Evidence map›Paper›PMID 39718586›Full record

ArticleRheumatology international2024

Remission induction therapies and long-term outcomes in granulomatosis with polyangiitis and microscopic polyangiitis: real-world data from a European cohort.

Stefan Krämer, Kristian Vogt, Theresa Maria Schreibing, Martin Busch, Tobias Schmitt, Raoul Bergner, Sebastian Mosberger, Thomas Neumann, Thomas Rauen

Abstract readMulticenter Study
In one paragraph

Article in Rheumatology international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
  4. Review
  5. Observational
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Stefan KrämerDepartment of Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany.ORCID 0009-0004-9485-0969
Kristian VogtDepartment of Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany.ORCID 0009-0001-0137-4464
Theresa Maria SchreibingDepartment of Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany.ORCID 0000-0003-0593-5123
Martin BuschDepartment of Internal Medicine III, University Hospital Jena, Friedrich-Schiller University, Jena, Germany.ORCID 0000-0002-7889-6156
Tobias SchmittDepartment of Internal Medicine III, University Hospital Jena, Friedrich-Schiller University, Jena, Germany.
Raoul BergnerDepartment of Internal Medicine A, Nephrology and Rheumatology, Municipal Hospital Ludwigshafen, Ludwigshafen, Germany.ORCID 0000-0002-7965-1273
Sebastian MosbergerDepartment of Internal Medicine A, Nephrology and Rheumatology, Municipal Hospital Ludwigshafen, Ludwigshafen, Germany.ORCID 0009-0001-1152-9925
Thomas Neumann *Department of Rheumatology and Immunology, Cantonal Hospital St. Gallen, St. Gallen, Switzerland.ORCID 0000-0003-3755-9038
Thomas Rauen *Department of Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074, Aachen, Germany. trauen@ukaachen.de.ORCID 0000-0002-6544-8901

Funding

Vifor Pharma IIS-NA2021-0615
6 · The paper itself

Abstract

To explore disease characteristics, renal involvement and induction treatment strategies over the last decades and evaluate relapse rates and renal outcomes in ANCA-associated vasculitides (AAV). We retrospectively analyzed remission, relapse rates and the occurrence of the composite endpoint (comprising death and renal failure) in newly diagnosed AAV cases in four tertial referral centers in Germany and Switzerland diagnosed between 1999 and 2022. Hazard ratios were computed by Cox proportional hazard and Kaplan-Meier curves were plotted to compare therapeutic strategies after propensity-matching. In our cohort of 358 AAV patients, 203 (58.1%) were classified as granulomatosis with polyangiitis (GPA) based on the novel 2022 ACR/EULAR criteria, 139 (38.8%) as microscopic polyangiitis (MPA). The proportion of MPA cases among all AAV patients increased from 28.9% between 1999 and 2013 up to 46.7% thereafter. Cyclophosphamide (CYC) was chosen most frequently for remission induction (74.8% before 2013 and 57.3% thereafter), whereas the use of rituximab (RTX) increased from 5 to 26% within these periods. GPA patients had a higher relapse rate as compared to MPA patients (41.3% vs. 25.9%, p = 0.006). However, in AAV patients with renal involvement, renal events (i.e. end-stage kidney disease or a persistent drop in the estimated glomerular filtration rate (eGFR) below 15 ml/min/1.73 m

Indexed as

CyclophosphamideGranulomatosis with PolyangiitisImmunosuppressive AgentsMicroscopic PolyangiitisRecurrenceRemission InductionRituximabAdultAgedFemaleGermanyHumansMaleMiddle AgedRetrospective StudiesSwitzerlandCyclophosphamideImmunosuppressive AgentsRituximabAAVANCACyclophosphamideGPAMPARelapseRenal outcomeRituximabVasculitis

Identifiers

PMID39718586
PMCPMC11668861

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Registered trials

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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.