Vulvar lichen sclerosus when topical calcineurin inhibitors have not achieved symptom control

This protocol is for patients with vulvar lichen sclerosus (EB60.0) whose symptoms persisted through a full course of topical calcineurin inhibitor therapy — and in whom escalation to the next treatment line is now being considered.

Prior targets not met

The preceding line used topical calcineurin inhibitors — tacrolimus 0.1% or pimecrolimus 1% cream — applied to the affected vulval skin. The defined goal was improvement in vulval pruritus and burning/pain within 12 weeks. Failure to achieve that improvement triggers escalation to the protocol described here.

At this stage the treatment strategy involves systemic or light-based interventions that go beyond topical application and require involvement of a relevant specialist. The complete sequencing, selection criteria, and all associated considerations are contained in the full protocol.

Instant Access to Structured Evidence-Based Regimens

References

DOI: 10.1111/jdv.18102

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