TY - JOUR
T1 - American College of Rheumatology Provisional Criteria for Clinically Relevant Improvement in Children and Adolescents With Childhood-Onset Systemic Lupus Erythematosus
AU - the Paediatric Rheumatology International Trial Organisation and Pediatric Rheumatology Collaborative Study Group
AU - Brunner, Hermine I.
AU - Holland, Michael J.
AU - Beresford, Michael W.
AU - Ardoin, Stacy P.
AU - Appenzeller, Simone
AU - Silva, Clovis A.
AU - Flores, Francisco
AU - Goilav, Beatrice
AU - Avar Aydin, Pinar Ozge
AU - Wenderfer, Scott E.
AU - Levy, Deborah M.
AU - Ravelli, Angelo
AU - Khubchandani, Raju
AU - Avcin, Tadej
AU - Klein-Gitelman, Marisa S.
AU - Ruperto, Nicolino
AU - Feldman, Brian M.
AU - Ying, Jun
AU - Battagliotti, Cristina
AU - Brusco, Maria Isabel
AU - Cuttica, Rubén
AU - De Cunto, Carmen
AU - Espada, Graciela
AU - Farfan, Maximiliano
AU - Garay, Stella
AU - Marcantoni, Maria
AU - Marcela, Alvarez
AU - Meiorin, Silvia
AU - Rama, Maria Elena
AU - Russo, Ricardo
AU - Torre Walsh, Carolina
AU - Zamparo, Celso
AU - Adib, Navid
AU - Akikusa, Jonathan
AU - Boros, Christina
AU - Lee, Senq J.
AU - Mckay, Damien
AU - Piper, Susan
AU - Joos, Rik
AU - Bica, Blanca
AU - Campos, Leonardo
AU - Cavalcanti, André
AU - do Prado, Rogerio
AU - Donner-Maliki, Amanda
AU - Fernandes, Taciana
AU - Fonseca, Adriana
AU - Gasparello de Almeida, Rozana
AU - Guariento, Andressa
AU - Gusman, Catherine
AU - Jusan Fiorot, Fernanda
N1 - Publisher Copyright:
© 2019, American College of Rheumatology
PY - 2019/5
Y1 - 2019/5
N2 - Objective: To develop a Childhood Lupus Improvement Index (CHILI) as a tool to measure response to therapy in childhood-onset systemic lupus erythematosus (cSLE), with a focus on clinically relevant improvement (CRI c SLE ). Methods: Pediatric nephrology and rheumatology subspecialists (n = 213) experienced in cSLE management were invited to define CRI c SLE and rate a total of 433 unique patient profiles for the presence/absence of CRI c SLE . Patient profiles included the following cSLE core response variables (CRVs): global assessment of patient well-being (patient-global), physician assessment of cSLE activity (MD-global), disease activity index score (here, we used the Systemic Lupus Erythematosus Disease Activity Index), urine protein-to-creatinine ratio, and Child Health Questionnaire physical summary score. Percentage and absolute changes in these cSLE-CRVs (baseline versus follow-up) were considered in order to develop candidate algorithms and validate their performance (sensitivity, specificity, area under the receiver operating characteristic curve [AUC]; range 0–1). Results: During an international consensus conference, unanimous agreement on a definition of CRI c SLE was achieved; cSLE experts (n = 13) concurred (100%) that the preferred CHILI algorithm considers absolute changes in the cSLE-CRVs. After transformation to a range of 0–100, a CHILI score of ≥54 had outstanding accuracy for identifying CRI c SLE (AUC 0.93, sensitivity 81.1%, and specificity 84.2%). CHILI scores also reflect minor, moderate, and major improvement for values exceeding 15, 68, and 92, respectively (all AUC ≥0.92, sensitivity ≥93.1%, and specificity ≥73.4%). Conclusion: The CHILI is a new, seemingly highly accurate index for measuring CRI in cSLE over time. This index is useful to categorize the degree of response to therapy in children and adolescents with cSLE.
AB - Objective: To develop a Childhood Lupus Improvement Index (CHILI) as a tool to measure response to therapy in childhood-onset systemic lupus erythematosus (cSLE), with a focus on clinically relevant improvement (CRI c SLE ). Methods: Pediatric nephrology and rheumatology subspecialists (n = 213) experienced in cSLE management were invited to define CRI c SLE and rate a total of 433 unique patient profiles for the presence/absence of CRI c SLE . Patient profiles included the following cSLE core response variables (CRVs): global assessment of patient well-being (patient-global), physician assessment of cSLE activity (MD-global), disease activity index score (here, we used the Systemic Lupus Erythematosus Disease Activity Index), urine protein-to-creatinine ratio, and Child Health Questionnaire physical summary score. Percentage and absolute changes in these cSLE-CRVs (baseline versus follow-up) were considered in order to develop candidate algorithms and validate their performance (sensitivity, specificity, area under the receiver operating characteristic curve [AUC]; range 0–1). Results: During an international consensus conference, unanimous agreement on a definition of CRI c SLE was achieved; cSLE experts (n = 13) concurred (100%) that the preferred CHILI algorithm considers absolute changes in the cSLE-CRVs. After transformation to a range of 0–100, a CHILI score of ≥54 had outstanding accuracy for identifying CRI c SLE (AUC 0.93, sensitivity 81.1%, and specificity 84.2%). CHILI scores also reflect minor, moderate, and major improvement for values exceeding 15, 68, and 92, respectively (all AUC ≥0.92, sensitivity ≥93.1%, and specificity ≥73.4%). Conclusion: The CHILI is a new, seemingly highly accurate index for measuring CRI in cSLE over time. This index is useful to categorize the degree of response to therapy in children and adolescents with cSLE.
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U2 - 10.1002/acr.23834
DO - 10.1002/acr.23834
M3 - Article
C2 - 30680946
AN - SCOPUS:85064810180
SN - 2151-464X
VL - 71
SP - 579
EP - 590
JO - Arthritis Care and Research
JF - Arthritis Care and Research
IS - 5
ER -