Evidence on treat to target strategies in polymyalgia rheumatica and giant cell arteritis: a systematic literature review

Author:

Hysa Elvis1ORCID,Bond Milena2ORCID,Ehlers Lisa3ORCID,Camellino Dario4ORCID,Falzon Louise5ORCID,Dejaco Christian26ORCID,Buttgereit Frank3ORCID,Aletaha Daniel7ORCID,Kerschbaumer Andreas7ORCID

Affiliation:

1. Laboratory of Experimental Rheumatology and Academic Division of Clinical Rheumatology, Department of Internal Medicine, San Martino Polyclinic, University of Genoa , Genoa, Italy

2. Department of Rheumatology, Hospital of Bruneck (ASAA-SABES), Teaching Hospital of the Paracelsius Medical University , Bruneck, Italy

3. Department of Rheumatology and Clinical Immunology, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin , Berlin, Germany

4. Division of Rheumatology, Local Health Trust 3 , Genoa, Italy

5. Health Economics and Decision Science, School of Health and Related Research, University of Sheffield , Sheffield, England

6. Department of Rheumatology, Medical University Graz , Graz, Austria

7. Division of Rheumatology, Department of Medicine III, Medical University of Vienna , Vienna, Austria

Abstract

Abstract Objectives To inform an international task force about current evidence on Treat to Target (T2T) strategies in PMR and GCA. Methods A systematic literature research (SLR) was conducted in Medline, EMBASE, Cochrane Library, clinicaltrials.gov from their inception date to May 2022, and in the EULAR/ACR abstract database (2019–2021). Randomised clinical trials (RCTs) and non-randomised interventional studies published in English and answering at least one of the eleven PICO questions on T2T strategies, treatment targets and outcomes, framed by the taskforce, were identified. Study selection process, data extraction and risk of bias assessment were conducted independently by two investigators. Results Of 7809 screened abstracts, 397 were selected for detailed review and 76 manuscripts were finally included (31 RCTs, eight subgroup/exploratory analyses of RCTs and 37 non-randomised interventional studies). No study comparing a T2T strategy against standard of care was identified. In PMR RCTs, the most frequently applied outcomes concerned treatment (90.9% of RCTs), particularly the cumulative glucocorticoids (GC) dose and GC tapering, followed by clinical, laboratory and safety outcomes (63.3% each). Conversely, the most commonly reported outcomes in RCTs in GCA were prevention of relapses (72.2%), remission as well as treatment-related and safety outcomes (67.0% each). Conclusions This SLR provides evidence and highlights the knowledge gaps on T2T strategies in PMR and GCA, informing the task force developing T2T recommendations for these diseases.

Funder

AbbVie

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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