# Avacopan for severe pulmonary hemorrhage requiring extracorporeal membrane oxygenation in a patient with MPO-ANCA positive vasculitis

**Authors:** Keita Endo, Koichi Hayashi, Yuki Hara, Akihiro Miyake, Keisuke Takano, Kaede Yoshino, Koichi Kitamura, Shinsuke Ito, Shigeki Fujitani, Toshihiko Suzuki

PMC · DOI: 10.1007/s13730-025-01068-0 · CEN Case Reports · 2026-02-03

## TL;DR

Avacopan, a drug that blocks C5a, helped a patient with severe lung bleeding from vasculitis recover and allowed early reduction of steroid use.

## Contribution

This case demonstrates avacopan's potential to manage severe pulmonary vasculitis and enable early steroid withdrawal.

## Key findings

- Avacopan use led to remission in a patient with severe pulmonary hemorrhage from MPO-ANCA vasculitis.
- Glucocorticoid withdrawal was safely achieved within six months of avacopan initiation.
- The beneficial effect of avacopan was sustained for at least six months post-steroid discontinuation.

## Abstract

Myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA)-positive vasculitis frequently affects the kidney and the lung, with alveolar hemorrhage being fatal. Whereas aggressive immunosuppressive therapies are conventionally used, recent studies have shown the beneficial effect of avacopan, a C5a antagonist, as an alternative to glucocorticoids for ANCA-associated vasculitis (AAV). In patients with pulmonary hemorrhage and severe respiratory failure, however, neither the efficacy of avacopan nor the contribution of this drug to early withdrawal of glucocorticoids is fully qualified. Here, we report a case of AAV presenting with alveolar hemorrhage requiring aggressive ventilatory support in which we experienced the favorable effect of early use of avacopan. A 31-year-old man was referred to our hospital because of a two-week history of blood sputum and positive MPO-ANCA. His respiratory failure deteriorated rapidly, necessitating both mechanical ventilation and extracorporeal membrane oxygenation. A combination therapy with glucocorticoids and rituximab was initiated and avacopan was started on hospital day 8, which resulted in successful remission within six months of admission (Birmingham Vasculitis Activity Score version 3 = 0), and the beneficial effect was sustained for at least 6 months following the discontinuation of glucocorticoid withdrawal (day 156). Thus, avacopan, in combination with immunosuppressives, may not only help suppress the disease activity of AAV but also facilitate early withdrawal of glucocorticoids even in case of life-threatening respiratory failure.

## Linked entities

- **Proteins:** MPO (myeloperoxidase), C5 (complement C5)
- **Chemicals:** avacopan (PubChem CID 49841217)
- **Diseases:** ANCA-associated vasculitis (MONDO:0012105)

## Full-text entities

- **Genes:** PRTN3 (proteinase 3) [NCBI Gene 5657] {aka ACPA, AGP7, C-ANCA, CANCA, MBN, MBT}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, MPO (myeloperoxidase) [NCBI Gene 4353], HLA-G (major histocompatibility complex, class I, G) [NCBI Gene 3135] {aka MHC-G}, C5AR1 (complement C5a receptor 1) [NCBI Gene 728] {aka C5A, C5AR, C5R1, CD88}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}
- **Diseases:** Vasculitis (MESH:D014657), lung infiltrates (MESH:D008171), common cold (MESH:D003139), pulmonary involvement (MESH:C566343), glomerulonephritis (MESH:D005921), kidney disease (MESH:D007674), inflammation (MESH:D007249), bone marrow suppression (MESH:D001855), MPA (MESH:D055953), allergies (MESH:D004342), mesangial proliferation (MESH:C537346), hemoptysis (MESH:D006469), hematuria (MESH:D006417), arteritis (MESH:D001167), death (MESH:D003643), uveitis (MESH:D014605), Hypoxemia (MESH:D000860), involvement (MESH:C564676), edema (MESH:D004487), alveolar (MESH:D002282), atopic dermatitis (MESH:D003876), toxicity (MESH:D064420), atrophy (MESH:D001284), heart murmur (MESH:D006337), alveolar hemorrhage (MESH:D006470), fatigue (MESH:D005221), proteinuria (MESH:D011507), joint pain (MESH:D018771), respiratory failure (MESH:D012131), fibrosis (MESH:D005355), anemia (MESH:D000740), interstitial pneumonia (MESH:D017563), pulmonary infiltrate (MESH:D017254), renal and pulmonary lesions (MESH:C538458), tenderness (MESH:D063806), hypertension (MESH:D006973), AAV (MESH:D056648), glomerular segmental necrosis (MESH:D005923), skin rash (MESH:D005076), acute kidney injury (MESH:D058186), sclerosis (MESH:D012598), MPO-ANCA positive (MESH:C562864), infection (MESH:D007239)
- **Chemicals:** triglyceride (MESH:D014280), Avacopan (MESH:C000620232), TG (MESH:D013866), steroid (MESH:D013256), oxygen (MESH:D010100), Rituximab (MESH:D000069283), Cr (MESH:D002857), urea nitrogen (MESH:C530477), creatinine (MESH:D003404), cyclophosphamide (MESH:D003520), Prednisolone (MESH:D011239), methylprednisolone (MESH:D008775)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12864564