<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Skin and Venereal Diseases</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Skin and Venereal Diseases</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский журнал кожных и венерических болезней</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1560-9588</issn><issn publication-format="electronic">2412-9097</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">114870</article-id><article-id pub-id-type="doi">10.17816/dv114870</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>DERMATOLOGY</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ДЕРМАТОЛОГИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Randomized study of the efficacy of monoclonal antibodies in patients with refractory psoriasis</article-title><trans-title-group xml:lang="ru"><trans-title>Изучение эффективности и переносимости ингибитора IL-17А у пациентов с вульгарным псориазом</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2482-1754</contrib-id><contrib-id contrib-id-type="spin">2500-7989</contrib-id><name-alternatives><name xml:lang="en"><surname>Olisova</surname><given-names>Olga Yu.</given-names></name><name xml:lang="ru"><surname>Олисова</surname><given-names>Ольга Юрьевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Dr. Sci. (Med.), Professor, Corresponding Member of the Russian Academy of Sciences</p></bio><bio xml:lang="ru"><p>д.м.н., профессор, чл.-корр. РАН</p></bio><email>olisovaolga@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4674-8327</contrib-id><name-alternatives><name xml:lang="en"><surname>Nikuradze</surname><given-names>Victoria O.</given-names></name><name xml:lang="ru"><surname>Никурадзе</surname><given-names>Виктория Олеговна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Graduate Student</p></bio><bio xml:lang="ru"><p>аспирант</p></bio><email>victorianikuradze@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7968-9829</contrib-id><contrib-id contrib-id-type="spin">8028-5545</contrib-id><name-alternatives><name xml:lang="en"><surname>Grekova</surname><given-names>Ekaterina V.</given-names></name><name xml:lang="ru"><surname>Грекова</surname><given-names>Екатерина Владимировна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Cand. Sci. (Med.), Assistant Lecturer</p></bio><bio xml:lang="ru"><p>к.м.н., ассистент кафедры</p></bio><email>grekova_kate@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">I.M. Sechenov First Moscow State Medical University (Sechenov University)</institution></aff><aff><institution xml:lang="ru">Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет)</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2023-01-29" publication-format="electronic"><day>29</day><month>01</month><year>2023</year></pub-date><pub-date date-type="pub" iso-8601-date="2022-12-17" publication-format="electronic"><day>17</day><month>12</month><year>2022</year></pub-date><volume>25</volume><issue>6</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>71</fpage><lpage>81</lpage><history><date date-type="received" iso-8601-date="2022-11-26"><day>26</day><month>11</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2023-01-07"><day>07</day><month>01</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Olisova O.Y., Nikuradze V.O., Grekova E.V.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, Олисова О.Ю., Никурадзе В.О., Грекова Е.В.</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Olisova O.Y., Nikuradze V.O., Grekova E.V.</copyright-holder><copyright-holder xml:lang="ru">Олисова О.Ю., Никурадзе В.О., Грекова Е.В.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2026-02-17"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc-nd/4.0/</ali:license_ref></license></permissions><self-uri xlink:href="https://rjsvd.com/1560-9588/article/view/114870">https://rjsvd.com/1560-9588/article/view/114870</self-uri><abstract xml:lang="en"><p><bold><italic>BACKGROUND:</italic></bold> The main vector of psoriasis therapy is suppression of proliferative activity of keratinocytes, normalization of their differentiation, neutralization of immune inflammation in the dermis and normalization of cytokine balance.</p> <p><bold><italic>AIM:</italic></bold> of the study was to study the efficacy and tolerability of an IL-17A inhibitor (secukinumab) as monotherapy and in combination with methotrexate in patients with moderate and severe psoriasis vulgaris.