Literature DB >> 24515813

Efficacy of tocilizumab in conventional treatment-refractory adult-onset Still's disease: multicenter retrospective open-label study of thirty-four patients.

Francisco Ortiz-Sanjuán1, Ricardo Blanco, Vanesa Calvo-Rio, Javier Narvaez, Esteban Rubio Romero, Alejandro Olivé, Santos Castañeda, Adela Gallego Flores, M Victoria Hernández, Cristina Mata, Inmaculada Ros Vilamajo, Walter Alberto Sifuentes Giraldo, Miguel A Caracuel, Mercedes Freire, Catalina Gómez Arango, José Llobet, Sara Manrique Arija, Carlos Marras, Concepción Moll-Tuduri, Chamaida Plasencia-Rodriguez, Rosa Roselló, Ana Urruticoechea, Maria L Velloso-Feijoo, Jordi Del Blanco, M Carmen González-Vela, Javier Rueda-Gotor, Trinitario Pina, Javier Loricera, Miguel A González-Gay.   

Abstract

OBJECTIVE: Adult-onset Still's disease (AOSD) is frequently refractory to standard therapy. Tocilizumab (TCZ) has demonstrated efficacy in single cases and in small series of patients with AOSD. The aim of this multicenter study was to assess the efficacy of TCZ in patients with AOSD refractory to conventional treatment.
METHODS: This was a retrospective open-label study of TCZ treatment in 34 patients with AOSD who had experienced an inadequate response to corticosteroids and at least 1 standard synthetic immunosuppressive drug and also, in many cases, biologic agents.
RESULTS: The mean ± SD age of the patients (8 men and 26 women) was 38.7 ± 16.1 years. The median duration of AOSD before TCZ was initiated was 4.2 years (interquartile range [IQR] 1-9 years). The initial dosages of intravenous TCZ were 8 mg/kg every 4 weeks in 22 patients, 4 mg/kg every 4 weeks in 2 patients, and 8 mg/kg every 2 weeks in 10 patients. TCZ treatment resulted in rapid and maintained improvement in both clinical and laboratory parameters. After 1 year of TCZ therapy, the incidence of joint manifestations had decreased from 97.1% at baseline to 32.4%, the incidence of both cutaneous manifestations and fever had decreased from 58.8% to 5.9%, and the incidence of lymphadenopathy had decreased from 29.4% to 0%. A dramatic reduction in laboratory markers of inflammation, including the C-reactive protein level, the erythrocyte sedimentation rate, and the ferritin level, was achieved. The median dosage of prednisone was also reduced, from 13.8 mg/day (IQR 5-45) at the initiation of TCZ to 2.5 mg/day (IQR 0-30) at 12 months. After a median followup of 19 months (IQR 12-31 months), only 2 patients required permanent discontinuation of TCZ therapy because of severe infections.
CONCLUSION: TCZ treatment was associated with rapid and maintained clinical and laboratory improvement in patients with AOSD refractory to standard treatment. However, joint manifestations seem to be more refractory to treatment compared with systemic manifestations.
Copyright © 2014 by the American College of Rheumatology.

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Year:  2014        PMID: 24515813     DOI: 10.1002/art.38398

Source DB:  PubMed          Journal:  Arthritis Rheumatol        ISSN: 2326-5191            Impact factor:   10.995


  34 in total

1.  A retrospective study of patients with adult-onset Still's disease: is pericarditis a possible predictor for biological disease-modifying anti-rheumatic drugs need?

Authors:  Francesca Dall'Ara; Micol Frassi; Angela Tincani; Paolo Airò
Journal:  Clin Rheumatol       Date:  2016-01-12       Impact factor: 2.980

Review 2.  Macrophage activation syndrome complicating rheumatic diseases in adults: case-based review.

Authors:  Mayan Gilboa; Gil Bornstein; Ilan Ben-Zvi; Chagai Grossman
Journal:  Rheumatol Int       Date:  2019-07-31       Impact factor: 2.631

3.  Complex presentation of adult-onset Still's disease.

Authors:  Muhammad Zafran; Nancy Wassef
Journal:  BMJ Case Rep       Date:  2019-04-25

Review 4.  Adult-Onset Still's Disease: Molecular Pathophysiology and Therapeutic Advances.

Authors:  Paolo Sfriso; Sara Bindoli; Paola Galozzi
Journal:  Drugs       Date:  2018-08       Impact factor: 9.546

Review 5.  [Still's disease in children and adults].

Authors:  C M Hedrich; C Günther; M Aringer
Journal:  Z Rheumatol       Date:  2017-09       Impact factor: 1.372

6.  Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes.

Authors:  R Sighart; J Rech; A Hueber; N Blank; S Löhr; A Reis; H Sticht; U Hüffmeier
Journal:  Rheumatol Int       Date:  2017-11-20       Impact factor: 2.631

Review 7.  A Review of Recent Advances Using Tocilizumab in the Treatment of Rheumatic Diseases.

Authors:  Andrea Rubbert-Roth; Daniel E Furst; Jan Michael Nebesky; Angela Jin; Erhan Berber
Journal:  Rheumatol Ther       Date:  2018-03-03

Review 8.  Tocilizumab-induced anaphylaxis in patients with adult-onset Still's disease and systemic juvenile idiopathic arthritis: a case-based review.

Authors:  Eun Hye Park; Eun Young Lee; Kichul Shin; Hyoun-Ah Kim
Journal:  Rheumatol Int       Date:  2019-10-09       Impact factor: 2.631

Review 9.  [Still's disease in children and adults].

Authors:  C M Hedrich; C Günther; M Aringer
Journal:  Hautarzt       Date:  2017-06       Impact factor: 0.751

Review 10.  [Still's syndrome-similarities and differences between the juvenile and adult forms].

Authors:  Andrea Regel; Dirk Föll; Martin A Kriegel
Journal:  Z Rheumatol       Date:  2021-11-04       Impact factor: 1.372

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