<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">medalphabet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский алфавит</journal-title><trans-title-group xml:lang="en"><trans-title>Medical alphabet</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2078-5631</issn><issn pub-type="epub">2949-2807</issn><publisher><publisher-name>ООО «Альфмед»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.33667/2078-5631-2020-38-29-33</article-id><article-id custom-type="elpub" pub-id-type="custom">medalphabet-1888</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>Статьи</subject></subj-group></article-categories><title-group><article-title>Молекулярно-генетические методы диагностики и таргетная терапия в педиатрической онкологии (обзор литературы)</article-title><trans-title-group xml:lang="en"><trans-title>Molecular diagnostics and targeted treatment approaches in pediatric oncology (literature review)</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>Рожков</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Rozhkov</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>студент Клинического института детского здоровья</p><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нуриев</surname><given-names>Р. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Nuriev</surname><given-names>R. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>аспирант кафедры онкологии, радиотерапии и пластической хирургии Института клинической медицины</p><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Секачева</surname><given-names>М. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Sekacheva</surname><given-names>M. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., проф. кафедры онкологии, радиотерапии и пластической хирургии Института клинической медицины, директор Института персонализированной медицины</p><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГАОУ ВО «Первый Московский государственный медицинский университет имени И.М. Сеченова» Минздрава России (Сеченовский университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>First Moscow State Medical University n.a. I.M. Sechenov</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГАОУ ВО «Первый Московский государственный медицинский университет имени И.М. Сеченова» Минздрава России (Сеченовский университет); ФГБУ «Научно-исследовательский институт вакцин и сывороток имени И.И. Мечникова» Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>First Moscow State Medical University n.a. I.M. Sechenov; Scientific and Research Institute for Vaccines and Sera n.a. I.I. Mechnikov</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>23</day><month>01</month><year>2021</year></pub-date><volume>0</volume><issue>38</issue><issue-title>Диагностика и онкотерапия (4)</issue-title><fpage>29</fpage><lpage>33</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Рожков А.А., Нуриев Р.И., Секачева М.И., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Рожков А.А., Нуриев Р.И., Секачева М.И.</copyright-holder><copyright-holder xml:lang="en">Rozhkov A.A., Nuriev R.I., Sekacheva M.I.</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.med-alphabet.com/jour/article/view/1888">https://www.med-alphabet.com/jour/article/view/1888</self-uri><abstract><p>Непрерывная эволюция технологий в области молекулярной диагностики и геномного анализа, разработка новых подходов в фармакогенетике и появление целого спектра различных таргетных препаратов расширили возможности клинической практики, позволяя персонализировать подход к каждому конкретному пациенту. Диагностика и терапия педиатрических онкологических заболеваний являются одним из ярких примеров успешного применения персонализированного подхода в клинической практике. На сегодняшний день множество педиатрических опухолевых заболеваний успешно лечатся с помощью таргетных препаратов, что значительно увеличивает выживаемость пациентов. Таргетная терапия позволяет подобрать конкретный препарат для каждого больного, повышая тем самым эффективность лечения, снижая риск возникновения побочных эффектов, а также уменьшая вероятность развития рецидива заболевания.