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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">lvrach</journal-id><journal-title-group><journal-title xml:lang="ru">Лечащий Врач</journal-title><trans-title-group xml:lang="en"><trans-title>Lechaschi Vrach</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1560-5175</issn><issn pub-type="epub">2687-1181</issn><publisher><publisher-name>ООО «Издательство "Открытые системы"»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.51793/OS.2025.28.9.006</article-id><article-id custom-type="elpub" pub-id-type="custom">lvrach-1464</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>АКТУАЛЬНАЯ ТЕМА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>TOPICAL THEME</subject></subj-group></article-categories><title-group><article-title>Цитокиногенетическая терапия в комбинированном лечении рака толстого кишечника</article-title><trans-title-group xml:lang="en"><trans-title>Cytokine therapy in combination treatment of colorectal 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/0000-0002-7973-5231</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Заркуа</surname><given-names>В. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Zarkua</surname><given-names>V. T.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Заркуа Владимир Тамазиевич, онколог</p><p>125047, Москва, ул. Фадеева, 4</p><p>Researcher ID (WOS): NFS – 4512-2025</p></bio><bio xml:lang="en"><p>Vladimir T. Zarkua, oncologist</p><p>4 Fadeev St., Moscow, 125047</p><p>Researcher ID (WOS): NFS – 4512-2025</p></bio><email xlink:type="simple">miro.zarkua@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9239-2539</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бен Аммар</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Ben Ammar</surname><given-names>А. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бен Аммар Амир Мохамед, онколог</p><p>125047, Москва, ул. Фадеева, 4</p><p>Researcher ID (WOS): NFS – 7043-2025</p></bio><bio xml:lang="en"><p>Аmir M. Ben Ammar, oncologist</p><p>4 Fadeev St., Moscow, 125047</p><p>Researcher ID (WOS): NFS – 7043-2025</p></bio><email xlink:type="simple">amirbenammar94095@gmail.com</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>Спирочкина</surname><given-names>Е. Э.</given-names></name><name name-style="western" xml:lang="en"><surname>Spirochkina</surname><given-names>E. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Спирочкина Елена Эдуардовна, онколог</p><p>125047, Москва, ул. Фадеева, 4</p></bio><bio xml:lang="en"><p>Elena E. Spirochkina, oncologist</p><p>4 Fadeev St., Moscow, 125047</p></bio><email xlink:type="simple">alena.dudka2016@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ОнкоКейр Клиник 308</institution><country>Россия</country></aff><aff xml:lang="en"><institution>OncoCare Clinic 308</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>24</day><month>09</month><year>2025</year></pub-date><volume>0</volume><issue>9</issue><fpage>36</fpage><lpage>41</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Заркуа В.Т., Бен Аммар А.М., Спирочкина Е.Э., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Заркуа В.Т., Бен Аммар А.М., Спирочкина Е.Э.</copyright-holder><copyright-holder xml:lang="en">Zarkua V.T., Ben Ammar А.M., Spirochkina E.E.</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://journal.lvrach.ru/jour/article/view/1464">https://journal.lvrach.ru/jour/article/view/1464</self-uri><abstract><sec><title>Введение</title><p>Введение. Лечение колоректального рака на поздних линиях лекарственной терапии представляет значительные сложности, поскольку арсенал возможностей противоопухолевой терапии ограничен. Для потенцирования действия повторно назначаемых цитостатиков привлекает возможность использования препаратов цитокиногенетической терапии.</p></sec><sec><title>Цель работы</title><p>Цель работы. Оценить у пациента с IV стадией прогрессирующего рака толстого кишечника эффективность и безопасность применения цитокиногенетической терапии в сочетании с цитостатической терапией в поздней линии противоопухолевого лечения.</p></sec><sec><title>Материал и методы</title><p>Материал и методы. Под наблюдением находился пациент 62 лет, поступивший с первично-множественным синхронным раком толстой кишки: рак поперечно-ободочной кишки, усТ3N2M1b (печень), оперативное вмешательство (27.09.2022), 4 линии терапии (FOLFOX-6, FOLFIRI + бевацизумаб, регорафиниб, цетуксимаб), прогрессия, рак прямой кишки рТ2N0M0, оперативные вмешательства (18.06.2020, 27.09.2022). При обследовании была использована магнитно-резонансная томография с контрастным усилением.</p></sec><sec><title>Результаты</title><p>Результаты. Пациент отметил улучшение самочувствия после трех курсов цитокиногенетической терапии, а после восьмого курса смог не только выполнять привычную работу по дому и самостоятельно добираться до больницы, но и стал немного заниматься своей профессиональной деятельностью. Применение противоопухолевой терапии по схеме ХЕLOX (пятая линия) в сочетании с цитокиногенетической терапией не сопровождалось выраженной токсичностью. По данным магнитно-резонансной томографии была достигнута частичная регрессия опухолевых очагов.</p></sec><sec><title>Заключение</title><p>Заключение. Совместное использование полихимиотерапии по схеме ХЕLOX и препаратов цитокиногенетической терапии позволило достичь частичной регрессии ранее прогрессирующей опухоли и увеличить продолжительность жизни больного.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Background</title><p>Background. Treatment of colorectal cancer in late lines of drug therapy presents significant challenges, since the arsenal of antitumor therapy options is limited. The possibility of using cytokinogenetic therapy drugs is attractive for potentiating the effect of re-administered cytostatics.</p></sec><sec><title>Objective</title><p>Objective. To evaluate the efficacy and safety of cytokinogenetic therapy in combination with cytostatic therapy in a patient with stage IV progressive colon cancer in the late line of antitumor treatment.</p></sec><sec><title>Material and methods</title><p>Material and methods. A 62-year-old patient was observed, admitted with a diagnosis of primary multiple synchronous colon cancer: transverse colon cancer, usT3N2M1b (liver), surgery (09/27/2022), 4 lines of therapy (FOLFOX-6, FOLFIRI + bevacizumab, regorafinib, cetuximab), progression, rectal cancer pT2N0M0, surgery (06/18/2020, 09/27/2022). During the examination, magnetic resonance imaging (MRI) with contrast enhancement was used.</p></sec><sec><title>Results</title><p>Results. The patient noted an improvement in his well-being after three courses of cytokinogenetic therapy, and after the 8th course he was able not only to do his usual housework and get to the hospital on his own, but also began to do his professional activities a little. The use of antitumor therapy according to the XELOX scheme (5th line) in combination with cytokinogenetic therapy was not accompanied by significant toxicity. According to MRI data, partial regression of tumor foci was achieved.</p></sec><sec><title>Conclusion</title><p>Conclusion. The combined use of polychemotherapy according to the XELOX scheme and cytokinogenetic therapy drugs made it possible to achieve partial regression of a previously progressing tumor and increase the patient's life expectancy.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>колоректальный рак</kwd><kwd>поздние линии лекарственной терапии</kwd><kwd>цитокиногенетическая терапия</kwd><kwd>цитостатики</kwd></kwd-group><kwd-group xml:lang="en"><kwd>colorectal cancer</kwd><kwd>late-line drug therapy</kwd><kwd>cytokinogenetic therapy</kwd><kwd>cytostatics</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">Cho Y. A., Lee J., Oh J. H., et al. Genetic Risk Score, Combined Lifestyle Factors and Risk of Colorectal Cancer. Cancer Res Treat. 2019; 51 (3): 1033-1040. https://doi.org/10.4143/crt.2018.447.</mixed-citation><mixed-citation xml:lang="en">Cho Y. A., Lee J., Oh J. 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