Oral treatment for multiple sclerosis

Summary Background The armamentarium for the treatment of relapsing-remitting multiple sclerosis (RRMS) is increasing rapidly. Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Lancet neurology 2011-11, Vol.10 (11), p.1026-1034
Hauptverfasser: Killestein, Joep, Dr, Rudick, Richard A, Prof, Polman, Chris H, Prof
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1034
container_issue 11
container_start_page 1026
container_title Lancet neurology
container_volume 10
creator Killestein, Joep, Dr
Rudick, Richard A, Prof
Polman, Chris H, Prof
description Summary Background The armamentarium for the treatment of relapsing-remitting multiple sclerosis (RRMS) is increasing rapidly. Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs will not necessarily translate into clinical effectiveness and safety. Here, we provide an interim report about the mechanisms of action, and efficacy and safety results that have been reported since January, 2010, for five new oral drugs. Additionally, we draw attention to issues that neurologists and patients will encounter when considering the use of new oral drugs. Recent developments Positive results have been reported for five new oral drugs for RRMS—fingolimod, cladribine, teriflunomide, laquinimod, and dimethyl fumarate—in phase 3 studies; a few new oral drugs are likely to be approved for RRMS soon. Where next? Emerging oral treatments are ushering in a new era in the treatment of MS, providing not only new treatment options but also new challenges. Since data for some of the new drugs have not been reported in peer-reviewed journals yet and safety profiles are not yet fully developed, opinions about the use of these new oral drugs in practice are preliminary and tentative. Practice will evolve with time as information and experience accumulates. Of importance will be results from comparator trials, information about management of patients with breakthrough disease, results from long-term safety studies, and results of studies to assess the potential for neuroprotective effects of the new drugs.
doi_str_mv 10.1016/S1474-4422(11)70228-9
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_904498238</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1474442211702289</els_id><sourcerecordid>904498238</sourcerecordid><originalsourceid>FETCH-LOGICAL-c478t-bc08ac6686ca35d40e111b40bf59148c92621452cf60675ae2d0ba6cfc34acc93</originalsourceid><addsrcrecordid>eNqNkE1P3DAQhq2qqHz1J7RaVUKUQ2DGcZzkAkKrUpCQOEDPljOZSKZOsrUTJP49ye52D1zaky3r8TvzPkJ8QThHQH3xiCpXiVJSfkc8y0HKIik_iIPts84-7u5S7ovDGJ8BJKoCP4l9KQGVSvMDcfIQrF8Mge3Qcjcsmj4s2tEPbuV5Eclz6KOLx2KvsT7y5-15JH7d_Hha3ib3Dz_vltf3Cam8GJKKoLCkdaHJplmtgBGxUlA1WTlNplLqaYNMUqNB55llWUNlNTWUKktUpkfidJO7Cv2fkeNgWheJvbcd92M0JShVFjIt_oMEnUKqYCK_vSOf-zF0U40ZUrnUhZqgbAPR1DcGbswquNaGV4NgZt9m7dvMMg2iWfs288Jft-Fj1XK9-_VX8ARcbQCetL04DiaS4464doFpMHXv_jni8l0Cedc5sv43v3LclUETpYFNyJyBuE4o0zeq_KGP</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>900472684</pqid></control><display><type>article</type><title>Oral treatment for multiple sclerosis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>ProQuest Central UK/Ireland</source><creator>Killestein, Joep, Dr ; Rudick, Richard A, Prof ; Polman, Chris H, Prof</creator><creatorcontrib>Killestein, Joep, Dr ; Rudick, Richard A, Prof ; Polman, Chris H, Prof</creatorcontrib><description>Summary Background The armamentarium for the treatment of relapsing-remitting multiple sclerosis (RRMS) is increasing rapidly. Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs will not necessarily translate into clinical effectiveness and safety. Here, we provide an interim report about the mechanisms of action, and efficacy and safety results that have been reported since January, 2010, for five new oral drugs. Additionally, we draw attention to issues that neurologists and patients will encounter when considering the use of new oral drugs. Recent developments Positive results have been reported for five new oral drugs for RRMS—fingolimod, cladribine, teriflunomide, laquinimod, and dimethyl fumarate—in phase 3 studies; a few new oral drugs are likely to be approved for RRMS soon. Where next? Emerging oral treatments are ushering in a new era in the treatment of MS, providing not only new treatment options but also new challenges. Since data for some of the new drugs have not been reported in peer-reviewed journals yet and safety profiles are not yet fully developed, opinions about the use of these new oral drugs in practice are preliminary and tentative. Practice will evolve with time as information and experience accumulates. Of importance will be results from comparator trials, information about management of patients with breakthrough disease, results from long-term safety studies, and results of studies to assess the potential for neuroprotective effects of the new drugs.