</p></abstract><trans-abstract xml:lang="en"><p>The continuous evolution of new technologies in the field of molecular diagnostics and genome analysis, the development of new approaches in pharmacogenetics and the emergence of a range of different targeted drugs have expanded the possibilities of clinical practice, resulting in personalized approaches to treatment. The diagnosis and therapy of pediatric oncological diseases are some of the vivid examples of the successful application of a personalized approach in clinical practice. Today, many pediatric neoplastic diseases are successfully treated with targeted drugs, which significantly increases patient survival. Targeted therapy allows to choose a specific drug for each patient, thereby increasing the effectiveness of treatment, reducing the risk of side effects, and also reducing the likelihood of a relapse of the disease.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>персонализированная медицина</kwd><kwd>онкология</kwd><kwd>таргетная терапия</kwd><kwd>молекулярная диагностика</kwd><kwd>детская онкология</kwd></kwd-group><kwd-group xml:lang="en"><kwd>personalized medicine</kwd><kwd>oncology</kwd><kwd>targeted therapy</kwd><kwd>molecular diagnostics</kwd><kwd>pediatric oncology</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">Localio AR, Mulrow CD, Griswold ME. Advancing Personalized Medicine Through Prediction. Ann Intern Med. 2020; 172: 63–64.</mixed-citation><mixed-citation xml:lang="en">Localio AR, Mulrow CD, Griswold ME. Advancing Personalized Medicine Through Prediction. Ann Intern Med. 2020; 172: 63–64.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">David Bick, Marilyn Jones, Stacie L Taylor, Ryan J Taft, John Belmont. HudsonAlpha institute for Biotechnology, Huntsville, Alabama, USA Rady Children’s Hospital San Diego, San Diego, California, USA illumina inc, San Diego, California, USA. Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases. Review 19 March 2019.</mixed-citation><mixed-citation xml:lang="en">David Bick, Marilyn Jones, Stacie L Taylor, Ryan J Taft, John Belmont. HudsonAlpha institute for Biotechnology, Huntsville, Alabama, USA Rady Children’s Hospital San Diego, San Diego, California, USA illumina inc, San Diego, California, USA. Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases. Review 19 March 2019.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">de Ligt J, Boone PM, Pfundt R, Vissers LE, Richmond T, Geoghegan J, et al. Detection of clinically relevant copy number variants with whole-exome sequencing. Hum Mutat. 2013; 34 (10): 1439–48.</mixed-citation><mixed-citation xml:lang="en">de Ligt J, Boone PM, Pfundt R, Vissers LE, Richmond T, Geoghegan J, et al. Detection of clinically relevant copy number variants with whole-exome sequencing. Hum Mutat. 2013; 34 (10): 1439–48.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Krumm N, Sudmant PH, Ko A, O’Roak BJ, Malig M, Coe BP, et al. Copy number variation detection and genotyping from exome sequence data. Genome Res. 2012; 22 (8): 1525–32.</mixed-citation><mixed-citation xml:lang="en">Krumm N, Sudmant PH, Ko A, O’Roak BJ, Malig M, Coe BP, et al. Copy number variation detection and genotyping from exome sequence data. Genome Res. 2012; 22 (8): 1525–32.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang F, Lupski JR. Non-coding genetic variants in human disease. Hum Mol Genet. 2015; 24 (R 1): R 102–10.</mixed-citation><mixed-citation xml:lang="en">Zhang F, Lupski JR. Non-coding genetic variants in human disease. Hum Mol Genet. 2015; 24 (R 1): R 102–10.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Jennifer E. Posey. Genome sequencing and implications for rare disorders. Posey Orphanet Journal of Rare Diseases. 2019.</mixed-citation><mixed-citation xml:lang="en">Jennifer E. Posey. Genome sequencing and implications for rare disorders. Posey Orphanet Journal of Rare Diseases. 2019.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Jeffrey E. Rubnitz, MD, PhD and William M. Crist, MD. Molecular Genetics of Childhood Cancer: Implications for Pathogenesis, Diagnosis, and Treatment. Review. March 13, 2015.