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Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder
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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4723136/ https://www.ncbi.nlm.nih.gov/pubmed/26819962 http://dx.doi.org/10.1212/NXI.0000000000000188 |
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author | Nosadini, Margherita Alper, Gulay Riney, Catherine J. Benson, Leslie A. Mohammad, Shekeeb S. Ramanathan, Sudarshini Nolan, Melinda Appleton, Richard Leventer, Richard J. Deiva, Kumaran Brilot, Fabienne Gorman, Mark P. Waldman, Amy T. Banwell, Brenda Dale, Russell C. |
author_facet | Nosadini, Margherita Alper, Gulay Riney, Catherine J. Benson, Leslie A. Mohammad, Shekeeb S. Ramanathan, Sudarshini Nolan, Melinda Appleton, Richard Leventer, Richard J. Deiva, Kumaran Brilot, Fabienne Gorman, Mark P. Waldman, Amy T. Banwell, Brenda Dale, Russell C. |
author_sort | Nosadini, Margherita |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4723136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-47231362016-01-27 Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder Nosadini, Margherita Alper, Gulay Riney, Catherine J. Benson, Leslie A. Mohammad, Shekeeb S. Ramanathan, Sudarshini Nolan, Melinda Appleton, Richard Leventer, Richard J. Deiva, Kumaran Brilot, Fabienne Gorman, Mark P. Waldman, Amy T. Banwell, Brenda Dale, Russell C. Neurol Neuroimmunol Neuroinflamm Article 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. Lippincott Williams & Wilkins 2016-01-21 /pmc/articles/PMC4723136/ /pubmed/26819962 http://dx.doi.org/10.1212/NXI.0000000000000188 Text en © 2016 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Article Nosadini, Margherita Alper, Gulay Riney, Catherine J. Benson, Leslie A. Mohammad, Shekeeb S. Ramanathan, Sudarshini Nolan, Melinda Appleton, Richard Leventer, Richard J. Deiva, Kumaran Brilot, Fabienne Gorman, Mark P. Waldman, Amy T. Banwell, Brenda Dale, Russell C. Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder |
title | Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder |
title_full | Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder |
title_fullStr | Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder |
title_full_unstemmed | Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder |
title_short | Rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder |
title_sort | rituximab monitoring and redosing in pediatric neuromyelitis optica spectrum disorder |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4723136/ https://www.ncbi.nlm.nih.gov/pubmed/26819962 http://dx.doi.org/10.1212/NXI.0000000000000188 |
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