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- W2908655339 abstract "Background There is international consensus around a core set of variables (cSLE-CRVs) to assess response to therapy with childhood-onset systemic lupus erythematosus (cSLE) [global assessment of patient well-being (Patient-global), physician assessment of cSLE activity (MD-global), disease activity index score, urine protein to creatinine ratio (PCR), Child Health Questionnaire physical function summary score (CHQ-Phs)]. Percentage changes of these cSLE-CRVs are used in the Provisional PRINTO-ACR- EULAR Criteria of Response to Therapy of cSLE (PCI). In a small dataset, we have previously shown that the PCI and the Systemic Lupus Responder Index only have fair accuracy in detecting cSLE improvement. The Objective of this research was to 1) validate the PCI and 2) develop for Children an Index of Lupus Improvement (CHILI) as a tool to measure response to therapy, with focus on clinically relevant improvement (CRIcSLE). Methods Pediatric subspecialists (n=213) in treating cSLE were invited to define CRIcSLE and rate a total of 433 unique patient profiles for the presence/absence of CRIcSLE and various levels of improvement. Patient profiles included the cSLE-CRVs and routine laboratory tests at a baseline and follow-up time-point. To measure CRIcSLE we tested the PCI, and developed the candidate CHILI criteria that considered a) absolute and b) percentage changes of the cSLE-CRVs (baseline vs follow-up) in a trainings-dataset and initially validated these criteria in the validation-dataset. Criteria accuracy was assessed by kappa statistics (PCI) and the area under the ROC curve (AUC; range: 0–1)], respectively. Results During an international consensus conference agreement on a definition of CRIcSLE was achieved. Response rate to patient profile ratings was 91% (194/214). The PIC had no more than fair accuracy (kappa 0.92, sensitivity: >93.1%; specificity: >73.4%), respectively. Conclusions The CHILI is a new highly accurate index to capture improvement in the overall course of cSLE. This index is also useful to categorize the degree of cSLE response to therapy. Acknowledgements For the Pediatric Rheumatology International Trial Network and the Pediatric Rheumatology Collaborative Study Group; the study is supported by NIH grants 5U01-AR51868, P30-AR AR47363 and 2UL1RR026314 and the PRCSG and PRINTO Coordinating Centers. This study is also supported by grants from Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP 2015/03756–4 to CAS), Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq 303422/2015–7 to CAS) and by Nucleo de Apoio a Pesquisa ‘Saude da Crianca e do Adolescente’ da USP (NAP-CriAd) to CAS." @default.
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- W2908655339 date "2018-08-01" @default.
- W2908655339 modified "2023-09-30" @default.
- W2908655339 title "CS-10 Criteria for clinically relevant improvement in children & adolescents with childhood-onset systemic lupus erythematosus" @default.
- W2908655339 doi "https://doi.org/10.1136/lupus-2018-lsm.45" @default.
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