Clinical case of successful treatment of granulomatosis with polyangiitis
- Авторлар: Frolova N.F.1,2, Mutovina Z.Y.1,3, Kobzar M.V.1, Arbolishvili G.N.1,4, Pavlov D.P.1, Shmeleva D.Y.1, Manerov F.F.1, Lysenko M.A.1,5
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Мекемелер:
- City Clinical Hospital No. 52, Moscow Health Department
- Russian University of Medicine
- Central State Medical Academy
- Lomonosov Moscow State University
- Pirogov Russian National Research Medical University named after N.I. Russian Ministry of Health
- Шығарылым: Том 16, № 3 (2024)
- Беттер: 36-43
- Бөлім: Clinical case
- URL: https://journals.eco-vector.com/2075-3594/article/view/637320
- DOI: https://doi.org/10.18565/nephrology.2024.3.36-43
- ID: 637320
Дәйексөз келтіру
Аннотация
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a systemic autoimmune disease characterized by the development of necrotizing inflammation in small blood vessels with damage to various organs and systems. Glucocorticosteroids (GCS) in combination with rituximab or cyclophosphamide are recommended as a pathogenetic therapy for ANCA vasculitis and help restore kidney function and reduce mortality. However, the use of these drugs is associated with certain side effects, primarily this concerns caution with respect to GCS. In this regard, there is a constant search for drugs that could ensure both the achievement of clinical remission of ANCA vasculitis (as the main goal of therapy) and a reduction in the dose, and, ideally, the cancellation of GCS. Based on the data obtained on the role of the alternative complement pathway in the pathogenesis of ANCA vasculitis, avacopan, C5a receptor inhibitor, was proposed for its treatment. In a clinical trial involving patients with ANCA-associated vasculitis, avacopan was non-inferior in achieving remission at week 26 and superior to the GCS therapy group in achieving sustained remission at week 52. All patients in the study also received cyclophosphamide or rituximab. Avacopan is recommended by KDIGO 2024 for inclusion in the induction phase of therapy to reduce the dose of GCS in patients with ANCA glomerulonephritis.
Description of the clinical case. The article presents a case of a patient with granulomatosis with polyangiitis (GPA), who was diagnosed at an advanced stage of the disease, with damage to vital organs and an extremely high risk of death. The severity of the patient's condition required mechanical ventilation with subsequent initiation of venovenous extracorporeal membrane oxygenation (ECMO), as well as renal replacement therapy. Therapy was initiated with a series of plasma exchange sessions, pulse therapy, followed by a transition to oral GCS. Taking into account the severity of glomerulonephritis and infectious complications, the decision of the council was to initiate therapy with avacopan, a drug unregistered in the Russian Federation (in combination with cyclophosphamide and rituximab).
Results. After 8 months from the start of pathogenetic therapy, the patient, who was constantly taking a minimum dose of GCS and avacopan, clinically demonstrated remission of GPA in relation to extrarenal manifestations and partial remission of glomerulonephritis.
