December 2022

Recommandations de l'EULAR pour la prise en charge de la polyarthrite rhumatoïde avec des antirhumatismaux modificateurs de la maladie synthétiques et biologiques : mise à jour 2022

Ann Rheum Dis. 2022. Epub ahead of print [05/12/2022] doi: 10.1136/ard-2022-223356

Smolen, et al. provide a 2022 update of the EULAR recommendations for the management of RA with synthetic and biological DMARDs.

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Sécurité des DMARD synthétiques et biologiques : une revue systématique de la littérature pour la mise à jour 2022 des recommandations de l'EULAR pour la prise en charge de la polyarthrite rhumatoïde

Ann Rheum Dis. 2022. Epub ahead of print doi: 10.1136/ard-2022-223357

Sepriano, et al. provide results of a systematic literature review (SLR) on the safety of synthetic and biological DMARDs, to inform the 2022 update of the EULAR recommendations for the management of rheumatoid arthritis.

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Efficacité des DMARD synthétiques et biologiques : une revue systématique de la littérature pour la mise à jour 2022 des recommandations de l'EULAR pour la prise en charge de la polyarthrite rhumatoïde

Ann Rheum Dis. 2022. Epub ahead of print. doi: 10.1136/ard-2022-223365

Kerschbaumer, et al. provide results of a systematic literature review (SLR) on efficacy of synthetic and biological DMARDs, to inform the 2022 update of the EULAR recommendations for the management of rheumatoid arthritis.

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November 2022

Efficacité et sécurité des DMARD biologiques : Une revue systématique de la littérature pour la mise à jour 2022 des recommandations ASAS-EULAR pour la prise en charge de la spondylarthrite axiale

Ann Rheum Dis 2022; online ahead of print doi:10.1136/ard-2022-223298

New evidence supports the efficacy and safety of TNFi (originators/biosimilars) and IL-17i in r-axSpA and nr-axSpA. This systematic literature review was conducted to inform the taskforce of the 2022 update of the ASAS-EULAR recommendations.

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Recommandations ASAS-EULAR pour la prise en charge de la spondylarthrite axiale : mise à jour 2022

Ann Rheum Dis 2022; online ahead of print doi:10.1136/ard-2022-223296

Since the last update in 2016, more data have become available on existing treatment options for axSpA, and particularly on IL-17i. The increasing availability of more drugs and with different modes of action raises questions around their positioning in the treatment pathway. This review sought to update the 2016 recommendations with newly available evidence.

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Efficacité et sécurité des interventions non pharmacologiques et non biologiques : Une revue systématique de la littérature pour la mise à jour 2022 des recommandations ASAS/EULAR pour la prise en charge de la spondylarthrite axiale

Ann Rheum Dis 2022; online ahead of print doi:10.1136/ard-2022-223297

Non-pharmacological interventions are important for any rheumatic disease, but especially axSpA, where they represent the cornerstone of treatment. The aim of this study was to produce a systematic literature review on efficacy and safety of non-pharmacological and non-biological pharmacological treatments was performed.

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Efficacité et sécurité du Filgotinib chez les patients présentant un risque élevé de mauvais pronostic et ayant montré une réponse inadéquate au MTX : Analyse post hoc de l'étude FINCH 1

Rheumatol Ther. 2022. Epub ahead of print doi: 10.1007/s40744-022-00498-x

Post hoc analysis from the FINCH 1 study highlights filgotinib as a potential beneficial treatment option for patients with RA who have had inadequate response to MTX and have high risk of disease progression and poor prognosis.

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October 2022

Taux de reprise et de retraitement avec l'Ixekizumab après l'arrêt du traitement chez les patients atteints de spondylarthrite axiale : Résultats à la semaine 104 d'une étude de retrait randomisée contrôlée par placebo

Ann Rheum Dis. 2022 doi: 10.1136/ard-2022-222731

The present analysis demonstrated that patients continuously treated with IXE were less likely to experience flare compared with patients receiving placebo. The aim of this study was to evaluate the recapture of response with open-label IXE retreatment at week 104 in patients with axSpA who flared after withdrawal of IXE therapy.

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May 2021

Évaluation de la progression radiographique chez les patients atteints de polyarthrite rhumatoïde traités par tofacitinib dans des études à long terme

Rheumatology (Oxford). 2021;60(4):1708-1716.

Long-term evaluation of tofacitinib has found limited progression of structural damage in patients with RA treated with tofacitinib for up to 5 years. Similar results were also observed for patients receiving tofacitinib monotherapy or combination therapy for up to 3 years.It is well known that inflammation in RA leads to structural damage over time, and therapies such as DMARDS have the ability to reduce inflammation whilst inhibiting the progression of structural damage. In this study, van der...

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February 2021

Filgotinib Versus Placebo ou Adalimumab Chez les Patients Atteints de Polyarthrite Rhumatoïde et Présentant une Réponse Inadéquate au Méthotrexate : Essai Clinique Randomisé De Phase III

Ann Rheum Dis. 2021 Jan 27:annrheumdis-2020-219214

Filgotinib improved RA signs and symptoms, physical function, and inhibited radiographic progression. FIL 200mg plus MTX, but not FIL 100mg plus MTX showed non-inferiority to ADA plus MTX, based on DAS28(CRP) low disease activity. FIL was also well tolerated in RA patients with inadequate response to MTX.This 52-week, phase 3 randomised clinical trial (FINCH 1) evaluated the efficacy and safety of FIL in patients with RA randomised to FIL 200 or 100mg, ADA 40mg, or placebo, all with background M...

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