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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="en"><front><journal-meta><journal-id journal-id-type="publisher-id">rpcardio</journal-id><journal-title-group><journal-title xml:lang="en">Rational Pharmacotherapy in Cardiology</journal-title><trans-title-group xml:lang="ru"><trans-title>Рациональная Фармакотерапия в Кардиологии</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1819-6446</issn><issn pub-type="epub">2225-3653</issn><publisher><publisher-name>«SILICEA-POLIGRAF» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20996/1819-6446-2020-04-10</article-id><article-id custom-type="elpub" pub-id-type="custom">rpcardio-2177</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="en"><subject>POINT OF VIEW</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ТОЧКА ЗРЕНИЯ</subject></subj-group></article-categories><title-group><article-title>The Current Status of Direct Oral Anticoagulants in Cancer-Related Venous Thromboembolism Treatment</article-title><trans-title-group xml:lang="ru"><trans-title>Актуальный статус прямых оральных антикоагулянтов при лечении венозных тромбоэмболических осложнений у онкологических больных</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>Лобастов</surname><given-names>К. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Lobastov</surname><given-names>К. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лобастов Кирилл Викторович – кандидат медицинских наук, доцент, кафедра общей хирургии и лучевой диагностики</p><p>117997 Москва, ул. Островитянова, 1 </p></bio><bio xml:lang="en"><p>Kirill V. Lobastov – MD, PhD, Associate Professor, Chair of General Surgery and Radiology</p><p>Ostrovitianova ul. 1, Moscow, 117997 </p></bio><email xlink:type="simple">lobastov_kv@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Счастливцев</surname><given-names>И. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Schastlivtsev</surname><given-names>I. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Счастливцев Илья Вениаминович – кандидат медицинских наук, доцент, кафедра общей хирургии и лучевой диагностики</p><p>117997 Москва, ул. Островитянова, 1 </p></bio><bio xml:lang="en"><p>Ilya V. Schastlivtsev – MD, PhD, Associate Professor, Chair of General Surgery and Radiology</p><p>Ostrovitianova ul. 1, Moscow, 117997 </p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Российский Национальный Исследовательский Медицинский Университет им. Н.И. Пирогова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Pirogov Russian National Research Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>01</day><month>05</month><year>2020</year></pub-date><volume>16</volume><issue>2</issue><fpage>286</fpage><lpage>295</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Lobastov К.V., Schastlivtsev I.V., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Лобастов К.В., Счастливцев И.В.</copyright-holder><copyright-holder xml:lang="en">Lobastov К.V., Schastlivtsev I.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.rpcardio.online/jour/article/view/2177">https://www.rpcardio.online/jour/article/view/2177</self-uri><abstract><p>This article is a review of epidemiology, pathogenesis and treatment of venous thromboembolism (VTE) in cancer patients. In accordance with actual guidelines, the duration of anticoagulant therapy of cancer-related venous thrombosis should be at least 6 months. The use of vitamin K antagonists (VKA) is associated with an increased risk of VTE recurrence and bleeding, so low molecular weight heparin (LMWH), in particular dalteparin, has been the "gold standard" until recently. Compared to VKA, prolonged use of LMWH can reduce the incidence of VTE recurrence without affecting the risk of bleeding or death. The main disadvantage of LMWH is low compliance, leading to premature discontinuation of treatment or switching to alternative anticoagulants. Direct oral anticoagulants (DOACs) have changed the situation. Compared to VKA, they demonstrated higher efficacy with a similar (or improved for individual DOACs) safety in patients with cancer-related VTE. Recently, the results of studies comparing the use of DOACs with dalteparin in cancer patients have been published: SELECT-D (rivaroxaban), HOKUSAI-VTE Cancer (edoxaban), ADAM VTE (apixaban), CARAVAGGIO (apixaban). Rivaroxaban showed higher efficacy than dalteparin with a similar risk of major bleeding, but an increased risk of clinically relevant non-major (CRNM) bleeding. Edoxaban had the same efficacy as dalteparin but increased risk of major but not CRNM bleeding. Apixaban showed similar efficacy and safety as dalteparin in the CARAVAGGIO study, but did not provide higher safety in the ADAM VTE study. It was noted that gastrointestinal and urogenital bleeding dominated in the structure of hemorrhagic complications of DOACs. The results of published trials are reflected in the current guidelines of the specialized societies. DOACs (particularly, rivaroxaban and edoxaban) are recommended for the VTE treatment in cancer patients.</p></abstract><trans-abstract xml:lang="ru"><p>Статья представляет собой обзор, посвященный вопросам эпидемиологии, патогенеза и лечения венозных тромбоэмболических осложнений (ВТЭО) у онкологических больных. В соответствии с современными рекомендациями антикоагулянтная терапия онко-ассоциированного венозного тромбоза должна продолжаться не менее 6 мес. Использование антагонистов витамина К (АВК) ассоциируется с повышенным риском рецидива ВТЭО и кровотечения, поэтому «золотым стандартом» до последнего времени являлись низкомолекулярные гепарины (НМГ), в частности, далтепарин. В сравнении с АВК длительное использование НМГ позволяет уменьшить риск рецидива ВТЭО без влияния на опасность геморрагических осложнений и летального исхода. Главным недостатком НМГ считается низкая комплаентность, приводящая к преждевременному завершению лечения или переходу на альтернативные препараты. Появление прямых оральных антикоагулянтов (ПОАК) изменило ситуацию. В сравнении с АВК они обладают более высокой эффективностью при сопоставимом (или улучшенном для отдельных препаратов) профиле безопасности при лечении онко-ассоциированных ВТЭО. Недавно были опубликованы результаты исследо-ваний, сравнивающих результаты применения ПОАК и далтепарина у онкологических пациентов: SELECT-D (ривароксабан), HOKUSAI-VTE Cancer (эдоксабан), ADAM VTE (апиксабан), CARAVAGGIO (апиксабан). Ривароксабан продемонстрировал бóльшую эффективность при сопоставимом риске больших кровотечений и увеличенной частоте не больших, но клинически значимых (НБКЗ) кровотечений. Эдоксабан оказался не менее эффективным, но увеличивал частоту развития больших (но не НБКЗ) кровотечений. Апиксабан продемонстрировал не меньшую эффективность и сопоставимую безопасность в исследовании CARAVAGGIO, но не смог доказать бóльшую безопасность в исследовании ADAM VTE. Было отмечено, что в структуре геморрагических осложнений при использовании ПОАК доминировали желудочно-кишечные и урогенитальные кровотечения. Результаты опубликованных исследований нашли отражение в современных рекомендациях специализированных сообществ. ПОАК (в частности, ривароксабан и эдоксабан) рекомендуются к применению для лечения ВТЭО у онкологических пациентов.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>венозный тромбоз</kwd><kwd>легочная эмболия</kwd><kwd>венозное тромбоэмболическое осложнение</kwd><kwd>злокачественное новообразование</kwd><kwd>прямые оральные антикоагулянты</kwd></kwd-group><kwd-group xml:lang="en"><kwd>venous thrombosis</kwd><kwd>pulmonary embolism</kwd><kwd>venous thromboembolism</kwd><kwd>malignancy</kwd><kwd>direct oral anticoagulants</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">Anderson, F.A., Jr., Spencer, F.A. 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