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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">oncotomsk</journal-id><journal-title-group><journal-title xml:lang="ru">Сибирский онкологический журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Siberian journal of oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1814-4861</issn><issn pub-type="epub">2312-3168</issn><publisher><publisher-name>Tomsk National Research Medical Сепtеr of the Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21294/1814-4861-2019-18-5-38-44</article-id><article-id custom-type="elpub" pub-id-type="custom">oncotomsk-1186</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>КЛИНИЧЕСКИЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL STUDIES</subject></subj-group></article-categories><title-group><article-title>КЛИНИЧЕСКИЕ ВАРИАНТЫ МЕТАБОЛИЧЕСКОГО СИНДРОМА У БОЛЬНЫХ РАКОМ ЭНДОМЕТРИЯ</article-title><trans-title-group xml:lang="en"><trans-title>CLINICAL OPTIONS FOR METABOLIC SYNDROME IN PATIENTS WITH ENDOMETRIAL CANCER</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2560-0996</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кишкина</surname><given-names>А. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Kishkina</surname><given-names>A. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кишкина Анастасия Юрьевна, аспирант отделения гинекологии</p><p>г. Томск, 634009, пер. Кооперативный, 5</p><p>Author ID (Scopus): 57201799990</p></bio><bio xml:lang="en"><p>Anastasia Yu. Kishkina, MD, Postgraduate, Department of Gynecology</p><p>5, Kooperativny Street, 634009-Tomsk</p><p>Author ID (Scopus): 57201799990</p></bio><email xlink:type="simple">kichkinaanastasia91@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6854-8940</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коломиец</surname><given-names>Л. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kolomiets</surname><given-names>L. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Коломиец Лариса Александровна, доктор медицинских наук, профессор, заведующая отделением гинекологии, Научноисследовательский институт онкологии, Томский национальный исследовательский медицинский центр Российской академии наук</p><p>г. Томск, 634009, пер. Кооперативный, 5, </p><p>г. Томск, 634050, Московский тракт, 2  </p><p>SPIN-код: 6316-1146</p><p>AuthorID (РИНЦ): 347966</p><p>Author ID (Scopus): 7004921120</p><p>Researcher ID (WOS): C-8573-2012</p></bio><bio xml:lang="en"><p>Larisa A. Kolomiets, MD, DSc, Professor, Head of Gynecology Department, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences</p><p>5, Kooperativny Street, 634009-Tomsk, </p><p>2, Moskovsky Tract, 634050-Tomsk</p><p>Author ID (Scopus): 7004921120</p><p>Researcher ID (WOS): C-85732012</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4595-4177</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Юнусова</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Yunusova</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Юнусова Наталья Валерьевна, доктор медицинских наук, старший научный сотрудник лаборатории биохимии опухолей</p><p>г. Томск, 634009, пер. Кооперативный, 5</p><p>SPIN-код: 3513-1888</p><p>AuthorID (РИНЦ): 558006</p><p>Author ID (Scopus): 845414400</p><p>Researcher ID (WOS): C-9275-2012</p></bio><bio xml:lang="en"><p>Natalia V. Yunusovа, MD, DSc, Leading Researcher, Laboratory of Tumor Biochemistry</p><p>5, Kooperativny Street, 634009-Tomsk</p><p>Author ID (Scopus): 845414400</p><p>Researcher ID (WOS): C-9275-2012</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт онкологии, Томский национальный исследовательский медицинский центр Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Научно-исследовательский институт онкологии, Томский национальный исследовательский медицинский центр Российской академии наук;&#13;
Сибирский государственный медицинский университет Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences;&#13;
