<?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="data-paper" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Allergy</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Allergy</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский Аллергологический Журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1810-8830</issn><issn publication-format="electronic">2686-682X</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">16913</article-id><article-id pub-id-type="doi">10.36691/RJA16913</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Технический отчёт</subject></subj-group><subj-group subj-group-type="article-type"><subject>Scientific Report</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Experience of lanadelumab usage for long-term prophylaxis of attacks in hereditary angioedema in patients of the Moscow region</article-title><trans-title-group xml:lang="ru"><trans-title>Опыт применения ланаделумаба для долгосрочной профилактики атак при наследственном ангиоотёке у пациентов Московской области</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0002-4865-433X</contrib-id><contrib-id contrib-id-type="spin">8105-7529</contrib-id><name-alternatives><name xml:lang="en"><surname>Proskurina</surname><given-names>Elena V.</given-names></name><name xml:lang="ru"><surname>Проскурина</surname><given-names>Елена Валерьевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>alberus17@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0004-5617-2335</contrib-id><name-alternatives><name xml:lang="en"><surname>Morozova</surname><given-names>Natalia V.</given-names></name><name xml:lang="ru"><surname>Морозова</surname><given-names>Наталья Викторовна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD</p></bio><email>natalya_morozova_63@bk.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6758-2389</contrib-id><contrib-id contrib-id-type="spin">7074-8300</contrib-id><name-alternatives><name xml:lang="en"><surname>Kokushkin</surname><given-names>Konstantin A.</given-names></name><name xml:lang="ru"><surname>Кокушкин</surname><given-names>Константин Александрович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD</p></bio><email>Kokushkinka@gmail.com</email><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Moscow Regional Research and Clinical Institute</institution></aff><aff><institution xml:lang="ru">Московский областной научно-исследовательский клинический институт имени М.Ф. Владимирского</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Scientific and Practical Center for Clinical and Economic Analysis of the Ministry of Health of the Moscow Region</institution></aff><aff><institution xml:lang="ru">Научно-практический центр клинико-экономического анализа Министерства здравоохранения Московской области</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2024-05-21" publication-format="electronic"><day>21</day><month>05</month><year>2024</year></pub-date><pub-date date-type="pub" iso-8601-date="2024-06-16" publication-format="electronic"><day>16</day><month>06</month><year>2024</year></pub-date><volume>21</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>254</fpage><lpage>264</lpage><history><date date-type="received" iso-8601-date="2024-01-23"><day>23</day><month>01</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-05-14"><day>14</day><month>05</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Pharmarus Print Media</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Фармарус Принт Медиа</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Pharmarus Print Media</copyright-holder><copyright-holder xml:lang="ru">Фармарус Принт Медиа</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2026-06-16"/></permissions><self-uri xlink:href="https://rusalljournal.ru/raj/article/view/16913">https://rusalljournal.ru/raj/article/view/16913</self-uri><abstract xml:lang="en"><p><italic>BACKGROUND: </italic>Hereditary angioedema is a rare disease with high frequency for orphan diseases. The autosomal dominant type of inheritance leads to a significant number of affected patients in families. Angioedema attacks significantly impair the quality of life. hereditary angioedema causes life-threatening conditions which depend on edema’s localization.</p> <p><italic>AIM: </italic>To evaluate the efficacy and safety of lanadelumab for long-term prophylaxis in hereditary angioedema in routine practice.</p> <p><italic>MATERIALS AND METHODS: </italic>16 patients with hereditary angioedema were enrolled in the observational single-center study. The data were researched: sex, patients age, age of symptoms onset, efficacy of previous methods of therapy, type of hereditary angioedema, genetics of the disease, contraindications for other prophylaxis methods. The efficacy of therapy was evaluated according to the duration of the course, the frequency of administration, the number of attacks of edema during the period of observation, and the improvement of the quality of life according to the AAS28 scale. Safety of use was evaluated by the presence of adverse events during the investigation.