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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">816</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2024-23-1-172-179</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LITERATURE REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Molecular pathogenesis of T-lymphoblastic lymphoma</article-title><trans-title-group xml:lang="ru"><trans-title>Молекулярный патогенез T-лимфобластной лимфомы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0002-3896-6612</contrib-id><name-alternatives><name xml:lang="en"><surname>Dneprovskii</surname><given-names>V. R.</given-names></name><name xml:lang="ru"><surname>Днепровский</surname><given-names>В. Р.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Владимир Романович Днепровский</p><p>Москва</p></bio><email>dneprovsky.vladimir@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4699-1730</contrib-id><name-alternatives><name xml:lang="en"><surname>Fedorova</surname><given-names>A. S.</given-names></name><name xml:lang="ru"><surname>Фёдорова</surname><given-names>А. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Анна Сергеевна Фёдорова</p><p>Москва</p></bio><email>fyodorova_hannah@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3664-2876</contrib-id><name-alternatives><name xml:lang="en"><surname>Abramov</surname><given-names>D. S.</given-names></name><name xml:lang="ru"><surname>Абрамов</surname><given-names>Д. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Дмитрий Сергеевич Абрамов</p><p>Москва</p></bio><email>abramovd_s@bk.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2574-1636</contrib-id><name-alternatives><name xml:lang="en"><surname>Volchkov</surname><given-names>E. V.</given-names></name><name xml:lang="ru"><surname>Волчков</surname><given-names>Е. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Egor V. Volchkov, a hematologist</p><p>Lymphoma Research Department</p><p>117997; 1 Samory Mashela St.; Moscow</p></bio><bio xml:lang="ru"><p>Егор Васильевич Волчков, врач-гематолог</p><p>отдел исследования лимфом</p><p>117997; ул. Саморы Машела, 1; Москва</p></bio><email>volchcov.egor@yandex.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4779-1896</contrib-id><name-alternatives><name xml:lang="en"><surname>Myakova</surname><given-names>N. V.</given-names></name><name xml:lang="ru"><surname>Мякова</surname><given-names>Н. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Наталья Валерьевна Мякова</p><p>Москва</p></bio><email>nmiakova@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">The Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology of Ministry of Healthсare of the Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Research Institute of Molecular and Cellular Medicine of the Patrice Lumumba Рeoples’ Friendship University of Russia</institution></aff><aff><institution xml:lang="ru">Научно-исследовательский институт молекулярной и клеточной медицины ФГАОУ ВО «Российский университет дружбы народов им. Патриса Лумумбы»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-04-19" publication-format="electronic"><day>19</day><month>04</month><year>2024</year></pub-date><volume>23</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>172</fpage><lpage>179</lpage><history><date date-type="received" iso-8601-date="2024-01-31"><day>31</day><month>01</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-04-08"><day>08</day><month>04</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://hemoncim.com/jour/article/view/816">https://hemoncim.com/jour/article/view/816</self-uri><abstract xml:lang="en"><p>   T-lymphoblastic lymphoma (T-LBL) is one of the most common non-Hodgkin lymphomas in children. According to the 2022 WHO classification, T-LBL and acute T-lymphoblastic leukemia are considered as a single disease since they both have T-cell precursors as a morphological substrate. In recent years, some progress has been made in the treatment of this disease, but the prognosis for relapses and refractory cases remains extremely unfavorable. One of the promising areas that can increase the effectiveness of therapy is the use of new treatment approaches that consider the molecular and biological features of this tumor. This review examines in detail the molecular aspects of the pathogenesis of T-LBL.</p></abstract><trans-abstract xml:lang="ru"><p>   Т-лимфобластная лимфома (Т-ЛБЛ) занимает одно из ведущих мест в структуре неходжкинских лимфом у детей. По классификации Всемирной организации здравоохранения 2022 г. Т-ЛБЛ и острый Т-лимфобластный лейкоз рассматриваются в рамках единой нозологической категории, так как они имеют один и тот же морфологический субстрат – предшественники Т-клеток. За последние годы в лечении этого заболевания достигнуты определенные успехи, однако прогноз при рецидивах и рефрактерном течении до сих пор остается крайне неблагоприятным. Одним из перспективных направлений, способных повысить эффективность терапии, является внедрение новых схем лечения, учитывающих молекулярно-генетические особенности данной опухоли. В настоящем обзоре подробно рассматриваются молекулярные аспекты патогенеза Т-ЛБЛ.</p></trans-abstract><kwd-group xml:lang="en"><kwd>T-lymphoblastic leukemia</kwd><kwd>T-lymphoblastic lymphoma</kwd><kwd>non-Hodgkin lymphomas</kwd><kwd>children</kwd><kwd>NOTCH1</kwd><kwd>FBXW7</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>Т-лимфобластный лейкоз</kwd><kwd>Т-лимфобластная лимфома</kwd><kwd>неходжкинские лимфомы</kwd><kwd>дети</kwd><kwd>NOTCH1</kwd><kwd>FBXW7</kwd></kwd-group><funding-group><funding-statement xml:lang="en">Not specified</funding-statement><funding-statement xml:lang="ru">Не указан</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Alaggio R., Amador C., Anagnostopoulos I., Attygalle A.D., Araujo I.B. de O., Berti E., et al. The 5<sup>th</sup> edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms. Leukemia 2022; 36 (7): 1720–48. 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