</mixed-citation><mixed-citation xml:lang="en">Jeffrey E. Rubnitz, MD, PhD and William M. Crist, MD. Molecular Genetics of Childhood Cancer: Implications for Pathogenesis, Diagnosis, and Treatment. Review. March 13, 2015.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Martin CL, Warburton D. Detection of chromosomal aberrations in clinical practice: from karyotype to genome sequence. Annu Rev Genomics Hum Genet. 2015; 16: 309–26.</mixed-citation><mixed-citation xml:lang="en">Martin CL, Warburton D. Detection of chromosomal aberrations in clinical practice: from karyotype to genome sequence. Annu Rev Genomics Hum Genet. 2015; 16: 309–26.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Ginsburg G. S., Kuderer N. M. Comparative effectiveness research, genomics-enabled personalized medicine, and rapid learning health care: A Common Bond. J. Clin. Oncol., 2012, 30 (34), 4233–4242.</mixed-citation><mixed-citation xml:lang="en">Ginsburg G. S., Kuderer N. M. Comparative effectiveness research, genomics-enabled personalized medicine, and rapid learning health care: A Common Bond. J. Clin. Oncol., 2012, 30 (34), 4233–4242.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Catenacci DVT. Next-generation clinical trials: novel strategies to address the challenge of tumor molecular heterogeneity. Mol Oncol 2015; 9: 967–96.</mixed-citation><mixed-citation xml:lang="en">Catenacci DVT. Next-generation clinical trials: novel strategies to address the challenge of tumor molecular heterogeneity. Mol Oncol 2015; 9: 967–96.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Servant N, Roméjon J, Gestraud P, La Rosa P, Lucotte G, Lair S, Bernard V, Zeitouni B, Coffin F, Jules-Clément G, Yvon F, Lermine A, Poullet P, Liva S, Pook, S, Popova T, Barette C, Prud’homme F, Dick J.G, Kamal M, Le Tourneau C, Barillot E, Hupé P. Bioinformatics for precision medicine in oncology: Principles and application to the SHIVA clinical trial. Front. Genet., 2014, 5, 152.</mixed-citation><mixed-citation xml:lang="en">Servant N, Roméjon J, Gestraud P, La Rosa P, Lucotte G, Lair S, Bernard V, Zeitouni B, Coffin F, Jules-Clément G, Yvon F, Lermine A, Poullet P, Liva S, Pook, S, Popova T, Barette C, Prud’homme F, Dick J.G, Kamal M, Le Tourneau C, Barillot E, Hupé P. Bioinformatics for precision medicine in oncology: Principles and application to the SHIVA clinical trial. Front. Genet., 2014, 5, 152.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Arne Van Hoeck, Niels H. Tjoonk, Ruben van Boxtel, Edwin Cuppen. Portrait of a cancer: mutational signature analyses for cancer diagnostics. Center for Molecular Medicine and Oncode Institute, University Medical Centre Utrecht, Heidelberglaan. review. 2019.</mixed-citation><mixed-citation xml:lang="en">Arne Van Hoeck, Niels H. Tjoonk, Ruben van Boxtel, Edwin Cuppen. Portrait of a cancer: mutational signature analyses for cancer diagnostics. Center for Molecular Medicine and Oncode Institute, University Medical Centre Utrecht, Heidelberglaan. review. 2019.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Khoury M.J, Iademarco M.F, Riley W.T. Precision public health for the era of precision medicine. Am. J. Prev. Med., 2016.</mixed-citation><mixed-citation xml:lang="en">Khoury M.J, Iademarco M.F, Riley W.T. Precision public health for the era of precision medicine. Am. J. Prev. Med., 2016.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Nita L. Seibel, Katherine Janeway, Carl E. Allen, Susan N. Chi, Y Jae Cho, Julia L. Glade Bender, AeRang Kim, Theodore W. Laetsch, Meredith S. Irwin, Naoko Takebe, James V. Tricoli and D. Williams Parsons, Pediatric Oncology Enters the Era of Precision Medicine, Current Problems in Cancer; 2017 September.</mixed-citation><mixed-citation xml:lang="en">Nita L. Seibel, Katherine Janeway, Carl E. Allen, Susan N. Chi, Y Jae Cho, Julia L. Glade Bender, AeRang Kim, Theodore W. Laetsch, Meredith S. Irwin, Naoko Takebe, James V. Tricoli and D. Williams Parsons, Pediatric Oncology Enters the Era of Precision Medicine, Current Problems in Cancer; 2017 September.