</description><identifier>ISSN: 1474-4422</identifier><identifier>EISSN: 1474-4465</identifier><identifier>DOI: 10.1016/S1474-4422(11)70228-9</identifier><identifier>PMID: 22014437</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject><![CDATA[Administration, Oral ; Attention ; cladribine ; Cladribine - administration & dosage ; Cladribine - therapeutic use ; Clinical trials ; Clinical Trials as Topic ; Crotonates - administration & dosage ; Crotonates - therapeutic use ; Cytokines ; Data processing ; Dimethyl Fumarate ; Drug dosages ; Drugs ; FDA approval ; Fingolimod Hydrochloride ; Fumarates - administration & dosage ; Fumarates - therapeutic use ; Humans ; Immunosuppressive Agents - administration & dosage ; Immunosuppressive Agents - therapeutic use ; Interferon ; Lymphocytes ; Multiple sclerosis ; Multiple Sclerosis, Relapsing-Remitting - drug therapy ; Neurology ; Neuroprotection ; Propylene Glycols - administration & dosage ; Propylene Glycols - therapeutic use ; Quinolones - administration & dosage ; Quinolones - therapeutic use ; Sphingosine - administration & dosage ; Sphingosine - analogs & derivatives ; Sphingosine - therapeutic use ; Toluidines - administration & dosage ; Toluidines - therapeutic use]]></subject><ispartof>Lancet neurology, 2011-11, Vol.10 (11), p.1026-1034</ispartof><rights>Elsevier Ltd</rights><rights>2011 Elsevier Ltd</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited Nov 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-bc08ac6686ca35d40e111b40bf59148c92621452cf60675ae2d0ba6cfc34acc93</citedby><cites>FETCH-LOGICAL-c478t-bc08ac6686ca35d40e111b40bf59148c92621452cf60675ae2d0ba6cfc34acc93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/900472684?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974,64362,64364,64366,72216</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22014437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Killestein, Joep, Dr</creatorcontrib><creatorcontrib>Rudick, Richard A, Prof</creatorcontrib><creatorcontrib>Polman, Chris H, Prof</creatorcontrib><title>Oral treatment for multiple sclerosis</title><title>Lancet neurology</title><addtitle>Lancet Neurol</addtitle><description>Summary Background The armamentarium for the treatment of relapsing-remitting multiple sclerosis (RRMS) is increasing rapidly. Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs will not necessarily translate into clinical effectiveness and safety. Here, we provide an interim report about the mechanisms of action, and efficacy and safety results that have been reported since January, 2010, for five new oral drugs. Additionally, we draw attention to issues that neurologists and patients will encounter when considering the use of new oral drugs. Recent developments Positive results have been reported for five new oral drugs for RRMS—fingolimod, cladribine, teriflunomide, laquinimod, and dimethyl fumarate—in phase 3 studies; a few new oral drugs are likely to be approved for RRMS soon. Where next? Emerging oral treatments are ushering in a new era in the treatment of MS, providing not only new treatment options but also new challenges. Since data for some of the new drugs have not been reported in peer-reviewed journals yet and safety profiles are not yet fully developed, opinions about the use of these new oral drugs in practice are preliminary and tentative. Practice will evolve with time as information and experience accumulates. Of importance will be results from comparator trials, information about management of patients with breakthrough disease, results from long-term safety studies, and results of studies to assess the potential for neuroprotective effects of the new drugs.