Толық мәтін

Авторлар туралы
Nadiya Frolova
City Clinical Hospital No. 52, Moscow Health Department; Russian University of Medicine
Email: nadiya.frolova@yandex.ru
ORCID iD: 0000-0002-6086-5220
Cand.Sci. (Med.), Deputy Chief Physician for Nephrology, Head of the Interdistrict Nephrology Center, City Clinical Hospital No. 52 of the Moscow Healthcare Department; Associate Professor at the Nephrology Department, Faculty of Continuous Professional Education, Russian University of Medicine (RosUniMed)
Ресей, Moscow; MoscowZinaida Mutovina
City Clinical Hospital No. 52, Moscow Health Department; Central State Medical Academy
Email: zmutovina@mail.ru
ORCID iD: 0000-0001-5809-6015
Cand.Sci. (Med.), Head of the Rheumatology Department No. 1, City Clinical Hospital No. 52 of the Moscow Healthcare Department; Associate Professor of the Department of Therapy, Cardiology and Functional Diagnostics with a course in Nephrology, Central State Medical Academy of the Administrative Dicrectorate of the President of the Russian Federation
Ресей, Moscow; MoscowMargarita Kobzar
City Clinical Hospital No. 52, Moscow Health Department
Email: m.v.kobzar@yandex.ru
ORCID iD: 0009-0004-0236-653X
Analyst of the Project Office
Ресей, MoscowGeorgy Arbolishvili
City Clinical Hospital No. 52, Moscow Health Department; Lomonosov Moscow State University
Email: geodoc@yandex.ru
ORCID iD: 0000-0002-2252-3975
Deputy Chief Physician for Anesthesiology and Critical Care, City Clinical Hospital No. 52 of the Moscow Healthcare Department; Associate Professor at the Department of Anesthesiology and Critical Care, Faculty of Fundamental Medicine, Lomonosov Moscow State University
Ресей, Moscow; MoscowDenis Pavlov
City Clinical Hospital No. 52, Moscow Health Department
Email: dr.pavlov@mail.ru
ORCID iD: 0009-0000-0572-8031
Head of the ICU No. 7
Ресей, MoscowDaria Shmeleva
City Clinical Hospital No. 52, Moscow Health Department
Email: dasha068@icloud.com
ORCID iD: 0009-0001-8310-2795
Neurologist of the Rheumatology Department
Ресей, MoscowFarid Manerov
City Clinical Hospital No. 52, Moscow Health Department
Email: faridmanerov036@gmail.com
ORCID iD: 0009-0004-6478-6652
Resuscitation Physician
Ресей, MoscowMaryana Lysenko
City Clinical Hospital No. 52, Moscow Health Department; Pirogov Russian National Research Medical University named after N.I. Russian Ministry of Health
Хат алмасуға жауапты Автор.
Email: gkb52@zdrav.mos.ru
ORCID iD: 0000-0001-6010-7975
Dr.Sci. (Med.), Professor, Chief Physician of the City Clinical Hospital No. 52 of the Moscow Healthcare Department; Professor at the Department of General Therapy, Pirogov Russian National Research Medical University
Ресей, Moscow; MoscowӘдебиет тізімі
- Hutton H.L., Holdsworth S.R., Kitching A.R. ANCA-Associated Vasculitis: Pathogenesis, Models, and Preclinical Testing. Semin. Nephrol. 2017;37(5):418–35. doi: 10.1016/j.semnephrol.2017.05.016. [PMID: 28863790].
- Al-Hussain T., Hussein M.H., Conca W., et al. Pathophysiology of ANCA-associated Vasculitis. Adv. Anat. Pathol. 2017;24(4):226–34. doi: 10.1097/PAP.0000000000000154. [PMID: 28537941].
- Watts R.A., Lane S.E., Bentham G., Scott D.G. Epidemiology of systemic vasculitis: a ten-year study in the United Kingdom. Arthrit. Rheum. 2000;43(2):414–9. doi: 10.1002/1529-0131(200002)43:2<414:AID-ANR23>3.0.CO;2-0. [PMID: 10693883].
- Watts R.A., Mahr A., Mohammad A.J., et al. Classification, epidemiology and clinical subgrouping of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Nephrol. Dial. Transplant. 2015;30(Suppl. 1):i14–22. doi: 10.1093/ndt/gfv022. [PMID: 25805746].
- Jennette J.C., Falk R.J., Bacon P.A., et al. 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthrit. Rheum. 2013;65(1):1–11. doi: 10.1002/art.37715. [PMID: 23045170].
- Gapud E.J., Seo P., Antiochos B. ANCA-Associated Vasculitis Pathogenesis: A Commentary. Curr. Rheum. Rep. 2017;19(4):15. doi: 10.1007/s11926-017-0641-0. [PMID: 28361331].
- Jennette J.C., Nachman P.H. ANCA Glomerulonephritis and Vasculitis. Clin. J. Am. Soc. Nephrol. 2017;12(10):1680–91. doi: 10.2215/CJN.02500317. [Epub 2017 Aug 25, PMID: 28842398, PMCID: PMC5628710].
- Jennette J.Ch., Nachman P.H. ANCA Glomerulonephritis and Vasculitis. Clin. J. Am. Soc. Nephrol. 2017;12(10):1680–91.
