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without authorization.
Standard care for antineutrophil cytoplasmic antibody (ANCA)-associated
.
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
58 mg/dL, gastrointestinal 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
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
as soon as possible is recommended.
Patients with AAV should be monitored and treated
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.