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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">Surgery and Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Surgery and Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Хирургия и онкология</trans-title></trans-title-group></journal-title-group><issn publication-format="electronic">2949-5857</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">26</article-id><article-id pub-id-type="doi">10.17650/2220-3478-2014-0-2-18-21</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРЫ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">THE HIGH ACTIVITY OF VECTIBIX IN PATIENTS WITH METASTATIC COLORECTAL CANCER WITH THE RAS WILD-TYPE GENE</article-title><trans-title-group xml:lang="ru"><trans-title>ВЫСОКАЯ АКТИВНОСТЬ ВЕКТИБИКСА У БОЛЬНЫХ МЕТАСТАТИЧЕСКИМ КОЛОРЕКТАЛЬНЫМ РАКОМ С ДИКИМ ТИПОМ ГЕНА RAS</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Semenov</surname><given-names>N. N.</given-names></name><name xml:lang="ru"><surname>Семёнов</surname><given-names>Н. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>Отделение химиотерапии и комбинированного лечения злокачественных опухолей</p></bio><email>niksemenov1969@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Department of Chemotherapy and Combination Treatment for Malignant Tumors, N.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences, Moscow</institution></aff><aff><institution xml:lang="ru">ФГБУ «РОНЦ им. Н. Н. Блохина» РАМН, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2014-05-25" publication-format="electronic"><day>25</day><month>05</month><year>2014</year></pub-date><volume>3</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>18</fpage><lpage>21</lpage><history><date date-type="received" iso-8601-date="2015-02-25"><day>25</day><month>02</month><year>2015</year></date><date date-type="accepted" iso-8601-date="2015-02-25"><day>25</day><month>02</month><year>2015</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2014, ABV-press</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2014, АБВ-пресс</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="en">ABV-press</copyright-holder><copyright-holder xml:lang="ru">АБВ-пресс</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://onco-surgery.info/jour/about/editorialPolicies</ali:license_ref></license></permissions><self-uri xlink:href="https://onco-surgery.info/jour/article/view/26">https://onco-surgery.info/jour/article/view/26</self-uri><abstract xml:lang="en"><p>High-efficiency inhibitors of EGFR (panitumumab and cetuximab) in combination with chemotherapy in patients with advanced colorectal cancer is the result of the targeting special group of the patients based on studies of genes. Previously it was shown that the presence of mutation in exon 2 of KRAS gene (40 % of patients) determines the effectivity of this group of drugs. However, the search for additional indicators was continued. The result is that the presence of mutations in exons 3 and 4 of KRAS gene and in exons 2, 3 and 4 of NRAS gene also predict EGFR inhibitors efficacy. These mutations are defined in 10 % of patients. Analysis showed that the efficiency of panitumumab and cetuximab in combination with chemotherapy significantly increased in patients with wild-type KRAS and NRAS.</p></abstract><trans-abstract xml:lang="ru"><p>Высокая эффективность ингибиторов EGFR (панитумумаба и цетуксимаба) в комбинации с химиотерапией (ХТ) у больных распространенным колоректальным раком обусловлена возможностью выделить специальную группу больных на основании исследований генов. Ранее было показано, что наличие мутации во 2-м экзоне гена KRAS (40 % больных) предопределяет неэффективность этой группы препаратов. Тем не менее поиск дополнительных показателей для более целевого назначения ингибиторов EGFR был продолжен. В результате определено, что наличие мутаций в 3-м и 4-м экзонах гена KRAS и во 2, 3 и 4-м экзонах гена NRAS равным образом предопределяет неэффективность ингибиторов EGFR. Эти мутации определяются у 10 % больных. Проведенный анализ показал, что эффективность панитумумаба и цетуксимаба в сочетании с ХТ значительно увеличивалась у больных с диким типом KRAS и NRAS.</p></trans-abstract><kwd-group xml:lang="en"><kwd>metastatic colorectal cancer</kwd><kwd>inhibitors of EGFR</kwd><kwd>chemotherapy</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>метастатический колоректальный рак</kwd><kwd>ингибиторы EGFR</kwd><kwd>химиотерапия</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. Douillard J. Y., Siena S., Cassidy J. et al. 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