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Eculizumab use in neuromyelitis optica spectrum disorders: routine clinical care data from a european cohort

Title: Eculizumab use in neuromyelitis optica spectrum disorders: routine clinical care data from a european cohort
Authors: Ringelstein, M.; Asseyer, S.; Lindenblatt, G.; Fischer, K.; Pul, R.; Skuljec, J.; Revie, L.; Giglhuber, K.; Häußler, V.; Karenfort, M.; Hellwig, K.; Paul, F.; Bellmann-Strobl, J.; Otto, C.; Ruprecht, K.; Ziemssen, T.; Emmer, A.; Rothhammer, V.; Nickel, F.T.; Angstwurm, K.; Linker, R.; Laurent, S.A.; Warnke, C.; Jarius, S.; Korporal-Kuhnke, M.; Wildemann, B.; Wolff, S.; Seipelt, M.; Yalachkov, Y.; Retzlaff, N.; Zettl, U.K.; Rommer, P.S.; Kowarik, M.C.; Wickel, J.; Geis, C.; Hümmert, M.W.; Trebst, C.; Senel, M.; Gold, R.; Klotz, L.; Kleinschnitz, C.; Meuth, S.G.; Aktas, O.; Berthele, A.; Ayzenberg, I.
Publisher Information: American Academy of Neurology
Publication Year: 2024
Collection: Max-Delbrueck-Center for Molecular Medicine, Berlin: MDC Repository
Subject Terms: Function and Dysfunction of the Nervous System; Topic 3: Integrative Biomedicine
Description: BACKGROUND AND OBJECTIVES: Attack prevention is crucial in managing neuromyelitis optica spectrum disorders (NMOSDs). Eculizumab (ECU), an inhibitor of the terminal complement cascade, was highly effective in preventing attacks in a phase III trial of aquaporin-4 (AQP4)-IgG seropositive(+) NMOSDs. In this article, we evaluated effectiveness and safety of ECU in routine clinical care. METHODS: We retrospectively evaluated patients with AQP4-IgG+ NMOSD treated with ECU between December 2014 and April 2022 at 20 German and 1 Austrian university center(s) of the Neuromyelitis Optica Study Group (NEMOS) by chart review. Primary outcomes were effectiveness (assessed using annualized attack rate [AAR], MRI activity, and disability changes [Expanded Disability Status Scale {EDSS}]) and safety (including adverse events, mortality, and attacks after meningococcal vaccinations), analyzed by descriptive statistics. RESULTS: Fifty-two patients (87% female, age 55.0 ± 16.3 years) received ECU for 16.2 (interquartile range [IQR] 9.6 - 21.7) months. Forty-five patients (87%) received meningococcal vaccination before starting ECU, 9 with concomitant oral prednisone and 36 without. Seven of the latter (19%) experienced attacks shortly after vaccination (median: 9 days, IQR 6-10 days). No postvaccinal attack occurred in the 9 patients vaccinated while on oral prednisone before starting ECU and in 25 (re-)vaccinated while on ECU. During ECU therapy, 88% of patients were attack-free. The median AAR decreased from 1.0 (range 0-4) in the 2 years preceding ECU to 0 (range 0-0.8; p < 0.001). The EDSS score from start to the last follow-up was stable (median 6.0), and the proportion of patients with new T2-enhancing or gadolinium-enhancing MRI lesions in the brain and spinal cord decreased. Seven patients (13%) experienced serious infections. Five patients (10%; median age 53.7 years) died on ECU treatment (1 from myocardial infarction, 1 from ileus with secondary sepsis, and 3 from systemic infection, including 1 meningococcal ...
Document Type: article in journal/newspaper
File Description: application/pdf; other
Language: English
Relation: https://edoc.mdc-berlin.de/id/eprint/24820/1/24820oa.pdf; https://edoc.mdc-berlin.de/id/eprint/24820/2/24820suppl.zip; Eculizumab use in neuromyelitis optica spectrum disorders: routine clinical care data from a european cohort. Ringelstein, M., Asseyer, S., Lindenblatt, G., Fischer, K., Pul, R., Skuljec, J., Revie, L., Giglhuber, K., Häußler, V., Karenfort, M., Hellwig, K., Paul, F., Bellmann-Strobl, J., Otto, C., Ruprecht, K., Ziemssen, T., Emmer, A., Rothhammer, V., Nickel, F.T., Angstwurm, K., Linker, R., Laurent, S.A., Warnke, C., Jarius, S., Korporal-Kuhnke, M., Wildemann, B., Wolff, S., Seipelt, M., Yalachkov, Y., Retzlaff, N., Zettl, U.K., Rommer, P.S., Kowarik, M.C., Wickel, J., Geis, C., Hümmert, M.W., Trebst, C., Senel, M., Gold, R., Klotz, L., Kleinschnitz, C., Meuth, S.G., Aktas, O., Berthele, A. and Ayzenberg, I. Neurology 103 (9): e209888. 12 November 2024; PMID:39353149; https://doi.org/10.1212/wnl.0000000000209888
DOI: 10.1212/wnl.0000000000209888
Availability: https://edoc.mdc-berlin.de/id/eprint/24820/; https://edoc.mdc-berlin.de/24820/; https://doi.org/10.1212/wnl.0000000000209888
Rights: cc_by_nc_nd_4
Accession Number: edsbas.ADA6476B
Database: BASE