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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">Oncohematology</journal-id><journal-title-group><journal-title xml:lang="en">Oncohematology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкогематология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1818-8346</issn><issn publication-format="electronic">2413-4023</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">367</article-id><article-id pub-id-type="doi">10.17650/1818-8346-2019-14-3-12-22</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Treatment-free remission in patients with chronic myeloid leukemia: literature review</article-title><trans-title-group xml:lang="ru"><trans-title>Ремиссия без лечения у больных хроническим миелолейкозом: обзор литературы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Petrova</surname><given-names>A. N.</given-names></name><name xml:lang="ru"><surname>Петрова</surname><given-names>А. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>4 Novyy Zykovskiy Proezd, Moscow 125167</italic></p></bio><bio xml:lang="ru"><p><bold>Анна Николаевна Петрова </bold></p><p><italic>125167 Москва, Новый Зыковский проезд, 4 </italic></p><p> </p></bio><email>ap996@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6423-1789</contrib-id><name-alternatives><name xml:lang="en"><surname>Chelysheva</surname><given-names>E. Yu.</given-names></name><name xml:lang="ru"><surname>Челышева</surname><given-names>Е. Ю.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>4 Novyy Zykovskiy Proezd, Moscow 125167</italic></p></bio><bio xml:lang="ru"><p><italic>125167 Москва, Новый Зыковский проезд, 4 </italic></p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9947-2371</contrib-id><name-alternatives><name xml:lang="en"><surname>Turkina</surname><given-names>A. G.</given-names></name><name xml:lang="ru"><surname>Туркина</surname><given-names>А. Г.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>4 Novyy Zykovskiy Proezd, Moscow 125167</italic></p></bio><bio xml:lang="ru"><p><italic>125167 Москва, Новый Зыковский проезд, 4 </italic></p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">National Research Center for Hematology, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр гематологии» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-10-20" publication-format="electronic"><day>20</day><month>10</month><year>2019</year></pub-date><volume>14</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>12</fpage><lpage>22</lpage><history><date date-type="received" iso-8601-date="2019-10-19"><day>19</day><month>10</month><year>2019</year></date><date date-type="accepted" iso-8601-date="2019-10-19"><day>19</day><month>10</month><year>2019</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncohematology.abvpress.ru/ongm/article/view/367">https://oncohematology.abvpress.ru/ongm/article/view/367</self-uri><abstract xml:lang="en"><p>Tyrosine kinase inhibitors have radically changed the course of chronic myeloid leukemia, significantly increasing survival and reducing the risk of disease progression. Nearly 50–70 % of patients achieve a consistently low or undetectable level of minimal residual disease – a deep molecular response. The long-term tyrosine kinase inhibitors treatment in about one-third of patients is accompanied by toxicity which impairs the quality of life. Therefore, the safe treatment discontinuation is relevant. The results of clinical trials have shown 40-60% possibility of maintaining treatment-free remission in patients with long-term deep molecular respons; however, all patients with molecular relapse regain molecular remission after the resumption of tyrosine kinase inhibitors therapy. Currently, clinical and biological factors associated with maintaining treatment-free remission are being studied. It is assumed that cessation of tyrosine kinase inhibitors therapy can improve the quality of life, but approximately 30 % of patients are reporting musculoskeletal pain – so called “withdrawal syndrome” – that begins or worsens after stopping tyrosine kinase inhibitors therapy. The mechanisms for the development of this phenomenon are currently unclear. Thus, many aspects concerning treatment-free remission require to be studied, which determines the importance of clinical trials in this area.</p></abstract><trans-abstract xml:lang="ru"><p>Терапия ингибиторами тирозинкиназ радикально изменила течение хронического миелолейкоза, значительно повысив выживаемость и снизив риск прогрессирования заболевания. У 50–70 % пациентов удается достичь низкого или неопределяемого уровня минимальной остаточной болезни – глубокого молекулярного ответа. Длительная терапия ингибиторами тирозинкиназ примерно у трети больных сопровождается развитием токсичности и снижает качество жизни, что определяет актуальность вопроса безопасного прекращения лечения. В условиях клинических исследований у больных с длительным глубоким молекулярным ответом показана возможность сохранения ремиссии без лечения примерно в 40–60 % случаев; при этом все пациенты с молекулярным рецидивом вновь достигают ремиссии после возобновления терапии ингибиторами тирозинкиназ. В настоящее время проводится поиск клинических и молекулярногенетических факторов для определения групп пациентов, имеющих наибольшую вероятность сохранения ремиссии без лечения. Предполагается, что прекращение терапии ингибиторами тирозинкиназ может улучшить качество жизни пациентов, однако в 30 % случаев наблюдается синдром отмены, проявляющийся возникновением или ухудшением ранее существующего болевого синдрома в суставах, мышцах и костях. Механизмы развития этого явления на данный момент неясны. Таким образом, многие вопросы, касающиеся ремиссии без лечения, требуют изучения, что определяет важность проведения клинических исследований в этой области.</p></trans-abstract><kwd-group xml:lang="en"><kwd>chronic myeloid leukemia</kwd><kwd>tyrosine kinase inhibitor</kwd><kwd>deep molecular response</kwd><kwd>treatment free remission</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>хронический миелолейкоз</kwd><kwd>ингибитор тирозинкиназ</kwd><kwd>глубокий молекулярный ответ</kwd><kwd>ремиссия без лечения</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">Turkina A.G., Chelysheva E.Yu. Therapeutic strategy for chronic myeloid leukemia: possibilities and prospects. Terapevticheskiy arkhiv = Therapeutic Archive 2013;85(7):4–9. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">Туркина А.Г., Челышева Е.Ю. 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