</p> <p><bold><italic>MATERIALS AND METHODS:</italic></bold> The severity of psoriasis was assessed by the Psoriasis Prevalence and Severity Index (Psoriasis Area and Severity Index, PASI). To assess the damage to the nail plates of the hands and feet in psoriasis, the NAPSI index (Nail Psoriasis Severity Index) was used. In order to assess the quality of life of patients with psoriasis, a Russian-language version of the dermatological quality of life index (DQLI) was used. Patients' quality of life was assessed before the prescribed therapy and at 12 weeks of treatment. Assessment of the severity of itching and its impact on the daily life of patients was carried out according to the Prurindex questionnaire.</p> <p><bold><italic>RESULTS:</italic></bold> All patients were divided into two groups by a randomized method. The first group included 25 patients who received therapy with secukinumab in the age category of 55 (30–67) years. The second group included 25 patients aged 56 (34–69) years of moderate and severe psoriasis who were treated with secukinumab after initiation (300 mg) 150 mg subcutaneously in combination with methotrexate 15 mg intramuscularly for 24 weeks. Thus, in the first group PASI 90 was achieved after 24 weeks ― in 69%, PASI 100 ― in 31% patients; in the second group ― PASI 90 ― in 68%, PASI 100 ― in 32% patients respectively. In both groups, it was possible to maintain clinical remission (PASI ≥90) in 87.3% of patients throughout the year. During therapy in patients of both groups, there was a decrease in DLQI values from 25.6±3.7 to 3.5±3.1 (<italic>p</italic> &lt;0.01) in the first group and from 23.3±3.7 up to 3.1±2.6 in the second group.</p> <p><bold><italic>CONCLUSIONS:</italic></bold> Treatment of patients with moderate and severe psoriasis vulgaris with secukinumab has shown its high efficacy and safety. Moreover, it was estimated that the combination of secukinumab and methotrexate is comparable in effectiveness to secukinumab monotherapy. It has been established that the use of secukinumab as monotherapy and in combination with methotrexate significantly improves the quality of life of patients with moderate and severe psoriasis vulgaris.</p></abstract><trans-abstract xml:lang="ru"><p><bold><italic>Обоснование.</italic></bold> Основными векторами терапии псориаза являются подавление пролиферативной активности кератиноцитов, нормализация их дифференцировки, нейтрализация иммунного воспаления в дерме и нормализация баланса цитокинов.</p> <p><bold><italic>Цель исследования</italic></bold> ― изучение эффективности и переносимости ингибитора IL-17A (секукинумаб) в виде монотерапии и в сочетании с метотрексатом у больных вульгарным псориазом средней и тяжёлой степени.</p> <p><bold><italic>Материал и методы.</italic></bold> Под наблюдением находилось 50 больных вульгарным псориазом. Оценка степени тяжести псориаза производилась по индексу распространённости и тяжести псориаза (Psoriasis Area and Severity Index, PASI). С целью изучения качества жизни больных псориазом была использована русскоязычная версия дерматологического индекса качества жизни (ДИКЖ). Оценку выраженности зуда и его воздействия на повседневную жизнь пациентов проводили по опроснику Пруриндекс. Для определения поражения ногтевых пластинок кистей и стоп при псориазе использовали индекс NAPSI (Nail Psoriasis Severity Index). В ходе проводимой терапии в каждой из групп определяли уровни показателей PASI, ДИКЖ и Пруриндекс до лечения, на 4, 12 и 24-й неделе, NAPSI ― на 0-й и 24-й неделе.</p> <p><bold><italic>Результаты.</italic></bold> Все пациенты были разделены на две группы рандомизированным методом. Первая группа включала 25 пациентов возрастной категории 55 (30–67) лет со средней и тяжёлой степенью течения заболевания, которые получали терапию секукинумабом в дозе 300 мг подкожно. Вторая группа состояла из 25 пациентов в возрасте 56 (34–69) лет со средней и тяжёлой степенью заболевания, получавших терапию секукинумабом после инициации (300 мг) по 150 мг подкожно в комбинации с метотрексатом по 15 мг внутримышечно в течение 24 недель. Спустя 24 недели лечения у пациентов первой группы в результате монотерапии секукинумабом было достигнуто PASI 90 в 69% случаев, PASI 100 ― в 31%; у пациентов второй группы (секукинумаб + метотрексат) ― в 68 и 32% соответственно. У 87,3% больных обеих групп удалось сохранить клиническую ремиссию (PASI ≥90) на протяжении года. В ходе терапии у пациентов первой группы отмечалось снижение показателей ДИКЖ с 25,6±3,7 до 3,5±3,1 (<italic>p</italic> &lt;0,01), во второй группе ― с 23,3±3,7 до 3,1±2,6.