REAL-WORLD LONG TERM OUTCOMES IN NATALIZUMAB TREATED PATIENTS
IntroductionThe aim of this prospective, observational, single centre study was to evaluate the effects of Natalizumab on cognition and disability measures in rapidly evolving relapsing remitting multiple sclerosis (REMS) patients treated for up to six years.MethodWe analysed data for 37 patients (2...
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Veröffentlicht in: | Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 2016-12, Vol.87 (12), p.e1-e1 |
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description | IntroductionThe aim of this prospective, observational, single centre study was to evaluate the effects of Natalizumab on cognition and disability measures in rapidly evolving relapsing remitting multiple sclerosis (REMS) patients treated for up to six years.MethodWe analysed data for 37 patients (26F) treated with Natalizumab for up to 6 years. Data recorded included 3-monthly assessments of expanded disability severity status (EDSS), 10 metre timed walk (10MTW) and Addenbrooke's cognitive examination (ACE-R).ResultsDisability (EDSS (SD)) improved from baseline (4.2 (1.8)) and at 3 months (−0.49), was maximal (−1.3) at 3 years, and sustained to 6 years (−1.0). Sustained disability improvement/progression was seen in 37% and 13% respectively.Cognition (mean ACE-R 88.3) improved at 3 months (mean change 2.2 points) and was sustained (7.8 at 3 years) to 6 years (7.0). The proportion with a sustained improvement in cognition (>4 on ACE-R) was 22% at 3 months and 59% overall.A clinically significant improvement (>20%) in the 10MTW was noted in 13.9% at 3 months and in 27% overall.ConclusionThe results demonstrate that Natalizumab may improve disability, walking and cognition in a significant proportion of REMS. Improvement was noted within 3 months and maintained throughout treatment. |
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Data recorded included 3-monthly assessments of expanded disability severity status (EDSS), 10 metre timed walk (10MTW) and Addenbrooke's cognitive examination (ACE-R).ResultsDisability (EDSS (SD)) improved from baseline (4.2 (1.8)) and at 3 months (−0.49), was maximal (−1.3) at 3 years, and sustained to 6 years (−1.0). Sustained disability improvement/progression was seen in 37% and 13% respectively.Cognition (mean ACE-R 88.3) improved at 3 months (mean change 2.2 points) and was sustained (7.8 at 3 years) to 6 years (7.0). The proportion with a sustained improvement in cognition (>4 on ACE-R) was 22% at 3 months and 59% overall.A clinically significant improvement (>20%) in the 10MTW was noted in 13.9% at 3 months and in 27% overall.ConclusionThe results demonstrate that Natalizumab may improve disability, walking and cognition in a significant proportion of REMS. Improvement was noted within 3 months and maintained throughout treatment.</description><identifier>ISSN: 0022-3050</identifier><identifier>EISSN: 1468-330X</identifier><identifier>DOI: 10.1136/jnnp-2016-315106.164</identifier><identifier>CODEN: JNNPAU</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><ispartof>Journal of neurology, neurosurgery and psychiatry, 2016-12, Vol.87 (12), p.e1-e1</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing</rights><rights>Copyright: 2016 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jnnp.bmj.com/content/87/12/e1.73.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttps://jnnp.bmj.com/content/87/12/e1.73.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3196,23571,27924,27925,77600,77631</link.rule.ids></links><search><creatorcontrib>Wynford-Thomas, Ray</creatorcontrib><creatorcontrib>Owen, Helen</creatorcontrib><creatorcontrib>Mulloch, Sue</creatorcontrib><creatorcontrib>Evans, Peter</creatorcontrib><creatorcontrib>Conway, Bernie</creatorcontrib><creatorcontrib>Watson, Lynne</creatorcontrib><creatorcontrib>Pearson, Owen</creatorcontrib><title>REAL-WORLD LONG TERM OUTCOMES IN NATALIZUMAB TREATED PATIENTS</title><title>Journal of neurology, neurosurgery and psychiatry</title><description>IntroductionThe aim of this prospective, observational, single centre study was to evaluate the effects of Natalizumab on cognition and disability measures in rapidly evolving relapsing remitting multiple sclerosis (REMS) patients treated for up to six years.MethodWe analysed data for 37 patients (26F) treated with Natalizumab for up to 6 years. Data recorded included 3-monthly assessments of expanded disability severity