- Бекетова Т.В., Фролова Н.Ф., Столяревич Е.С. и др. Проблемы диагностики и лечения АНЦА-ассоциированных системных васкулитов: в фокусе АНЦА-негативный pauci-иммунный гломерулонефрит. Научно-практическая ревматология. 2016;54(5):543–52. [Beketova T.V., Frolova N.F., Stolyarevich E.S., et al. Problems of diagnosis and treatment of ANCA-associated systemic vasculitis: the focus is ANCA-negative pauci-immune glomerulonephritis. Sci. Pract. Rheum. 2016;54(5):543–52 (In Russ.)].
- Wallace Z.S., Miloslavsky E.M. Management of ANCA associated vasculitis. BMJ. 2020;368:m421. doi: 10.1136/bmj.m421. [PMID: 32188597].
- Hellmich B., Flossmann O., Gross W.L., et al. EULAR recommendations for conducting clinical studies and/or clinical trials in systemic vasculitis: focus on anti-neutrophil cytoplasm antibody-associated vasculitis. Ann. Rheum. Dis. 2007;66(5):605–17. doi: 10.1136/ard.2006.062711. [Epub 2006 Dec 14, PMID: 17170053, PMCID: PMC2703775].
- Yates M., Watts R.A., Bajema I.M., et al. EULAR/ERA-EDTA recommendations for the management of ANCA-associated vasculitis. Ann. Rheum. Dis. 2016;75(9):1583–94. doi: 10.1136/annrheumdis-2016-209133. [PMID: 27338776].
- Jennette J.Ch., Nachman P.H. ANCA Glomerulonephritis and Vasculitis. Clin. J. Am. Soc. Nephrol. 2017;12(10):1680–91. doi: 10.2215/CJN.02500317.
- Лысенко М.А., Фролова Н.Ф., Кецкало М.В. и др. Экстракорпоральная мембранная оксигенация при жизнеугрожающем ANCA-позитивном диффузном некротизирующем геморрагическом альвеолите. Клин. Нефрология. 2018;3. Doi: https://dx.doi.org/10.18565/nephrology.2018.3.57-62. [Lysenko M.A., Frolova N.F., Ketskalo M.V., et al. ECMO in life-threatening ANCA-positive diffuse necrotizing hemorrhagic alveolitis. Clin. Nephrol. 2018;3 (In Russ.)].
- Kronbichler A., Lee K.H., Denicolò S., et al. Immunopathogenesis of ANCA-Associated Vasculitis. Int. J. Mol. Sci. 2020;21(19):7319. doi: 10.3390/ijms21197319. [PMID: 33023023, PMCID: PMC7584042].
- Xiao H., Schreiber A., Heeringa P., et al. Alternative complement pathway in the pathogenesis of disease mediated by anti-neutrophil cytoplasmic autoantibodies. Am. J. Pathol. 2007;170:52–64.
- Hutton H.L., Holdsworth S.R., Kitching A.R. ANCA-Associated Vasculitis: Pathogenesis, Models, and Preclinical Testing. Semin. Nephrol. 2017;37(5):418–35. doi: 10.1016/j.semnephrol.2017.05.016. [PMID: 28863790].
- Jennette J.Ch., Nachman P.H. ANCA Glomerulonephritis and Vasculitis. Clin J. Am. Soc. Nephrol. 2017;12(10):1680–91. doi: 10.2215/CJN.02500317.
- Huugen D., van Esch A., Xiao H., еt al. Inhibition of complement factor C5 protects against anti-myeloperoxidase antibody-mediated glomerulonephritis in mice. Kidney Int. 2007;71:646–54.
- Chen M., Jayne D.R., Zhao M.H. Complement in ANCA-associated vasculitis: mechanisms and implications for management. Nat. Rev. Nephrol. 2017;13:359–67.
- Quintana L.F., Kronbichler A., Blasco M., et al. ANCA associated vasculitis: The journey to complement-targeting therapies. Mol. Immunol. 2019;112:394–8. https://doi. org/10.1016/j.molimm.2019.06.018.
