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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">107</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2011-7-1-66-72</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>PROSTATE CANCER</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>РАК ПРЕДСТАТЕЛЬНОЙ ЖЕЛЕЗЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">ROLE OF DEGARELIX (FIRMAGON) IN THE TREATMENT OF DISSEMINATED PROSTATE CANCER: CAN THE QUALITY OF CASTRATION THERAPY BE IMPROVED?</article-title><trans-title-group xml:lang="ru"><trans-title>РОЛЬ ДЕГАРЕЛИКСА (ФИРМАГОН) В ЛЕЧЕНИИ РАСПРОСТРАНЕННОГО РАКА ПРЕДСТАТЕЛЬНОЙ ЖЕЛЕЗЫ: МОЖНО ЛИ УЛУЧШИТЬ КАЧЕСТВО КАСТРАЦИОННОЙ ТЕРАПИИ?</trans-title></trans-title-group></title-group><contrib-group><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>mivolkova@rambler.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Volkova</surname><given-names>M. I.</given-names></name><name xml:lang="ru"><surname>Волкова</surname><given-names>М. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>mivolkova@rambler.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Department of Urology, N.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences, Moscow</institution></aff><aff><institution xml:lang="ru">Отделение урологии РОНЦ им. Н.Н. Блохина РАМН, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2011-03-30" publication-format="electronic"><day>30</day><month>03</month><year>2011</year></pub-date><volume>7</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>66</fpage><lpage>72</lpage><history><date date-type="received" iso-8601-date="2014-07-27"><day>27</day><month>07</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-07-27"><day>27</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/107">https://oncourology.abvpress.ru/oncur/article/view/107</self-uri><abstract xml:lang="en"><p>Degarelix (Firmagon) (Ferring Pharmaceuticals) is a new gonadotropin-releasing hormone (GnRH) antagonist permitted and approved for use in the treatment of hormone-dependent prostate cancer. It is recommended to administer the drug subcutaneously in the abdomen in a starting dose of 240 mg, followed by monthly maintenance doses of 80 mg. The Phase III randomized trial demonstrated that degarelix had advantages over the GnRH agonist leuprorelin in the reduction rates for testosterone to castration levels and for prostate-specific antigen (PSA) levels and in the absence of the initial increase and variations of androgen concentrations during treatment. A one-year follow-up showed that the risk of PSA recurrence and death with leuprorelin was significantly higher than that with degarelix. There was a significant reduction in the risk of PSA recurrence in patients switched from leuproprorelin to degarelix. The rates of adverse reactions and treatment discontinuation in the degarelix treatment group do not differ from that in the leuprorelin group. Long-term follow-up studies are required to draw final conclusions.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>prostate cancer</kwd><kwd>castration therapy</kwd><kwd>degarelix</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>рак предстательной железы</kwd><kwd>кастрационная терапия</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. Huggins C., Hodges C.V. Studies on prostatic cancer: effect of castration, of estrogen and of androgen injection on serum phosphatases in metastatic carcinoma of the prostate. Cancer Res 1941;1:293–7.</mixed-citation><mixed-citation xml:lang="ru">Huggins C., Hodges C.V. Studies on prostatic cancer: effect of castration, of estrogen and of androgen injection on serum phosphatases in metastatic carcinoma of the prostate. 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