</p> <p><bold><italic>Заключение.</italic></bold> Лечение пациентов с вульгарным псориазом средней и тяжёлой степени тяжести секукинумабом показало высокую эффективность и безопасность препарата. Учитывая полученные данные, комбинация секукинумаба и метотрексата сопоставима по эффективности с монотерапией секукинумабом. Установлено, что применение секукинумаба в виде монотерапии и в сочетании с метотрексатом значительно улучшает качество жизни пациентов с вульгарным псориазом средней и тяжёлой степени.</p></trans-abstract><kwd-group xml:lang="en"><kwd>secukinumab</kwd><kwd>methotrexate</kwd><kwd>psoriasis vulgaris</kwd><kwd>monoclonal antibody</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>секукинумаб</kwd><kwd>метотрексат</kwd><kwd>вульгарный псориаз</kwd><kwd>моноклональное антитело</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">Sobolewski P, Błaszczak A, Szymańska E, Walecka I. Psoriasis in special localizations. Reumatologia. 2018;56(6):392–398. doi: 10.5114/reum.2018.80718</mixed-citation><mixed-citation xml:lang="ru">Sobolewski P., Błaszczak A., Szymańska E., Walecka I. Psoriasis in special localizations // Reumatologia. 2018. Vol. 56, N 6. Р. 392–398. doi: 10.5114/reum.2018.80718</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Kubanov AA, Bogdanova EV. The results of the activities of medical organizations providing medical care in the field of dermatovenerology in 2020: Work in a pandemic. Bulletin Dermatology Venereology. 2021;(4):8–32. (In Russ). doi: 10.25208/vdv1261</mixed-citation><mixed-citation xml:lang="ru">Кубанов А.А., Богданова Е.В. Итоги деятельности медицинских организаций, оказывающих медицинскую помощь по профилю дерматовенерология, в 2020 году: работа в условиях пандемии // Вестник дерматологии и венерологии. 2021. № 4. С. 8–32. doi: 10.25208/vdv1261</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Olisova OY, Garanyan LG. Epidemiology, etiopathogenesis and comorbidity in psoriasis: new facts. Russ J Skin Venereal Diseases. 2017;20(4):214–219. (In Russ). doi: 10.18821/1560-9588-2017-20-4-214-219</mixed-citation><mixed-citation xml:lang="ru">Олисова О.Ю., Гаранян Л.Г. Эпидемиология, этиопатогенез и коморбидность при псориазе ― новые факты // Российский журнал кожных и венерических болезней. 2017. Т. 20, № 4. С. 214–219. doi: 10.18821/1560-9588-2017-20-4-214-219</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Chang YT, Chen TJ, Liu PC, et al. Epidemiological study of psoriasis in the national health insurance database in Taiwan. Acta Derm Venereol. 2009;89(3):262–266. doi: 10.2340/00015555-0642</mixed-citation><mixed-citation xml:lang="ru">Chang Y.T., Chen T.J., Liu P.C., et al. Epidemiological study of psoriasis in the national health insurance database in Taiwan // Acta Derm Venereol. 2009. Vol. 89, N 3. Р. 262–266. doi: 10.2340/00015555-0642</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Parisi R, Iskandar IY, Kontopantelis E, et al. National, regional, and worldwide epidemiology of psoriasis: Systematic analysis and modelling study. Bmj. 2020:(369):m1590. doi: 10.1136/bmj.m1590</mixed-citation><mixed-citation xml:lang="ru">Parisi R., Iskandar I.Y., Kontopantelis E., et al. National, regional, and worldwide epidemiology of psoriasis: Systematic analysis and modelling study // Bmj. 2020. N 369. Р. m1590. doi: 10.1136/bmj.m1590</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Rojas M, Restrepo-Jiménez P, Monsalve DM, et al. Molecular mimicry and autoimmunity. J Autoimmunity. 2018;(95):100–123. doi: 10.1016/j.jaut.2018.10.012</mixed-citation><mixed-citation xml:lang="ru">Rojas M., Restrepo-Jiménez P., Monsalve D.M., et al. Molecular mimicry and autoimmunity // J Autoimmunity. 2018. N 95. Р. 100–123. doi: 10.1016/j.jaut.2018.10.012</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Parkhouse AR. Experiences of stigma-stress among people living with psoriasis in the United States. Am J Health Behav. 