Loading…
3149 Real-world Australian experience with Ofatumumab in the MSBase registry
ObjectivesTo characterize the use of ofatumumab (OFA), a fully human self-administered anti-CD20 monoclonal antibody, in a real-world setting in Australia by assessing the profile of relapsing multiple sclerosis (RMS) patients initiating OFA through an evaluation of patient demographics, background...
Saved in:
Published in: | BMJ neurology open 2024-08, Vol.6 (Suppl 1), p.A45-A46 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | A46 |
container_issue | Suppl 1 |
container_start_page | A45 |
container_title | BMJ neurology open |
container_volume | 6 |
creator | Migocki, Margaret Walt, Anneke Van der Butzkueven, Helmut Spelman, Tim Kermode, Allan Fabis-Pedrini, Marzena Carroll, William M Lechner-Scott, Jeannette John, Nevin Barnett, Michael Hodgkinson, Suzanne McCombe, Pamela Kalincik, Tomas Macdonell, Richard Slee, Mark Schmitt, Birte |
description | ObjectivesTo characterize the use of ofatumumab (OFA), a fully human self-administered anti-CD20 monoclonal antibody, in a real-world setting in Australia by assessing the profile of relapsing multiple sclerosis (RMS) patients initiating OFA through an evaluation of patient demographics, background MS disease characteristics and prior therapy history as recorded in MSBase.MethodsThis is a retrospective secondary use of MSBase Registry data study, describing the baseline characteristics of RMS patients in Australia initiated on OFA treatment, including demographics, disease duration, expanded disability status scale (EDSS), treatment history with disease-modifying therapies (DMTs) prior to commencing OFA and proportion of naïve patients initiating ofatumumab relative to patients having received a prior DMT.ResultsAs of 1st January 2024, MSBase has included 320 eligible patients initiated on OFA, with 22.2% treatment naïve, 30.9% switching from ocrelizumab, 14.7% switching from natalizumab, 3.1% from alemtuzumab and 27.7% from oral DMTs. The reasons for switching DMT to OFA included scheduled stop (13.1%), evidence of disease activity (9.1%), convenience (6.9%), side effects/intolerance (6.2%), JCV antibody positive (2.8%), pregnancy planned/confirmed (2.5%) and not reported (37.2%). The median age of patients initiating OFA was 42.67 [36.65, 51.98] years, with a median disease duration of 9.19 [3.61, 17.11] years and median EDSS of 2 [1.5, 3.5].ConclusionThe real-world data from this secondary use of data MSBase registry analysis provides a valuable snapshot of the Australian experience of relapsing MS patients initiated on OFA, with 22% of patients treated as first line therapy. |
doi_str_mv | 10.1136/bmjno-2024-ANZAN.127 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_706454ebc05847b9b6160577b6ab227b</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_706454ebc05847b9b6160577b6ab227b</doaj_id><sourcerecordid>3099106571</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1351-8e1e66937cfed2811e6ccbadd5202519debc8928216da2dbcd39a5ad466f149a3</originalsourceid><addsrcrecordid>eNpFkMtKw0AUhoMgWGrfwEXAderck1nG4qVQW_CycTOcyUzahFzqJKF258YX9UmctoKrwzn85-PnC4IrjKYYU3Gj67JpI4IIi9Lle7qcYhKfBSMiKIkEZugimHRdiRAiHLFEslGwpJjJn6_vZwtVtGtdZcJ06HoHVQFNaD-31hW2yWy4K_pNuMqhH-qhBh0WTdhvbPj0cgudDZ1dF_5rfxmc51B1dvI3x8Hb_d3r7DFarB7ms3QRaUw5jhKLrRCSxlluDUmw37JMgzHcd-dYGquzRJKEYGGAGJ0ZKoGDYULkvi_QcTA_cU0Lpdq6oga3Vy0U6nho3VqB64ussipGgnHmgYgnLNZSCywQj2MtQBMSa8-6PrG2rv0YbNersh1c4-sriqTESPAY-xQ6pbzj_wBG6iBeHcWrg3h1FK-8ePoL2ep5WQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3099106571</pqid></control><display><type>article</type><title>3149 Real-world Australian experience with Ofatumumab in the MSBase registry</title><source>BMJ Journals (Open Access)</source><source>PubMed Central</source><creator>Migocki, Margaret ; Walt, Anneke Van der ; Butzkueven, Helmut ; Spelman, Tim ; Kermode, Allan ; Fabis-Pedrini, Marzena ; Carroll, William M ; Lechner-Scott, Jeannette ; John, Nevin ; Barnett, Michael ; Hodgkinson, Suzanne ; McCombe, Pamela ; Kalincik, Tomas ; Macdonell, Richard ; Slee, Mark ; Schmitt, Birte</creator><creatorcontrib>Migocki, Margaret ; Walt, Anneke Van der ; Butzkueven, Helmut ; Spelman, Tim ; Kermode, Allan ; Fabis-Pedrini, Marzena ; Carroll, William M ; Lechner-Scott, Jeannette ; John, Nevin ; Barnett, Michael ; Hodgkinson, Suzanne ; McCombe, Pamela ; Kalincik, Tomas ; Macdonell, Richard ; Slee, Mark ; Schmitt, Birte</creatorcontrib><description>ObjectivesTo characterize the use of ofatumumab (OFA), a fully human self-administered anti-CD20 monoclonal antibody, in a real-world setting in Australia by assessing the profile of relapsing multiple sclerosis (RMS) patients initiating OFA through an evaluation of patient demographics, background MS disease characteristics and prior therapy history as recorded in MSBase.MethodsThis is a retrospective secondary use of MSBase Registry data study, describing the baseline characteristics of RMS patients in Australia initiated on OFA treatment, including demographics, disease duration, expanded disability status scale (EDSS), treatment history with disease-modifying therapies (DMTs) prior to commencing OFA and proportion of naïve patients initiating ofatumumab relative to patients having received a prior DMT.ResultsAs of 1st January 2024, MSBase has included 320 eligible patients initiated on OFA, with 22.2% treatment naïve, 30.9% switching from ocrelizumab, 14.7% switching from natalizumab, 3.1% from alemtuzumab and 27.7% from oral DMTs. The reasons for switching DMT to OFA included scheduled stop (13.1%), evidence of disease activity (9.1%), convenience (6.9%), side effects/intolerance (6.2%), JCV antibody positive (2.8%), pregnancy planned/confirmed (2.5%) and not reported (37.2%). The median age of patients initiating OFA was 42.67 [36.65, 51.98] years, with a median disease duration of 9.19 [3.61, 17.11] years and median EDSS of 2 [1.5, 3.5].ConclusionThe real-world data from this secondary use of data MSBase registry analysis provides a valuable snapshot of the Australian experience of relapsing MS patients initiated on OFA, with 22% of patients treated as first line therapy.</description><identifier>EISSN: 2632-6140</identifier><identifier>DOI: 10.1136/bmjno-2024-ANZAN.127</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>Monoclonal antibodies ; Poster Abstracts</subject><ispartof>BMJ neurology open, 2024-08, Vol.6 (Suppl 1), p.A45-A46</ispartof><rights>Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2024 Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://neurologyopen.bmj.com/content/6/Suppl_1/A45.3.full.pdf$$EPDF$$P50$$Gbmj$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://neurologyopen.bmj.com/content/6/Suppl_1/A45.3.full$$EHTML$$P50$$Gbmj$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,27922,27923,55348,77430,77456</link.rule.ids></links><search><creatorcontrib>Migocki, Margaret</creatorcontrib><creatorcontrib>Walt, Anneke Van der</creatorcontrib><creatorcontrib>Butzkueven, Helmut</creatorcontrib><creatorcontrib>Spelman, Tim</creatorcontrib><creatorcontrib>Kermode, Allan</creatorcontrib><creatorcontrib>Fabis-Pedrini, Marzena</creatorcontrib><creatorcontrib>Carroll, William M</creatorcontrib><creatorcontrib>Lechner-Scott, Jeannette</creatorcontrib><creatorcontrib>John, Nevin</creatorcontrib><creatorcontrib>Barnett, Michael</creatorcontrib><creatorcontrib>Hodgkinson, Suzanne</creatorcontrib><creatorcontrib>McCombe, Pamela</creatorcontrib><creatorcontrib>Kalincik, Tomas</creatorcontrib><creatorcontrib>Macdonell, Richard</creatorcontrib><creatorcontrib>Slee, Mark</creatorcontrib><creatorcontrib>Schmitt, Birte</creatorcontrib><title>3149 Real-world Australian experience with Ofatumumab in the MSBase registry</title><title>BMJ neurology open</title><addtitle>BMJ Neurol Open</addtitle><description>ObjectivesTo characterize the use of ofatumumab (OFA), a fully human self-administered anti-CD20 monoclonal antibody, in a real-world setting in Australia by assessing the profile of relapsing multiple sclerosis (RMS) patients initiating OFA through an evaluation of patient demographics, background MS disease characteristics and