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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">tumors</journal-id><journal-title-group><journal-title xml:lang="ru">Malignant tumours</journal-title><trans-title-group xml:lang="en"><trans-title>Malignant tumours</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2224-5057</issn><issn pub-type="epub">2587-6813</issn><publisher><publisher-name>Rosoncoweb</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18027/2224-5057-2012-2-5-13</article-id><article-id custom-type="elpub" pub-id-type="custom">tumors-7</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>ОБЗОРЫ И АНАЛИТИКА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS AND ANALYSIS</subject></subj-group></article-categories><title-group><article-title>ИНГИБИТОРЫ ТИРОЗИНКИНАЗЫ РЕЦЕПТОРА ЭПИДЕРМАЛЬНОГО ФАКТОРА РОСТА У БОЛЬНЫХ НЕМЕЛКОКЛЕТОЧНЫМ РАКОМ ЛЕГКОГО: 10 ЛЕТ СПУСТЯ</article-title><trans-title-group xml:lang="en"><trans-title></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>Тюляндин</surname><given-names>С. А.</given-names></name></name-alternatives><bio xml:lang="ru"><p>отделение клинической фармакологии, Каширское ш. 24, Москва, Россия 115478 Тел. (499) 324 98 44.</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Носов</surname><given-names>Д. А.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Российский онкологический научный центр им. Н.Н.  Блохина РАМН</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>19</day><month>05</month><year>2015</year></pub-date><volume>1</volume><issue>2</issue><fpage>5</fpage><lpage>13</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Тюляндин С.А., Носов Д.А., 2015</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="ru">Тюляндин С.А., Носов Д.А.</copyright-holder><copyright-holder xml:lang="en">Тюляндин С.А., Носов Д.А.</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://www.malignanttumors.org/jour/article/view/7">https://www.malignanttumors.org/jour/article/view/7</self-uri><abstract><p>Опыт применения ингибиторов тирозинкиназы рецептора эпидермального фактора роста (EGFR) насчитывает около 10 лет. За это время произошла серьезная эволюция наших представлений о месте и показаниях к назначению ингибиторов EGFR при немелкоклеточном раке легкого (НМРЛ). Эти лекарства были в первом ряду таргетных препаратов, идеология применения которых подразумевала точечное поражение мишени, имеющее важное значение для жизнедеятельности опухолевой клетки. Назначение таргетных препаратов показано только тем больным, у которых в опухоли содержится мишень поражения. Обнаружение активирующих мутаций в гене EGFR или мутаций, повышающих связывающую способность ингибиторов тирозинкиназы EGFR, позволило выделить тех (не более 10% от общего числа больных НМРЛ) больных, у которых наблюдается выраженный эффект от назначения этих препаратов. Таким образом, терапия ингибиторами EGFR стала таргетной не только по определению, но и по смыслу.</p></abstract><kwd-group xml:lang="ru"><kwd>немелкоклеточный рак легкого</kwd><kwd>рецептор эпидермального фактора роста</kwd><kwd>гиперэкспрессия</kwd><kwd>мутация</kwd><kwd>эрлотиниб</kwd><kwd>гефитиниб</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">Давыдов М.И., Аксель Е.М. Статистика злокачественных новообразований в России и странах СНГ в 2008 г. Вестник РОНЦ им. Н.Н.Блохина РАМН, т. 21, приложение №1, 2010.</mixed-citation><mixed-citation xml:lang="en">Давыдов М.И., Аксель Е.М. Статистика злокачественных новообразований в России и странах СНГ в 2008 г. Вестник РОНЦ им. Н.Н.Блохина РАМН, т. 21, приложение №1, 2010.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Rusch, v. et al. 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