6533b7ddfe1ef96bd1273a1a

RESEARCH PRODUCT

ASSESSING THE CLINICAL RELEVANCE AND RISK MINIMIZATION OF ANTIBODIES TO BIOLOGICS IN JUVENILE IDIOPATHIC ARTHRITIS (JIA) (ABIRISK) - PRELIMINARY RESULTS

Martina FinettiGabriella GiancaneFrancesca BagnascoPavla DolezalovaElena TsitsamiMaria TrachanaIsabelle Koné-pautDespoina MaritsiErkan DemirkayaGiovanni FilocamoPierre QuartierOlga VougioukaRolando CimazRebecca NicolaiHelga SannerAlina L. BoteanuAlma N. OlivieriElzbieta SmolewskaElisabeth Solau GervaisMaria C. MaggioValda StanevichaSeza OzenMichael HoferMihaela SpirchezMaria G. MagnoliaVeronika VargovaDenis MullemanFlorian DeisenhammerMarc PallardyXavier MarietteLaura CareniniMariangela RinaldiAlberto MartiniNicolino Ruperto

subject

Settore MED/38 - Pediatria Generale E SpecialisticaJIA ABIRISK

description

Introduction: ABIRISK is a project funded by Innovative Medicine Initiative, with the aim to investigate anti-drug antibody (ADA) formation in the treatment of JIA with biologics (BPs). A major limitation to the use of biologics is the development of ADA that may decrease the efficacy of BPs. Objectives: The aim of this project is to improve the capability to predict biologic immunogenicity in JIA patients. Methods: JIA Patients (by ILAR criteria) followed by 24 PRINTO centres in 12 countries were prospectively enrolled and treated with Etanercept, Adalimumab or Tocilizumab. Patient’s data were obtained from Pharmachild, a pharmacovigilance data registry of JIA patients. For each patient detailed demographic and clinical information were reported; biologic samples were collected for PK and ADA detection before therapy start as well as at periodic visits up to month 18 of follow-up. Disease activity was assessed with Juvenile Arthritis Disease Activity Score-10 (JADAS10) and JIA American College of Rheumatology (JIA ACR) criteria. Results: 148 patients were included in the analysis. Five patients were considered twice because treated with 2 different sequential biologics. Demographic and clinical data by therapy are represented in the table. 54% of the patients were treated with Adalimumab. Disease duration was higher in the group receiving Tocilizumab. Disease activity showed a pattern of improvement over time both globally and for each treatment group (Table 1). Anti-adalimumab and antitocilizumab antibodies were detected respectively in 14 and 3 patients, while no patient developed antibodies anti-etanercept. Conclusion: Preliminary data show a global improvement of disease activity during follow-up period. Analysis of the correlation between drug concentration/ADA development and clinical information will help to determine which patients will respond best to which biologic.

http://hdl.handle.net/10447/369317