI: 10.1148/rg.2018180109.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Ryall S, Zapotocky M, Fukuoka K, et al. Integrated molecular and clinical analysis of 1,000 pediatric low-grade gliomas. Cancer Cell.2020; 37: 569–583. DOI: 10.1016/j.ccell.2020.03.011.</mixed-citation><mixed-citation xml:lang="en">Ryall S, Zapotocky M, Fukuoka K, et al. Integrated molecular and clinical analysis of 1,000 pediatric low-grade gliomas. Cancer Cell.2020; 37: 569–583. DOI: 10.1016/j.ccell.2020.03.011.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Lin A, Rodriguez FJ, Karajannis MA, et al. BRAF alterations in primary glial and glioneuronal neoplasms of the central nervous system with identification of 2 novel KIAA1549: BRAF fusion variants. J Neuropathol Exp Neurol. 2012; 71: 66–72. DOI: 10.1097/NEN.0b013e31823f2cb0.</mixed-citation><mixed-citation xml:lang="en">Lin A, Rodriguez FJ, Karajannis MA, et al. BRAF alterations in primary glial and glioneuronal neoplasms of the central nervous system with identification of 2 novel KIAA1549: BRAF fusion variants. J Neuropathol Exp Neurol. 2012; 71: 66–72. DOI: 10.1097/NEN.0b013e31823f2cb0.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Bag AK, Chiang J, Patay Z. Radiohistogenomics of pediatric low-grade neuroepithelial tumors. Neuroradiology. 2021; 63(8):1185–1213. DOI: 10.1007/s00234-021-02691-1.</mixed-citation><mixed-citation xml:lang="en">Bag AK, Chiang J, Patay Z. Radiohistogenomics of pediatric low-grade neuroepithelial tumors. Neuroradiology. 2021; 63(8):1185–1213. DOI: 10.1007/s00234-021-02691-1.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Kumar V, Abbas AK, Fausto N, et al. Robbins and Cotran Pathologic Basis of Disease, Professional Edition E-Book. Philadelphia, PA: Elsevier Health Sciences, 2014.</mixed-citation><mixed-citation xml:lang="en">Kumar V, Abbas AK, Fausto N, et al. Robbins and Cotran Pathologic Basis of Disease, Professional Edition E-Book. Philadelphia, PA: Elsevier Health Sciences, 2014.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">de Blank PMK, Fisher MJ, Liu GT, et al. Optic pathway gliomas in neurofibromatosis Type 1: An update: surveillance, treatment indications, and biomarkers of vision. J Neuroophthalmol. 2017; 37 (Suppl.1): 23–32. URL: https://journals.lww.com/jneuro-ophthalmology/abstract/2017/09001/optic_pathway_gliomas_in_neurofibromatosis_type_1_.4.aspx.</mixed-citation><mixed-citation xml:lang="en">de Blank PMK, Fisher MJ, Liu GT, et al. Optic pathway gliomas in neurofibromatosis Type 1: An update: surveillance, treatment indications, and biomarkers of vision. J Neuroophthalmol. 2017; 37 (Suppl.1): 23–32. URL: https://journals.lww.com/jneuro-ophthalmology/abstract/2017/09001/optic_pathway_gliomas_in_neurofibromatosis_type_1_.4.aspx.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Hartmann C, Meyer J, Balss J, et al. Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: A study of 1,010 diffuse gliomas. Acta Neuropathol. 2009; 118: 469–474. DOI: 10.1007/s00401-009-0561-9.</mixed-citation><mixed-citation xml:lang="en">Hartmann C, Meyer J, Balss J, et al. Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: A study of 1,010 diffuse gliomas. Acta Neuropathol. 2009; 118: 469–474. DOI: 10.1007/s00401-009-0561-9.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Leu S, von Felten S, Frank S, et al. IDH mutation is associated with higher risk of malignant transformation in low-grade glioma. J Neurooncol. 2016; 127: 363–372. DOI: 10.1007/s11060-015-2048-y.