Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2016
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
_version_ 1782411465768042496
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
work_keys_str_mv AT nosadinimargherita rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT alpergulay rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT rineycatherinej rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT bensonlesliea rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT mohammadshekeebs rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT ramanathansudarshini rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT nolanmelinda rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT appletonrichard rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT leventerrichardj rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT deivakumaran rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT brilotfabienne rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT gormanmarkp rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT waldmanamyt rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT banwellbrenda rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder
AT dalerussellc rituximabmonitoringandredosinginpediatricneuromyelitisopticaspectrumdisorder