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    Home > Active Ingredient News > Immunology News > ANCA-associated vasculitis has recurred, how to deal with it? Latest roundup

    ANCA-associated vasculitis has recurred, how to deal with it? Latest roundup

    • Last Update: 2023-01-07
    • Source: Internet
    • Author: User
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    Standard care for antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) consists of two phases, starting with glucocorticoids (GC) plus cyclophosphamide or rituximab to induce remission, followed by remission maintenance therapy to prevent relapse
    .
    Still, there is a significant risk of
    relapse.
    This article discusses new strategies for the prevention and treatment of AAV recurrence, with a focus on granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA).


    Evaluation for suspected recurrence of AAV


    AAV has a tendency to spontaneously recur, sometimes severe and potentially organ-endangering or life-threatening
    .
    There is currently insufficient evidence to predict episodes or recurrence, and there are no reliable indicators to guide risk stratification
    of recurrence.
    Therefore, ongoing and regular clinical monitoring of patients with AAV after remission induction is recommended for early detection of recurrence, when symptoms and signs are generally milder
    than when relapse is confirmed.


    For patients with suspected recurrence of AAV, the clinical manifestations need to be determined first, then the diagnosis should be clarified, the differential diagnosis should be excluded, and the severity of the recurrence should be determined, and the corresponding treatment plan
    should be formulated.
    Once relapse is diagnosed, its severity must be thoroughly assessed for organ or vital manifestations
    .
    About one-third of relapses are severe conditions
    that affect the kidneys and patient survival.


    To help clinicians determine the best treatment strategy and avoid overtreatment, a five-factor score (FFS) can be used to assess patient outcomes
    .
    Five factors include proteinuria > 1 g/day, renal insufficiency with serum creatinine >1.
    58 mg/dL, gastrointestinal involvement, cardiomyopathy, and central nervous system involvement
    .
    The higher the FFS score, the worse
    the prognosis.


    Principles of treatment of recurrence of AAV


    Patients with relapse should follow the same principles of treatment as newly diagnosed patients, taking into account several factors: classification of disease, expected outcome, severity, previous treatment, comorbidities, and age
    .
    Its management includes rapid initiation of therapy to avoid organ damage and early death, followed by maintenance remission therapy
    with less toxic immunosuppressive regimens.


    Treatment with recurrence of organ-threatening or life-threatening manifestations of AAV


    For recurrence of AAV with organ-threatening or life-threatening manifestations, it is recommended to reintroduce or intensify the GC dose in conjunction with cyclophosphamide or rituximab
    .
    Rituximab is preferred, in contrast, with a better response to treatment in patients with recurrent disease
    .
    After completion of induction with cyclophosphamide, maintenance therapy with cyclophosphamide should be spaced 2-4 weeks
    apart, regardless of the choice of drug maintenance therapy.
    Cyclophosphamide can be taken orally, but oral administration is not recommended as first-line therapy because oral administration is more likely to cause adverse effects
    than infusion.


    The role of plasmapheresis in the treatment of AAV has been a research hotspot, especially for refractory or severe AAV
    .
    The latest evidence shows that plasmapheresis has no significant effect on mortality in patients with AAV and reduces the risk of end-stage renal disease up to 12 months, but increases the risk of
    serious infection.
    Therefore, plasmapheresis is more appropriate for selected patients with AAV: with antiglomerular basement disease or rapidly progressive glomerulonephritis but minimal scarring and/or ANCA-induced pulmonary hemorrhage
    .


    Treatment of mild recurrent AAV


    GPA carries a clear risk of recurrence, so immunosuppressants or immunomodulators should be used in combination with GC
    in all patients with active disease, regardless of severity.
    For non-severe active MPA, first-line GC monotherapy such as ≤ 1 mg/kg/day of prednisone or other equivalent corticosteroids
    is recommended.
    Immunosuppressants may be used monotherapy in patients with MPA who cannot be controlled, or as an alternative to GC, or in cases of intolerance to GC
    .


    Long-term management of AAV


    ANCA is an important biomarker for AAV, but for patients with GPA or MPA, it is not recommended to adjust immunosuppressants
    based solely on ANCA titer results.
    Elevated ANCA titers can only be used as an indicator of AAV activity with limited information, and it is not a reliable predictor
    of recurrence in individual patients.
    Strengthening immunosuppressive therapy based solely on ANCA titer or its change may cause unwanted immunosuppression and thus adverse events
    .
    In addition, a persistent positive ANCA does not necessarily mean the need to continue immunosuppressive therapy
    .


    Once remission is achieved, prolonged maintenance therapy is recommended and prophylactic therapy is recommended: low-dose (500 mg) rituximab
    is administered every 6 months.
    For patients with AAV receiving rituximab or cyclophosphamide, measures to prevent Pneumocystis jirovecii pneumonia are recommended, and vaccination
    as soon as possible is recommended.
    Patients with AAV should be monitored and treated for hypertension, high cholesterol, and diabetes
    as appropriate.
    Patients should also be strongly discouraged from smoking and advised to adopt a healthy lifestyle
    .


    References: Puéchal X, Guillevin L.
    How best to manage relapse and remission in ANCA-associated vasculitis[J].
    Expert Rev Clin Immunol.
    2022 Sep 14.
    doi: 10.
    1080/1744666X.
    2022.
    2122954.
    Epub ahead of print.
    PMID: 36102147.

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