</mixed-citation><mixed-citation xml:lang="en">Leu S, von Felten S, Frank S, et al. IDH mutation is associated with higher risk of malignant transformation in low-grade glioma. J Neurooncol. 2016; 127: 363–372. DOI: 10.1007/s11060-015-2048-y.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Ryall S, Krishnatry R, Arnoldo A, et al. Targeted detection of genetic alterations reveal the prognostic impact of H3K27M and MAPK pathway aberrations in paediatric thalamic glioma. Acta Neuropathol Commun. 2016; 4: 93. DOI: 10.1186/s40478-016-0353-0.</mixed-citation><mixed-citation xml:lang="en">Ryall S, Krishnatry R, Arnoldo A, et al. Targeted detection of genetic alterations reveal the prognostic impact of H3K27M and MAPK pathway aberrations in paediatric thalamic glioma. Acta Neuropathol Commun. 2016; 4: 93. DOI: 10.1186/s40478-016-0353-0.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Mistry M, Zhukova N, Merico D, et al. BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade glioma. J Clin Oncol. 2015; 33(9):1015–1022. DOI: 10.1200/JCO.2014.58.3922.</mixed-citation><mixed-citation xml:lang="en">Mistry M, Zhukova N, Merico D, et al. BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade glioma. J Clin Oncol. 2015; 33(9):1015–1022. DOI: 10.1200/JCO.2014.58.3922.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Mackay A, Burford A, Carvalho D, et al. Integrated molecular metaanalysis of 1,000 pediatric high-grade and diffuse intrinsic Pontine Glioma. Cancer Cell. 2017; 32: 520–537. DOI: 10.1016/j.ccell.2017.08.017.</mixed-citation><mixed-citation xml:lang="en">Mackay A, Burford A, Carvalho D, et al. Integrated molecular metaanalysis of 1,000 pediatric high-grade and diffuse intrinsic Pontine Glioma. Cancer Cell. 2017; 32: 520–537. DOI: 10.1016/j.ccell.2017.08.017.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Chiang J, Harreld JH, Tinkle CL, et al. A single-center study of the clinicopathologic correlates of gliomas with a MYB or MYBL1 alteration. Acta Neuropathol. 2019; 138: 1091–1092. DOI: 10.1007/s00401-019-02081-1.</mixed-citation><mixed-citation xml:lang="en">Chiang J, Harreld JH, Tinkle CL, et al. A single-center study of the clinicopathologic correlates of gliomas with a MYB or MYBL1 alteration. Acta Neuropathol. 2019; 138: 1091–1092. DOI: 10.1007/s00401-019-02081-1.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Collins VP, Jones DTW, Giannini C. Pilocytic astrocytoma: Pathology, molecular mechanisms and markers. Acta Neuropathol. 2015; 129: 775–788. DOI: 10.1007/s00401-015-1410-7.</mixed-citation><mixed-citation xml:lang="en">Collins VP, Jones DTW, Giannini C. Pilocytic astrocytoma: Pathology, molecular mechanisms and markers. Acta Neuropathol. 2015; 129: 775–788. DOI: 10.1007/s00401-015-1410-7.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Raybaud C, Ramaswamy V, Taylor MD, et al. Posterior fossa tumors in children: Developmental anatomy and diagnostic imaging. Child’s Nervous System. 2015; 31: 1661–1676. DOI: 10.1007/s00381-015-2834-z.</mixed-citation><mixed-citation xml:lang="en">Raybaud C, Ramaswamy V, Taylor MD, et al. Posterior fossa tumors in children: Developmental anatomy and diagnostic imaging. Child’s Nervous System. 2015; 31: 1661–1676. DOI: 10.1007/s00381-015-2834-z.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Broniscer A, Gajjar A. Supratentorial high-grade astrocytoma and diffuse brainstem glioma: Two challenges for the pediatric oncologist. Oncologist. 2004; 9:197–206. DOI: 10.1634/theoncologist.9-2-197.