Rituximab Monitoring and Redosing in Pediatric Neuromyelitis Optica Spectrum Disorder
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Objective: To study rituximab in pediatric neuromyelitis optica (NMO)/NMO spectrum disorders (NMOSD) and the relationship between rituximab, B cell repopulation, and relapses in order to improve rituximab monitoring and redosing.
Methods: Multicenter retrospective study of 16 children with NMO/NMOSD receiving ≥2 rituximab courses. According to CD19 counts, events during rituximab were categorized as "repopulation," "depletion," or "depletion failure" relapses (repopulation threshold CD19 ≥10 × 10(6) cells/L).
Results: The 16 patients (14 girls; mean age 9.6 years, range 1.8-15.3) had a mean of 6.1 events (range 1-11) during a mean follow-up of 6.1 years (range 1.6-13.6) and received a total of 76 rituximab courses (mean 4.7, range 2-9) in 42.6-year cohort treatment. Before rituximab, 62.5% had received azathioprine, mycophenolate mofetil, or cyclophosphamide. Mean time from rituximab to last documented B cell depletion and first repopulation was 4.5 and 6.8 months, respectively, with large interpatient variability. Earliest repopulations occurred with the lowest doses. Significant reduction between pre- and post-rituximab annualized relapse rate (ARR) was observed (p = 0.003). During rituximab, 6 patients were relapse-free, although 21 relapses occurred in 10 patients, including 13 "repopulation," 3 "depletion," and 4 "depletion failure" relapses. Of the 13 "repopulation" relapses, 4 had CD19 10-50 × 10(6) cells/L, 10 had inadequate monitoring (≤1 CD19 in the 4 months before relapses), and 5 had delayed redosing after repopulation detection.
Conclusion: Rituximab is effective in relapse prevention, but B cell repopulation creates a risk of relapse. Redosing before B cell repopulation could reduce the relapse risk further.
Classification Of Evidence: This study provides Class IV evidence that rituximab significantly reduces ARR in pediatric NMO/NMOSD. This study also demonstrates a relationship between B cell repopulation and relapses.
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Wu H, Gombolay G, Yang J, Graves J, Christy A, Xiang X Curr Neurol Neurosci Rep. 2024; 24(10):479-494.
PMID: 39259430 DOI: 10.1007/s11910-024-01366-7.
Tisavipat N, Juan H, Chen J Saudi J Ophthalmol. 2024; 38(1):2-12.
PMID: 38628414 PMC: 11017007. DOI: 10.4103/sjopt.sjopt_102_23.
Eva L, Ples H, Covache-Busuioc R, Glavan L, Bratu B, Bordeianu A Biomedicines. 2023; 11(9).
PMID: 37760930 PMC: 10526343. DOI: 10.3390/biomedicines11092489.
Wang R, Sun D, Du Q, Shi Z, Chen H, Zhou H J Neurol. 2023; 270(10):5085-5089.
PMID: 37204456 DOI: 10.1007/s00415-023-11776-1.
Therapeutic Response in Pediatric Neuromyelitis Optica Spectrum Disorder.
Pizzolato Umeton R, Waltz M, Aaen G, Benson L, Gorman M, Goyal M Neurology. 2022; 100(9):e985-e994.
PMID: 36460473 PMC: 9990442. DOI: 10.1212/WNL.0000000000201625.