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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">medsovet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский Совет</journal-title><trans-title-group xml:lang="en"><trans-title>Meditsinskiy sovet = Medical Council</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-701X</issn><issn pub-type="epub">2658-5790</issn><publisher><publisher-name>REMEDIUM GROUP Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21518/2079-701X-2017-6-104-109</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-1894</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>Онкоурология</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Oncourology</subject></subj-group></article-categories><title-group><article-title>МЕСТО ЭНЗАЛУТАМИДА В ПОСЛЕДОВАТЕЛЬНОМ ЛЕЧЕНИИ КАСТРАЦИОННО-РЕЗИСТЕНТНОГО РАКА ПРЕДСТАТЕЛЬНОЙ ЖЕЛЕЗЫ</article-title><trans-title-group xml:lang="en"><trans-title>THE PLACE OF ENZALUTAMIDE IN THE SERIAL TREATMENT OF TREATMENT-RESISTANT PROSTATE 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>ГРИЦКЕВИЧ</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>GRITSKEVICH</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н.</p></bio><bio xml:lang="en"><p>PhD in medicine</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>МИШУГИН</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>MISHUGIN</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н.</p></bio><bio xml:lang="en"><p>PhD in medicine</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>РУСАКОВ</surname><given-names>И. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>RUSAKOV</surname><given-names>I. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор</p></bio><bio xml:lang="en"><p>MD, Prof.</p></bio><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт хирургии им. А.В. Вишневского</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Vishnevsky Institute of Surgery</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Городская клиническая больница №57</institution><country>Россия</country></aff><aff xml:lang="en"><institution>City Clinical Hospital No. 57</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Городская клиническая больница №57&#13;
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Национальный медицинский исследовательский радиологический центр</institution><country>Россия</country></aff><aff xml:lang="en"><institution>City Clinical Hospital No. 57&#13;
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National Medical Research and Radiological Center</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>20</day><month>06</month><year>2017</year></pub-date><volume>0</volume><issue>6</issue><fpage>104</fpage><lpage>109</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; ГРИЦКЕВИЧ А.А., МИШУГИН С.В., РУСАКОВ И.Г., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">ГРИЦКЕВИЧ А.А., МИШУГИН С.В., РУСАКОВ И.Г.</copyright-holder><copyright-holder xml:lang="en">GRITSKEVICH A.A., MISHUGIN S.V., RUSAKOV I.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.med-sovet.pro/jour/article/view/1894">https://www.med-sovet.pro/jour/article/view/1894</self-uri><abstract><p>Рак предстательной железы первоначально отвечает на андроген-депривационную терапию, но у большинства пациентов в конечном итоге развивается кастрационно-резистентная форма заболевания. Энзалутамид является суперселективным ингибитором андрогенного рецептора (AР), который блокирует несколько этапов сигнального пути AР. Препарат показал значительную эффективность в лечении метастатического кастрационно-резистентного рака предстательной железы (КРРПЖ) как в 1-й линии терапии, так и во 2-й линии после предшествующей цитотоксической терапии доцетакселом. Чтобы обеспечить оптимальное лечение, важно понять последствия применения энзалутамида в контексте других методов лечения, так как недавние исследования показали, что перекрестная резистентность возникает между классами препаратов и внутри них. Мутации и сплайс-варианты AР также влияют на течение рака предстательной железы. Будущие стратегии лечения, включающие энзалутамид, должны учитывать предшествующий уровень воздействия таксанов или антиандрогенной терапии и наличие вариантов АР, которые могут повлиять на эффективность.</p></abstract><trans-abstract xml:lang="en"><p>Prostate cancer initially responds to androgen-deprivation therapy, but most patients eventually develop a castration-resistant form of disease. Enzalutamid is the superselective inhibitor of the androgen receptor (AR), which blocks several stages of the AR signal path. The drug showed significant effectiveness in the treatment of metastatic castration-resistant prostate cancer (MCRPC) in both the first line therapy and the second line therapy after the previous cytotoxic therapy of Docetaxel. To ensure optimum treatment, it is important to understand the impact of Enzalutamide in the context of other therapies, as recent studies have shown that cross-resistance occurs between and within classes of drugs. Mutations and AR splice-variants also affect prostate cancer. Future treatment strategies, including enzalutamide, should take into account the previous level of exposure to taxanes or anti-androgen therapy and the existence of variants of AR that may affect efficiency.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>метастатический рак предстательной железы</kwd><kwd>энзалутамид</kwd><kwd>абиратерона ацетат</kwd><kwd>кастрационная резистентность.</kwd></kwd-group><kwd-group xml:lang="en"><kwd>metastatic cancer</kwd><kwd>Enzalutamide</kwd><kwd>abiraterone acetate</kwd><kwd>castration resistance</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">Zarif JC, Miranti CK. The importance of nonnuclear AR signaling in prostate cancer progression and therapeutic resistance. Cell Signal, 2016, 28: 348-356.</mixed-citation><mixed-citation xml:lang="en">Zarif JC, Miranti CK. 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