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The edition · Rheumatology

In controlled RA, tapering raised flare risk by half and withdrawal more than doubled it

A meta-analysis of 27 publications and 5262 patients found de-escalation, especially of biologics, brought flares and radiographic progression without fewer adverse events. Plus who to keep on rituximab in ANCA vasculitis, statin-associated necrotising myopathy and a tocilizumab biosimilar supplement.

The edition in brief

A meta-analysis of randomised trials covering 5262 patients with rheumatoid arthritis in sustained control found that tapering DMARDs raised flare risk by about half (RR 1.56, 1.26 to 1.98), mostly from biologic tapering in the first nine months, while stopping them more than doubled it (RR 2.23, 1.83 to 2.94) at every time point. Both were linked to radiographic progression over longer follow-up, and neither reduced adverse events. Gradual tapering can be discussed with stable patients, but stopping is best avoided. External validation in 217 patients from the MAINRITSAN trials showed that a model using sex, age, ANCA status, relapsing disease, ENT involvement and prednisone dose predicted major relapse, mainly in PR3-ANCA disease, while an infection model including lung disease, diabetes, prior infections and IgG level predicted serious infection more strongly (HR 2.93). Together they can frame the decision to extend rituximab beyond 18 months. In a US cohort of 142 people with myositis, statin-associated necrotising myopathy carried higher mortality, but the excess faded after adjustment for age and cardiometabolic disease. The FDA approved a supplement to the licence of the tocilizumab biosimilar Avtozma on 29 September; the notice does not describe the change. The pearl covers infection screening before biologics.

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