Evidence map›Paper›PMID 32601673›Full record

ArticleNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association2021

PR3-ANCAs predict relapses in ANCA-associated vasculitis patients after rituximab.

Laura S van Dam, Ebru Dirikgil, Edwin W Bredewold, Argho Ray, Jaap A Bakker, Cees van Kooten, Ton J Rabelink, Yoe K Onno Teng

Open access · greenAbstract read
In one paragraph

Article in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 4% of its field
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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

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  17. New Biomarkers for Systemic Necrotizing Vasculitides.Journal of clinical medicine · 2024
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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

8 authors at 1 institution in 1 country.

Laura S van DamCentre of Expertise for Lupus-, Vasculitis-, and Complement-Mediated Systemic Autoimmune Diseases Leiden, The Netherlands, Department of Internal Medicine, Section of Nephrology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0001-6373-7673
Ebru DirikgilCentre of Expertise for Lupus-, Vasculitis-, and Complement-Mediated Systemic Autoimmune Diseases Leiden, The Netherlands, Department of Internal Medicine, Section of Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
Edwin W BredewoldCentre of Expertise for Lupus-, Vasculitis-, and Complement-Mediated Systemic Autoimmune Diseases Leiden, The Netherlands, Department of Internal Medicine, Section of Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
Argho RayCentre of Expertise for Lupus-, Vasculitis-, and Complement-Mediated Systemic Autoimmune Diseases Leiden, The Netherlands, Department of Internal Medicine, Section of Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
Jaap A BakkerDepartment of Clinical Chemistry and Laboratory Medicine, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0002-2918-7361
Cees van KootenCentre of Expertise for Lupus-, Vasculitis-, and Complement-Mediated Systemic Autoimmune Diseases Leiden, The Netherlands, Department of Internal Medicine, Section of Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
Ton J RabelinkCentre of Expertise for Lupus-, Vasculitis-, and Complement-Mediated Systemic Autoimmune Diseases Leiden, The Netherlands, Department of Internal Medicine, Section of Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
Yoe K Onno TengCentre of Expertise for Lupus-, Vasculitis-, and Complement-Mediated Systemic Autoimmune Diseases Leiden, The Netherlands, Department of Internal Medicine, Section of Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe primary challenge of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) patient care is the early detection of relapses to prevent organ damage and increase survival. Potential biomarkers for relapses are ANCA and B cells, but their predictive value is a matter of debate. Therefore this study investigated how ANCA and B-cell status related to relapses in AAV patients treated with rituximab (RTX) as remission induction (RI).

methodsThis single-centre cohort study identified 110 ANCA-positive AAV patients treated with RTX between 2006 and 2018. Serial ANCA, CD19+ B-cell status and relapses were assessed >2 years.

resultsPatients (31/110) relapsed within 2 years after RTX RI treatment. Patients who achieved and maintained PR3-ANCA negativity (n = 29) had few relapses (3%), while persistent proteinase 3 (PR3)-ANCA positivity (n = 49) and reappearance of PR3-ANCAs (n = 10) associated significantly with more relapses (37%, P = 0.002 and 50%, P = 0.002). Patients with incomplete B-cell depletion (n = 11) had significantly more relapses (54%) as compared with patients with B-cell depletion [n = 76 (26%), P = 0.02]. Also, patients with repopulation of B cells (n = 58) had significantly more relapses (41%) as compared with patients without B-cell repopulation [n = 27 (15%), P = 0.03]. Overall, the absence of PR3- or myeloperoxidase (MPO)-ANCA positivity was highly predictive for remaining relapse-free. In PR3-ANCA-positive patients, 96% of the relapses occurred with persistent or reappearance of PR3-ANCAs and 81% with B-cell repopulation. In MPO-ANCA-positive patients, all relapses were restricted to patients with persistent MPO-ANCAs and B-cell repopulation.

conclusionsUpon RI treatment with RTX in AAV patients, ANCA and B-cell status were predictive of the majority of relapses and specifically their absence strongly predicted a relapse-free status. Therefore the implementation of ANCA and B-cell monitoring could guide therapeutic decision-making to prevent relapses in AAV patients treated with RTX.

Indexed as

Antibodies, Antineutrophil CytoplasmicAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisCohort StudiesHumansMyeloblastinPeroxidaseRecurrenceRituximabAntibodies, Antineutrophil CytoplasmicMyeloblastinPeroxidaseRituximabANCAbiomarkerscrescentic glomerulonephritisimmunomonitoringrituximabvasculitis

Identifiers

PMID32601673
PMCPMC8311572
OpenAlexW3040421122

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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.