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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">surgonco</journal-id><journal-title-group><journal-title xml:lang="ru">Креативная хирургия и онкология</journal-title><trans-title-group xml:lang="en"><trans-title>Creative surgery and oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2076-3093</issn><issn pub-type="epub">2307-0501</issn><publisher><publisher-name>Башкирский государственный медицинский университет</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.24060/2076-3093-2019-9-4-261-265</article-id><article-id custom-type="elpub" pub-id-type="custom">surgonco-432</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>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group></article-categories><title-group><article-title>Лимфомы клеток мантийной зоны. Новые возможности диагностики и лечения (эпидемиологическое исследование)</article-title><trans-title-group xml:lang="en"><trans-title>Mantle Zone Cell Lymphomas. New Opportunities for Diagnosis and Treatment (Epidemiological Research)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8323-3181</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Канкумашева</surname><given-names>Э. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Kankumasheva</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Канкумашева Эльза Ильдаровна — врач-онколог</p><p>450054, Уфа, пр-т Октября, 73/1</p></bio><bio xml:lang="en"><p>Kankumasheva Elza Ildarovna — Oncologist</p><p>73/1 Oktyabrya ave., Ufa, 450054</p></bio><email xlink:type="simple">elsa-2011@mail.ru</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>Валиахметова</surname><given-names>Ч. Х.</given-names></name><name name-style="western" xml:lang="en"><surname>Valiakhmetova</surname><given-names>Ch. Kh.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Валиахметова Чулпан Хусаеновна — к.м.н., врачонколог, зав. онкологическим отделением противоопухолевой лекарственной терапии</p><p>450054, Уфа, пр-т Октября, 73/1</p></bio><bio xml:lang="en"><p>Valiakhmetova Chulpan Khusaenovna — Candidate of Medical Sciences, Oncologist, Head of the Oncology Department of Antineoplastic Drug Therapy</p><p>73/1 Oktyabrya ave., Ufa, 450054</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Республиканский клинический онкологический диспансер</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Republican Clinical Oncology Center</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>23</day><month>01</month><year>2020</year></pub-date><volume>9</volume><issue>4</issue><fpage>261</fpage><lpage>265</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Канкумашева Э.И., Валиахметова Ч.Х., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Канкумашева Э.И., Валиахметова Ч.Х.</copyright-holder><copyright-holder xml:lang="en">Kankumasheva E.I., Valiakhmetova C.K.</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.surgonco.ru/jour/article/view/432">https://www.surgonco.ru/jour/article/view/432</self-uri><abstract><sec><title>Введение</title><p>Введение. Лимфома клеток мантийной зоны — редко встречающийся вариант В-клеточной неходжкинской лимфомы. По статистике из 100 000 человек заболевает 2–3, что составляет примерно 6 % от общего количества больных неходжкинскими лимфомами. Известно, что различные молекулярно-генетические характеристики пациентов с лимфомой мантийной зоны могут обеспечить персонифицированный подход при определении прогноза болезни и тактики лечения.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. Проведен ретроспективный анализ 45 пациентов с лимфомой зоны мантии, наблюдавшихся в ГАУЗ РКОД Минздрава в период с 2015 г. по настоящее время. При анализе учитывались данные клинико-лабораторного обследования, позитронно-эмиссионная томография, цитологическое, гистологическое и иммуногистохимическое исследования биоптата опухоли и костного мозга. Проанализированы эпидемиологические данные, клинические характеристики пациентов, терапевтические подходы, непосредственные и отдаленные результаты лечения.</p></sec><sec><title>Результаты и обсуждение</title><p>Результаты и обсуждение. Установлено, что наиболее часто в патологический процесс вовлекается костный мозг (44 %) и селезенка (41 %). Распределение MIPI: высокий у 14 (30 %), средний у 20 (45 %), низкий у 11 (25 %). Ki67 в 4 случаях менее 30 %, в остальных более 30 %. Пациентам c 2015 по 2017 г. в первой линии проводилась химиотерапия в режиме R-CHOP с последующей поддержкой ритуксимабом. Средняя БПВ составила 20 месяцев, 8 (17 %) пациентов в статусе длительной ремиссии (с 2015 г.). С 2017 г. в первой линии терапии начали применяться режимы R-BAC (схема с высокодозным цитарабином для кандидатов на ТСК) и R-B (для пожилых и коморбидных). С 2018 г. 8 пациентам проведена аутоТСК (в 1-м позднем рецидиве) как этап консолидации лечения. На данный момент обследование на del17p и мутацию TP53 проведено 13 пациентам в федеральных центрах.</p></sec><sec><title>Заключение</title><p>Заключение. Продемонстрирована необходимость и варианты терапии в зависимости от результатов молекулярно-генетического анализа лимфомы клеток мантийной зоны.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. Mantle cell lymphoma is a rare type of B-cell non-Hodgkin lymphoma. According to statistics the incidence of this disorder amounts to 2-3 per 100,000 people; this is about 6% of all non-Hodgkin lymphomas. It has been established that various molecular genetic characteristics of mantle cell lymphoma patients may present opportunities for a patient-specific approach to the disease prognosis and treatment strategy.</p></sec><sec><title>Materials and methods</title><p>Materials and methods. The paper presents a retrospective analysis of 45 mantle cell lymphoma patients treated at the GAUZ RKOD of the Ministry of Healthcare from 2015 until now. The data used in the analysis included clinical examination, lab panels, PET CT, tumour and bone marrow biopsy specimen cytology, histology and immunohistochemistry. We analysed the epidemiological data, the patients’ clinical presentation characteristics, treatment approaches, immediate and long-term outcomes.</p></sec><sec><title>Results and discussion</title><p>Results and discussion. We have established that the pathological process most frequently involves bone marrow (44%) and spleen (41%). The MIPI scores distribution was as follows: high in 14 (30%), medium in 20 (45%), low in 11 (41%). Ki67 was recorded at under 30% in four cases, in others it amounted to over 30%. In 2015–2017 patients were treated with the R-CHOP protocol with the following support with rituximab. PFS averaged at 20 months, 8 (17%) of patients remain in lasting remission (since 2015). In 2017 the R-BAC (high dose cytarabine for SCT candidates) and R-B (for the elderly and comorbid patients) became protocols of first line. Since 2018 eight patients have undergone auto-SCT (at the first late recurrence) as a treatment consolidation stage. As of now 13 patients have been examined in federal centres for del17p and the TP53 mutation.</p></sec><sec><title>Conclusion</title><p>Conclusion. We have demonstrated the need for and the option of treatment depending on the results of molecular genetic testing of mantle cell lymphomas.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>лимфома клеток мантийной зоны</kwd><kwd>неходжкинская лимфома</kwd><kwd>иммуногистохимия</kwd><kwd>циклин d1</kwd><kwd>генетическая транслокация</kwd><kwd>флюоресцентная in situ гибридизация</kwd><kwd>цитарабин</kwd><kwd>бортезомиб</kwd></kwd-group><kwd-group xml:lang="en"><kwd>mantle cell lymphoma</kwd><kwd>non-Hodgkin lymphoma</kwd><kwd>immunohistochemistry</kwd><kwd>cyclin D1</kwd><kwd>genetic translocation</kwd><kwd>fluorescence in situ hybridization</kwd><kwd>cytarabine</kwd><kwd>bortezomib</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">Поддубная И.В., Савченко В.Г. (ред.) Российские клинические рекомендации по диагностике и лечению лимфопролиферативных заболеваний. 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