</description><subject>Administration, Oral</subject><subject>Attention</subject><subject>cladribine</subject><subject>Cladribine - administration &amp; dosage</subject><subject>Cladribine - therapeutic use</subject><subject>Clinical trials</subject><subject>Clinical Trials as Topic</subject><subject>Crotonates - administration &amp; dosage</subject><subject>Crotonates - therapeutic use</subject><subject>Cytokines</subject><subject>Data processing</subject><subject>Dimethyl Fumarate</subject><subject>Drug dosages</subject><subject>Drugs</subject><subject>FDA approval</subject><subject>Fingolimod Hydrochloride</subject><subject>Fumarates - administration &amp; dosage</subject><subject>Fumarates - therapeutic use</subject><subject>Humans</subject><subject>Immunosuppressive Agents - administration &amp; dosage</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Interferon</subject><subject>Lymphocytes</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis, Relapsing-Remitting - drug therapy</subject><subject>Neurology</subject><subject>Neuroprotection</subject><subject>Propylene Glycols - administration &amp; dosage</subject><subject>Propylene Glycols - therapeutic use</subject><subject>Quinolones - administration &amp; dosage</subject><subject>Quinolones - therapeutic use</subject><subject>Sphingosine - administration &amp; dosage</subject><subject>Sphingosine - analogs &amp; derivatives</subject><subject>Sphingosine - therapeutic use</subject><subject>Toluidines - administration &amp; dosage</subject><subject>Toluidines - therapeutic use</subject><issn>1474-4422</issn><issn>1474-4465</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkE1P3DAQhq2qqHz1J7RaVUKUQ2DGcZzkAkKrUpCQOEDPljOZSKZOsrUTJP49ye52D1zaky3r8TvzPkJ8QThHQH3xiCpXiVJSfkc8y0HKIik_iIPts84-7u5S7ovDGJ8BJKoCP4l9KQGVSvMDcfIQrF8Mge3Qcjcsmj4s2tEPbuV5Eclz6KOLx2KvsT7y5-15JH7d_Hha3ib3Dz_vltf3Cam8GJKKoLCkdaHJplmtgBGxUlA1WTlNplLqaYNMUqNB55llWUNlNTWUKktUpkfidJO7Cv2fkeNgWheJvbcd92M0JShVFjIt_oMEnUKqYCK_vSOf-zF0U40ZUrnUhZqgbAPR1DcGbswquNaGV4NgZt9m7dvMMg2iWfs288Jft-Fj1XK9-_VX8ARcbQCetL04DiaS4464doFpMHXv_jni8l0Cedc5sv43v3LclUETpYFNyJyBuE4o0zeq_KGP</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Killestein, Joep, Dr</creator><creator>Rudick, Richard A, Prof</creator><creator>Polman, Chris H, Prof</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0TZ</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20111101</creationdate><title>Oral treatment for multiple sclerosis</title><author>Killestein, Joep, Dr ; Rudick, Richard A, Prof ; Polman, Chris H, Prof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-bc08ac6686ca35d40e111b40bf59148c92621452cf60675ae2d0ba6cfc34acc93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Administration, Oral</topic><topic>Attention</topic><topic>cladribine</topic><topic>Cladribine - administration &amp; dosage</topic><topic>Cladribine - therapeutic use</topic><topic>Clinical trials</topic><topic>Clinical Trials as Topic</topic><topic>Crotonates - administration &amp; dosage</topic><topic>Crotonates - therapeutic use</topic><topic>Cytokines</topic><topic>Data processing</topic><topic>Dimethyl Fumarate</topic><topic>Drug dosages</topic><topic>Drugs</topic><topic>FDA approval</topic><topic>Fingolimod Hydrochloride</topic><topic>Fumarates - administration &amp; dosage</topic><topic>Fumarates - therapeutic use</topic><topic>Humans</topic><topic>Immunosuppressive Agents - administration &amp; dosage</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Interferon</topic><topic>Lymphocytes</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis, Relapsing-Remitting - drug therapy</topic><topic>Neurology</topic><topic>Neuroprotection</topic><topic>Propylene Glycols - administration &amp; dosage</topic><topic>Propylene Glycols - therapeutic use</topic><topic>Quinolones - administration &amp; dosage</topic><topic>Quinolones - therapeutic use</topic><topic>Sphingosine - administration &amp; dosage</topic><topic>Sphingosine - analogs &amp; derivatives</topic><topic>Sphingosine - therapeutic use</topic><topic>Toluidines - administration &amp; dosage</topic><topic>Toluidines - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Killestein, Joep, Dr</creatorcontrib><creatorcontrib>Rudick, Richard A, Prof</creatorcontrib><creatorcontrib>Polman, Chris H, Prof</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Lancet