Literature DB >> 21103985

Criteria to define response to therapy in paediatric rheumatic diseases.

Nicolino Ruperto1, Angela Pistorio, Angelo Ravelli, Rachana Hasija, Dinara Guseinova, Giovanni Filocamo, Erkan Demirkaya, Clara Malattia, Alberto Martini.   

Abstract

PURPOSE: In this review we describe the general methodology and the results of the international projects, conducted by the Paediatric Rheumatology International Trials Organisation (PRINTO), in collaboration with the Paediatric Rheumatology Collaborative Study Group (PRCSG). The aim of these projects were to identify and validate criteria for the evaluation of response to therapy in clinical trials and in daily clinical practice in patients with the three major paediatric rheumatic diseases (PRD): juvenile idiopathic arthritis (JIA), juvenile dermatomyositis (JDM) and juvenile systemic lupus erythematosus (JSLE).
METHODS: The methodological approach to identify and validate outcome measures can be divided into three main phases: (1) the development of a preliminary core set of measures to evaluate the outcome (e.g. response to therapy, remission criteria, disease activity or damage etc.) through literature review and consensus techniques; (2) a large-scale data collection for a prospectively evidence-based validation of the preliminary findings; (3) the final development of a validated criteria for the evaluation of the outcome.
RESULTS: The core sets for three diseases included domains that are common to all diseases (physician's global assessment of disease activity; parent's global assessment of the overall patient's well-being; disability and/or health-related quality of life) plus additional domains that are specific for each disease. In order to be classified as a responder to a given treatment, a patient should demonstrate a different minimum level of improvement (≥30% in JIA, ≥20% in JDM, and ≥50% in JSLE) with no more than one of the remaining variables worsening by more than 30%.
CONCLUSIONS: The proposed core sets and definitions of improvement incorporate clinically meaningful change in a composite endpoint for the evaluation of global response to therapy in the major PRD. The definitions are proposed for use in PRD clinical trials and may help physicians to decide if a child has responded adequately to therapy.

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Year:  2010        PMID: 21103985     DOI: 10.1007/s00228-010-0937-8

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  42 in total

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Authors:  J D Connor
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Authors:  A Ravelli; S Viola; N Ruperto; B Corsi; G Ballardini; A Martini
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4.  Preliminary definition of improvement in juvenile arthritis.

Authors:  E H Giannini; N Ruperto; A Ravelli; D J Lovell; D T Felson; A Martini
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5.  Development of validated disease activity and damage indices for the juvenile idiopathic inflammatory myopathies. II. The Childhood Myositis Assessment Scale (CMAS): a quantitative tool for the evaluation of muscle function. The Juvenile Dermatomyositis Disease Activity Collaborative Study Group.

Authors:  D J Lovell; C B Lindsley; R M Rennebohm; S H Ballinger; S L Bowyer; E H Giannini; J E Hicks; J E Levinson; R Mier; L M Pachman; M H Passo; M D Perez; A M Reed; K N Schikler; M Smith; L S Zemel; L G Rider
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6.  Evaluation of 21-numbered circle and 10-centimeter horizontal line visual analog scales for physician and parent subjective ratings in juvenile idiopathic arthritis.

Authors:  Giovanni Filocamo; Sergio Davì; Angela Pistorio; Marta Bertamino; Nicolino Ruperto; Bianca Lattanzi; Alessandro Consolaro; Silvia Magni-Manzoni; Roberta Galasso; Giulia Camilla Varnier; Alberto Martini; Angelo Ravelli
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Authors:  J S Smolen; V Strand; M Cardiel; S Edworthy; D Furst; D Gladman; C Gordon; D A Isenberg; J H Klippel; M Petri; L Simon; P Tugwell; F Wolfe
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8.  Outcome measures to be used in clinical trials in systemic lupus erythematosus.

Authors:  V Strand; D Gladman; D Isenberg; M Petri; J Smolen; P Tugwell
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Review 9.  International research networks in pediatric rheumatology: the PRINTO perspective.

