Evaluate the Remission MAINtenance Using Extended Administration of Prednisone in Systemic Anti-neutrophil Cytoplasmic Antibodies (ANCA)-Associated Vasculitis.

Last updated: November 20, 2019
Sponsor: Hospices Civils de Lyon
Overall Status: Active - Recruiting

Phase

N/A

Condition

Vascular Diseases

Lupus

Dermatomyositis (Connective Tissue Disease)

Treatment

N/A

Clinical Study ID

NCT03290456
69HCL17_0020
  • Ages > 18
  • All Genders

Study Summary

Immunosuppressive therapy of granulomatosis with polyangiitis (GPA, Wegener's) and microscopic polyangiitis (MPA) has transformed the outcome from death to a strong likelihood of disease control and temporary remission. However, most patients have recurrent relapses that lead to damage and require repeated treatment associated with long-term morbidity and death.

Rituximab has been shown to be as effective as cyclophosphamide to induce remission and maintenance of remission in severe GPA and MPA patients, with an acceptable safety profile . Although rituximab is becoming the standard of care for maintenance therapy in these patients, relapse still occurs and the optimal duration of prednisone therapy remains debated.

On the one hand, most US studies use early withdrawal (6-12 months) because of feared side effects. On the other hand, most European trials propose late withdrawal (>18 months) given a lower observed relapse rate on long-term low dose glucocorticoids treatment.

In a systematic review and meta-analysis, glucocorticoids regimen was the most significant variable explaining the variability between the proportions of ANCA-associated vasculitis patients with relapses. Nevertheless, it was an indirect estimation of treatment effect because of the absence of dedicated randomized trial. This meta-analysis concluded that combined longer-term (i.e. >12 months) use of low dose prednisone or nonzero glucocorticoids target is associated with a 20% reduction of relapse compared to early withdrawal (i.e. ≤12 months).

The relapse rate in patients with early glucocorticoids (10-12 months) withdrawal was provided in two studies and was of 37 and 34%, respectively. By contrast, the relapse rate in patients with late prednisone withdrawal (18-24 months) and receiving rituximab as maintenance treatment was 14% at 24 months in the MAINRITSAN trial. Of note, the decision to withdraw glucocorticoids after 18 months was left to physician's discretion in this study and two thirds of the nonsevere relapses occurred when patients were off prednisone.

The trial detailed here is the first prospective trial evaluating the length of glucocorticoid administration as remission adjunctive treatment for patients with GPA or MPA.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients with a diagnosis of MPA or GPA independently of ANCA status,

  • Patient aged of 18 years or older,

  • Patients with newly-diagnosed disease or relapsing disease at the time of screening,with an inactive disease defined as a BVAS = 0,

  • Patients receiving maintenance infusion of rituximab 500 mg at 6 and 12 months afterthe start of vasculitis induction

  • Patients receiving 5-10 mg/day of prednisone at screening,

  • Patient able to give written informed consent prior to participation in the study.

  • At Inclusion visit day, patient must be between 5 and 10 mg/day prednisone and atrandomization visit day (D1), patient must be at 5 mg/day prednisone

Exclusion

Exclusion Criteria:

  • Patients with EGPA, or other vasculitides, defined by the ACR criteria and/or theChapel Hill Consensus Conference,

  • Patients with vasculitis with active disease defined as a BVAS >0,

  • Patients with acute infections or chronic active infections (including HIV, HBV orHCV),

  • Patients with active cancer or recent cancer (<5 years), except basocellular carcinomaand prostatic cancer of low activity controlled by hormonal treatment,

  • Pregnant women and lactation. Patients with childbearing potential should havereliable contraception for the all duration of the study,

  • Patients with other uncontrolled diseases, including drug or alcohol abuse, severepsychiatric diseases, that could interfere with participation in the trial accordingto the protocol,

  • Patients included in other investigational therapeutic study within the previous 3months,

  • Patients suspected not to be observant to the proposed treatments,

  • Patients who have white blood cell count ≤4,000/mm3,

  • Patients who have platelet count ≤100,000/mm3,

  • Patients who have ALT or AST level greater than 3 times the upper limit of normal thatcannot be attributed to underlying MPA-GPA disease,

  • Patients unable to give written informed consent prior to participation in the study.

  • Patients with contraindication to use rituximab,

Study Design

Total Participants: 146
Study Start date:
August 20, 2019
Estimated Completion Date:
June 04, 2024

Study Description

Immunosuppressive therapy of granulomatosis with polyangiitis (GPA, Wegener's) and microscopic polyangiitis (MPA) has transformed the outcome from death to a strong likelihood of disease control and temporary remission. However, most patients have recurrent relapses that lead to damage and require repeated treatment associated with long-term morbidity and death.

Rituximab has been shown to be as effective as cyclophosphamide to induce remission and maintenance of remission in severe GPA and MPA patients, with an acceptable safety profile. Although rituximab is becoming the standard of care for maintenance therapy in these patients, relapse still occurs and the optimal duration of prednisone therapy remains debated.

On the one hand, most US studies use early withdrawal (6-12 months) because of feared side effects. On the other hand, most European trials propose late withdrawal (>18 months) given a lower observed relapse rate on long-term low dose glucocorticoids treatment.

