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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">Cancer Urology</journal-id><journal-title-group><journal-title xml:lang="en">Cancer Urology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкоурология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-9776</issn><issn publication-format="electronic">1996-1812</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">351</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2012-8-4-22-26</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>DIAGNOSIS AND TREATMENT OF URINARY SYSTEM TUMORS. RENAL CANCER</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ДИАГНОСТИКА И ЛЕЧЕНИЕ ОПУХОЛЕЙ МОЧЕПОЛОВОЙ СИСТЕМЫ. Рак почки</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">OPTIMIZATION OF SECOND-LINE TARGETED THERAPY FOR METASTATIC RENAL CELL CARCINOMA CANCER AFTER USE OF VEGF RECEPTOR – TYROSINE KINASE INHIBITORS (LITERATURE REVIEW)</article-title><trans-title-group xml:lang="ru"><trans-title>ОПТИМИЗАЦИЯ ВТОРОЙ ЛИНИИ ТАРГЕТНОЙ ТЕРАПИИ МЕТАСТАТИЧЕСКОГО РАКА ПОЧКИ ПОСЛЕ ПРИМЕНЕНИЯ ИНГИБИТОРОВ ТИРОЗИНКИНАЗ РЕЦЕПТОРОВ VEGF (ОБЗОР ЛИТЕРАТУРЫ)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Savkov</surname><given-names>R. V.</given-names></name><name xml:lang="ru"><surname>Савков</surname><given-names>Р. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>Отделение онкоурологии</p></bio><email>dr.savkov@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Department of Urological Oncology, Moscow Regional Oncology Dispensary, Balashikha</institution></aff><aff><institution xml:lang="ru">ГБУЗ МООД, Балашиха</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2012-12-30" publication-format="electronic"><day>30</day><month>12</month><year>2012</year></pub-date><volume>8</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>22</fpage><lpage>26</lpage><history><date date-type="received" iso-8601-date="2014-08-07"><day>07</day><month>08</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-08-07"><day>07</day><month>08</month><year>2014</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncourology.abvpress.ru/oncur/article/view/351">https://oncourology.abvpress.ru/oncur/article/view/351</self-uri><abstract xml:lang="en"><p><italic>Sequential targeted therapy is now the standard of treatment for metastatic renal cell carcinoma (mRCC). A switch into a different mechanism of action of mTOR inhibitor after vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitors (TKI) in second-line therapy helps to elude cumulative toxicity and cross-resistance, which may occur in the sequential use of different anti-VEGFR agents through the overlapping mechanisms of action. After VEGFR TKI therapy failure, treatment with the mTOR inhibitor everolimus in second-line therapy is recognized to be effective and safe, substantially increasing progression-free survival, without worsening its quality. Everolimus is recommended as second-line targeted treatment for patients with progressive mRCC after primary VEGFR TKI use. Switching to everolimus is warranted especially in patients who have a poor response to or a high toxicity of first-line antiangiogenic therapy.</italic></p></abstract><trans-abstract xml:lang="ru"><p><italic>В настоящее время последовательная таргетная терапия является стандартом лечения метастатического почечно-клеточ ного рака (мПКР). Смена механизма действия при использовании ингибитора mTOR после ингибиторов тирозинкиназы (ИТК) рецепторов VEGF (VEGFR) во 2-й линии терапии позволяет избежать кумулятивной токсичности и перекрестной резистентности, возможных при последовательном применении различных анти-VEGFR-агентов за счет частично перекрывающихся механизмов действия. Лечение ингибитором mTOR эверолимусом во 2-й линии терапии при безуспешности лечения ИТК VEGFR признано эффективным и безопасным, позволяющим существенно увеличить выживаемость без прогрессирования без ухудшения ка чества жизни пациентов. Эверолимус – рекомендованный стандарт 2-й линии таргетного лечения пациентов с мПКР при прогрессировании заболевания после первичного применения ИТК VEGFR. Переход на эверолимус в особенности оправдан у пациентов с прогрессированием или высокой токсичностью антиангиогенной терапии 1-й линии.</italic></p></trans-abstract><kwd-group xml:lang="en"><kwd>sequential targeted therapy</kwd><kwd>second-line therapy</kwd><kwd>everolimus</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>последовательная таргетная терапия</kwd><kwd>2-я линия терапии</kwd><kwd>эверолимус</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. Escudier B., Pluzanska A., Koralewski P. et al. AVOREN Trial investigators. Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial. 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