The Risk of Severe Infections Following Rituximab Administration in Patients With Autoimmune Kidney Diseases: Austrian ABCDE Registry Analysis.
Authors
Odler, Balazs
Windpessl, Martin
Krall, Marcell
Steiner, Maria
Riedl, Regina
Hebesberger, Carina
Ursli, Martin
Zitt, Emanuel
Lhotta, Karl
Antlanger, Marlies
Cejka, Daniel
Gauckler, Philipp
Wiesholzer, Martin
Saemann, Marcus
Rosenkranz, Alexander R
Eller, Kathrin
Publication Date
2021Journal Title
Front Immunol
ISSN
1664-3224
Publisher
Frontiers Media SA
Volume
12
Language
en
Type
Article
This Version
VoR
Metadata
Show full item recordCitation
Odler, B., Windpessl, M., Krall, M., Steiner, M., Riedl, R., Hebesberger, C., Ursli, M., et al. (2021). The Risk of Severe Infections Following Rituximab Administration in Patients With Autoimmune Kidney Diseases: Austrian ABCDE Registry Analysis.. Front Immunol, 12 https://doi.org/10.3389/fimmu.2021.760708
Abstract
OBJECTIVE: To characterize the incidence, type, and risk factors of severe infections (SI) in patients with autoimmune kidney diseases treated with rituximab (RTX). METHODS: We conducted a multicenter retrospective cohort study of adult patients with immune-related kidney diseases treated with at least one course of RTX between 2015 and 2019. As a part of the ABCDE Registry, detailed data on RTX application and SI were collected. SI were defined by Common Terminology Criteria for Adverse Events v5.0 as infectious complications grade 3 and above. Patients were dichotomized between "nephrotic" and "nephritic" indications. The primary outcome was the incidence of SI within 12 months after the first RTX application. RESULTS: A total of 144 patients were included. Twenty-five patients (17.4%) presented with SI, mostly within the first 3 months after RTX administration. Most patients in the nephritic group had ANCA-associated vasculitis, while membranous nephropathy was the leading entity in the nephrotic group. Respiratory infections were the leading SI (n= 10, 40%), followed by urinary tract (n=3, 12%) and gastrointestinal infections (n=2, 8%). On multivariable analysis, body mass index (BMI, 24.6 kg/m2versus 26.9 kg/m2, HR: 0.88; 95%CI: 0.79-0.99; p=0.039) and baseline creatinine (HR: 1.25; 95%CI: 1.04-1.49; p=0.017) were significantly associated with SI. All patients in the nephritic group (n=19; 100%) who experienced a SI received oral glucocorticoid (GC) treatment at the time of infection. Hypogammaglobulinemia was frequent (58.5%) but not associated with SI. CONCLUSIONS: After RTX administration, impaired kidney function and lower BMI are independent risk factors for SI. Patients with nephritic glomerular diseases having concomitant GC treatment might be at higher risk of developing SI.
Keywords
glomerular disease, infections, lupus, nephritic, nephrotic, rituximab, vasculitis, Adult, Aged, Aged, 80 and over, Austria, Autoimmune Diseases, Body Mass Index, Female, Humans, Immunologic Factors, Incidence, Infections, Kaplan-Meier Estimate, Kidney Diseases, Male, Middle Aged, Proportional Hazards Models, Registries, Retrospective Studies, Risk Factors, Rituximab, Young Adult
Identifiers
External DOI: https://doi.org/10.3389/fimmu.2021.760708
This record's URL: https://www.repository.cam.ac.uk/handle/1810/330767
Rights
Licence:
http://creativecommons.org/licenses/by/4.0/
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