In a systematic review and meta-analysis, glucocorticoids regimen was the most significant variable explaining the variability between the proportions of ANCA-associated vasculitis patients with relapses. Nevertheless, it was an indirect estimation of treatment effect because of the absence of dedicated randomized trial. This meta-analysis concluded that combined longer-term (i.e. >12 months) use of low dose prednisone or nonzero glucocorticoids target is associated with a 20% reduction of relapse compared to early withdrawal (i.e. ≤12 months).

The relapse rate in patients with early glucocorticoids (10-12 months) withdrawal was provided in two studies and was of 37 and 34%, respectively. By contrast, the relapse rate in patients with late prednisone withdrawal (18-24 months) and receiving rituximab as maintenance treatment was 14% at 24 months in the MAINRITSAN trial. Of note, the decision to withdraw glucocorticoids after 18 months was left to physician's discretion in this study and two thirds of the nonsevere relapses occurred when patients were off prednisone.

The trial detailed here is the first prospective trial evaluating the length of glucocorticoid administration as remission adjunctive treatment for patients with GPA or MPA.

Connect with a study center

  • CHU Amiens-Hôpital Nord

    Amiens, 80054
    France

    Active - Recruiting

  • CHU Angers

    Angers, 49933
    France

    Active - Recruiting

  • Clinique Rhône-Durance

    Avignon, 84000
    France

    Site Not Available

  • Hôpital Jeanne d'Arc

    Bar-le-Duc, 55000
    France

    Site Not Available

  • Hôpital Avicenne

    Bobigny, 93009
    France

    Site Not Available

  • Hôpital La Cavale Blanche

    Brest, 29200
    France

    Active - Recruiting

  • Hôpital Louis Pradel

    Bron, 69500
    France

    Active - Recruiting

  • CHU de Caen - Cote de Nacre

    Caen, 14033
    France

    Active - Recruiting

  • Hôpital Louis Pasteur

    Chartres, 28018
    France

    Site Not Available

  • CHU Estaing

    Clermont-Ferrand, 63003
    France

    Active - Recruiting

  • CHU Gabriel Montpied

    Clermont-Ferrand, 63003
    France

    Active - Recruiting

  • CHIC Créteil

    Créteil, 94010
    France

    Site Not Available

  • CHRU François Mitterrand

    Dijon, 21000
    France

    Site Not Available

  • CHRU Lille - Hôpital Claude Huriez

    Lille, 59037
    France

    Site Not Available

  • Centre Hospitalier Croix Rousse

    Lyon, 69004
    France

    Active - Recruiting

  • Hôpital Edouard Herriot

    Lyon, 69137
    France

    Site Not Available

  • Hôpital La Timone

    Marseille, 13385
    France

    Site Not Available

  • Hôpital de la Conception

    Marseille, 13005
    France

    Site Not Available

  • HP Site Belle Isle

    Metz, 57045
    France

    Site Not Available

  • CHU Nantes - Hôtel Dieu

    Nantes, 44093
    France

    Active - Recruiting

  • CHU de Nice - Hôpital Pasteur 2

    Nice, 06001
    France

    Active - Recruiting

  • Hôpital Cochin

    Paris, 75014
    France

    Active - Recruiting

  • Hôpital Européen G. Pompidou

    Paris, 75015
    France

    Site Not Available

  • Hôpital Saint Louis

    Paris, 75475
    France

    Site Not Available

  • Hôpital la Pitié Salpêtrière

    Paris, 75013
    France

    Active - Recruiting

  • Hôpital Haut Lévêque

    Pessac, 33600
    France

    Site Not Available

  • CH Lyon Sud

    Pierre-Bénite, 69495
    France

    Active - Recruiting

  • Centre Hospitalier Lyon Sud

    Pierre-Bénite, 69310
    France

    Active - Recruiting

  • CHU de Poitiers

    Poitiers, 86021
    France

    Site Not Available

  • CHRU Rennes - Hôpital Sud

    Rennes, 35200
    France

    Active - Recruiting

  • Hôpital Charles Nicolle

    Rouen, 76031
    France

    Active - Recruiting

  • CHRU Hautepierre

    Strasbourg, 67098
    France

    Site Not Available

  • CHU Strasbourg

    Strasbourg, 67000
    France

    Site Not Available

  • Hopitaux Universaitaire de Strasbourg Hopitaux

    Strasbourg,
    France

    Active - Recruiting

  • Hôpital Foch

    Suresnes, 92150
    France

    Site Not Available

  • CHRU Bretonneau

    Tours, 37044
    France

    Site Not Available

  • CH de Troyes

    Troyes, 10003
    France

    Active - Recruiting

  • CH Valenciennes

    Valenciennes, 59322
    France

    Active - Recruiting

  • Hôpitaux de Brabois

    Vandœuvre-lès-Nancy, 54511
    France

    Site Not Available

  • CH Bretagne Atlantique

    Vannes, 56017
    France

    Active - Recruiting

  • CH de Verdun

    Verdun, 55100
    France

    Site Not Available

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