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The edition · Rheumatology

After a JAK inhibitor fails, why it stopped should pick what comes next

A Japanese registry links the reason for stopping a JAK inhibitor to how well each next drug is kept; alongside, 48-week structural data for guselkumab in erosive psoriatic arthritis and deep renal responses with belimumab in lupus nephritis.

The edition in brief

In 500 treatment courses from the Japanese ANSWER registry started after a JAK inhibitor was stopped in rheumatoid arthritis, abatacept (CTLA4-Ig) was associated with more discontinuation for ineffectiveness than cycling to another JAK inhibitor when the first had failed (HR 2.83, 95% CI 1.20 to 6.70). When the JAK inhibitor had been stopped for toxicity, TNF inhibitors and IL-6 receptor antibodies were associated with fewer subsequent toxicity-related stops than another JAK inhibitor. Disease activity trajectories over 12 months did not differ. In the phase 3b APEX trial of 1,020 biologic-naive adults with active, erosive psoriatic arthritis, guselkumab sustained ACR20 responses of 71% to 74% at 48 weeks with low radiographic progression, and progression slowed in placebo patients after they switched. A single-centre cohort of 43 patients with lupus nephritis given add-on belimumab reached a stringent deep renal response (protein-to-creatinine ratio under 200 mg/g, no active haematuria) in 53.8% by 24 months. The pearl covers hydroxychloroquine dosing and retinal screening.

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