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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">650</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2017-13-1-101-111</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">Combined chemohormonalradiation treatment of highand very-high-risk non-metastatic prostate cancer</article-title><trans-title-group xml:lang="ru"><trans-title>Комплексное гормонохимиолучевое лечение больных неметастатическим раком предстательной железы группы высокого и очень высокого риска прогрессирования</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kaprin</surname><given-names>A. D.</given-names></name><name xml:lang="ru"><surname>Каприн</surname><given-names>А. Д.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>4 Korolyova St., Obninsk 249031</p></bio><bio xml:lang="ru"><p>Андрей Дмитриевич Каприн, доктор медицинских наук, профессор, академик РАН, генеральный директор ФГБУ «НМИРЦ» Минздрава России</p></bio><email>alex_troy@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Troyanov</surname><given-names>A. V.</given-names></name><name xml:lang="ru"><surname>Троянов</surname><given-names>А. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>4 Korolyova St., Obninsk 249031</p></bio><bio xml:lang="ru"><p>Контакты: Алексей Владимирович Троянов </p><p>SPIN-код: <ext-link ext-link-type="uri" xlink:href="http://elibrary.ru/author_info.asp?isold=1">4504-1800</ext-link></p></bio><email>alex_troy@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ivanov</surname><given-names>S. A.</given-names></name><name xml:lang="ru"><surname>Иванов</surname><given-names>С. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>4 Korolyova St., Obninsk 249031</p></bio><bio xml:lang="ru"><p>Сергей Анатольевич Иванов, доктор медицинских наук, заместитель директора по научной и лечебной работе МРНЦ им.А.Ф.Цыба</p></bio><email>alex_troy@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Karyakin</surname><given-names>O. V.</given-names></name><name xml:lang="ru"><surname>Карякин</surname><given-names>О. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>4 Korolyova St., Obninsk 249031</p></bio><bio xml:lang="ru"><p>Олег Борисович Карякин, доктор медицинских наук, профессор, заведущий отделением лучевого и хирургического лечения урологических заболеваний с группой брахитерапии рака предстательной железы МРНЦ им.А.Ф.Цыба.</p></bio><email>alex_troy@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">A.F. Tsyb Medical Radiological Research Center – branch of the National Medical Research Radiological Center</institution></aff><aff><institution xml:lang="ru">Медицинский радиологический научный центр им А.Ф. Цыба – филиал ФГБУ «Национальный медицинский исследовательский радиологический центр»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2017-03-30" publication-format="electronic"><day>30</day><month>03</month><year>2017</year></pub-date><volume>13</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>101</fpage><lpage>111</lpage><history><date date-type="received" iso-8601-date="2017-01-26"><day>26</day><month>01</month><year>2017</year></date><date date-type="accepted" iso-8601-date="2017-03-17"><day>17</day><month>03</month><year>2017</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/650">https://oncourology.abvpress.ru/oncur/article/view/650</self-uri><abstract xml:lang="en"><p><bold>Introduction</bold>. Treatment of highand very-high-risk prostate cancer appears to be extremely difficult. External beam radiation therapy combined with long-term androgen deprivation therapy (ADT) plays the main role, though low treatment effectiveness compared to one of intermediateand low-risk groups pushes towards finding new treatment options and modalities.</p><p><bold>Objective</bold>: to enlighten data from modern publications and reviews concerning combined treatment uncluding (or not) chemotherapy and different types of radiation therapy.</p><p><bold>Risk stratification</bold>. Several organizations (NCCN, NICE, ESMO, AUA, EAU and others) offer risk stratification systems. The NCCN system includes the very-high-risk group (Т3b–T4). Nowadays high-risk is set (EAU) when stages ≥ T2c or prostatic specific antigen &gt; 20 ng/ml or Gleason score 8–10 appear.</p><p><bold>External beam radiation therapy</bold>. Recommended dose is ≥ 74 Gy not depending on risk group. Low overall 10-years survival rate makes searching for new effective treatments inevitable.</p><p><bold>ADT.</bold> Long-term regimens (2–3 years) of ADT in high-risk prostate cancer is undoubtable and neccecary. Biochemical progression-free survival can be achieved by using luteinizing hormone-releasing hormone antagonists in long-term regimens.