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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">436</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2020-19-4-198-204</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">Prognostic markers of lymphoblastic lymphoma</article-title><trans-title-group xml:lang="ru"><trans-title>Прогностические маркеры лимфобластной лимфомы</trans-title></trans-title-group></title-group><contrib-group><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><bold>Egor V. Volchcov</bold>, a research technician at the Lymphoma Research Department</p><p>1 Samory Mashela St., Moscow 117997 </p></bio><bio xml:lang="ru"><p><bold>Волчков Егор Васильевич</bold>, лаборант-исследователь отдела исследования лимфом</p><p>117997, Москва, ул. Саморы Машела, 1 </p></bio><email>volchcov.egor@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2352-7716</contrib-id><name-alternatives><name xml:lang="en"><surname>Olshanskaya</surname><given-names>Yu. V.</given-names></name><name xml:lang="ru"><surname>Ольшанская</surname><given-names>Ю. 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>Москва</p></bio><xref ref-type="aff" rid="aff1"/></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>Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology of Ministry of Healthcare 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><pub-date date-type="pub" iso-8601-date="2020-12-08" publication-format="electronic"><day>08</day><month>12</month><year>2020</year></pub-date><volume>19</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>198</fpage><lpage>204</lpage><history><date date-type="received" iso-8601-date="2020-12-22"><day>22</day><month>12</month><year>2020</year></date><date date-type="accepted" iso-8601-date="2020-12-22"><day>22</day><month>12</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2025</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/436">https://hemoncim.com/jour/article/view/436</self-uri><abstract xml:lang="en"><p>Lymphoblastic lymphoma (LBL) is the second most common non-Hodgkin's lymphoma in childhood. According to modern concepts LBL and acute lymphoblastic leukemia (ALL) are considered as manifestations of the same disease given the similar morphological substrate of the tumor – T and B lymphoblasts. The standard for the treatment of LBL is currently ALL-like riskadapted treatment protocols that allow achieving overall and event-free survival rates of 80–90%. The division into risk groups is based on the stage of the disease and the response to induction therapy. However, the problem of relapse/refractory course of the disease remains a serious problem due to the lack of sufficiently effective therapeutic options. Currently, there is a sufficient amount of clinical data that reliably shows that a number of molecular biological factors can be used to create a new system of into risk groups stratification of patients with LBL. This review focuses on the analysis of various factors that may be responsible for the prognosis of LBL in children.</p></abstract><trans-abstract xml:lang="ru"><p>Лимфобластная лимфома (ЛБЛ) – вторая по частоте встречаемости неходжкинская лимфома у детей. Согласно современным представлениям, ЛБЛ и острый лимфобластный лейкоз (ОЛЛ) рассматривают как проявления одного и того же заболевания, учитывая сходный морфологический субстрат опухоли – Т- и В-лимфобласты. Стандартом терапии ЛБЛ в настоящее время являются ОЛЛ-подобные риск-адаптированные протоколы лечения, позволяющие добиться показателей общей и бессобытийной выживаемости, достигающие 80–90%. Разделение на группы риска основано на стадии заболевания и ответе на терапию индукции. Однако проблема рецидивов/ рефрактерного течения заболевания остается серьезной ввиду отсутствия достаточно эффективных терапевтических опций. На сегодняшний день имеется достаточное количество клинических данных, достоверно показывающих, что ряд молекулярно-биологических факторов может быть использован для создания новой системы стратификации на группы риска пациентов с ЛБЛ. Настоящий обзор посвящен анализу различных факторов, которые могут быть ответственны за прогноз ЛБЛ у детей.</p></trans-abstract><kwd-group xml:lang="en"><kwd>lymphoblastic lymphoma</kwd><kwd>acute lymphoblastic leukemia</kwd><kwd>non-Hodgkin lymphoma</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>лимфобластная лимфома</kwd><kwd>острый лимфобластный лейкоз</kwd><kwd>неходжкинские лимфомы</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Arber D., Orazi A., Hasserjian R., Thiele J., Borowitz M.J., Le Beau M.M., et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 2016;127 (20): 2391–405. DOI: 10.1182/blood-2016-03-643544</mixed-citation><mixed-citation xml:lang="ru">Arber D., Orazi A., Hasserjian R., Thiele J., Borowitz M.J., Le Beau M.M., et al. 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