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Journal:  Curr Opin Rheumatol       Date:  2004-09       Impact factor: 5.006

10.  Development and testing of reduced joint counts in juvenile idiopathic arthritis.

Authors:  Anna Bazso; Alessandro Consolaro; Nicolino Ruperto; Angela Pistorio; Stefania Viola; Silvia Magni-Manzoni; Clara Malattia; Antonella Buoncompagni; Anna Loy; Alberto Martini; Angelo Ravelli
Journal:  J Rheumatol       Date:  2009-01       Impact factor: 4.666

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1.  Paediatric rheumatic disease: Defining clinically inactive disease in juvenile dermatomyositis.

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Journal:  Nat Rev Rheumatol       Date:  2012-10-02       Impact factor: 20.543

2.  2016 American College of Rheumatology/European League Against Rheumatism Criteria for Minimal, Moderate, and Major Clinical Response in Juvenile Dermatomyositis: An International Myositis Assessment and Clinical Studies Group/Paediatric Rheumatology International Trials Organisation Collaborative Initiative.

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Review 3.  Innovative Research Design to Meet the Challenges of Clinical Trials for Juvenile Dermatomyositis.

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4.  2016 American College of Rheumatology/European League Against Rheumatism Criteria for Minimal, Moderate, and Major Clinical Response in Adult Dermatomyositis and Polymyositis: An International Myositis Assessment and Clinical Studies Group/Paediatric Rheumatology International Trials Organisation Collaborative Initiative.

Authors:  Rohit Aggarwal; Lisa G Rider; Nicolino Ruperto; Nastaran Bayat; Brian Erman; Brian M Feldman; Chester V Oddis; Anthony A Amato; Hector Chinoy; Robert G Cooper; Maryam Dastmalchi; David Fiorentino; David Isenberg; James D Katz; Andrew Mammen; Marianne de Visser; Steven R Ytterberg; Ingrid E Lundberg; Lorinda Chung; Katalin Danko; Ignacio García-De la Torre; Yeong Wook Song; Luca Villa; Mariangela Rinaldi; Howard Rockette; Peter A Lachenbruch; Frederick W Miller; Jiri Vencovsky
Journal:  Arthritis Rheumatol       Date:  2017-04-06       Impact factor: 10.995

5.  2016 American College of Rheumatology/European League Against Rheumatism Criteria for Minimal, Moderate, and Major Clinical Response in Juvenile Dermatomyositis: An International Myositis Assessment and Clinical Studies Group/Paediatric Rheumatology International Trials Organisation Collaborative Initiative.

Authors:  Lisa G Rider; Rohit Aggarwal; Angela Pistorio; Nastaran Bayat; Brian Erman; Brian M Feldman; Adam M Huber; Rolando Cimaz; Rubén J Cuttica; Sheila Knupp de Oliveira; Carol B Lindsley; Clarissa A Pilkington; Marilynn Punaro; Angelo Ravelli; Ann M Reed; Kelly Rouster-Stevens; Annet van Royen-Kerkhof; Frank Dressler; Claudia Saad Magalhaes; Tamás Constantin; Joyce E Davidson; Bo Magnusson; Ricardo Russo; Luca Villa; Mariangela Rinaldi; Howard Rockette; Peter A Lachenbruch; Frederick W Miller; Jiri Vencovsky; Nicolino Ruperto
Journal:  Arthritis Rheumatol       Date:  2017-04-06       Impact factor: 10.995

6.  Time to focus on outcome assessment tools for childhood vasculitis.

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Review 7.  Disease activity measures in paediatric rheumatic diseases.

Authors:  Nadia J Luca; Brian M Feldman
Journal:  Int J Rheumatol       Date:  2013-09-08

8.  Dynamic knee joint function in children with juvenile idiopathic arthritis (JIA).

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9.  Exercise in children with joint hypermobility syndrome and knee pain: a randomised controlled trial comparing exercise into hypermobile versus neutral knee extension.

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10.  Muscle Biopsy Findings in Combination With Myositis-Specific Autoantibodies Aid Prediction of Outcomes in Juvenile Dermatomyositis.

Authors:  Claire T Deakin; Shireena A Yasin; Stefania Simou; Katie A Arnold; Sarah L Tansley; Zoe E Betteridge; Neil J McHugh; Hemlata Varsani; Janice L Holton; Thomas S Jacques; Clarissa A Pilkington; Kiran Nistala; Lucy R Wedderburn
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