Evidence map›Paper›PMID 41895800›Full record

ArticleRMD open2026

Complete PET/CT extinction and subsequent risk of aortic dilation in patients with giant cell arteritis-related large vessel vasculitis treated with tocilizumab.

Anaël Dumont, Olivier Espitia, Maxime Samson, Chloé Comarmond-Ortoli, Laurent Sailler, Emilie Berthoux, Jean-François Alexandra, Marie Morard, Sophie Gallou, Rémi Philip and 8 more

Abstract readMulticenter Study
In one paragraph

Article in RMD open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Anaël DumontDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France dumont-an@chu-caen.fr.ORCID 0000-0003-1105-7662
Olivier EspitiaNantes Université, CHU Nantes, CNRS UMR 6291, INSERM UMR 1087, l'institut du thorax Team III Vascular and Pulmonary Diseases, Nantes, France.ORCID 0000-0003-0821-9990
Maxime SamsonDepartment of Internal Medicine and Clinical Immunology, Referral Center for Rare Systemic Autoimmune and Autoinflammatory Diseases, Dijon-Bourgogne University Hospital, University EPE Bourgogne Europe, Dijon, France.
Chloé Comarmond-OrtoliDepartment of Internal Medicine, Département Médico-Universitaire INVICTUS, Lariboisière Hospital, Assistance Publique-Hôpitaux de Paris (APHP), Nord-Université Paris Cité, Paris, France.ORCID 0009-0000-0272-4633
Laurent SaillerDepartment of Internal Medicine, Toulouse University Hospital, Toulouse, France.
Emilie BerthouxDepartment of Internal Medicine, Saint-Joseph and Saint-Luc Hospital, Lyon, France.
Jean-François AlexandraDepartment of Internal Medicine, Hôpital Bichat, Université Paris Cité, Assistance Publique Hôpitaux de Paris, Paris, France.
Marie MorardNantes Université, CHU Nantes, CNRS UMR 6291, INSERM UMR 1087, l'institut du thorax Team III Vascular and Pulmonary Diseases, Nantes, France.ORCID 0009-0003-2842-6695
Sophie GallouDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
Rémi PhilipDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
Nicolas Martin-SilvaDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
Gwénola MaignéDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
Jonathan BoutemyDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
Claire DelacotteDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
Samuel DeshayesDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
Achille AoubaDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
Hubert de BoyssonDepartment of Internal Medicine, Caen University Hospital, Avenue de la Côte de Nacre, Caen, France.
French Study Group for Large Vessel Vasculitis (GEFA)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe proportion of patients with giant cell arteritis (GCA)-related large vessel vasculitis (LVV) treated with tocilizumab (TCZ) who achieve a complete metabolic response on repeated 18 F-fluorodeoxyglucose positron emission tomography (

methodsWe conducted a retrospective multicentre study that enrolled patients with GCA-related LVV demonstrated on PET/CT, who were treated with TCZ and underwent at least one repeated PET/CT. The primary endpoint was the proportion of patients with vascular extinction on repeated PET/CT during or after TCZ treatment (grade 0 or 1 on the visual vascular to liver FDG uptake grading scale).

resultsA total of 91 patients (64 women (70%), median age: 69 (54-83) years) were included. Clinical remission and a complete metabolic response on PET/CT were observed in 69 patients (76%). Among these, 30 had discontinued all GCA treatments and had not relapsed after >12 months of follow-up post negative PET/CT; the remaining 39 patients were still treated or had <12 months of follow-up after the negative PET/CT.13 (14%) patients experienced a relapse of LVV on a third PET/CT within 12 months after TCZ discontinuation. During follow-up, an aortic dilation occurred in one (1%) patient with complete metabolic extinction and in four (18%) patients who did not show complete and persisting PET/CT extinction (p=0.006 by log-rank test).

conclusionThis study suggests that TCZ is an interesting therapeutic option for achieving complete metabolic response on PET/CT in patients with GCA-related LVV. The subsequent risk of aortic dilation may be reduced.

Indexed as

Antibodies, Monoclonal, HumanizedAortaGiant Cell ArteritisPositron Emission Tomography Computed TomographyAgedAged, 80 and overDilatation, PathologicFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedFluorodeoxyglucose F18tocilizumabGiant Cell ArteritisTreatmentVasculitis

Identifiers

PMID41895800
PMCPMC13034310

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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.