Immune checkpoint inhibitors-associated vasculitis: a heterogeneous condition with possible severe disease course

Rheumatology (Oxford). 2024 Dec 23:keae711. doi: 10.1093/rheumatology/keae711. Online ahead of print.

Abstract

Objective: To describe presentation, treatment and outcome of immune checkpoint inhibitor (ICI) associated-vasculitis in cancer patients in a multicentre study.

Methods: Thanks to the ImmunoCancer International Registry (ICIR), a multidisciplinary network focused on the research of the immune related adverse events related to cancer immunotherapies, patients presenting with a clinical and/or radiological suspicion of vasculitis, and histological evidence of vasculitis after being exposed to ICIs were retrospectively identified.

Results: Twenty eight cases were identified in the ICIR registry. The median interval between starting ICI treatment and vasculitis diagnosis was 4 months. Small vessel vasculitis were predominant (n = 21), followed by large vessel (n = 4) and medium vessel (n = 3). The small vessel vasculitis included 10 unclassified vasculitis either with limited cutaneous involvement (n = 6) or systemic involvement (n = 4), 5 IgA vasculitis, 3 cryoglobulinemic vasculitis, and 3 ANCA+ vasculitis. At presentation or during the evolution, renal and neurologic manifestations were evidenced in 7 cases each (25%). Renal biopsies documented immune glomerulopathies in 6 cases. Only seven patients (25%) fulfilled the 2022 ACR/EULAR classification criteria (4 giant cell arteritis, 2 EGPA, and one GPA). Most patients (90%) required systemic corticosteroid and an additional drug was given in 10 patients (36%). Vasculitis outcome was good: 22 patients had vasculitis complete response, no patient died due to vasculitis. Nine patients (32%) were rechallenged with immunotherapy with only one relapse.

Conclusion: ICI-associated vasculitis are rare, heterogeneous, but can be severe requiring urgent multidisciplinary management with aggressive treatment.

Keywords: Aortitis; Cancer immunotherapy; Glomerulonephritis; Immune check-point inhibitor; Immune-related adverse events; Large vessels vasculitis; Purpura; Small vessels vasculitis; Vasculitis.