18F-FDG PET-CT in rheumatoid arthritis patients tapering TNFi: reliability, validity and predictive value.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
18 04 2022
Historique:
received: 08 09 2021
accepted: 03 11 2021
pubmed: 19 11 2021
medline: 21 4 2022
entrez: 18 11 2021
Statut: ppublish

Résumé

To investigate the reliability and validity of fluorine-18 fluorodeoxyglucose (18F-FDG) PET-CT scanning (FDG-PET) in RA patients with low disease activity tapering TNF inhibitors (TNFis) and its predictive value for successful tapering or discontinuation. Patients in the tapering arm of the Dose REduction Strategies of Subcutaneous TNFi study, a randomized controlled trial of TNFi tapering in RA, underwent FDG-PET before tapering (baseline) and after maximal tapering. A total of 48 joints per scan were scored both visually [FDG-avid joint (FAJ), yes/no] and quantitatively [maximal and mean standardized uptake values (SUVmax and SUVmean)]. Interobserver agreement was calculated in 10 patients at baseline. Quantitative and visual FDG-PET scores were investigated for (multilevel) association with clinical parameters both on a joint and patient level and for the predictive value at baseline and the change between baseline and maximal tapering (Δ) for successful tapering and discontinuation at 18 months. A total of 79 patients underwent FDG-PET. For performance of identification of FAJs on PET, Cohen's κ was 0.49 (range 0.35-0.63). For SUVmax and SUVmean, intraclass correlation coefficients were 0.80 (range 0.77-0.83) and 0.96 (0.9-1.0), respectively. On a joint level, swelling was significantly associated with SUVmax and SUVmean [B coefficients 1.0 (95% CI 0.73, 1.35) and 0.2 (0.08, 0.32), respectively]. On a patient level, only correlation with acute phase reactants was found. FDG-PET scores were not predictive of successful tapering or discontinuation. Quantitative FDG-PET arthritis scoring in RA patients with low disease activity is reliable and has some construct validity. However, no predictive values were found for FDG-PET parameters for successful tapering and/or discontinuation of TNFi.

Identifiants

pubmed: 34791068
pii: 6427647
doi: 10.1093/rheumatology/keab842
doi:

Substances chimiques

Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

SI6-SI13

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Chantal A M Bouman (CAM)

Department of Rheumatology, Rijnstate Hospital, Arnhem.
Department of Rheumatology, Sint Maartenskliniek.

Noortje van Herwaarden (N)

Department of Rheumatology, Sint Maartenskliniek.
Department of Farmacology-Toxicology, Radboudumc, Nijmegen.

Annelies B Blanken (AB)

Department of Rheumatology, Amsterdam UMC-Location VU Medical Center.
Department of Rheumatology, Reade, Amsterdam.

Conny J Van der Laken (CJ)

Department of Rheumatology, Amsterdam UMC-Location VU Medical Center.

Martin Gotthardt (M)

Department of Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

Wim J G Oyen (WJG)

Department of Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.
Department of Nuclear Medicine, Humanitas University and Clinical and Research Center, Milan, Italy.
Department of Nuclear Medicine, Rijnstate Hospital, Arnhem.

Alfons A den Broeder (AA)

Department of Rheumatology, Sint Maartenskliniek.
Department of Rheumatology, Radboudumc, Nijmegen, The Netherlands.

Aatke van der Maas (A)

Department of Rheumatology, Sint Maartenskliniek.

Cornelia H van den Ende (CH)

Department of Rheumatology, Sint Maartenskliniek.
Department of Rheumatology, Radboudumc, Nijmegen, The Netherlands.

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