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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">10.18027/2224-5057-2016-3-54-59</article-id><article-id custom-type="elpub" pub-id-type="custom">tumors-261</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</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL REPORTS</subject></subj-group></article-categories><title-group><article-title>Рецептор эпидермального фактора роста как мишень молекулярно-направленной терапии у непредлеченных пациентов с немелкоклеточным раком легкого</article-title><trans-title-group xml:lang="en"><trans-title>Epidermal growth factor receptor as target of moleculartargeted therapy in patients with primary non-small cell lung cancer</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>САКАЕВА</surname><given-names>Д. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>SAKAEVA</surname><given-names>D. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д. м.н., профессор, заместитель главного врача</p></bio><bio xml:lang="en"><p>MD, RhD, DSc, professor, deputy chief doctor</p></bio><email xlink:type="simple">d_sakaeva@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>ГОРДИЕВ</surname><given-names>М. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>GORDIEV</surname><given-names>M. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>заведующий молекулярно-диагностической лабораторией </p></bio><bio xml:lang="en"><p>chief of molecular-diagnostic laboratory</p></bio><email xlink:type="simple">marat7925@gmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГБУЗ РКОД МЗ РБ г. Уфа</institution><country>Россия</country></aff><aff xml:lang="en"><institution>SBHI Republican clinical oncology dispensary of MoH of Bashkortostan Republic in Ufa</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ГБУЗ РКОД МЗ РТ г. Казань</institution><country>Россия</country></aff><aff xml:lang="en"><institution>SAHI, Republican clinical oncology dispensary of MoH of Tatarstan Republic, Kazan</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>16</day><month>10</month><year>2016</year></pub-date><volume>0</volume><issue>3</issue><fpage>54</fpage><lpage>59</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; САКАЕВА Д.Д., ГОРДИЕВ М.Г., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">САКАЕВА Д.Д., ГОРДИЕВ М.Г.</copyright-holder><copyright-holder xml:lang="en">SAKAEVA D.D., GORDIEV M.G.</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/261">https://www.malignanttumors.org/jour/article/view/261</self-uri><abstract><p>Рецептор эпидермального фактора роста (EGFR) – один из наиболее важных и наиболее изученных сигнальных путей, регулирующий рост, выживаемость, пролиферативную активность и дифференцировку клеток у млекопитающих [<xref ref-type="bibr" rid="cit1">1</xref>]. В тоже время EGFR и семейство белков – эпидермальных факторов роста, играют центральную роль в патогенезе и прогрессии различных видов опухолей [<xref ref-type="bibr" rid="cit2">2</xref>]. В 80-х годах прошлого века была выдвинута гипотеза о том, что данный сигнальный путь может стать мишенью для лекарственной терапии [<xref ref-type="bibr" rid="cit1">1</xref>]. В настоящее время существует 3 поколения ингибиторов тирозинкиназ (ИТК) EGFR. Препараты данного класса активно используются в клинической практике для лечения больных распространенным НМРЛ с наличием мутации гена EGFR. Исследования этих препаратов продолжаются. В данном обзоре освещены возможности использования ИТК в 1-й линии терапии распространенного НМРЛ, а также в адъювантном режиме.</p></abstract><trans-abstract xml:lang="en"><p>Epidermal Grows factor receptor (EGFR) is one of the most significant and studied signaling pathway, regulating growth, survival, proliferation and differentiation of mamllian cells. At the same time EGFR and its protein family play a central role in pathogenesis and progression of different type of tumors. In the 80-s, it was proposed that this signaling pathway could be the target for the therapy. Today there are 3 generations of tyrosine kinase inhibitors (TKIs). This drug class is actively used in clinical practice for therapy of patients with EGFR mutation positive advanced non small cell lung cancer (NSCLC). Investigation of TKIs is continuing. In this review, the options of TKI use in the adjuvant setting and the 1st line treatment of advanced NSCLC are highlighted.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>EGFR мутация</kwd><kwd>ИТК</kwd><kwd>НМРЛ</kwd></kwd-group><kwd-group xml:lang="en"><kwd>EGFR mutation</kwd><kwd>TKIs</kwd><kwd>NSCLC</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">D.S. Salomon, R. Brandt, F. Ciardiello, N. 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