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Fabio Girardi, Claudia Allemani, and Michel P. Coleman. Worldwide Trends in Survival From Common Childhood Brain Tumors: A Systematic Review. Journal of Global Oncology, 2019: 5, 1–25.</mixed-citation><mixed-citation xml:lang="en">Fabio Girardi, Claudia Allemani, and Michel P. Coleman. Worldwide Trends in Survival From Common Childhood Brain Tumors: A Systematic Review. Journal of Global Oncology, 2019: 5, 1–25.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Buzdin A, Sorokin M, Garazha A, Sekacheva M, Kim E, Zhukov N, et al. Molecular pathway activation – new type of biomarkers for tumor morphology and personalized selection of target drugs. Semin Cancer Biol. (2018) 53: 110–24.</mixed-citation><mixed-citation xml:lang="en">Buzdin A, Sorokin M, Garazha A, Sekacheva M, Kim E, Zhukov N, et al. Molecular pathway activation – new type of biomarkers for tumor morphology and personalized selection of target drugs. Semin Cancer Biol. (2018) 53: 110–24.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Christophe Le Tourneau, Jean-Pierre Delord, Anthony Gonçalves, Céline Gavoille, Coraline Dubot, Nicolas Isambert, Mario Campone, Olivier Trédan, Marie-Ange Massiani, Cécile Mauborgne, Sebastien Armanet, Nicolas Servant, Ivan Bièche, Virginie Bernard, David Gentien, Pascal Jezequel, Valéry Attignon, Sandrine Boyault, Anne Vincent-Salomon, Vincent Servois, Marie-Paule Sablin, Maud Kamal, Xavier Paoletti, for the SHIVA investigators. Molecularly targeted therapy based on tumour molecular profiling versus conventional therapy for advanced cancer (SHIVA): a multicentre, open-label, proof-of-concept, randomised, controlled phase 2 trial. Articles; September 3, 2015.</mixed-citation><mixed-citation xml:lang="en">Christophe Le Tourneau, Jean-Pierre Delord, Anthony Gonçalves, Céline Gavoille, Coraline Dubot, Nicolas Isambert, Mario Campone, Olivier Trédan, Marie-Ange Massiani, Cécile Mauborgne, Sebastien Armanet, Nicolas Servant, Ivan Bièche, Virginie Bernard, David Gentien, Pascal Jezequel, Valéry Attignon, Sandrine Boyault, Anne Vincent-Salomon, Vincent Servois, Marie-Paule Sablin, Maud Kamal, Xavier Paoletti, for the SHIVA investigators. Molecularly targeted therapy based on tumour molecular profiling versus conventional therapy for advanced cancer (SHIVA): a multicentre, open-label, proof-of-concept, randomised, controlled phase 2 trial. Articles; September 3, 2015.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Tremblay, J, Hamet, P. Role of genomics on the path to personalized medicine. Metabolism, 2013, 62 (Suppl. 1), S 2–5.</mixed-citation><mixed-citation xml:lang="en">Tremblay, J, Hamet, P. Role of genomics on the path to personalized medicine. Metabolism, 2013, 62 (Suppl. 1), S 2–5.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Boeldt DL, Cheung C, Ariniello L, Darst BF, Topol S, Schork NJ, Philis-Tsimikas A, Torkamani A, Fortmann AL, Bloss CS. Patient perspectives on whole-genome sequencing for undiagnosed diseases. Personalized Medicine 2017; 14: 17–25.</mixed-citation><mixed-citation xml:lang="en">Boeldt DL, Cheung C, Ariniello L, Darst BF, Topol S, Schork NJ, Philis-Tsimikas A, Torkamani A, Fortmann AL, Bloss CS. Patient perspectives on whole-genome sequencing for undiagnosed diseases. Personalized Medicine 2017; 14: 17–25.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">М. А. Масчан, Н. В. Мякова; Острый лимфобластный лейкоз: Онкогематология; 2006.</mixed-citation><mixed-citation xml:lang="en">М. А. Масчан, Н. В. Мякова; Острый лимфобластный лейкоз: Онкогематология; 2006.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">А. Г. Румянцев. Эволюция лечения острого лимфобластного лейкоза у детей: Детская гематология/онкология. ФГБУ Федеральный научно-клинический центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева МЗ РФ, Москва, РФ; 2016.