2019;43(2):243–257. doi: 10.5993/ajhb.43.2.2</mixed-citation><mixed-citation xml:lang="ru">Parkhouse A.R. Experiences of stigma-stress among people living with psoriasis in the United States // Am J Health Behav. 2019. Vol. 43, N 2. Р. 243–257. doi: 10.5993/ajhb.43.2.2</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Danielsen K. Increased risk of death in patients with psoriasis: Disease or lifestyle? Br J Dermatol. 2019;180(1):3–4. doi: 10.1111/bjd.17141</mixed-citation><mixed-citation xml:lang="ru">Danielsen K. Increased risk of death in patients with psoriasis: Disease or lifestyle? // Br J Dermatol. 2019. Vol. 180, N 1. Р. 3–4. doi: 10.1111/bjd.17141</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Pilon D, Teeple A, Zhdanava M, et al. The economic burden of psoriasis with high comorbidity among privately insured patients in the United States. J Med Econ. 2019;22(2):196–203. doi: 10.1080/13696998.2018.1557201</mixed-citation><mixed-citation xml:lang="ru">Pilon D., Teeple A., Zhdanava M., et al. The economic burden of psoriasis with high comorbidity among privately insured patients in the United States // J Med Econ. 2019. Vol. 22, N 2. Р. 196–203. doi: 10.1080/13696998.2018.1557201</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Kvist-Hansen A, Kaiser H, Skov L, Hansen PR. [Comorbidity in connection with psoriasis is more than psoriatic arthritis]. Ugeskr Laeger. 2018;180(2):V07170526. (In Danish).</mixed-citation><mixed-citation xml:lang="ru">Kvist-Hansen A., Kaiser H., Skov L., Hansen P.R. [Comorbidity in connection with psoriasis is more than psoriatic arthritis] // Ugeskr Laeger. 2018. Vol. 180, N 2. Р. V07170526. Danish.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Pilon D, Teeple A, Zhdanava M, et al. The economic burden of psoriasis with high comorbidity among privately insured patients in the United States. J Med Econ. 2019;22(2):196–203. doi: 10.1080/13696998.2018.1557201</mixed-citation><mixed-citation xml:lang="ru">Pilon D., Teeple A., Zhdanava M., et al. The economic burden of psoriasis with high comorbidity among privately insured patients in the United States // J Med Econ. 2019. Vol. 22, N 2. Р. 196–203. doi: 10.1080/13696998.2018.1557201</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Langley RG, Elewski BE, Lebwohl M, et al. Secukinumab in plaque psoriasis-results of two phase 3 trials. N Engl J Med. 2014;371(4):326–338. doi: 10.1056/nejmoa1314258</mixed-citation><mixed-citation xml:lang="ru">Langley R.G., Elewski B.E., Lebwohl M., et al. Secukinumab in plaque psoriasis-results of two phase 3 trials // N Engl J Med. 2014. Vol. 371, N 4. Р. 326–338. doi: 10.1056/nejmoa1314258</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Lebwohl M, Strober B, Menter A, et al. Phase 3 studies comparing brodalumab with ustekinumab in psoriasis. N Engl J Med. 2015;373(14):1318–1328. doi: 10.1056/nejmoa1503824</mixed-citation><mixed-citation xml:lang="ru">Lebwohl M., Strober B., Menter A., et al. Phase 3 studies comparing brodalumab with ustekinumab in psoriasis // N Engl J Med. 2015. Vol. 373, N 14. Р. 1318–1328. doi: 10.1056/nejmoa1503824</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Leonardi CL, Kimball AB, Papp KA, et al. Efficacy and safety of ustekinumab, a human interleukin-12/23 monoclonal antibody, in patients with psoriasis: 76-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 1). Lancet Lond Engl. 2008;371(9625):1665–1674. doi: 10.1016/s0140-6736(08)60725-4</mixed-citation><mixed-citation xml:lang="ru">Leonardi C.L., Kimball A.B., Papp K.A., et al. Efficacy and safety of ustekinumab, a human interleukin-12/23 monoclonal antibody, in patients with psoriasis: 76-week results from a randomised, double-blind, placebo-controlled trial (PHOENIX 1) // Lancet Lond Engl. 2008. Vol. 371, N 9625. Р. 1665–1674. doi: 10.1016/s0140-6736(08)60725-4</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Marzano AV, Derlino F, Berti EF. Pathogenesis of psoriasis: Focus on autoinflammation. Dermatopathology. 2018;5(1):14–15. doi: 10.1159/000486304</mixed-citation><mixed-citation xml:lang="ru">Marzano A.V., Derlino F., Berti E.F. Pathogenesis of psoriasis: Focus on autoinflammation // Dermatopathology. 2018. Vol. 5, N 1. Р. 14–15. doi: 10.1159/000486304</mixed-citation></citation-alternatives></ref></ref-list></back></article>