</mixed-citation><mixed-citation xml:lang="en">Broniscer A, Gajjar A. Supratentorial high-grade astrocytoma and diffuse brainstem glioma: Two challenges for the pediatric oncologist. Oncologist. 2004; 9:197–206. DOI: 10.1634/theoncologist.9-2-197.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Perkins SM, Rubin JB, Leonard JR, et al. Glioblastoma in children: A single-institution experience. Int J Radiat Oncol Biol Phys. 2011; 80: 1117–1121. DOI: 10.1016/j.ijrobp.2010.03.013.</mixed-citation><mixed-citation xml:lang="en">Perkins SM, Rubin JB, Leonard JR, et al. Glioblastoma in children: A single-institution experience. Int J Radiat Oncol Biol Phys. 2011; 80: 1117–1121. DOI: 10.1016/j.ijrobp.2010.03.013.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Kline C, Felton E, Allen IE, et al. Survival outcomes in pediatric recurrent high-grade glioma: Results of a 20-year systematic review and meta-analysis. J Neurooncol. 2018; 137:103–110. DOI: 10.1007/s11060-017-2701-8.</mixed-citation><mixed-citation xml:lang="en">Kline C, Felton E, Allen IE, et al. Survival outcomes in pediatric recurrent high-grade glioma: Results of a 20-year systematic review and meta-analysis. J Neurooncol. 2018; 137:103–110. DOI: 10.1007/s11060-017-2701-8.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Chatwin HV, Cruz J, Green AL. Pediatric high-grade glioma: Moving toward subtype-specific multimodal therapy. FEBS J. 2021; 288: 6127–6141. DOI: 10.1111/febs.15739.</mixed-citation><mixed-citation xml:lang="en">Chatwin HV, Cruz J, Green AL. Pediatric high-grade glioma: Moving toward subtype-specific multimodal therapy. FEBS J. 2021; 288: 6127–6141. DOI: 10.1111/febs.15739.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Schwartzentruber J, Korshunov A, Liu XY, et al. Driver mutations in histone H3. 3 and chromatin remodelling genes in paediatric glioblastoma. Nature. 2012; 482: 226–231. DOI: 10.1038/nature10833.</mixed-citation><mixed-citation xml:lang="en">Schwartzentruber J, Korshunov A, Liu XY, et al. Driver mutations in histone H3. 3 and chromatin remodelling genes in paediatric glioblastoma. Nature. 2012; 482: 226–231. DOI: 10.1038/nature10833.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Sun Y, Bailey CP, Sadighi Z, et al. Pediatric high-grade glioma: Aberrant epigenetics and kinase signaling define emerging therapeutic opportunities. J Neurooncol. 2020; 150: 17–26. DOI: 10.1007/s11060-020-03546-0.</mixed-citation><mixed-citation xml:lang="en">Sun Y, Bailey CP, Sadighi Z, et al. Pediatric high-grade glioma: Aberrant epigenetics and kinase signaling define emerging therapeutic opportunities. J Neurooncol. 2020; 150: 17–26. DOI: 10.1007/s11060-020-03546-0.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Jones C, Baker SJ. Unique genetic and epigenetic mechanisms driving paediatric diffuse high-grade glioma. Nat Rev Cancer. 2014; 14: 651–661. DOI: 10.1038/nrc3811.</mixed-citation><mixed-citation xml:lang="en">Jones C, Baker SJ. Unique genetic and epigenetic mechanisms driving paediatric diffuse high-grade glioma. Nat Rev Cancer. 2014; 14: 651–661. DOI: 10.1038/nrc3811.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Clarke M, Mackay A, Ismer B, et al. Infant high-grade gliomas comprise multiple subgroups characterized by novel targetable gene fusions and favorable outcomes. Cancer Discovery. 2020; 10: 942–963. DOI: 10.1158/2159-8290.CD-19-1030.