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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">rsp</journal-id><journal-title-group><journal-title xml:lang="ru">Научно-практическая ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Rheumatology Science and Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1995-4484</issn><issn pub-type="epub">1995-4492</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47360/1995-4484-2021-192-200</article-id><article-id custom-type="elpub" pub-id-type="custom">rsp-3022</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>ПРОГРЕСС В РЕВМАТОЛОГИИ В XXI ВЕКЕ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PROGRESS IN RHEUMATOLOGY IN THE XXI CENTURY</subject></subj-group></article-categories><title-group><article-title>Перспективы применения танезумаба при хронической боли</article-title><trans-title-group xml:lang="en"><trans-title>Use of tanezumab for chronic pain treatment</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1391-0711</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каратеев</surname><given-names>А. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Karateev</surname><given-names>A. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Каратеев Андрей Евгеньевич, д.м.н, заведующий лаборатории патофизиологии боли и полиморфизма скелетномышечных заболеваний</p><p>115522, Москва, Каширское шоссе, 34а</p></bio><bio xml:lang="en"><p>Andrey E. Karateev</p><p>115522, Moscow, Kashirskoye Highway, 34A</p></bio><email xlink:type="simple">aekarat@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6068-3080</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лила</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Lila</surname><given-names>A. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н, профессор, директор ФГБНУ НИИР им. В.А. Насоновой, заведующий кафедрой ревматологии ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России</p><p>115522, Москва, Каширское шоссе, 34а125993, Москва, ул. Баррикадная, 2/1, стр. 1</p></bio><bio xml:lang="en"><p>Aleksander M. Lila</p><p>115522, Moscow, Kashirskoye Highway, 34A125993, Moscow, Barrikadnaya str., 2/1, building 1</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7017-0898</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Алексеева</surname><given-names>Л. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Alekseeva</surname><given-names>L. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н, заведующая лабораторией остеоартроза</p><p>115522, Москва, Каширское шоссе, 34а</p></bio><bio xml:lang="en"><p>Lyudmila I. Alekseeva</p><p>115522, Moscow, Kashirskoye Highway, 34A</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»<country>Россия</country></aff><aff xml:lang="en">V.A. Nasonova Research Institute of Rheumatology<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»; ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России<country>Россия</country></aff><aff xml:lang="en">V.A. Nasonova Research Institute of Rheumatology; Russian Medical Academy of Continuous Professional Education of the Ministry of Healthcare of the Russian Federation<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>12</day><month>05</month><year>2021</year></pub-date><volume>59</volume><issue>2</issue><fpage>192</fpage><lpage>200</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Каратеев А.Е., Лила А.М., Алексеева Л.И., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Каратеев А.Е., Лила А.М., Алексеева Л.И.</copyright-holder><copyright-holder xml:lang="en">Karateev A.E., Lila A.M., Alekseeva L.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://rsp.mediar-press.net/rsp/article/view/3022">https://rsp.mediar-press.net/rsp/article/view/3022</self-uri><abstract><p>Проблема хронической скелетно-мышечной боли, определяющей тяжелые страдания и инвалидизацию сотен миллионов жителей нашей планеты, далека от своего решения. Особенно сложным контроль боли представляется у пациентов с тяжелыми формами остеоартрита (ОА) и хронической неспецифической болью в спине (ХНБС). Популярные анальгетики – нестероидные противовоспалительные препараты (НПВП) и опиоиды – демонстрируют при этой патологии умеренную эффективность и высокий риск нежелательных явлений (НЯ). Это заставляет искать новые подходы для анальгетической терапии. Танезумаб – генно-инженерный биологический препарат (моноклональное антитело), специфически блокирующий фактор роста нервов, который играет ключевую роль в развитии хронической боли. Серия исследований II и III фазы оказали, что танезумаб при внутривенном или подкожном введении в дозе от 2,5 до 20 мг 1 раз через 8 недель у больных ОА или ХНБС оказывает выраженное и стойкое обезболивающее действие, превосходящее действие плацебо и равное или превосходящее эффект многомесячного ежедневного приема напроксена, целекоксиба, диклофенака, оксикодона и трамадола. Танезумаб может вызывать различные НЯ, прежде всего быстрое прогрессирование ОА (у 2,6–6,0%) и неврологические нарушения (парестезии и гипостезии, у ≈5%). При этом прогрессирование ОА значительно чаще отмечалось при комбинированном использовании танезумаба и НПВП. Тем не менее, учитывая сложную категорию больных, у которых использовался танезумаб (пациенты с болью, рефрактерной к стандартному лечению; пациенты с тяжелыми формами ОА), хороший анальгетический потенциал танезумаба позволяет рассматривать его как перспективное средство для контроля хронической скелетно-мышечной боли, которое будет широко востребовано в реальной клинической практике.</p></abstract><trans-abstract xml:lang="en"><p>The problem of chronic musculoskeletal pain, the cause of severe suffering and disability of hundreds of millions of people on our planet, is far from being solved. Pain control is particularly difficult in patients with severe forms of osteoarthritis (OA) and chronic non-specific low back pain (CLBP). Popular analgesics – nonsteroidal anti-inflammatory drugs (NSAIDs) and opioids, demonstrate moderate effectiveness and a high risk of adverse events (AE). This leads to the search for new approaches for analgesic therapy. Tanezumab is a monoclonal antibody that specifically blocks nerve growth factor, which plays a key role in the development of chronic pain. A series of phase II and III studies showed that tanezumab was administered intravenously or subcutaneously at a dose of 2.5 mg to 20 mg once every 8 weeks. In patients with OA or CNSLBP, it has a pronounced and persistent analgesic effect that exceeds the effect of placebo, and is equal to or superior to the effect of many months of daily intake of naproxen, celecoxib, diclofenac, oxycodone and tramadol. Tanezumab can cause various AE, primarily rapid progression of OA (in 2.6–6.0%) and neurological disorders (paresthesia and hyposthesia, in ≈5%). At the same time, the progression of OA was significantly more often observed with the combined use of tanezumab and NSAIDs. Nevertheless, taking into account the characteristics of patients who used tanezumab (patients with pain refractory to standard treatment; severe forms of OA), the good analgesic potential of tanezumab allows us to consider it as a promising tool for the control of chronic musculoskeletal pain, which will be widely used in real clinical practice.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>хроническая скелетно-мышечная боль</kwd><kwd>остеоартрит</kwd><kwd>боль в нижней части спины</kwd><kwd>танезумаб</kwd><kwd>эффективность</kwd><kwd>безопасность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>chronic musculoskeletal pain</kwd><kwd>osteoarthritis</kwd><kwd>lower back pain</kwd><kwd>tanezumab</kwd><kwd>efficacy</kwd><kwd>safety</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">Насонов ЕЛ. Достижения ревматологии в XXI в. 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