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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">medsovet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский Совет</journal-title><trans-title-group xml:lang="en"><trans-title>Meditsinskiy sovet = Medical Council</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-701X</issn><issn pub-type="epub">2658-5790</issn><publisher><publisher-name>REMEDIUM GROUP Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21518/2079-701X-2018-19-32-41</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-2744</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>ТАРГЕТНАЯ ТЕРАПИЯ ОПУХОЛЕЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Target therapy of tumors</subject></subj-group></article-categories><title-group><article-title>Цетуксимаб в терапии метастатического колоректального рака: история вопроса и клиническое наблюдение</article-title><trans-title-group xml:lang="en"><trans-title>Cetuximab in treatment of metastatic colorectal cancer: background and clinical observation</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>Даренская</surname><given-names>А. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Darenskaya</surname><given-names>A. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н., младший научный сотрудник отделения химиотерапии и комбинированного лечения злокачественных опухолей НИИ клинической онкологии</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Доброва</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Dobrova</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н., старший научный сотрудник отделения химиотерапии и комбинированного лечения злокачественных опухолей НИИ клинической онкологии</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Медведева</surname><given-names>Б. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Medvedeva</surname><given-names>B. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., ведущий научный сотрудник рентгенодиагностического отделения НИИ клинической и экспериментальной радиологии</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н.Н. Блохина» Минздрава России, Москва</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Blokhin National Medical Cancer Research Center of the Ministry of Healthcare of Russia, Moscow</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>11</day><month>11</month><year>2018</year></pub-date><volume>0</volume><issue>19</issue><fpage>32</fpage><lpage>41</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Даренская А.Д., Доброва Н.В., Медведева Б.М., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Даренская А.Д., Доброва Н.В., Медведева Б.М.</copyright-holder><copyright-holder xml:lang="en">Darenskaya A.D., Dobrova N.V., Medvedeva B.M.</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.med-sovet.pro/jour/article/view/2744">https://www.med-sovet.pro/jour/article/view/2744</self-uri><abstract><p>В настоящее время продолжается поиск наиболее оптимальных режимов лекарственной терапии метастатического колоректального рака (мКРР), в результате использования которых предполагаются увеличение выживаемости без прогрессирования (ВБП) и общей выживаемости (ОВ); улучшение качества жизни пациентов. Благодаря значительному прогрессу в химиотерапии (ХТ) и хирургическом лечении мКРР, использованию мультидисциплинарного подхода алгоритмы лечения больных изменились. Увеличение продолжительности жизни пациентов наблюдается при использовании всех трех наиболее активных при данном заболевании химиопрепаратов: оксалиплатина (Oxa), иринотекана (Iri), фторпиримидинов. Включение таргетного препарата цетуксимаба в современные режимы лечения мКРР привело к статистически достоверному увеличению частоты объективных ответов (ЧОО), медианы ВБП и ОВ. В статье приводятся результаты наиболее значимых клинических исследований, посвященных изучению эффективности анти-EGFR препарата цетуксимаба в комбинации со стандартными режимами ХТ в I и II линиях лекарственного лечения мКРР, а также представлено клиническое наблюдение успешного использования цетуксимаба в терапии мКРР.</p></abstract><trans-abstract xml:lang="en"><p>Today, the researchers continue the search for the most optimal regimens of drug therapy for metastatic colorectal cancer (mCRC) which are supposed to increase progression-free survival (PFS) and overall survival (OS), improve patient quality of life. Due to significant progress in chemotherapy (CT) and surgical treatment of mCRC, and the multidisciplinary approach, the treatment algorithms have changed. The increase in life expectancy of patients is observed when all three of the most active chemotherapy drugs in this disease: oxaliplatin (Oxa), irinotecan (Iri), fluoropyrimidines are administered. The inclusion of the targeted drug cetuximab in modern mCRC treatment regimens led to a statistically significant increase in the objective response rate (ORR), median PFS and OS. The article presents the results of the most significant clinical studies of the eficacy of the antiEGFR drug cetuximab in combination with standard CT regimens for the first- and second-line treatment of mCRC, and describes a clinical case of the successful use of cetuximab in mCRC therapy.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>метастатический колоректальный рак (мКРР)</kwd><kwd>таргетная терапия</kwd><kwd>рецептор эпидермального фактора роста (EGFR)</kwd><kwd>моноклональное антитело (МКА)</kwd><kwd>цетуксимаб</kwd><kwd>химиотерапия (ХТ)</kwd><kwd>иринотекан</kwd><kwd>оксалиплатин</kwd><kwd>фторпиримидины</kwd></kwd-group><kwd-group xml:lang="en"><kwd>metastatic colorectal cancer (mCRC)</kwd><kwd>targeted therapy</kwd><kwd>epidermal growth factor receptor (EGFR)</kwd><kwd>monoclonal antibody (MAB)</kwd><kwd>cetuximab</kwd><kwd>chemotherapy (CT)</kwd><kwd>irinotecan</kwd><kwd>oxaliplatin</kwd><kwd>fluoropyrimidines</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">Goldstein N et al. 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