This protocol applies to children with juvenile idiopathic arthritis and non-systemic polyarthritis — five or more joints ever involved — in whom the second biologic agent did not achieve low disease activity and a further treatment step is required.
JIA with polyarthritis (≥5 joints ever involved), excluding systemic arthritis and sacroiliitis. This group may include children across different ILAR JIA categories who share widespread joint involvement without systemic or axial features.
The preceding step involved switching to a non-TNFi biologic (tocilizumab or abatacept) — or, for patients with secondary failure of a first TNFi, a second TNFi. That treatment did not achieve the required target: low disease activity (clinical JADAS-10 ≤2.5). This protocol defines the appropriate next step following that failure.
DOI: 10.1002/acr.23870
This group includes children with JIA and polyarthritis (≥5 joints ever involved) and may include children from different ILAR JIA categories but excludes children with systemic arthritis or sacroiliitis.
In patients with JIA and polyarthritis and moderate or high disease activity despite a second biologic, using a TNFi, abatacept, or tocilizumab (depending upon prior biologics received) is conditionally recommended over rituximab.
Good disease control, with therapeutic escalation to achieve low disease activity, was recommended.
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