status (EDSS), 10 metre timed walk (10MTW) and Addenbrooke's cognitive examination (ACE-R).ResultsDisability (EDSS (SD)) improved from baseline (4.2 (1.8)) and at 3 months (−0.49), was maximal (−1.3) at 3 years, and sustained to 6 years (−1.0). Sustained disability improvement/progression was seen in 37% and 13% respectively.Cognition (mean ACE-R 88.3) improved at 3 months (mean change 2.2 points) and was sustained (7.8 at 3 years) to 6 years (7.0). The proportion with a sustained improvement in cognition (>4 on ACE-R) was 22% at 3 months and 59% overall.A clinically significant improvement (>20%) in the 10MTW was noted in 13.9% at 3 months and in 27% overall.ConclusionThe results demonstrate that Natalizumab may improve disability, walking and cognition in a significant proportion of REMS. Improvement was noted within 3 months and maintained throughout treatment.</description><issn>0022-3050</issn><issn>1468-330X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkD1PwzAURS0EEqXwDxgisbCkff6I4wwMoQ0lUpqg1hWIxXJSRyJqkxLTgX-PozIx8Za3nHt1dRC6xTDBmPJp07YHnwDmPsUBBj7BnJ2hEWZc-JTC2zkaARDiUwjgEl1Z28BwIhqhh1USZ_5rscrmXlbkC08mq6VXbOSsWCZrL829PJZxlr5vlvGjJx0tk7n3Ess0yeX6Gl3UemfNze8fo81TImfPflYs0pkrLt0G8DWENdEmLEVFA0KDugxNKPSWiYhRqmnItSBbTSONQ1JVPDJlwCkGA1Rg0AEdo_tT76HvPo_Gfqn9h63Mbqdb0x2twoJxRkAAOPTuD9p0x7516wYqIAyHlDuKnaiq76ztTa0O_cde998KgxqcqsGpGpyqk1PlnLrY9BQr983_Ej9onHFI</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Wynford-Thomas, Ray</creator><creator>Owen, Helen</creator><creator>Mulloch, Sue</creator><creator>Evans, Peter</creator><creator>Conway, Bernie</creator><creator>Watson, Lynne</creator><creator>Pearson, Owen</creator><general>BMJ Publishing Group LTD</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7TK</scope></search><sort><creationdate>201612</creationdate><title>REAL-WORLD LONG TERM OUTCOMES IN NATALIZUMAB TREATED PATIENTS</title><author>Wynford-Thomas, Ray ; Owen, Helen ; Mulloch, Sue ; Evans, Peter ; Conway, Bernie ; Watson, Lynne ; Pearson, Owen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1460-a07f2ae7b8c35235fb7e78ad489433a376a82da39a172cc69eb56310e03810a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wynford-Thomas, Ray</creatorcontrib><creatorcontrib>Owen, Helen</creatorcontrib><creatorcontrib>Mulloch, Sue</creatorcontrib><creatorcontrib>Evans, Peter</creatorcontrib><creatorcontrib>Conway, Bernie</creatorcontrib><creatorcontrib>Watson, Lynne</creatorcontrib><creatorcontrib>Pearson, Owen</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wynford-Thomas, Ray</au><au>Owen, Helen</au><au>Mulloch, Sue</au><au>Evans, Peter</au><au>Conway, Bernie</au><au>Watson, Lynne</au><au>Pearson, Owen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>REAL-WORLD LONG TERM OUTCOMES IN NATALIZUMAB TREATED PATIENTS</atitle><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle><date>2016-12</date><risdate>2016</risdate><volume>87</volume><issue>12</issue><spage>e1</spage><epage>e1</epage><pages>e1-e1</pages><issn>0022-3050</issn><eissn>1468-330X</eissn><coden>JNNPAU</coden><abstract>IntroductionThe aim of this prospective, observational, single centre study was to evaluate the effects of Natalizumab on cognition and disability measures in rapidly evolving relapsing remitting multiple sclerosis (REMS) patients treated for up to six years.MethodWe analysed data for 37 patients (26F) treated with Natalizumab for up to 6 years. Data recorded included 3-monthly assessments of expanded disability severity status (EDSS), 10 metre timed walk (10MTW) and Addenbrooke's cognitive examination (ACE-R).ResultsDisability (EDSS (SD)) improved from baseline (4.2 (1.8)) and at 3 months (−0.49), was maximal (−1.3) at 3 years, and sustained to 6 years (−1.0). Sustained disability improvement/progression was seen in 37% and 13% respectively.Cognition (mean ACE-R 88.3) improved at 3 months (mean change 2.2 points) and was sustained (7.8 at 3 years) to 6 years (7.0). The proportion with a sustained improvement in cognition (>4 on ACE-R) was 22% at 3 months and 59% overall.A clinically significant improvement (>20%) in the 10MTW was noted in 13.9% at 3 months and in 27% overall.ConclusionThe results demonstrate that Natalizumab may improve disability, walking and cognition in a significant proportion of REMS. Improvement was noted within 3 months and maintained throughout treatment.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/jnnp-2016-315106.164</doi></addata></record> |
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