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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">Bone and soft tissue sarcomas, tumors of the skin</journal-id><journal-title-group><journal-title xml:lang="en">Bone and soft tissue sarcomas, tumors of the skin</journal-title><trans-title-group xml:lang="ru"><trans-title>Саркомы костей, мягких тканей и опухоли кожи</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2219-4614</issn><issn publication-format="electronic">2782-3687</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">199</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Alkylguanine-DNA alkyltransferase as predictive factor of efficacy of dacarbazine+cisplatin+nidran regimen in patients with metastatic skin mela-
noma</article-title><trans-title-group xml:lang="ru"><trans-title>Алкилгуанин алкилтрансфераза как фактор предсказания эффек-
тивности режима дакарбазин+цисплатин+нидран у больных мета-
статической меланомой кожи</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name><surname>Степанова</surname><given-names>Е. В.</given-names></name><address><country country="RU">Russian Federation</country></address><email>e_stepanova@nm.ru</email></contrib><contrib contrib-type="author"><name><surname>Абрамов</surname><given-names>М. Е.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Барышников</surname><given-names>А. Ю.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Личиницер</surname><given-names>М. Р.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Stepanova</surname><given-names>E. V.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Abramov</surname><given-names>M. E.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Baryshnikov</surname><given-names>A. Yu.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Lichinitser</surname><given-names>M. R.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="ru">Российский онкологический научный центр им. Н.Н. Блохина РАМН</institution></aff><aff><institution xml:lang="en">N.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Science</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2011-01-11" publication-format="electronic"><day>11</day><month>01</month><year>2011</year></pub-date><volume>3</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>50</fpage><lpage>54</lpage><history><date date-type="received" iso-8601-date="2022-01-11"><day>11</day><month>01</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2011, ., ., ., ., Stepanova E.V., Abramov M.E., Baryshnikov A.Y., Lichinitser M.R.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2011, Степанова Е.В., Абрамов М.Е., Барышников А.Ю., Личиницер М.Р., Stepanova E., Abramov M., Baryshnikov A., Lichinitser M.</copyright-statement><copyright-year>2011</copyright-year><copyright-holder xml:lang="en">., ., ., ., Stepanova E.V., Abramov M.E., Baryshnikov A.Y., Lichinitser M.R.</copyright-holder><copyright-holder xml:lang="ru">Степанова Е.В., Абрамов М.Е., Барышников А.Ю., Личиницер М.Р., Stepanova E., Abramov M., Baryshnikov A., Lichinitser M.</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://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://sarbon.abvpress.ru/jour/article/view/199">https://sarbon.abvpress.ru/jour/article/view/199</self-uri><abstract xml:lang="en"><p><italic>Background. </italic>The goal of this study was to analyze significance of AGT expression as predictive marker of efficacy of Dacar bazine+Cisplatin+Nidran regimen in patients with metastatic skin melanoma <italic>Methods. </italic>26 patients with metastatic skin melanoma were enrolled in the retrospective study. Immunohistochemical analysis of AGT expression was performed on paraffin-embedded tissue sections of primary tumor or available metastasis. <italic>Results. </italic>High AGT expression in tumor cells was associated with low efficacy of Dacarbazine+Cisplatin+Nidran regimen. Disease progression was observed in 85,7% patient with AGT-positive tumor and 29,4% - AGT-negative (р=0,023). There was a not significant difference of time without progression between two groups of patients. <italic>Conclusion. </italic>AGT expression could be potentially useful tool for predicting response of metastatic melanoma patients to Dacarbazine+Cisplatin+Nidran regimen.</p></abstract><trans-abstract xml:lang="ru"><p><italic>Цельработы. </italic>Целью работы было изучить значение экспрессии АГТ в опухолевых клетках для предсказания эффективности режима с включением дакарбазина, цисплатина и нидрана для лечения метастатической меланомы кожи. <italic>Материалы и методы. </italic>В ретроспективное исследование включены 26 больных метастатической меланомой кожи. Было проведено исследование экспрессии АГТ иммуногистохимическим методом в парафиновых блоках опухоли (первичный очаг или доступный метастаз). <italic>Результаты. </italic>Экспрессия АГТ в опухоли ассоциировалась с низким эффектом режима дакарбазин+цисплатин+ нидран. Прогрессирование наблюдалось у 85,7% больных с АГТ-положительными опухолями и 29,4% - с АГТ-от-рицательными (р=0,023). Различия в выживаемости без прогрессировать больных не достигали достоверности. <italic>Заключение. </italic>Экспрессия АГТ может рассматриваться как перспективный маркер для предсказания эффективности режима дакарбазин+цисплатин+нидран у больных метастатической меланомой кожи.</p></trans-abstract><kwd-group xml:lang="en"><kwd>metastatic skin melanoma</kwd><kwd>chemotherapy</kwd><kwd>AGT</kwd><kwd>predictive factor</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>метастатическая меланома кожи</kwd><kwd>химиотерапия</kwd><kwd>АГТ</kwd><kwd>предсказывающие факторы</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Tsao H., Atkins M.B., Sober A.J. Management of cutaneous melanoma. N. Engl. J. 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