- Xiao H, Dairaghi D.J., Powers J.P., et al. C5a receptor (CD88) blockade protects against MPO-ANCA GN. J. Am. Soc. Nephrol. 2014;25(2):225–31. doi: 10.1681/ASN.2013020143. [Epub 2013 Oct 31, PMID: 24179165, PMCID: PMC3904560].
- Bekker P., Dairaghi D., Seitz L., et al. Characterization of Pharmacologic and Pharmacokinetic Properties of CCX168, a Potent and Selective Orally Administered Complement 5a Receptor Inhibitor, Based on Preclinical Evaluation and Randomized Phase 1 Clinical Study. PLoS One. 2016;11(10):e0164646. doi: 10.1371/journal.pone.0164646. Erratum in: PLoS One. 2019;14(1):e0210593. [PMID: 27768695, PMCID: PMC5074546].
- Alihosseini C., Kopelman H., Zaino M., Feldman S.R. Avacopan for the Treatment of Anti-Neutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis. Ann. Pharmacother. 2023;57(12):1449–54. doi: 10.1177/10600280231161592. [Epub 2023 Mar 28, PMID: 36975183].
- Brilland B., Garnier A.S., Chevailler A., et al. Complement alternative pathway in ANCA-associated vasculitis: Two decades from bench to bedside. Autoimmun. Rev. 2020;19(1):102424. doi: 10.1016/j.autrev.2019.102424. [Epub 2019 Nov 15, PMID: 31734405].
- Vifor. Tavneos 10 mg hard capsules (Avacopan). Summary of product characteristics. 2022. https://www.ema.europa.eu/en/documents/product-information/tavneos-epar-product-information_en.pdf.
- Jayne D.R.W., Bruchfeld A.N., Harper L., et al. CLEAR Study Group. Randomized Trial of C5a Receptor Inhibitor Avacopan in ANCA-Associated Vasculitis. J. Am. Soc. Nephrol. 2017;28(9):2756–67. doi: 10.1681/ASN.2016111179. [Epub 2017 Apr 11, PMID: 28400446, PMCID: PMC5576933].
- Merkel P.A., Niles J., Jimenez R., et al. CLASSIC Investigators. Adjunctive Treatment With Avacopan, an Oral C5a Receptor Inhibitor, in Patients With Antineutrophil Cytoplasmic Antibody-Associated Vasculitis. ACR. Open Rheumatol. 2020;2(11):662–71. doi: 10.1002/acr2.11185. [Epub 2020 Oct 31, PMID: 33128347, PMCID: PMC7672305].
- Jayne D.R.W., Merkel P.A., Schall T.J., Bekker P. ADVOCATE Study Group. Avacopan for the Treatment of ANCA-Associated Vasculitis. N. Engl. J. Med. 2021;384(7):599–609. doi: 10.1056/NEJMoa2023386. Erratum in: N. Engl. J. Med. 2024;390(4):388. [PMID: 33596356].
- Geetha D., Dua A., Yue H., et al. ADVOCATE Study Group. Efficacy and safety of avacopan in patients with ANCA-associated vasculitis receiving rituximab in a randomised trial. Ann. Rheum. Dis. 2024;83(2):223– 32. doi: 10.1136/ard-2023-224816. [PMID: 37979959, PMCID: PMC10850685].
- https://www.fda.gov/drugs/news-events-human-drugs/fda-approves-add-drug-adults-rare-form-blood-vessel-inflammation.
- https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu-3-14-1372.
- KDIGO ANCA Vasculitis Work Group. KDIGO 2024 Clinical Practice Guideline for the Management of Antineutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis. Kidney Int. 2024;105(3S):S71–116. Доступно по ссылке: https://kdigo.org/wp-content/uploads/2024/02/ KDIGO-2024-ANCA-Vasculitis-Guideline.pdf. Accessed February 2024.
- Zonozi R., Aqeel F., Le D., et al. Real-World Experience With Avacopan in Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis. Kidney Int. Rep. 2024;9(6):1783–91. doi: 10.1016/j.ekir.2024.03.022.
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