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https://repository.monashhealth.org/monashhealthjspui/handle/1/51386| Conference/Presentation Title: | Real-world experience with ocrelizumab in the msbase registry - Australian RRMS cohort. | Authors: | Butzkueven H.;Spelman T.;Kalincik T.;Buzzard K.;Van Der Walt A.;Lechner-Scott J.;Hodgkinson S.;Butler E. ;Macdonell R.;Slee M.;Marcel B. | Monash Health Department(s): | Neurology | Institution: | (Butzkueven, Van Der Walt) Monash University, Melbourne, VIC, Australia (Butzkueven, Spelman) MSBase Foundation, Melbourne, VIC, Australia (Kalincik) University of Melbourne, Melbourne, VIC, Australia (Buzzard) Box Hill Hospital, Box Hill, VIC, Australia (Lechner-Scott) University of Newcastle, Newcastle, NSW, Australia (Hodgkinson) Liverpool Hospital, Sydney, NSW, Australia (Butler) Monash Medical Centre, Melbourne, VIC, Australia (Macdonell) Austin Health, Melbourne, VIC, Australia (Slee) Flinders University, Adelaide, SA, Australia (Marcel) Roche Products Pty Ltd, Sydney, NSW, Australia |
Presentation/Conference Date: | 23-Mar-2024 | Copyright year: | 2021 | Publisher: | BMJ Publishing Group | Publication information: | BMJ Neurology Open. Conference: Australian and New Zealand Association of Neurologists Annual Scientific Meeting, Anzan 2021. Virtual. 3(supplement 1) (pp A4-a5), 2021. Date of Publication: August 2021. | Journal: | BMJ Neurology Open | Abstract: | Introduction Ocrelizumab (OCR) is a humanised anti-CD20+ monoclonal antibody for the treatment of Multiple Sclerosis. Objectives In Australian MSBase clinics, we describe baseline characteristics of relapsing-remitting MS (RRMS) patients treated with OCR, treatment pathways and early clinical outcomes. Methods Secondary analysis using MSBase Registry data for RRMS patients with OCR initiation within 3 months of MSBase recorded visit. Descriptive statistics included demographics, disease course/duration, prior disease modifying therapies (DMT) and EDSS. Relapse data was described in patients with -6 months follow-up. Results As of 4 June 2020, MSBase included 624 eligible Australian RRMS patients newly treated with OCR. Median age at OCR initiation was 42.5 years. OCR was first line therapy in 18.9% of patients. Most frequent DMT's in the 12 months prior to OCR were natalizumab (32.1%) and fingolimod (24.8%). Of 434 RRMS patients with -6 months follow-up, 392 remained relapse free (90.3%; 95% CI 81.6, 99.7) over a mean OCR exposure of 1.35 years. In this group, the annualized relapse rate (ARR) was 0.10 (95% CI 0.08-0.13), compared to an ARR of 0.83 in the 24 months pre-OCR start. Treatment discontinuation was recorded for 20 of these 434 patients In the overall RRMS cohort, treatment persistence at 12 and 24 months was 94.3% (95%CI: 90.9%- 96.1%%) and 88.7% (95%CI 77.2%-94.0%), respectively. Conclusion Almost 20% of RRMS patients treated with OCR in Australian MSBase centres received OCR as a first line treatment. During OCR treatment, relapses and OCR discontinuations were rare. | Conference Name: | Australian and New Zealand Association of Neurologists Annual Scientific Meeting, ANZAN 2021 | Conference Start Date: | 2021-05-19 | Conference End Date: | 2021-05-21 | Conference Location: | Virtual | DOI: | http://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1136/bmjno-2021-ANZAN.10 | URI: | https://repository.monashhealth.org/monashhealthjspui/handle/1/51386 | Type: | Conference Abstract | Subjects: | multiple sclerosis | Type of Clinical Study or Trial: | Observational study (cohort, case-control, cross sectional, or survey) |
| Appears in Collections: | Conference Abstracts |
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