Background: Lichen sclerosus (LS) is a chronic inflammatory condition mainly affecting genital skin. It causes distressing symptoms that impact daily quality of life (QoL). It causes progressive anatomical changes and a potential risk of cancer. Published randomised controlled trials are of varying methodological quality and difficult to combine in meta-analyses. This is partly due to lack of agreed outcome measures to assess treatment response. Identification of core outcome sets (COSs), which standardise key outcomes to be measured in all future trials, is a solution to this problem.
Objectives: To obtain international agreement on which outcome domains should be measured in interventional trials of genital LS.
Methods: Recommended best practice for COS domain development was followed: 1) Identification of potential outcome domains: a long-list was generated through up-to-date LSliterature search, including information collected during the LS Priority Setting Partnership. 2) Provisional agreement of outcome domains: A 3-stage multi-stakeholder international electronic-Delphi consensus study; 3) Final agreement of outcome domains: Online consensus meeting with international stakeholders including anonymised voting.
Results: In total, 123 participants (77 patients, 44 health professionals, 2 researchers) from 20 countries completed 3 rounds of the electronic-Delphi study. 11 outcome domains were rated as ‘critical’ and were discussed at the online consensus meetings. The first set of consensus meetings involved 42 participants from 13 countries. Consensus was met for ‘symptoms’ (100% agreed) and ‘quality of lif –LS specific’ (92% agreed). After set two of meetings, involving 29 participants from 12 countries, ‘Clinical (visible) signs’ also met consensus (97% agreed). Conclusions: The international community have agreed upon 3 key outcome domains to measure in all future LS clinical trials. We recommend that trialists and systematic reviewers incorporate these domains into study protocols with immediate effect. CORALS will now work with stakeholders to select an outcome measurement instrument per prioritised core domain.
The aim of this stage of CORALS was to obtain international agreement on which domains should be measured as a minimum requirement in interventional trials of genital LS.
ContributorsRosalind C Simpson, Gudula Kirtschig, Amanda Selk, Suzanne von Seitzberg, Gitte Vittrup, Ione Bissonnette, Jan Kottner, Jaclyn Lanthier, Chris Stanton, David Foster, Martin Promm, Angelo Augenti, Stefano Lauretti, Kim S Thomas, The Core Outcomes for Research in Lichen Sclerosus (CORALS) initiative steering group
Disease Category: Skin
Disease Name: lichen sclerosus
Age Range: Unknown
Sex: Either
Nature of Intervention:
- Clinical experts
- Consumers (patients)
- Journal editors
- Other
- Patient/ support group representatives
- Researchers
- COS for clinical trials or clinical research
- Consensus meeting
- Delphi process
- Literature review
Development of domains took a three-stage process: 1. Identification of possible domains using key documents in the literature 2. Provisional agreement of the most important domains via a 3-stage e-Delphi consensus study 3. Final agreement of domains: international virtual consensus meetings