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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">phgenomics</journal-id><journal-title-group><journal-title xml:lang="ru">Фармакогенетика и фармакогеномика</journal-title><trans-title-group xml:lang="en"><trans-title>Pharmacogenetics and Pharmacogenomics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2588-0527</issn><issn pub-type="epub">2686-8849</issn><publisher><publisher-name>LLC "Izdatelstvo OKI"</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">phgenomics-163</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>АКТУАЛЬНЫЕ ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CURRENT REVIEW</subject></subj-group></article-categories><title-group><article-title>Перспективы разработки фармакогенетических и фармакокинетических подходов к персонализации применения таргетных препаратов при хроническом миелолейкозе</article-title><trans-title-group xml:lang="en"><trans-title>The perspectives of development for pharmacogenetic and pharmacokinetic approaches to personalized use of target therapy in chronic myeloid leukemia</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Савельева</surname><given-names>М. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Savelyeva</surname><given-names>M. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Савельева Марина Ивановна — д.м.н., профессор кафедры клинической фармакологии и терапии, ведущий научный сотрудник группы клинико-фармакологических технологий НИЦ.</p><p>г. Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><email xlink:type="simple">marinasavelyeva@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">ГБОУ ДПО «Российская медицинская академия последипломного образования» Минздрава России<country>Россия</country></aff><aff xml:lang="en">Russian Medical Academy of Postgraduate Study<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>25</day><month>03</month><year>2020</year></pub-date><volume>0</volume><issue>1</issue><fpage>9</fpage><lpage>12</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Савельева М.И., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Савельева М.И.</copyright-holder><copyright-holder xml:lang="en">Savelyeva M.I.</copyright-holder><license 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.pharmacogenetics-pharmacogenomics.ru/jour/article/view/163">https://www.pharmacogenetics-pharmacogenomics.ru/jour/article/view/163</self-uri><abstract><p>Цель терапии хронического миелолейкоза (ХМЛ) на современном этапе — достижение цитогенетических и молекулярных ремиссий. Основная проблема, возникающая в процессе терапии ХМЛ — развитие фармакологической резистентности при применении ингибиторов тирозинкиназ (ИТК). Пероральный приём обуславливает целый комплекс последовательных фармакокинетических процессов, влияющих на судьбу ИТК в организме пациента. Очень выраженная индивидуальная фармакокинетическая вариабельность ИТК и вариабельность в ответе на терапию обуславливаются не только генетической гетерогенностью мишеней для действия лекарств, но также фармакогенетическими характеристиками пациента, приверженностью пациента к лечению и влиянием межлекарственных взаимодействий. Поэтому выбор лечения онкологических пациентов требует тщательного мониторинга новых видов таргетной терапии и развития инновационных (фармакогенетических и фармакокинетических) подходов к индивиуализации лечения.</p></abstract><trans-abstract xml:lang="en"><p>The objective of chronic myeloid leukemia therapy today is the achievement of cytogenetic and molecular remissions. The main problem of the CML therapy is the development of pharmacological resistance on tyrosine kinase inhibitors (TKI). Oraladministration generates a complex step in the pharmacokinetics (PK) of these drugs. Interindividual PK variability is often large and variability observed in response is influencednot only by the genetic heterogeneity of drug targets, but also by the pharmacogenetic backgroundof the patient (e.g. cytochome P450 and ABC transporter polymorphisms), patient characteristics such as adherence to treatment and environmental factors (drug—drug interactions).The appropriate management of oncology patients thus requires careful monitoring of newer targeted therapies and the development of innovative pharmacokinetic and pharmacogenetic approaches to treatment individualization.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>хронический миелоидный лейкоз</kwd><kwd>терапевтический лекарственный мониторинг</kwd><kwd>фармакогенетика</kwd><kwd>фармакокинетика</kwd><kwd>фармакодинамика</kwd><kwd>ингибиторытирозинкиназ</kwd><kwd>иматиниб</kwd><kwd>дазатиниб</kwd><kwd>нилотиниб</kwd><kwd>бозутиниб</kwd><kwd>лекарственный метаболизм</kwd><kwd>транспортеры лекарственных средств</kwd></kwd-group><kwd-group xml:lang="en"><kwd>chronic myeloid leukemia</kwd><kwd>therapeutic drug monitoring</kwd><kwd>pharmacogenetics</kwd><kwd>pharmacokinetics</kwd><kwd>pharmacodynamics</kwd><kwd>tyrosine kinase inhibitors</kwd><kwd>imatinib</kwd><kwd>dasatinib</kwd><kwd>nilotinib</kwd><kwd>bosutinib</kwd><kwd>generic imatinib</kwd><kwd>drug metabolism</kwd><kwd>drug transporters</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">O’Brien S., Guilhot F., Larson R., et al. 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