Effectiveness of a two-year tapered course of tocilizumab in patients with giant cell arteritis: A single-centre prospective study.


Journal

Seminars in arthritis and rheumatism
ISSN: 1532-866X
Titre abrégé: Semin Arthritis Rheum
Pays: United States
ID NLM: 1306053

Informations de publication

Date de publication:
04 2023
Historique:
received: 13 11 2022
revised: 01 02 2023
accepted: 06 02 2023
pmc-release: 01 04 2024
pubmed: 13 2 2023
medline: 4 3 2023
entrez: 12 2 2023
Statut: ppublish

Résumé

To evaluate the feasibility of tocilizumab tapering and withdrawal in patients with giant cell arteritis (GCA). GCA patients eligible for tocilizumab were prospectively enrolled. Tocilizumab was administered weekly for the first 12 months, every-other-week for an additional 12 months, then discontinued. Relapses on tocilizumab were managed with temporary increases in systemic glucocorticoids or addition of methotrexate. Primary outcome was relapse-free survival at month 6 after tocilizumab suspension. Relapse-free survival on tocilizumab, imaging response, and adverse events were evaluated. 23 GCA patients were enrolled. Reasons for tocilizumab start were relapse (n = 14), persistence of activity (n = 5), or steroid-related adverse events (n = 4). At tocilizumab start, two patients were on methotrexate, which was maintained. Fourteen patients had extracranial vascular involvement on Tocilizumab tapered over a two-year period was effective to induce and maintain remission in GCA. Relapses on tocilizumab were minor and responded to incremental changes in therapy. A significant proportion of patients relapsed in the 6 months after therapy suspension.

Identifiants

pubmed: 36774660
pii: S0049-0172(23)00014-8
doi: 10.1016/j.semarthrit.2023.152174
pmc: PMC9992325
mid: NIHMS1873790
pii:
doi:

Substances chimiques

tocilizumab I031V2H011
Methotrexate YL5FZ2Y5U1
Fluorodeoxyglucose F18 0Z5B2CJX4D
Glucocorticoids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

152174

Subventions

Organisme : Intramural NIH HHS
ID : Z99 AR999999
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

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Auteurs

Alessandro Tomelleri (A)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele Hospital, Via Olgettina 60, Milan 20132, Italy; Vita-Salute San Raffaele University, Milan, Italy. Electronic address: tomelleri.alessandro@hsr.it.

Corrado Campochiaro (C)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele Hospital, Via Olgettina 60, Milan 20132, Italy; Vita-Salute San Raffaele University, Milan, Italy.

Nicola Farina (N)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele Hospital, Via Olgettina 60, Milan 20132, Italy; Vita-Salute San Raffaele University, Milan, Italy.

Letizia Mariotti (L)

Vita-Salute San Raffaele University, Milan, Italy.

Elena Baldissera (E)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele Hospital, Via Olgettina 60, Milan 20132, Italy.

Peter C Grayson (PC)

National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland.

Marco Matucci-Cerinic (M)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele Hospital, Via Olgettina 60, Milan 20132, Italy.

Lorenzo Dagna (L)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele Hospital, Via Olgettina 60, Milan 20132, Italy; Vita-Salute San Raffaele University, Milan, Italy.

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Classifications MeSH