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Ocrelizumab-induced neutropenia: severity, recurrence, and management. A French national pharmacovigilance study
Vincent Brochard1, Benjamin Le Vavasseur2, Sylvine Pinel3
1Department of Neurology, Hôpital Fondation Adolphe de Rothschild, Paris, France.
Background:
Ocrelizumab, an anti-CD20 monoclonal antibody, has proven effective in reducing relapses and disease progression in multiple sclerosis. While neutropenia is a known adverse effect of anti-CD20 therapies, data on the clinical severity, recurrence risk, and management of ocrelizumab-induced neutropenia (OIN) remain limited.
Objectives:
Describe clinical severity, recurrence risk and management of OIN.
Methods:
We performed a retrospective observational study based on OIN reports from the French Pharmacovigilance Database. A questionnaire was sent to clinicians who had reported cases. Patients with moderate or severe neutropenia (< 1.0 G/L) were included.
Results:
Thirty-four cases of OIN were analysed. Neutropenia was mostly late-onset (>4 weeks post-cycle, 94.1 %) and occurred mainly after the first (32.4 %), second or third cycle (26.5 %). Most patients (55.9 %) were asymptomatic, 32.4 % developed infections and 11.8 % presented agranulocytosis symptoms. Ocrelizumab was reintroduced in 15 patients, with recurrence in 4 cases (26.6 %). Two cases of recurrent neutropenia were reported after switching to ofatumumab.
Conclusion:
OIN is an intermittent adverse event, often discovered incidentally and generally not severe. Most cases are likely to go undetected as asymptomatic. With a recurrence rate of 25 %, rechallenging with ocrelizumab should be considered based on MS condition of the patient and available alternative treatment.
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