Comparative effectiveness of TNF inhibitors and tocilizumab with and without conventional synthetic disease-modifying antirheumatic drugs in a pan-European observational cohort of bio-naïve patients with rheumatoid arthritis.


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:
02 2020
Historique:
received: 22 03 2019
revised: 07 06 2019
accepted: 24 06 2019
pubmed: 10 7 2019
medline: 5 2 2021
entrez: 9 7 2019
Statut: ppublish

Résumé

To compare treatment effectiveness in rheumatoid arthritis (RA) patients naïve to biological disease-modifying antirheumatic drugs (bDMARDs) treated with tocilizumab (TCZ) or TNF-inhibitor (TNFi) with (-combo) or without (-mono) conventional synthetic DMARDs (csDMARDs). Patients with RA across 7 European registries, naïve to bDMARDs who initiated treatment with TCZ or TNFi from 2009 to 2016 were included. Drug retention rate was analyzed using Kaplan-Meier and Cox models, and CDAI over time by mixed models. The proportions of patients reaching CDAI low disease activity (LDA) and remission after one year were corrected for attrition. 6713 TNFi-combo, 3762 TNFi-mono, 646 TCZ-combo and 384 TCZ-mono were eligible. Crude median retention was 3.67 years (95%CI 3.41-3.83) for TNFi-combo, 4.14 (3.77-4.62) for TNFi-mono, 2.98 (2.76-3.34) for TCZ-combo and 3.63 years (3.34-5.03) for TCZ-mono. After adjustment for covariates, country and year of treatment initiation stratification, hazards of discontinuation were lower for TCZ-mono (0.60, 95% CI 0.52-0.69) and TCZ-combo (0.66, 95% CI 0.54-0.81) compared to TNFi-combo. Adjusted CDAI evolution was not significantly different between groups. CDAI LDA and remission corrected for attrition were similar between TCZ with or without csDMARDs and TNFi-combo. In routine care across 7 European countries, the adjusted drug retention, adjusted CDAI over time and attrition-corrected response proportion for RA patients were similar for bio-naïve patients if treated with TNFi-combo, TCZ-combo or TCZ-mono.

Identifiants

pubmed: 31280937
pii: S0049-0172(19)30203-3
doi: 10.1016/j.semarthrit.2019.06.020
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antirheumatic Agents 0
Tumor Necrosis Factor Inhibitors 0
tocilizumab I031V2H011

Types de publication

Comparative Study Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

17-24

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Kim Lauper (K)

Geneva University Hospitals, Division of Rheumatology, 1205 Geneva, Switzerland. Electronic address: kim.lauper@hcuge.ch.

Denis Mongin (D)

Geneva University Hospitals, Division of Rheumatology, 1205 Geneva, Switzerland.

Florenzo Iannone (F)

GISEA, University Hospital of Bari, Bari, Italy.

Eirik K Kristianslund (EK)

Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.

Tore K Kvien (TK)

Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.

Dan C Nordström (DC)

ROB-FIN Helsinki University Hospital and Helsinki University, Helsinki, Finland.

Karel Pavelka (K)

Institut of Rheumatology, Prague and Clinic of Rheumatology Charles University, Prague, Czech Republic.

Manuel Pombo-Suarez (M)

Rheumatology Unit, Clinical University Hospital, University of Santiago de Compostela, Santiago de Compostela, Spain.

Ziga Rotar (Z)

BioRx.si, University Medical Centre Ljubljana, Ljubljana, Slovenia.

Maria J Santos (MJ)

Rheumatology Department, Hospital Garcia de Orta, Almada, Portugal.

Catalin Codreanu (C)

Center of Rheumatic Diseases, University of Medicine and Pharmacy, Bucharest, Romania.

Galina Lukina (G)

ARBITER, Institute of Rheumatology, Moscow, Russian Federation.

Sara L Gale (SL)

Genentech, South San Francisco, CA, United States.

Markus John (M)

F. Hoffmann-La Roche, Basel, Switzerland.

Yves Luder (Y)

F. Hoffmann-La Roche, Basel, Switzerland.

Delphine S Courvoisier (DS)

Geneva University Hospitals, Division of Rheumatology, 1205 Geneva, Switzerland.

Cem Gabay (C)

Geneva University Hospitals, Division of Rheumatology, 1205 Geneva, Switzerland.

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Classifications MeSH