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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">253</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">MALIGNANT FIBROUS HISTIOCYTOMA. THE RESULTS OF COMBINED TREATMENT OF RESECTABLE FORMS</article-title><trans-title-group xml:lang="ru"><trans-title>Злокачественные фиброзные гистиоцитомы. результаты комбинированного лечения резектабельных форм</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name><surname>Сехина</surname><given-names>О. В.</given-names></name><address><country country="RU">Russian Federation</country></address><email>doc-sehina@mail.ru</email></contrib><contrib contrib-type="author"><name><surname>Федянин</surname><given-names>М. Ю.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Яковлева</surname><given-names>Е. С.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Буланов</surname><given-names>А. А.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Бохян</surname><given-names>Б. Ю.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Sekhina</surname><given-names>O. V.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Fedyanin</surname><given-names>M. U.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Yakovleva</surname><given-names>E. S.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Bulanov</surname><given-names>A. A.</given-names></name><address><country country="RU">Russian Federation</country></address></contrib><contrib contrib-type="author"><name><surname>Bokhyan</surname><given-names>B. Y.</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 Sciences</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2011-11-11" publication-format="electronic"><day>11</day><month>11</month><year>2011</year></pub-date><volume>3</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>37</fpage><lpage>40</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, ., ., ., ., ., Sekhina O.V., Fedyanin M.U., Yakovleva E.S., Bulanov A.A., Bokhyan B.Y.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2011, Сехина О.В., Федянин М.Ю., Яковлева Е.С., Буланов А.А., Бохян Б.Ю., Sekhina O., Fedyanin M., Yakovleva E., Bulanov A., Bokhyan B.</copyright-statement><copyright-year>2011</copyright-year><copyright-holder xml:lang="en">., ., ., ., ., Sekhina O.V., Fedyanin M.U., Yakovleva E.S., Bulanov A.A., Bokhyan B.Y.</copyright-holder><copyright-holder xml:lang="ru">Сехина О.В., Федянин М.Ю., Яковлева Е.С., Буланов А.А., Бохян Б.Ю., Sekhina O., Fedyanin M., Yakovleva E., Bulanov A., Bokhyan B.</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/253">https://sarbon.abvpress.ru/jour/article/view/253</self-uri><abstract xml:lang="en"><p><italic>Background. </italic>We studied the patients' outcome with respectable forms of malignant fibrous histiocytoma according to the
type of chemotherapy. <italic>Methods. </italic>We performed a retrospective analysis of 53 patients with malignant fibrous histiocytoma treated in the N.N. Blokhins
Russian Cancer Research Center from 2000 to 2010. All patients underwent radical surgery. Neoadjuvant chemotherapy
was administered in 7 (13%) patients, adjuvant chemotherapy - in 5 (9%), neo and adjuvant chemotherapy - in 13 (24%)
patients, chemotherapy was not done in 28 (54%) patients. <italic>Result. </italic>Progression of the disease was revealed in 6/7 (86%), 7/18 (39%), 17/28 (60%) respectively. <italic>Conclusion. </italic>Patients with MFH should be prescribed adjuvant chemotherapy for reducing the risk of relapse.</p></abstract><trans-abstract xml:lang="ru"><p><italic>Цельработы. </italic>Оценить влияние химиотерапии на риск возникновения прогрессирования у больных резектабельными формами злокачественными фиброзными гистиоцитомами. <italic>Материалы и методы. </italic>Проведен ретроспективный анализ данных 53 пациентов со ЗФГ, получавших лечение в РОНЦ с 2000-го по 2010 г. Всем пациентам выполнено радикальное хирургическое вмешательство. Неоадъювантную химиотерапию получили 7 (13%) пациентов, 5 (9%) пациентов получили адъювантную химиотерапию, 13 (24%) пациентов получили нео- и адъювантную химиотерапию, 28 (54%) пациентам химиотерапия не проводилась. <italic>Результаты. </italic>Частота прогрессирования в группе пациентов, получавших только неоадъювантную XT, составила 6/7 (86%), при назначении нео- и адъювантной XT, прогрессирование наступало у 7/18 (39%) пациентов. При отсутствии XT прогрессирование отмечено у 17/28 (60%) пациентов.
Заключение. С целью снижения риска рецидива пациентам со злокачественной фиброзной гистиоцитомой следует назначать адъювантную химиотерапию.</p></trans-abstract><kwd-group xml:lang="en"><kwd>malignant fibrous histiocytoma</kwd><kwd>adjuvant chemotherapy</kwd><kwd>neoadjuvant chemotherapy</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>злокачественная фиброзная гистиоцитома</kwd><kwd>химиотерапия</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Давыдов М.И., Аксель Е.М. Статистика злокачественных новообразований в России и странах СНГ в 2007 г. Вестник онкологического научного центра им. Н.Н. Бло-хина РАМН. 2009, т. 20 (3), приложение 1.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>O'Brien J.E., Stout А.Р. Malignant fibrous xanthomas. Cancer. 1964, No. 17, p. 1445-1455.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Алиев М.Д. Современные подходы к лечению сарком мягких тканей. Практическая онкология. 2004, т. 5, № 4, с. 250-255.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Франк Г.А. Проблемы морфологической классификации диагностики опухолей мягких тканей. Практическая онкология. 2004, т. 5, № 4.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Pervaiz N., Colterjohn N. et al. A Systematic Meta-Analysis of Randomized Controlled Trials of Adjuvant Chemotherapy for Localized Resectable Soft-Tissue Sarcoma. Cancer. 2008, v. 113, p. 573-581.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Ferrari A., Gronchi A., Casanova M. et al. Synovial sarcoma: a retrospective analysis of 271 patients of all ages treated at a single institution. Cancer. 2004, v. 101 (3), p. 627-634.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Eilber F.C., Eilber F.R. et al. The impact of chemotherapy on the survival of patients with high-grade primary extremity liposarcoma. Ann. Surg. 2004, v. 240 (4), p. 686-695.</mixed-citation></ref></ref-list></back></article>
