Evidence map›Paper›PMID 42185210›Full record

ArticleRheumatology (Oxford, England)2026

Incorporating frailty and disease severity into treatment decisions for older patients with ANCA-associated vasculitis.

Mark E McClure, Ayonija Sundararajan, Karl Emil Nelveg-Kristensen, Maya Leibowitz, Matthew L Coates, Dominic McGovern, Michael Chen-Xu, Iftach Sagy, Karol Granak, Tom Quarrell and 7 more

Abstract read
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Article in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Mark E McClureVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
Ayonija SundararajanVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
Karl Emil Nelveg-KristensenDepartment of Nephrology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Maya LeibowitzDepartment of Medicine, University of Cambridge, Cambridge, UK.
Matthew L CoatesVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
Dominic McGovernVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.ORCID 0000-0003-3127-2052
Michael Chen-XuVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
Iftach SagyVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
Karol GranakVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
Tom QuarrellDepartment of Medicine, University of Cambridge, Cambridge, UK.
Shreehari SureshDepartment of Medicine, University of Cambridge, Cambridge, UK.
Martha WatsonDepartment of Medicine, University of Cambridge, Cambridge, UK.
Andreas KronbichlerVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.ORCID 0000-0002-2945-2946
Lisa WillcocksVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
Rona SmithVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.
David R W JayneVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.ORCID 0000-0002-1712-0637
Rachel B JonesVasculitis and Lupus Clinic, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveOlder patients with anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) are underrepresented in clinical trials, and long-term outcome data in this group are limited. We evaluated treatment approaches and outcomes among hospitalized older patients with AAV.

methodsWe retrospectively collected clinical and laboratory data on all hospitalized patients aged 75 years or older who commenced remission induction with cyclophosphamide- or rituximab-based regimens for severe AAV between 2014 and 2021.

resultsEighty-four patients were included (median age 79, range 75-93), with a median follow-up of 21 months (interquartile range 12-44). Choice of induction regimen was influenced by age and frailty: the rituximab-cyclophosphamide combination was more commonly used in younger patients within the cohort, while low-dose rituximab was favoured for the oldest and most frail, including those requiring residential or nursing home care. The distribution of regimens was as follows: rituximab-cyclophosphamide combination (11.9%), cyclophosphamide (26.2%), standard-dose rituximab (39.6%) and low-dose rituximab (22.3%). Serious infection requiring hospital readmission occurred in 27% of patients within the first year, with rates of 37.5%, 23.8%, 25.8% and 31.6% across the respective treatment groups. One-year mortality was 20% overall (by treatment group: 10%, 23%, 14% and 26%). Increasing age was associated with higher mortality (hazard ratio [HR] 4.15; 95% CI: 1.62, 10.6), but not with serious infection (HR 1.18; 95% CI: 0.47, 2.93).

conclusionConsidering the enrichment for hospitalized patients with severe disease and advanced age, a mortality rate of 20% at 1 year that is comparable to less severe and younger cohorts suggests tailoring remission induction strategy according to a holistic assessment of frailty and disease activity may partially mitigate the higher risk of infection and mortality with advancing age.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisClinical Decision-MakingCyclophosphamideFrailtyImmunosuppressive AgentsRituximabAgedAged, 80 and overAge FactorsDrug Therapy, CombinationFemaleFrail ElderlyHumansMaleRemission InductionRetrospective StudiesCyclophosphamideImmunosuppressive AgentsRituximabANCA-associated vasculitiscomorbiditycyclophosphamideelderlyfrailtyglucocorticoidsinfectionmortalityremission inductionrituximab

Identifiers

PMID42185210
PMCPMC13290483

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.