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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">25</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2014-10-1-76-81</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">ANDROGEN DEPRIVATION THERAPY WITH LUTEINIZING HORMONE-RELEASING HORMONE ANTAGONISTS FOR PROSTATE CANCER: BEST DISEASE CONTROL WITH A LOWER RISK OF SIDE EFFECTS. RESULTS OF ANALYSIS OF 6 COMPARATIVE RANDOMIZED PHASE III TRIALS OF DEGARELIX AND LUTEINIZIN</article-title><trans-title-group xml:lang="ru"><trans-title>АНДРОГЕНДЕПРИВАЦИОННАЯ ТЕРАПИЯ АНТАГОНИСТАМИ ЛГРГ ПРИ РАКЕ ПРЕДСТАТЕЛЬНОЙ ЖЕЛЕЗЫ: ЛУЧШИЙ КОНТРОЛЬ НАД ЗАБОЛЕВАНИЕМ ПРИ МЕНЬШЕМ РИСКЕ ПОБОЧНЫХ ЭФФЕКТОВ. РЕЗУЛЬТАТЫ АНАЛИЗА 6 СРАВНИТЕЛЬНЫХ РАНДОМИЗИРОВАННЫХ ИССЛЕДОВАНИЙ III ФАЗЫ ДЕГАРЕЛИКСА И АГОНИСТОВ ЛГРГ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Markova</surname><given-names>A. S.</given-names></name><name xml:lang="ru"><surname>Маркова</surname><given-names>А. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>mark-an1@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Matveev</surname><given-names>V. B.</given-names></name><name xml:lang="ru"><surname>Матвеев</surname><given-names>В. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>mark-an1@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N.N. Blokhin Russian Cancer Research Cancer, Russian Academy of Medical Sciences, Moscow</institution></aff><aff><institution xml:lang="ru">ФГБУ «РОНЦ им. Н. Н. Блохина» РАМН, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2014-03-30" publication-format="electronic"><day>30</day><month>03</month><year>2014</year></pub-date><volume>10</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>76</fpage><lpage>81</lpage><history><date date-type="received" iso-8601-date="2014-07-24"><day>24</day><month>07</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-07-24"><day>24</day><month>07</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/25">https://oncourology.abvpress.ru/oncur/article/view/25</self-uri><abstract xml:lang="en"><p>Androgen deprivation therapy with luteinizing hormone-releasing hormone (LHRH) antagonists versus therapy with agonists of this hormone ensures a better disease control due to the rapider and persistent suppression of testosterone levels without a flare phenomenon and requires no preventive use of antiandrogens. The third-generation LHRH antagonist degarelix shows a good tolerability and causes no systemic al-lergic reactions inherent in the earlier known drugs of this group. As indicated, the use of degarelix was characterized by the longer response of prostate-specific antigen (PSA) with a lower risk of adverse reactions, namely, serious cardiovascular and osseous complications, urinary tract infections (UTI). Thus, in males with a history of cardiovascular diseases, the risk of serious cardiovascular events or death decreased by 56% just within the first year of degarelix therapy. The findings allow degarelix to be regarded as the drug of choice for first-line hormone therapy in patients with advanced PC, particularly in males with cardiovascular disease or a high risk for UTI and osseous complications.</p><p> </p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>prostate cancer</kwd><kwd>androgen deprivation therapy</kwd><kwd>luteinizing hormone releasing hormone antagonists</kwd><kwd>degarelix</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>рак предстательной железы</kwd><kwd>андрогендепривационная терапия</kwd><kwd>антагонисты лютеинизирующего гормона рилизинг-гормона</kwd><kwd>дегареликс</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. Heidenreich A., Bastian P. J., Bellmunt J. et al. EAU Guidelines 2013; p. 1–154.</mixed-citation><mixed-citation xml:lang="ru">Heidenreich A., Bastian P. 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