Titles</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>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>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Nursing &amp; 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 Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Lancet neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Killestein, Joep, Dr</au><au>Rudick, Richard A, Prof</au><au>Polman, Chris H, Prof</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral treatment for multiple sclerosis</atitle><jtitle>Lancet neurology</jtitle><addtitle>Lancet Neurol</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>10</volume><issue>11</issue><spage>1026</spage><epage>1034</epage><pages>1026-1034</pages><issn>1474-4422</issn><eissn>1474-4465</eissn><coden>LANCAO</coden><abstract>Summary Background The armamentarium for the treatment of relapsing-remitting multiple sclerosis (RRMS) is increasing rapidly. Several oral treatments have shown benefit and will generate much interest because of the convenience of such administration. However, availability of convenient oral drugs will not necessarily translate into clinical effectiveness and safety. Here, we provide an interim report about the mechanisms of action, and efficacy and safety results that have been reported since January, 2010, for five new oral drugs. Additionally, we draw attention to issues that neurologists and patients will encounter when considering the use of new oral drugs. Recent developments Positive results have been reported for five new oral drugs for RRMS—fingolimod, cladribine, teriflunomide, laquinimod, and dimethyl fumarate—in phase 3 studies; a few new oral drugs are likely to be approved for RRMS soon. Where next? Emerging oral treatments are ushering in a new era in the treatment of MS, providing not only new treatment options but also new challenges. Since data for some of the new drugs have not been reported in peer-reviewed journals yet and safety profiles are not yet fully developed, opinions about the use of these new oral drugs in practice are preliminary and tentative. Practice will evolve with time as information and experience accumulates. Of importance will be results from comparator trials, information about management of patients with breakthrough disease, results from long-term safety studies, and results of studies to assess the potential for neuroprotective effects of the new drugs.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>22014437</pmid><doi>10.1016/S1474-4422(11)70228-9</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1474-4422
ispartof Lancet neurology, 2011-11, Vol.10 (11), p.1026-1034
issn 1474-4422
1474-4465
language eng
recordid cdi_proquest_miscellaneous_904498238
source MEDLINE; Elsevier ScienceDirect Journals; ProQuest Central UK/Ireland
subjects Administration, Oral
Attention
cladribine
Cladribine - administration & dosage
Cladribine - therapeutic use
Clinical trials
Clinical Trials as Topic
Crotonates - administration & dosage
Crotonates - therapeutic use
Cytokines
Data processing
Dimethyl Fumarate
Drug dosages
Drugs
FDA approval
Fingolimod Hydrochloride
Fumarates - administration & dosage
Fumarates - therapeutic use
Humans
Immunosuppressive Agents - administration & dosage
Immunosuppressive Agents - therapeutic use
Interferon
Lymphocytes
Multiple sclerosis
Multiple Sclerosis, Relapsing-Remitting - drug therapy
Neurology
Neuroprotection
Propylene Glycols - administration & dosage
Propylene Glycols - therapeutic use
Quinolones - administration & dosage
Quinolones - therapeutic use
Sphingosine - administration & dosage
Sphingosine - analogs & derivatives
Sphingosine - therapeutic use
Toluidines - administration & dosage
Toluidines - therapeutic use
title Oral treatment for multiple sclerosis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T10%3A55%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Oral%20treatment%20for%20multiple%20sclerosis&rft.jtitle=Lancet%20neurology&rft.au=Killestein,%20Joep,%20Dr&rft.date=2011-11-01&rft.volume=10&rft.issue=11&rft.spage=1026&rft.epage=1034&rft.pages=1026-1034&rft.issn=1474-4422&rft.eissn=1474-4465&rft.coden=LANCAO&rft_id=info:doi/10.1016/S1474-4422(11)70228-9&rft_dat=%3Cproquest_cross%3E904498238%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=900472684&rft_id=info:pmid/22014437&rft_els_id=S1474442211702289&rfr_iscdi=true