</mixed-citation><mixed-citation xml:lang="en">Clarke M, Mackay A, Ismer B, et al. Infant high-grade gliomas comprise multiple subgroups characterized by novel targetable gene fusions and favorable outcomes. Cancer Discovery. 2020; 10: 942–963. DOI: 10.1158/2159-8290.CD-19-1030.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Guerreiro Stucklin AS, Ryall S, Fukuoka K, et al. Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas. Nat Commun. 2019; 10: 1–13. DOI: 10.1038/s41467-019-12187-5.</mixed-citation><mixed-citation xml:lang="en">Guerreiro Stucklin AS, Ryall S, Fukuoka K, et al. Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas. Nat Commun. 2019; 10: 1–13. DOI: 10.1038/s41467-019-12187-5.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Goncalves FG, Viaene AN, Vossough A. Advanced magnetic resonance imaging in pediatric glioblastomas. Front Neurol. 2012; 12. DOI: 10.3389/fneur.2021.733323.</mixed-citation><mixed-citation xml:lang="en">Goncalves FG, Viaene AN, Vossough A. Advanced magnetic resonance imaging in pediatric glioblastomas. Front Neurol. 2012; 12. DOI: 10.3389/fneur.2021.733323.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Panigrahy A, Bleuml S. Neuroimaging of pediatric brain tumors: From basic to advanced magnetic resonance imaging (MRI). J Child Neurol. 2009; 24: 1343–1365. 38. DOI: 10.1177/0883073809342129.</mixed-citation><mixed-citation xml:lang="en">Panigrahy A, Bleuml S. Neuroimaging of pediatric brain tumors: From basic to advanced magnetic resonance imaging (MRI). J Child Neurol. 2009; 24: 1343–1365. 38. DOI: 10.1177/0883073809342129.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Aboian MS, Solomon DA, Felton E, et al. Imaging characteristics of pediatric diffuse midline gliomas with histone H3 K27M mutation. AJNR. 2017; 38:795. DOI: 10.3174/ajnr.A5076.</mixed-citation><mixed-citation xml:lang="en">Aboian MS, Solomon DA, Felton E, et al. Imaging characteristics of pediatric diffuse midline gliomas with histone H3 K27M mutation. AJNR. 2017; 38:795. DOI: 10.3174/ajnr.A5076.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Hales PW, d’Arco F, Cooper J, et al. Arterial spin labelling and diffusion-weighted imaging in paediatric brain tumours. NeuroImage Clin. 2019; 22: 101696. DOI: 10.1016/j.nicl.2019.101696.</mixed-citation><mixed-citation xml:lang="en">Hales PW, d’Arco F, Cooper J, et al. Arterial spin labelling and diffusion-weighted imaging in paediatric brain tumours. NeuroImage Clin. 2019; 22: 101696. DOI: 10.1016/j.nicl.2019.101696.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Yamasaki F, Kurisu K, Kajiwara Y, et al. Magnetic resonance spectroscopic detection of lactate is predictive of a poor prognosis in patients with diffuse intrinsic pontine glioma. Neuro-Oncology. 2011; 13: 791. DOI: 10.1093/neuonc/nor038.</mixed-citation><mixed-citation xml:lang="en">Yamasaki F, Kurisu K, Kajiwara Y, et al. Magnetic resonance spectroscopic detection of lactate is predictive of a poor prognosis in patients with diffuse intrinsic pontine glioma. Neuro-Oncology. 2011; 13: 791. DOI: 10.1093/neuonc/nor038.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Simon M, Hosen I, Gousias K, et al. TERT promoter mutations: A novel independent prognostic factor in primary glioblastomas. NeuroOncol. 2015; 17: 45–52.43. DOI: 10.1093/neuonc/nou158.</mixed-citation><mixed-citation xml:lang="en">Simon M, Hosen I, Gousias K, et al. TERT promoter mutations: A novel independent prognostic factor in primary glioblastomas. NeuroOncol. 2015; 17: 45–52.43. DOI: 10.1093/neuonc/nou158.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