</p> <p><italic>RESULTS: </italic>The long-term prophylaxis with lanadelumab was effectively and safety for all of 16 patients. Single attacks during of therapy were provoked by the influence of significant triggers. Life-threatening attacks were not registered. The frequency of lanadelumab injections was reduced after 12 months of usage for 50% of patients. The improvement of the quality of life (from 6 to 38 according to AAS28 scale) was confirmed for all patients. Adverse events weren’t registered during the period of treatment.</p> <p><italic>CONCLUSION: </italic>The long-term prophylaxis of edema in hereditary angioedema with lanadelumab usage was approved as efficiently and safety.</p></abstract><trans-abstract xml:lang="ru"><p>Обоснование. Наследственный ангиоотёк относится к орфанным заболеваниям и имеет достаточно высокую распространённость в этой группе болезней. Аутосомно-доминантный тип наследования определяет частоту заболевания членов семьи и, в частности, мутации, вызывающие наследственный ангиоотёк. Приступы ангиоотёка значительно ухудшают качество жизни пациента и в зависимости от локализации могут иметь жизнеугрожающий характер.</p> <p>Цель исследования ― оценить эффективность и безопасность применения нового препарата ланаделумаб для долговременной профилактики при наследственном ангиоотёке.</p> <p>Материалы и методы. В обсервационном одноцентровом исследовании приняли участие 16 пациентов с тяжёлой формой наследственного ангиоотёка. В исследуемой группе выполнена оценка следующих характеристик: пол, возраст на момент наблюдения, возраст дебюта симптоматики, эффективность применяемой до этого терапии, тип наследственного ангиоотёка, генетика заболевания, наличие противопоказаний или неэффективность других препаратов, рекомендованных для долгосрочной профилактики. Оценивалась эффективность терапии в зависимости от длительности курса, кратности введения, наличия приступов за период наблюдения, улучшения качества жизни по шкале AAS28. Безопасность применения оценивали по развитию нежелательных реакций на препарат.</p> <p>Результаты. У всех 16 пациентов оценка долгосрочной профилактики ланаделумабом оказалась эффективной и безопасной. Единичные отёки на фоне терапии были спровоцированы выраженным влиянием триггеров, при этом жизнеугрожающих отёков не зарегистрировано. Через 12 месяцев применения ланаделумаба у 50% пациентов удалось снизить кратность введения препарата. Улучшение качества жизни по шкале AAS28 отмечено у всех пациентов (6–38 баллов). Нежелательных реакций на фоне применения ланаделумаба не зарегистрировано.</p> <p>Заключение. Применение ланаделумаба для долгосрочной профилактики ангиоотёков при наследственной форме заболевания доказало свою эффективность и безопасность в исследовании группы пациентов, наблюдающихся в Центре орфанных заболеваний Московской области.</p></trans-abstract><kwd-group xml:lang="en"><kwd>hereditary angioedema</kwd><kwd>HAE</kwd><kwd>bradykinin</kwd><kwd>C1 Inhibitor</kwd><kwd>lanadelumab</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>наследственный ангиоотёк</kwd><kwd>НАО</kwd><kwd>брадикинин</kwd><kwd>С1-ингибитор</kwd><kwd>ланаделумаб</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">Maurer M, Magerl M, Ansotegui I, et al. The international WAO/EAACI guideline for the management of hereditary angioedema-The 2017 revision and update. Allergy. 2018;73(8):1575–1596. doi: 10.1111/all.13384</mixed-citation><mixed-citation xml:lang="ru">Maurer M., Magerl M., Ansotegui I., et al. The international WAO/EAACI guideline for the management of hereditary angioedema: The 2017 revision and update // Allergy. 2018. Vol. 73, N 8. P. 1575–1596. doi: 10.1111/all.13384</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Cicardi M, Aberer W, Banerji A, et al.; HAWK under the patronage of EAACI (European Academy of Allergy and Clinical Immunology). Classification, diagnosis, and approach to treatment for angioedema: Consensus report from the Hereditary Angioedema International Working Group. Allergy. 2014;69(5):602–616. doi: 10.1111/all.12380</mixed-citation><mixed-citation xml:lang="ru">Cicardi M., Aberer W., Banerji A., et al.; HAWK under the patronage of EAACI (European Academy of Allergy and Clinical Immunology). Classification, diagnosis, and approach to treatment for angioedema: Consensus report from the Hereditary Angioedema International Working Group // Allergy. 2014. Vol. 69, N 5. P. 602–616. doi: 10.1111/all.12380</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Caccia S, Suffritti C, Cicardi M. Pathophysiology of hereditary angioedema. Pediatr Allergy Immunol Pulmonol. 2014;27(4):159–163. doi: 10.1089/ped.2014.0425</mixed-citation><mixed-citation xml:lang="ru">Caccia S., Suffritti C., Cicardi M. Pathophysiology of hereditary angioedema // Pediatr Allergy Immunol Pulmonol. 2014. Vol. 27, N 4. P. 159–163. doi: 10.1089/ped.2014.0425</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Farkas H, Martinez-Saguer I, Bork K, et al.; HAWK. International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency. Allergy. 2017;72(2):300–313. doi: 10.1111/all.13001</mixed-citation><mixed-citation xml:lang="ru">Farkas H., Martinez-Saguer I., Bork K., et al.; HAWK. International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency // Allergy. 