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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-2016-10-34-37</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-1402</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>Онкология</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Oncology</subject></subj-group></article-categories><title-group><article-title>Эволюция изучения и клинического применения антиандрогенов в лечении распространенного рака предстательной железы</article-title><trans-title-group xml:lang="en"><trans-title>DEVELOPMENT AND CLINICAL EFFECTIVENESS OF ANTIANDROGENS IN THE TREATMENT OF ADVANCED 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>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><p>Москва</p></bio><bio xml:lang="en"><p>PhD in medicine</p><p>Moscow</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>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><p>Москва</p></bio><bio xml:lang="en"><p>PhD in medicine</p><p>Moscow</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><p>Москва</p></bio><bio xml:lang="en"><p>MD</p><p>Moscow</p></bio><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Городская клиническая больница им. Д.Д. Плетнева<country>Россия</country></aff><aff xml:lang="en">City Clinical Hospital №57<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">Институт хирургии им. А.В. Вишневского<country>Россия</country></aff><aff xml:lang="en">Vishnevsky Institute of Surgery<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru">Московский научно-исследовательский онкологический институт им. П.А. Герцена<country>Россия</country></aff><aff xml:lang="en">МНИОИ им. П.А. Герцена<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>30</day><month>12</month><year>2016</year></pub-date><volume>0</volume><issue>10</issue><fpage>34</fpage><lpage>37</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; МИШУГИН С.В., ГРИЦКЕВИЧ А.А., РУСАКОВ И.Г., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">МИШУГИН С.В., ГРИЦКЕВИЧ А.А., РУСАКОВ И.Г.</copyright-holder><copyright-holder xml:lang="en">MISHUGIN S.V., GRITSKEVICH A.A., RUSAKOV I.G.</copyright-holder><license 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/1402">https://www.med-sovet.pro/jour/article/view/1402</self-uri><abstract><p>Рак предстательной железы (РПЖ) является гормончувствительной опухолью. Благодаря открытию андрогенного рецептора (АР) в клинической практике появились препараты группы антиандрогенов, воздействующие на связывание тестостерона с АР. На протяжении ряда лет появилось несколько поколений данных препаратов и значительно изменились возможности применения данных препаратов. Первые поколения препаратов данной группы (ципротерон, флутамид и бикалутамид) используются в основном при лечении распространенного гормончувствительного РПЖ в комбинации с кастрационной терапией. Однако применение данных препаратов не приводит к увеличению выживаемости у пациентов с РПЖ и не показано при наступлении кастрационной резистентности. Появление энзалутамида (антиандроген II поколения), действующего на уровне ядра опухолевой клетки, позволило достоверно увеличить выживаемость пациентов с метастатическим кастрационно-резистентным РПЖ (мКРРПЖ) и значительно улучшить результаты лечения пациентов с мКРРПЖ. В настоящее время идет изучение возможности применения энзалутамида вместе с кастрационной терапией у пациентов с гормончувствительным РПЖ.</p></abstract><trans-abstract xml:lang="en"><p>Prostate cancer (PCa) is a hormonsensitive tumor. Due to the discovery of the androgen receptor (AR) it became possible to implement the antiandrogens as drugs blocking testosterone Binding to the AR into routine clinical practice. There have been discovered several generations of the antiandrogens over the years and the possibility of using these drugs in clinical practice has significantly changed. First generations of the antiandrogens (cyproterone, flutamid, bicalutamid) are used mainly for the treatment of advanced hormonsensitive PCa in combination with castration therapy. However these drugs do not increase survival in patients with PCa and are not indicated in terms of castration resistant PCa. Discovery of the enzalutamide (antiandrogen of 2’d generation), acting on the nuclear level of the tumor cell, allowed to increase significantly survival in patients with metastatic castration-resistant prostate cancer (mCRPC) and improve treatment results in patients with mCRPC. At the moment enzalutamide is being studied in combination with castration therapy in patients with hormonsensitive PCa.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>метастатический кастрационно-резистентный рак предстательной железы</kwd><kwd>андрогенный рецептор</kwd><kwd>антиандрогены</kwd><kwd>ципротерон</kwd><kwd>флутамид</kwd><kwd>нилутамид</kwd><kwd>бикалутамид</kwd><kwd>энзалутамид</kwd></kwd-group><kwd-group xml:lang="en"><kwd>metastatic castration-resistant prostate cancer</kwd><kwd>androgen receptor</kwd><kwd>antiandrogens</kwd><kwd>cyproteron</kwd><kwd>flutamid</kwd><kwd>bicalutamid</kwd><kwd>nilutamid</kwd><kwd>enzalutamid</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">Denmeade SR, Isaacs JT. 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