Siberian State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>31</day><month>10</month><year>2019</year></pub-date><volume>18</volume><issue>5</issue><fpage>38</fpage><lpage>44</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Кишкина А.Ю., Коломиец Л.А., Юнусова Н.В., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Кишкина А.Ю., Коломиец Л.А., Юнусова Н.В.</copyright-holder><copyright-holder xml:lang="en">Kishkina A.Y., Kolomiets L.A., Yunusova N.V.</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.siboncoj.ru/jour/article/view/1186">https://www.siboncoj.ru/jour/article/view/1186</self-uri><abstract><p>Эпидемиологические исследования выявили ассоциации между риском развития рака эндометрия (РЭ) и отдельными компонентами метаболического синдрома (МС). Учитывая высокую распространенность отдельных компонентов МС в общей популяции, подразумевается, что большой процент пациентов, особенно в пожилом возрасте, может иметь один или несколько компонентов на момент диагностики рака.</p><p>Цель исследования – выявить клинико-морфологические особенности рака эндометрия в зависимости от варианта метаболического синдрома: трех-, черырех и пятикомпонентного.</p><sec><title>Материал и методы</title><p>Материал и методы. В исследование были включены 60 больных морфологически верифицированным раком эндометрия I–II стадии (T1–3aN0–1M0), которым проведен стандартный объем обследования. Все больные в зависимости от наличия метаболического синдрома или метаболических нарушений были разделены на три группы: первая группа – больные РЭ с МС, вторая группа – больные РЭ с ожирением или избыточной массой тела, третья группа – больные РЭ без МС. Больные РЭ с МС были распределены на три подгруппы: больные РЭ с 3-компонентным МС, с 4-компонентным МС и с 5-компонентным МС.</p></sec><sec><title>Результаты</title><p>Результаты. Удельный вес больных раком эндометрия с метаболическим синдромом составил 53,3 %, средний возраст больных – 61,0 ± 2,1 года. Наиболее распространенным вариантом была 4-компонентная форма МС. Особенностями течения РЭ на фоне МС явилась умеренная степень дифференцировки В 71,8 % случаев, глубина инвазии до ½ миометрия у 65,3 %. Значимыми факторами безрецидивной выживаемости явились наличие или отсутствие МС, уровень тиреоглобулина и уровень глюкозы плазмы натощак, что еще раз подчеркивает влияние МС не только на развитие РЭ, но и на выживаемость больных.</p></sec><sec><title>Заключение</title><p>Заключение. Проведенное нами исследование и результаты ранних исследований свидетельствуют о необходимости разработки стратегий снижения распространенности компонентов МС, которые смогут оказать влияние как на снижение заболеваемости РЭ, так и на показатели выживаемости.</p></sec></abstract><trans-abstract xml:lang="en"><p>Many epidemiological studies have revealed the association between the risk of developing endometrial cancer (EС) and metabolic syndrome (MS) components. A large percentage of patients, especially elderly patients, may have one or more MS components at the time of cancer diagnosis.</p><sec><title>Objective</title><p>Objective: to identify the clinical and morphological features of EС, depending on the number of MS components: three-, fourand five-components.</p></sec><sec><title>Material and Methods</title><p>Material and Methods. The study included 60 patients with morphologically verified endometrial cancer (T1–3aN0–1M0). All endometrial cancer patients were divided into three groups. Group I included patients with MS, group II – patients with obesity or overweight (ICU ), and group III – patients without MS. Endometrial cancer patients with MS were divided into three subgroups: patients with 3 MS components, with 4 MS components and with 5 MS components.</p></sec><sec><title>Results</title><p>Results. The proportion of endometrial cancer patients with MS was 53.3 %. The median age of the patients was 61.0 ± 2.1 years. The majority of patients had 4 components of MS. Moderately differentiated tumor was observed in 71.8 % of cases, and invasion of less than one-half of the myometrium was observed in 65.3 % of cases. Significant factors of relapse-free survival were: the presence/absence of MS, TG level and the fasting plasma glucose level, thus underlining the effect of MS not only on the development of EС, but also the survival of patients.</p></sec><sec><title>Conclusions</title><p>Conclusions. Our study and many previous studies indicate that the strategies for reducing the prevalence of the components of MS are needed to be developed.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>рак эндометрия</kwd><kwd>метаболический синдром</kwd><kwd>ожирение</kwd><kwd>избыточная масса тела</kwd><kwd>выживаемость</kwd></kwd-group><kwd-group xml:lang="en"><kwd>endometrial cancer</kwd><kwd>metabolic syndrome</kwd><kwd>obesity</kwd><kwd>overweight</kwd><kwd>survival</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">World Cancer Research Fund. Endometrial cancer. How diet, nutrition and physical activity affect endometrial (womb) cancer risk [Internet]. URL: https://www.wcrf.org/dietandcancer/endometrial-cancer (cited 1.05.2019).</mixed-citation><mixed-citation xml:lang="en">World Cancer Research Fund. Endometrial cancer. 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