</p><p><bold>Brachytherapy</bold>. Brachytherapy alone and its combination with external beam radiation therapy show high effectiveness concerning progressionfree survival. In high-risk group survival rates are significantly lower. Improvement can be achieved by using adjuvant long-term ADT and other systemic therapy. Nowadays the results of such clinical trials are not available.</p><p><bold>Chemotherapy</bold>. Chemotherapy as part of combination treatment of non-metastatic hormonal-sensitive high-risk prostate cancer is proved to be effective (increasing progression-free and overall survival), but still rarely used treatment option.</p><p><bold>Conclusion</bold>. Reviews, meta-analyses and phase III clinical trials results show improvement of progression-free survival (and some – overall survival) when using a multimodal approach with chemotherapy. Combination treatment of taxane-base chemotherapy, luteinizing hormonereleasing hormone antagonists as ADT and brachytherapy alone or with external beam radiation therapy seems to be extremely perspective and needing further investigation. </p></abstract><trans-abstract xml:lang="ru"><p><bold>Введение.</bold> Лечение больных раком предстательной железы (РПЖ) группы высокого и очень высокого риска прогрессирования представляет большую сложность. Лучевая терапия в сочетании с длительной гормональной терапией (ГТ) играет ключевую роль, однако низкая эффективность лечения по сравнению с таковой в группе пациентов промежуточного и низкого риска прогрессирования вынуждает искать новые лечебные алгоритмы и подходы.</p><p><bold>Цель работы</bold> – анализ существующих публикаций и обзоров касательно комплексного лечения как с включением химиотерапии, так и без него, а также различных видов лучевой терапии.</p><p><bold>Оценка риска прогрессирования</bold>. Системы классификации и оценки риска прогрессирования предложены различными организациями (NCCN, NICE, ESMO, AUA, EAU и др.). Система классификации NCCN включает группу очень высокого риска (Т3b–4). В настоящее время принадлежность к группе высокого риска (EAU) определяется при стадии ≥ T2c, или при уровне простатического специфического антигена &gt; 20 нг/мл, или при сумме баллов по шкале Глисона 8–10.</p><p><bold>Лучевая терапия</bold>. Рекомендованная доза облучения составляет ≥ 74 Гр вне зависимости от группы риска. Низкий уровень 10-летней общей выживаемости при РПЖ высокого риска прогрессирования вынуждает искать более эффективные подходы терапии. ГТ. Применение режимов длительной (2–3 года) ГТ при РПЖ высокого риска прогрессирования не вызывает сомнений и является обязательным. Увеличение выживаемости без биохимического рецидива возможно при использовании антагонистов лютеинизирующего гормона рилизинг-гормона в долгосрочных режимах.</p><p><bold>Внутритканевая лучевая терапия</bold>. Брахитерапия, как и сочетание ее с дистанционной лучевой терапией, показывает высокие результаты в отношении безрецидивной выживаемости. В группе высокого риска отмечается значительно более низкая выживаемость, поэтому возможно улучшение эффективности лечения при использовании длительной адъювантной ГТ и иной системной терапии. В настоящее время результаты подобных исследований не опубликованы.</p><p><bold>Химиотерапия.</bold> Химиотерапия как часть комплексного лечения неметастатического гормоночувствительного РПЖ высокого и очень высокого риска прогрессирования является доказанно эффективным (увеличивая безрецидивную и общую выживаемость пациентов), но еще мало распространенным видом лечения.</p><p><bold>Заключение</bold>. Обзоры, метаанализы и результаты рандомизированных исследований III фазы сообщают о преимуществах в отношении безрецидивной выживаемости при использовании мультимодального подхода с включением химиотерапии. Комбинация химиотерапии на основе таксанов, ГТ в виде антагонистов лютеинизирующего гормона рилизинг-гормона и лучевой терапии в виде брахитерапии или сочетанной терапии видится крайне перспективной и требующей дальнейшего изучения. </p></trans-abstract><kwd-group xml:lang="en"><kwd>prostate cancer</kwd><kwd>non-metastatic cancer</kwd><kwd>high-risk of progression</kwd><kwd>combination treatment</kwd><kwd>chemohormonalradiation treatment</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>рак предстательной железы</kwd><kwd>неметастатический рак</kwd><kwd>высокий риск прогрессирования</kwd><kwd>комплексное лечение</kwd><kwd>гормонохимиолучевое лечение</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.	Карякин О.Б., Бирюков В.А. Новые тенденции в применении таксотера (доцетаксела) при раке предстательной железы. Онкоурология 2009;5(4):58–62. [Karyakin O.B., Biryukov V.A. 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