Sponsor-page-banner-GIRO

[scavanger-hunt]

Towards Personalised Treatment in Early Psoriatic Arthritis: Efficacy and Subgroup Identification from a Pooled Analysis of Four Strategy Trials

Authors

University of Oxford
Ji-Hyoun  Kang
University of Oxford, NDORMS, Oxford
Yunxuan  Jiang
University of Oxford, NDORMS, Oxford
Gabriele  De Marco
University of Leeds, NIHR Leeds Biomedical Research Centre, The Leeds Teaching Hospitals NHS Trust, Leeds, University of Leeds, Leeds Institute of Rheumatic and Musculoskeletal Medicine, Leeds, Mid Yorkshire Teaching NHS Trust, Division of Medicine, Department of Rheumatology, Wakefield
A.A.  den Broeder
Sint Maartenskliniek, Department of Rheumatology, Nijmegen
Noortje van Herwaarden
Sint Maartenskliniek, Department of Rheumatology, Nijmegen
Gonul  Hazal Koc
Erasmus MC, Department of Rheumatology, Rotterdam
Marc R. Kok
Maasstad Hospital, Department of Rheumatology and Clinical Immunology, Rotterdam
Jolanda J. Luime
Erasmus MC, Department of Rheumatology, Rotterdam
Helena Marzo-Ortega
University of Leeds, NIHR Leeds Biomedical Research Centre, The Leeds Teaching Hospitals NHS Trust, Leeds, University of Leeds, Leeds Institute of Rheumatic and Musculoskeletal Medicine, Leeds
Marijn Vis
Erasmus MC, Department of Rheumatology, Rotterdam
Michelle L.M. Mulder
Sint Maartenskliniek, Department of Rheumatology, Nijmegen
Ilja Tchetverikov
Albert Schweitzer Hospital, Department of Rheumatology, Dordrecht
Sofia Massa
University of Oxford, NDORMS, Oxford, University of Oxford, Oxford Clinical Trials Research Unit, Oxford
Laura C Coates
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford

Keywords

Causal Inference; Machine Learning, Meta-Analysis; Intensive Therapy; Psoriatic Arthritis; Personalisation; Precision Medicine

    Psoriatic arthritis (PsA) is a long-term condition that causes joint pain, swelling, and skin problems. When PsA is caught early, doctors have a choice: start with a standard step-up approach, gradually increasing treatment if needed, or begin more intensively from the outset, using a combination of drugs or biologic medicines straight away. Previous trials have given mixed answers about which approach works better, with some studies showing intensive treatment offers a clear advantage and others showing only a modest benefit.
    To make sense of these differing results, we combined individual-level data from four separate clinical trials, creating a larger and more detailed dataset of 441 patients with early, untreated PsA. Pooling the data allowed us to estimate the overall benefit of intensive treatment more precisely than any single trial could alone. We found that, on average, intensive treatment led to meaningfully better disease control than standard care.
    However, an "average" benefit doesn't mean intensive treatment helps everyone equally. Using newer statistical and machine learning methods, we looked beyond the average to ask: which patients benefit most? We found that factors such as age, baseline disease activity, and body weight (BMI) played an important role in how much a patient was likely to gain from intensive treatment. From this, we built simple decision rules to help identify which patients are good candidates for intensive treatment versus those who may do just as well with a standard approach.
    These findings are an early but encouraging step towards more personalised treatment in PsA.