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Anti-IgE Monoclonal Antibody (Omalizumab) in Refractory and Relapsing Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss): Data on Seventeen Patients.
Jachiet, Marie; Samson, Maxime; Cottin, Vincent; Kahn, Jean-Emmanuel; Le Guenno, Guillaume; Bonniaud, Philippe; Devilliers, Hervé; Bouillet, Laurence; Gondouin, Anne; Makhlouf, Fatma; Meaux-Ruault, Nadine; Gil, Helder; Bienvenu, Boris; Coste, André; Groh, Matthieu; Giraud, Violaine; Dominique, Stéphane; Godeau, Bertrand; Puéchal, Xavier; Khouatra, Chahera; Ruivard, Marc; Le Jeunne, Claire; Mouthon, Luc; Guillevin, Loïc; Terrier, Benjamin.
Afiliación
  • Jachiet M; National Referral Center for Systemic and Autoimmune Diseases, Hôpital Cochin, AP-HP, and Université Paris Descartes, Paris, France.
  • Samson M; Centre Hospitalier Universitaire (CHU) de Dijon, Dijon, France.
  • Cottin V; Hôpital Edouard Herriot Herriot, Lyon, France.
  • Kahn JE; Hôpital Foch, Université Versailles Saint-Quentin en Yvelines, Suresnes, France.
  • Le Guenno G; Hôpital Estaing, Clermont-Ferrand, France.
  • Bonniaud P; National Referral Center for Systemic and Autoimmune Diseases, Hôpital Cochin, AP-HP, and Université Paris Descartes, Paris, France.
  • Devilliers H; Centre Hospitalier Universitaire (CHU) de Dijon, Dijon, France.
  • Bouillet L; CHU de Grenoble and Michallon Hospital, Grenoble, France.
  • Gondouin A; CHU de Besançon, Besançon, France.
  • Makhlouf F; CHU de Grenoble and Michallon Hospital, Grenoble, France.
  • Meaux-Ruault N; CHU de Besançon, Besançon, France.
  • Gil H; CHU de Besançon, Besançon, France.
  • Bienvenu B; CHU de Caen, Caen, France.
  • Coste A; Hôpital Intercommunal, Créteil, France.
  • Groh M; National Referral Center for Systemic and Autoimmune Diseases, Hôpital Cochin, AP-HP, and Université Paris Descartes, Paris, France.
  • Giraud V; Hôpital Ambroise Paré, AP-HP, Boulogne-Billancourt, France.
  • Dominique S; CHU de Rouen, Rouen, France.
  • Godeau B; Hôpital Henri Mondor, AP-HP, Créteil, France.
  • Puéchal X; National Referral Center for Systemic and Autoimmune Diseases, Hôpital Cochin, AP-HP, and Université Paris Descartes, Paris, France.
  • Khouatra C; Centre Hospitalier Universitaire (CHU) de Dijon, Dijon, France.
  • Ruivard M; Hôpital Estaing, Clermont-Ferrand, France.
  • Le Jeunne C; National Referral Center for Systemic and Autoimmune Diseases, Hôpital Cochin, AP-HP, and Université Paris Descartes, Paris, France.
  • Mouthon L; National Referral Center for Systemic and Autoimmune Diseases, Hôpital Cochin, AP-HP, and Université Paris Descartes, Paris, France.
  • Guillevin L; National Referral Center for Systemic and Autoimmune Diseases, Hôpital Cochin, AP-HP, and Université Paris Descartes, Paris, France.
  • Terrier B; National Referral Center for Systemic and Autoimmune Diseases, Hôpital Cochin, AP-HP, and Université Paris Descartes, Paris, France.
Arthritis Rheumatol ; 68(9): 2274-82, 2016 09.
Article en En | MEDLINE | ID: mdl-26946346
ABSTRACT

OBJECTIVE:

To describe the efficacy and safety of omalizumab, an anti-IgE monoclonal antibody, in patients with refractory and/or relapsing eosinophilic granulomatosis with polyangiitis (Churg-Strauss) (EGPA).

METHODS:

We conducted a nationwide retrospective study including EGPA patients who received omalizumab. Response was defined as the absence of asthma and/or sinonasal exacerbations with a prednisone dosage of ≤7.5 mg/day (complete response) or >7.5 mg/day (partial response).

RESULTS:

Seventeen patients (median age 45 years) received omalizumab for severe steroid-dependent asthma (88%) and/or sinonasal involvement (18%). After a median follow-up of 22 months, 6 patients (35%) achieved a complete response, 5 patients (30%) achieved a partial response, and 6 patients (35%) had no improvement. The median Birmingham Vasculitis Activity Score decreased from 2.5 at baseline to 0.5 at 12 months. The median number of exacerbations per month decreased from 1 at baseline to 0 at 12 months, and the median forced expiratory volume in 1 second increased from 63% of the percent predicted at baseline to 85% of the percent predicted at 12 months. The median prednisone dosage decreased from 16 mg/day at baseline to 11 mg/day at 6 months and 9 mg/day at 12 months. Omalizumab was discontinued in 8 patients (47%) during follow-up, because of remission (12.5%), adverse event despite disease remission (12.5%), refractory disease (25%), or relapse (50%). Relapses included retrobulbar optic neuritis attributable to EGPA in 2 patients and severe asthma flare in 2 others.

CONCLUSION:

The results of this study suggest that omalizumab may have a corticosteroid-sparing effect in EGPA patients with asthmatic and/or sinonasal manifestations, but reducing the corticosteroid dose may also increase the risk of severe EGPA flares, which raises the question of the safety of omalizumab in patients with EGPA.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Churg-Strauss / Antialérgicos / Omalizumab Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Arthritis Rheumatol Año: 2016 Tipo del documento: Article País de afiliación: Francia Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Churg-Strauss / Antialérgicos / Omalizumab Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Arthritis Rheumatol Año: 2016 Tipo del documento: Article País de afiliación: Francia Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA