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Induction failure in granulomatosis with polyangiitis: a nationwide case-control study of risk factors and outcomes.
Sorin, Boris; Iudici, Michele; Guerry, Mary-Jane; Samson, Maxime; Bielefeld, Philip; Maillet, Thibault; Nouvier, Mathilde; Karras, Alexandre; Meyer, Lara; Lavigne, Christian; Régent, Alexis; Durel, Cécile-Audrey; Fabre, Marc; Charles, Pierre; Raimbourg, Quentin; Lanteri, Aurélia; Pugnet, Grégory; Rivière, Frédéric; Pineton de Chambrun, Marc; Cacoub, Patrice; Le Guenno, Guillaume; Jourdain, Pierre; Mekinian, Arsène; Paule, Romain; Dion, Jérémie; Legendre, Paul; Cohen, Pascal; Guillevin, Loïc; Puéchal, Xavier; Terrier, Benjamin.
Afiliação
  • Sorin B; Department of Internal Medicine, Hôpital Cochin, Paris, France.
  • Iudici M; National Reference Center for Rare Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  • Guerry MJ; National Reference Center for Rare Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  • Samson M; Division of Rheumatology, Department of Internal Medicine and Department of Medicine, Faculty of Medicine, Geneva University Hospitals, Geneve, Switzerland.
  • Bielefeld P; Department of Nephrology, Centre Hospitalier de Valenciennes, Valenciennes, France.
  • Maillet T; Department of Internal Medicine and Clinical Immunology, Hôpital François Mitterrand, Dijon, France.
  • Nouvier M; Department of Nephrology and Systemic Diseases, Hôpital François Mitterrand, Dijon, France.
  • Karras A; Department of Internal Medicine and Clinical Immunology, Hôpital François Mitterrand, Dijon, France.
  • Meyer L; Department of Nephrology, Centre Hospitalier Lyon Sud, Lyon, France.
  • Lavigne C; Department of Nephrology, Hôpital Européen Georges Pompidou, Paris, France.
  • Régent A; Department of Nephrology, Hôpital Européen Georges Pompidou, Paris, France.
  • Durel CA; Department of Internal Medicine-Clinical Immunology, Centre Hospitalier Universitaire d'Angers, Angers, France.
  • Fabre M; Department of Internal Medicine, Hôpital Cochin, Paris, France.
  • Charles P; National Reference Center for Rare Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  • Raimbourg Q; Department of Internal Medicine, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
  • Lanteri A; Department of Internal Medicine, Centre Hospitalier Pierre Oudot, Bourgouin, France.
  • Pugnet G; Department of Internal Medicine, Institut Mutualiste Montsouris, Paris, France.
  • Rivière F; Department of Nephrology, Hôpital Bichat Claude Bernard, Paris, France.
  • Pineton de Chambrun M; Department of Internal Medicine-Infectious Diseases, Centre Hospitalier d'Antibes, Antibes, France.
  • Cacoub P; Department of Internal Medicine and Clinical Immunology, Hôpital Rangueil, Toulouse, France.
  • Le Guenno G; Department of Pneumology, Hôpital d'Instruction des Armées Percy, Clamart, France.
  • Jourdain P; Department of Internal Medicine 2, Hôpital Pitié Salpêtrière, Paris, France.
  • Mekinian A; Department of Internal Medicine and Clinical Immunology, Hôpital Pitié Salpêtrière, Paris, France.
  • Paule R; Department of Internal Medicine, Hôpital d'Estaing, Clermont-Ferrand, France.
  • Dion J; Department of Nephrology, Centre Hospitalier Universitaire de Limoges, Limoges, France.
  • Legendre P; Department of Internal Medicine, Hôpital Saint-Antoine, Paris, France.
  • Cohen P; Department of Internal Medicine, Hôpital Foch, Suresnes, France.
  • Guillevin L; Department of Internal Medicine, Hôpital Cochin, Paris, France.
  • Puéchal X; National Reference Center for Rare Systemic and Autoimmune Diseases, Hôpital Cochin, Paris, France.
  • Terrier B; Department of Internal Medicine, Hôpital Cochin, Paris, France.
Rheumatology (Oxford) ; 62(11): 3662-3671, 2023 11 02.
Article em En | MEDLINE | ID: mdl-36847447
ABSTRACT

OBJECTIVE:

To identify characteristics of granulomatosis with polyangiitis (GPA) associated with induction failure, describe salvage therapies and their efficacy.

METHODS:

We conducted a nationwide retrospective case-control study of GPA with induction failure between 2006 and 2021. Each patient with induction failure was randomly paired to three controls matched for age, sex and induction treatment.

RESULTS:

We included 51 patients with GPA and induction failure (29 men and 22 women). At induction therapy, median age was 49 years. Twenty-seven patients received intravenous cyclophosphamide (ivCYC) and 24 rituximab (RTX) as induction therapy. Patients with ivCYC induction failure more frequently had PR3-ANCA (93% vs 70%, P = 0.02), relapsing disease (41% vs 7%, P < 0.001) and orbital mass (15% vs 0%, P < 0.01) compared with controls. Patients with disease progression despite RTX induction therapy more frequently had renal involvement (67% vs 25%, P = 0.02) with renal failure (serum creatinine >100 µmol/l in 42% vs 8%, P = 0.02) compared with controls. After salvage therapy, remission was achieved at 6 months in 35 (69%) patients. The most frequent salvage therapy was switching from ivCYC to RTX (or vice versa), showing an efficacy in 21/29 (72%). Remission was achieved in nine (50%) patients with inappropriate response to ivCYC, while in patients with progression after RTX induction, remission was achieved in four (100%) who received ivCYC (with or without immunomodulatory therapy), but only in three (50%) after adding immunomodulatory therapy alone.

CONCLUSION:

In patients with induction failure, characteristics of GPA, salvage therapies and their efficacy vary according to induction therapy and failure modality.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Granulomatose com Poliangiite / Vasculite Associada a Anticorpo Anticitoplasma de Neutrófilos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Granulomatose com Poliangiite / Vasculite Associada a Anticorpo Anticitoplasma de Neutrófilos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França