</mixed-citation><mixed-citation xml:lang="en">А. Г. Румянцев. Эволюция лечения острого лимфобластного лейкоза у детей: Детская гематология/онкология. ФГБУ Федеральный научно-клинический центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева МЗ РФ, Москва, РФ; 2016.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Bash RO, Crist WM, Shuster JJ, et al. Clinical features and outcome of T-cell acute lymphoblastic leukemia in childhood with respect to alterations at the TAL1 locus: a Pediatric Oncology Group study. Blood. 1993; 81: 2110–2117.</mixed-citation><mixed-citation xml:lang="en">Bash RO, Crist WM, Shuster JJ, et al. Clinical features and outcome of T-cell acute lymphoblastic leukemia in childhood with respect to alterations at the TAL1 locus: a Pediatric Oncology Group study. Blood. 1993; 81: 2110–2117.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Е. Н. Имянитов. Общие представления о таргетной терапии: Практическая онкология; НИИ онкологии им. Н. Н. Петрова, 2010.</mixed-citation><mixed-citation xml:lang="en">Е. Н. Имянитов. Общие представления о таргетной терапии: Практическая онкология; НИИ онкологии им. Н. Н. Петрова, 2010.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Hunger SP, Mullighan CG. Acute lymphoblastic leukemia in children. N. Engl. J. Med. 2015; 373 (16): 1541–1552.</mixed-citation><mixed-citation xml:lang="en">Hunger SP, Mullighan CG. Acute lymphoblastic leukemia in children. N. Engl. J. Med. 2015; 373 (16): 1541–1552.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Soverini S., Bassan R. &amp; Lion T. Treatment and monitoring of Philadelphia chromosome-positive leukemia patients: recent advances and remaining challenges. J Hematol Oncol 12, 39 (2019). https://doi.org/10.1186/s13045-019-0729-2</mixed-citation><mixed-citation xml:lang="en">Soverini S., Bassan R. &amp; Lion T. Treatment and monitoring of Philadelphia chromosome-positive leukemia patients: recent advances and remaining challenges. J Hematol Oncol 12, 39 (2019). https://doi.org/10.1186/s13045-019-0729-2</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Druker BJ, Talpaz M, Resta DJ, et al. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N Engl J Med 2001; 344: 1031–37.</mixed-citation><mixed-citation xml:lang="en">Druker BJ, Talpaz M, Resta DJ, et al. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N Engl J Med 2001; 344: 1031–37.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Авдеева Ж. И., Солдатов А. А., Киселевский М. В., Медуницын Н. В. Противоопухолевые моноклональные антитела: Иммунология. 2017. № 5. С. 256–270.</mixed-citation><mixed-citation xml:lang="en">Авдеева Ж. И., Солдатов А. А., Киселевский М. В., Медуницын Н. В. Противоопухолевые моноклональные антитела: Иммунология. 2017. № 5. С. 256–270.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">А. И. Карачунский, Ю. В. Румянцева, А. фон Штакельберг. Анти-CD19-моноклональные антитела при острой лимфобластной лейкемии у детей: Российский журнал детской гематологии и онкологии; ФГБУ «ФНКЦ ДГОИ им. Дмитрия Рогачева» Минздрава России, Москва.</mixed-citation><mixed-citation xml:lang="en">А. И. Карачунский, Ю. В. Румянцева, А. фон Штакельберг. Анти-CD19-моноклональные антитела при острой лимфобластной лейкемии у детей: Российский журнал детской гематологии и онкологии; ФГБУ «ФНКЦ ДГОИ им. Дмитрия Рогачева» Минздрава России, Москва.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Нуриев Р.И., Караулов А.В., Киселевский М.В. Новые стратегии лечениия пациентов с онкологическими заболеваниями: иммунотерапевтическуий родход: Иммунология. 2017; 38 (1): 39–48.</mixed-citation><mixed-citation xml:lang="en">Нуриев Р.И., Караулов А.В., Киселевский М.В. Новые стратегии лечениия пациентов с онкологическими заболеваниями: иммунотерапевтическуий родход: Иммунология. 2017; 38 (1): 39–48.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Noah Federman &amp; Ray McDermott (2019) Larotrectinib, a highly selective tropomyosin receptor kinase (TRK) inhibitor for the treatment of TRK fusion cancer, Expert Review of Clinical Pharmacology, 12: 10, 931–939, DOI: 10.1080/17512433.2019.1661775.</mixed-citation><mixed-citation xml:lang="en">Noah Federman &amp; Ray McDermott (2019) Larotrectinib, a highly selective tropomyosin receptor kinase (TRK) inhibitor for the treatment of TRK fusion cancer, Expert Review of Clinical Pharmacology, 12: 10, 931–939, DOI: 10.1080/17512433.2019.1661775.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Bergethon K, Shaw AT, Ou SH, et al. ROS 1 rearrangements define a unique molecular class of lung cancers. J Clin Oncol. 2012; 30 (8): 863–70.</mixed-citation><mixed-citation xml:lang="en">Bergethon K, Shaw AT, Ou SH, et al. ROS 1 rearrangements define a unique molecular class of lung cancers. J Clin Oncol. 2012; 30 (8): 863–70.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Theodore W Laetsch, Steven G DuBois, Leo Mascarenhas, Brian Turpin, Noah Federman, Catherine M Albert, et al. Larotrectinib for paediatric solid tumours harbouring NTRK gene fusions: phase 1 results from a multicentre, open-label, phase 1/2 study: The Lancet Oncology; Volume 19, Issue 5, May 2018, Pages 705–714.</mixed-citation><mixed-citation xml:lang="en">Theodore W Laetsch, Steven G DuBois, Leo Mascarenhas, Brian Turpin, Noah Federman, Catherine M Albert, et al. Larotrectinib for paediatric solid tumours harbouring NTRK gene fusions: phase 1 results from a multicentre, open-label, phase 1/2 study: The Lancet Oncology; Volume 19, Issue 5, May 2018, Pages 705–714.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Сулейманова А.М., Сагоян Г.Б., Киргизов К.И.. Новые подходы в терапии солидных опухолей у детей и подростков с использованием таргетного препарата энтректиниб: Российский журнал детской гематологии и онкологии; 2019; 6 (4): 62–8.</mixed-citation><mixed-citation xml:lang="en">Сулейманова А.М., Сагоян Г.Б., Киргизов К.И.. Новые подходы в терапии солидных опухолей у детей и подростков с использованием таргетного препарата энтректиниб: Российский журнал детской гематологии и онкологии; 2019; 6 (4): 62–8.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Anna F. Farago, Long P. Le, Zongli Zheng, Alona Muzikansky, Alexander Drilon, Manish Patel. Durable Clinical Response to Entrectinib in NTRK1-Rearranged Non-Small Cell Lung Cancer: Journal of Thoracic Oncology Volume 10, Number 12, December 2015.</mixed-citation><mixed-citation xml:lang="en">Anna F. Farago, Long P. Le, Zongli Zheng, Alona Muzikansky, Alexander Drilon, Manish Patel. Durable Clinical Response to Entrectinib in NTRK1-Rearranged Non-Small Cell Lung Cancer: Journal of Thoracic Oncology Volume 10, Number 12, December 2015.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Ahn M-J, Cho BC, Siena S, et al. Entrectinib in patients with locally advanced or metastatic ROS1 fusion-positive non-small cell lung cancer (NSCLC). Presented at: IASLC 18th World Conference on Lung Cancer; October 15–18, 2017; Yokohama, Japan. Abstract 8564.</mixed-citation><mixed-citation xml:lang="en">Ahn M-J, Cho BC, Siena S, et al. Entrectinib in patients with locally advanced or metastatic ROS1 fusion-positive non-small cell lung cancer (NSCLC). Presented at: IASLC 18th World Conference on Lung Cancer; October 15–18, 2017; Yokohama, Japan. Abstract 8564.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Demetri GD et al. Efficacy and Safety of Entrectinib in Patients with NTRK Fusion-Positive (NTRK-fp) Tumors: Pooled Analysis of STARTRK-2, STARTRK-1 and ALKA-372–001. Presented at ESMO 2018; October 19–23, 2018; Munich, Germany. Abstract LBA17.</mixed-citation><mixed-citation xml:lang="en">Demetri GD et al. Efficacy and Safety of Entrectinib in Patients with NTRK Fusion-Positive (NTRK-fp) Tumors: Pooled Analysis of STARTRK-2, STARTRK-1 and ALKA-372–001. Presented at ESMO 2018; October 19–23, 2018; Munich, Germany. Abstract LBA17.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Rolfo, et al. Entrectinib: a potent new TRK, ROS 1, and ALK inhibitor. Expert Opin Investig Drugs. 2015; 24 (11): 1493–500.</mixed-citation><mixed-citation xml:lang="en">Rolfo, et al. Entrectinib: a potent new TRK, ROS 1, and ALK inhibitor. Expert Opin Investig Drugs. 2015; 24 (11): 1493–500.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
