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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">nodgo</journal-id><journal-title-group><journal-title xml:lang="ru">Российский журнал детской гематологии и онкологии (РЖДГиО)</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Journal of Pediatric Hematology and Oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2311-1267</issn><issn pub-type="epub">2413-5496</issn><publisher><publisher-name>LTD “Graphica”</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17650/2311-1267-2016-3-3-47-51</article-id><article-id custom-type="elpub" pub-id-type="custom">nodgo-246</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>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ/ОБЗОРЫ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL INVESTIGATIONS/LITERATURE REVIEWS</subject></subj-group></article-categories><title-group><article-title>Современные стратегии лечения острого миелоидного лейкоза</article-title><trans-title-group xml:lang="en"><trans-title>Modern strategies in AML treatment</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рубнитц</surname><given-names>Дж.Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Rubnitz</surname><given-names>J.E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Отдел онкологии, </p><p>38105-2794, Теннесси, Мемфис, ул. Дэнни Томаса, 262</p></bio><bio xml:lang="en"><p>Department of Oncology, </p><p>262 Danny Thomas Place, Memphis, TN 38105-2794</p></bio><email xlink:type="simple">jeffrey.rubnitz@stjude.org</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Исследовательский госпиталь Святого Иуды</institution><country>Соединённые Штаты Америки</country></aff><aff xml:lang="en"><institution>St. Jude Children’s Research Hospital</institution><country>United States</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>22</day><month>09</month><year>2016</year></pub-date><volume>3</volume><issue>3</issue><fpage>47</fpage><lpage>51</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Рубнитц Д., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Рубнитц Д.</copyright-holder><copyright-holder xml:lang="en">Rubnitz J.</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://journal.nodgo.org/jour/article/view/246">https://journal.nodgo.org/jour/article/view/246</self-uri><abstract><p>Острый миелоидный лейкоз (ОМЛ) – это комплексное заболевание, которое характеризуется широким спектром генетических и эпигенетических аномалий. Гетерогенность подтипов ОМЛ подразумевает, что улучшение клинических исходов требует разработки методов терапии, которые будут специфичными для каждого подтипа, и создания новых клинических исследований для подтверждения их целесообразности. В данном обзоре кратко представлены последние клинические исследования, генетическое разнообразие ОМЛ и мониторинг минимальной остаточной болезни.</p><p>Авторы перевода: К.И. Киргизов, Т.В. Шаманская</p></abstract><trans-abstract xml:lang="en"><p>Acute myeloid leukemia (AML) is a complex disease that is characterized by diverse genetic and epigenetic abnormalities. The heterogeneity of AML subtypes implies that improvements in clinical outcome will require the development of therapies that are specific for each subtype of the disease and the design of novel clinical trials to test these strategies. In this review, we briefly summarize recent clinical trials, the genetic diversity of AML, and the use of minimal residual disease in the treatment of AML.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>острый миелоидный лейкоз</kwd><kwd>дети</kwd><kwd>лечение</kwd><kwd>минимальная остаточная болезнь</kwd></kwd-group><kwd-group xml:lang="en"><kwd>acute myeloid leukemia</kwd><kwd>children</kwd><kwd>treatment</kwd><kwd>minimal residual disease</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Zwaan C.M., Kolb E.A., Reinhardt D. et al. Collaborative Efforts Driving Progress in Pediatric Acute Myeloid Leukemia. J Clin Oncol 2015;33:2949–62.</mixed-citation><mixed-citation xml:lang="en">Zwaan C.M., Kolb E.A., Reinhardt D. et al. Collaborative Efforts Driving Progress in Pediatric Acute Myeloid Leukemia. 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