2017. Vol. 72, N 2. P. 300–313. doi: 10.1111/all.13001</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Clinical guidelines. Hereditary angioedema (HAE). Russian Association of Allergists and Clinical Immunologists, National Society of Experts in Primary Immunodeficiencies, Union of Paediatricians of Russia; 2019. (In Russ). Available from: https://raaci.ru/dat/pdf/КР%20НАО%20%2015.02.19.pdf. Accessed: 23.11.2023.</mixed-citation><mixed-citation xml:lang="ru">Клинические рекомендации. Наследственный ангионевротический отёк (НАО). Российская ассоциация аллергологов и клинических иммунологов, Национальное общество экспертов в области первичных иммунодефицитов, Союз педиатров России, 2019. Режим доступа: https://raaci.ru/dat/pdf/КР%20НАО%20%2015.02.19.pdf. Дата обращения 23.11.2023.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Banerji A, Bernstein JA, Johnston DT, et al.; HELP OLE Investigators. Long-term prevention of hereditary angioedema attacks with lanadelumab: The HELP OLE study. Allergy. 2022;77(3):979–990. doi: 10.1111/all.15011</mixed-citation><mixed-citation xml:lang="ru">Banerji A., Bernstein J.A., Johnston D.T., et al.; HELP OLE Investigators. Long-term prevention of hereditary angioedema attacks with lanadelumab: The HELP OLE Study // Allergy. 2022. Vol. 77, N 3. P. 979–990. doi: 10.1111/all.15011</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Lumry W, Bernstein J, Tachdjian R, et al. Efficacy of lanadelumab at fixed and modified dosing regimens in patients aged 2 to &lt;12 years old with hereditary angioedema (HAE) in the phase 3, open-label, multicenter SPRING Study. J Allergy Clin Immunol. 2023;151(2):AB140. doi: 10.1016/j.jaci.2022.12.437</mixed-citation><mixed-citation xml:lang="ru">Lumry W., Bernstein J., Tachdjian R., et al. Efficacy of lanadelumab at fixed and modified dosing regimens in patients aged 2 to &lt;12 years old with hereditary angioedema (HAE) in the phase 3, open-label, multicenter SPRING study // J Allergy Clin Immunol. 2023. Vol. 151, N 2. P. AB140. doi: 10.1016/j.jaci.2022.12.437</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Cicardi M, Levy RJ, McNeil DL, et al. Ecallantide for the treatment of acute attacks in hereditary angioedema. N Engl J Med. 2010;363(6):523–531. doi: 10.1056/NEJMoa0905079</mixed-citation><mixed-citation xml:lang="ru">Cicardi M., Levy R.J., McNeil D.L., et al. Ecallantide for the treatment of acute attacks in hereditary angioedema // N Engl J Med. 2010. Vol. 363, N 6. P. 523–531. doi: 10.1056/NEJMoa0905079</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Kotian PL, Wu M, Vadlakonda S, et al. Berotralstat (BCX7353): Structure-guided design of a potent, selective, and oral plasma kallikrein inhibitor to prevent attacks of hereditary angioedema (HAE). J Med Chem. 2021;64(17):12453–12468. doi: 10.1021/acs.jmedchem.1c00511</mixed-citation><mixed-citation xml:lang="ru">Kotian P.L., Wu M., Vadlakonda S., et al. Berotralstat (BCX7353): Structure-guided design of a potent, selective, and oral plasma kallikrein inhibitor to prevent attacks of hereditary angioedema (HAE) // J Med Chem. 2021. Vol. 64, N 17. P. 12453–12468. doi: 10.1021/acs.jmedchem.1c00511</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Weller K, Groffik A, Magerl M, et al. Development, validation, and initial results of the Angioedema Activity Score. Allergy. 2013;68(9):1185–1192. doi: 10.1111/all.12209</mixed-citation><mixed-citation xml:lang="ru">Weller K., Groffik A., Magerl M., et al. Development, validation, and initial results of the angioedema activity score // Allergy. 2013. Vol. 68, N 9. P. 1185–1192. doi: 10.1111/all.12209</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Manto IA, Latysheva EA, Sorokina LE, Latysheva TV. The place of scales and questionnaires in assessing the disease’s severity and the long-term prophylaxis’s prescribing in patients with hereditary angioedema. Ther Arch. 2021;93(12):1498–1509. EDN: XCEJKF doi: 10.26442/00403660.2021.12.201294</mixed-citation><mixed-citation xml:lang="ru">Манто И.А., Латышева Е.А., Сорокина Л.Е., Латышева Т.В. Место шкал и опросников в оценке тяжести течения и подборе долгосрочной профилактики у пациентов с наследственным ангио-отёком // Терапевтический архив. 2021. Т. 93, № 12. C. 1498–1509. EDN: XCEJKF doi: 10.26442/00403660.2021.12.201294</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Latysheva EA, Manto IA, Aleshina LV, et al. Preliminary results of a non-interventional single-center study evaluating the efficacy of long-term use of lanadelumab in routine clinical practice in the Russian Federation. Russ J Allergy. 2023;20(2):164–176. EDN: BORDLE doi: 10.36691/RJA5493</mixed-citation><mixed-citation xml:lang="ru">Латышева Е.А., Манто И.А., Алешина Л.В., и др. Предварительные результаты неинтервенционного одноцентрового исследования по оценке эффективности применения ланаделумаба в рутинной клинической практике в Российской Федерации // Российский аллергологический журнал. 2023. Т. 20, № 2. С. 164–176. EDN: BORDLE doi: 10.36691/RJA5493</mixed-citation></citation-alternatives></ref></ref-list></back></article>
