Occurrence of Late-Onset Neurotropenia After Anti-CD20 Therapy: Tianrong Yeo, PhD, MBBS, MRCP, MMED, FAMS, MCI
The senior consultant for the department of neurology at the National Neuroscience Institute discussed a report on two patients who developed an uncommon adverse event of late-onset neurotropenia after anti-CD20 therapy treatment. [WATCH TIME: 8 minutes]
WATCH TIME: 8 minutes
“For both of our patients in the report, we actually reinitiated the anti-CD 20 therapy, and they did well in a sense that it didn't reoccur, and they still continue to use the drugs.”
Anti-CD20 therapies have become increasingly used to treat neuroinflammatory conditions such as multiple sclerosis (MS) and neuromyelitis optica spectrum disorders (NMOSD). It has been described that late-onset neurotropenia (LON), a rare adverse event, can be found following use of treatments such as rituximab (Rituxan; Genentech/Biogen) and ocrelizumab (Ocrevus; Genentech).
A recently conducted report on two patients treated with an anti-CD20 therapy who developed LON was published in Neuroimmunology Reports.1 After the report on the two patients, a retrospective chart review was conducted on patients with neuroinflammatory conditions on anti-CD20 therapies from January 2015 to December 2021. The review identified 77 patients as having multiple sclerosis (MS; n = 41) or NMOSD(n = 26). In addition, 9 patients with MS were given ocrelizumab and the rest of the patients received rituximab (MS and NMOSD, n = 58).
The data was collected over a 7-year period and the incidence rate was 11% for the two patients reported with LON.1 In addition, the rate for using the treatments of ocrelizumab and rituximab for patients with LON was 1.7%, respectively. There was a 3.0% rate for the overall use of anti-CD20 treatment with the patients in the report.
Recently in an interview with NeurologyLive®, coauthor
REFERENCES
1. Lim CS, Tye JS, Tan K, Yeo T. Late-onset neutropenia following anti-CD20 therapies in Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorders: A report on two patients. Neuroimmunol Rep. 2022; 100136. doi:10.1016/j.nerep.2022.100136
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