prior therapy history as recorded in MSBase.MethodsThis is a retrospective secondary use of MSBase Registry data study, describing the baseline characteristics of RMS patients in Australia initiated on OFA treatment, including demographics, disease duration, expanded disability status scale (EDSS), treatment history with disease-modifying therapies (DMTs) prior to commencing OFA and proportion of naïve patients initiating ofatumumab relative to patients having received a prior DMT.ResultsAs of 1st January 2024, MSBase has included 320 eligible patients initiated on OFA, with 22.2% treatment naïve, 30.9% switching from ocrelizumab, 14.7% switching from natalizumab, 3.1% from alemtuzumab and 27.7% from oral DMTs. The reasons for switching DMT to OFA included scheduled stop (13.1%), evidence of disease activity (9.1%), convenience (6.9%), side effects/intolerance (6.2%), JCV antibody positive (2.8%), pregnancy planned/confirmed (2.5%) and not reported (37.2%). The median age of patients initiating OFA was 42.67 [36.65, 51.98] years, with a median disease duration of 9.19 [3.61, 17.11] years and median EDSS of 2 [1.5, 3.5].ConclusionThe real-world data from this secondary use of data MSBase registry analysis provides a valuable snapshot of the Australian experience of relapsing MS patients initiated on OFA, with 22% of patients treated as first line therapy.</description><subject>Monoclonal antibodies</subject><subject>Poster Abstracts</subject><issn>2632-6140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>DOA</sourceid><recordid>eNpFkMtKw0AUhoMgWGrfwEXAderck1nG4qVQW_CycTOcyUzahFzqJKF258YX9UmctoKrwzn85-PnC4IrjKYYU3Gj67JpI4IIi9Lle7qcYhKfBSMiKIkEZugimHRdiRAiHLFEslGwpJjJn6_vZwtVtGtdZcJ06HoHVQFNaD-31hW2yWy4K_pNuMqhH-qhBh0WTdhvbPj0cgudDZ1dF_5rfxmc51B1dvI3x8Hb_d3r7DFarB7ms3QRaUw5jhKLrRCSxlluDUmw37JMgzHcd-dYGquzRJKEYGGAGJ0ZKoGDYULkvi_QcTA_cU0Lpdq6oga3Vy0U6nho3VqB64ussipGgnHmgYgnLNZSCywQj2MtQBMSa8-6PrG2rv0YbNersh1c4-sriqTESPAY-xQ6pbzj_wBG6iBeHcWrg3h1FK-8ePoL2ep5WQ</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Migocki, Margaret</creator><creator>Walt, Anneke Van der</creator><creator>Butzkueven, Helmut</creator><creator>Spelman, Tim</creator><creator>Kermode, Allan</creator><creator>Fabis-Pedrini, Marzena</creator><creator>Carroll, William M</creator><creator>Lechner-Scott, Jeannette</creator><creator>John, Nevin</creator><creator>Barnett, Michael</creator><creator>Hodgkinson, Suzanne</creator><creator>McCombe, Pamela</creator><creator>Kalincik, Tomas</creator><creator>Macdonell, Richard</creator><creator>Slee, Mark</creator><creator>Schmitt, Birte</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>K9.</scope><scope>DOA</scope></search><sort><creationdate>20240801</creationdate><title>3149 Real-world Australian experience with Ofatumumab in the MSBase registry</title><author>Migocki, Margaret ; Walt, Anneke Van der ; Butzkueven, Helmut ; Spelman, Tim ; Kermode, Allan ; Fabis-Pedrini, Marzena ; Carroll, William M ; Lechner-Scott, Jeannette ; John, Nevin ; Barnett, Michael ; Hodgkinson, Suzanne ; McCombe, Pamela ; Kalincik, Tomas ; Macdonell, Richard ; Slee, Mark ; Schmitt, Birte</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1351-8e1e66937cfed2811e6ccbadd5202519debc8928216da2dbcd39a5ad466f149a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Monoclonal antibodies</topic><topic>Poster Abstracts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Migocki, Margaret</creatorcontrib><creatorcontrib>Walt, Anneke Van der</creatorcontrib><creatorcontrib>Butzkueven, Helmut</creatorcontrib><creatorcontrib>Spelman, Tim</creatorcontrib><creatorcontrib>Kermode, Allan</creatorcontrib><creatorcontrib>Fabis-Pedrini, Marzena</creatorcontrib><creatorcontrib>Carroll, William M</creatorcontrib><creatorcontrib>Lechner-Scott, Jeannette</creatorcontrib><creatorcontrib>John, Nevin</creatorcontrib><creatorcontrib>Barnett, Michael</creatorcontrib><creatorcontrib>Hodgkinson, Suzanne</creatorcontrib><creatorcontrib>McCombe, Pamela</creatorcontrib><creatorcontrib>Kalincik, Tomas</creatorcontrib><creatorcontrib>Macdonell, Richard</creatorcontrib><creatorcontrib>Slee, Mark</creatorcontrib><creatorcontrib>Schmitt, Birte</creatorcontrib><collection>BMJ Journals (Open Access)</collection><collection>BMJ Journals:Open Access</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Directory of Open Access Journals</collection><jtitle>BMJ neurology open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Migocki, Margaret</au><au>Walt, Anneke Van der</au><au>Butzkueven, Helmut</au><au>Spelman, Tim</au><au>Kermode, Allan</au><au>Fabis-Pedrini, Marzena</au><au>Carroll, William M</au><au>Lechner-Scott, Jeannette</au><au>John, Nevin</au><au>Barnett, Michael</au><au>Hodgkinson, Suzanne</au><au>McCombe, Pamela</au><au>Kalincik, Tomas</au><au>Macdonell, Richard</au><au>Slee, Mark</au><au>Schmitt, Birte</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>3149 Real-world Australian experience with Ofatumumab in the MSBase registry</atitle><jtitle>BMJ neurology open</jtitle><stitle>BMJ Neurol Open</stitle><date>2024-08-01</date><risdate>2024</risdate><volume>6</volume><issue>Suppl 1</issue><spage>A45</spage><epage>A46</epage><pages>A45-A46</pages><eissn>2632-6140</eissn><abstract>ObjectivesTo characterize the use of ofatumumab (OFA), a fully human self-administered anti-CD20 monoclonal antibody, in a real-world setting in Australia by assessing the profile of relapsing multiple sclerosis (RMS) patients initiating OFA through an evaluation of patient demographics, background MS disease characteristics and prior therapy history as recorded in MSBase.MethodsThis is a retrospective secondary use of MSBase Registry data study, describing the baseline characteristics of RMS patients in Australia initiated on OFA treatment, including demographics, disease duration, expanded disability status scale (EDSS), treatment history with disease-modifying therapies (DMTs) prior to commencing OFA and proportion of naïve patients initiating ofatumumab relative to patients having received a prior DMT.ResultsAs of 1st January 2024, MSBase has included 320 eligible patients initiated on OFA, with 22.2% treatment naïve, 30.9% switching from ocrelizumab, 14.7% switching from natalizumab, 3.1% from alemtuzumab and 27.7% from oral DMTs. The reasons for switching DMT to OFA included scheduled stop (13.1%), evidence of disease activity (9.1%), convenience (6.9%), side effects/intolerance (6.2%), JCV antibody positive (2.8%), pregnancy planned/confirmed (2.5%) and not reported (37.2%). The median age of patients initiating OFA was 42.67 [36.65, 51.98] years, with a median disease duration of 9.19 [3.61, 17.11] years and median EDSS of 2 [1.5, 3.5].ConclusionThe real-world data from this secondary use of data MSBase registry analysis provides a valuable snapshot of the Australian experience of relapsing MS patients initiated on OFA, with 22% of patients treated as first line therapy.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><doi>10.1136/bmjno-2024-ANZAN.127</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | EISSN: 2632-6140 |
ispartof | BMJ neurology open, 2024-08, Vol.6 (Suppl 1), p.A45-A46 |
issn | 2632-6140 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_706454ebc05847b9b6160577b6ab227b |
source | BMJ Journals (Open Access); PubMed Central |
subjects | Monoclonal antibodies Poster Abstracts |
title | 3149 Real-world Australian experience with Ofatumumab in the MSBase registry |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T13%3A06%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=3149%E2%80%85Real-world%20Australian%20experience%20with%20Ofatumumab%20in%20the%20MSBase%20registry&rft.jtitle=BMJ%20neurology%20open&rft.au=Migocki,%20Margaret&rft.date=2024-08-01&rft.volume=6&rft.issue=Suppl%201&rft.spage=A45&rft.epage=A46&rft.pages=A45-A46&rft.eissn=2632-6140&rft_id=info:doi/10.1136/bmjno-2024-ANZAN.127&rft_dat=%3Cproquest_doaj_%3E3099106571%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-b1351-8e1e66937cfed2811e6ccbadd5202519debc8928216da2dbcd39a5ad466f149a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3099106571&rft_id=info:pmid/&rfr_iscdi=true |