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Inicio temprano de alemtuzumab: cambio en el paradigma de tratamiento en esclerosis múltiple. Análisis intermedio del estudio LEMVIDA
Early beginning of alemtuzumab: changing the multiple sclerosis treatment paradigm. Interim analysis of the LEMVIDA study
J.E. Meca-Lallanaa,b,
Autor para correspondencia
pmecal@gmail.com

Autor para correspondencia.
, J.C. Álvarez-Cermeñoc, B. Casanova Estruchd, G. Izquierdo Ayusoe, R. Ortiz Castillof, A. Rodríguez-Antigüedadg, C. Calles Hernándezh, en nombre del Grupo de Estudio LEMVIDA
a CSUR Esclerosis Múltiple, Hospital Virgen de la Arrixaca (IMIB-Arrixaca), Murcia, España
b Cátedra de Neuroinmunología Clínica y Esclerosis Múltiple, UCAM-Universidad Católica San Antonio de Murcia, Murcia, España
c Unidad de Esclerosis Múltiple. Instituto de Investigación Ramón y Cajal, Hospital Universitario Ramón y Cajal, Madrid, España
d Unidad de Neuroinmunología Clínica, Hospital Universitario y Politécnico La Fe, Valencia, España
e Unidad de Investigación y Tratamiento de la Esclerosis Múltiple, Hospital Vithas Nisa, Sevilla, España
f Unidad de Esclerosis Múltiple, Sanofi, Madrid, España
g Servicio de Neurología, Hospital Universitario Cruces-Osakidetza, Bizkaia, España
h Unidad de Esclerosis Múltiple, Hospital Universitario Son Espases, Palma de Mallorca, España
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Alemtuzumab tambi&#233;n juega un papel importante en la estrategia de escalado terap&#233;utico en pacientes con respuesta sub&#243;ptima a un TME por persistencia de la actividad cl&#237;nica y&#47;o radiol&#243;gica<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">1</span></a>&#46; La indicaci&#243;n en la ficha t&#233;cnica &#40;FT&#41; europea anterior a noviembre de 2019 ha permitido a los cl&#237;nicos cierta flexibilidad en la decisi&#243;n de tratar con alemtuzumab ya que no se establec&#237;a una clara definici&#243;n del candidato ideal ni del nivel de actividad cl&#237;nica o radiol&#243;gica para su uso<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">7</span></a>&#46; En noviembre de 2019&#44; tras conocerse el resultado del informe peri&#243;dico sobre farmacovigilancia&#44; en el que se comunicaron reacciones adversas poco frecuentes pero graves&#44; se inici&#243; una evaluaci&#243;n del balance riesgo-beneficio en sus indicaciones autorizadas en virtud del Art&#237;culo 20 del Reglamento &#40;CE&#41; n&#46;&#176; 726&#47;2004&#44; y se restringi&#243; su indicaci&#243;n a pacientes con enfermedad muy activa a pesar de haber recibido un ciclo completo con al menos un TME&#44; o pacientes que evolucionan r&#225;pidamente a una EMRR grave&#44; definida por &#8805;&#160;2 brotes incapacitantes en un a&#241;o&#44; y con &#8805;&#160;1 lesiones realzadas con gadolinio &#40;Gd&#41; o un aumento significativo de la carga lesional en T2&#46; Actualmente&#44; la pr&#225;ctica m&#225;s com&#250;n en nuestro entorno es el escalado a alemtuzumab por falta de respuesta al TME previo&#44; aunque la falta de estudios publicados impide concluir cu&#225;l es la mejor secuencia de utilizaci&#243;n de los f&#225;rmacos inmunosupresores en EM de alta actividad&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">El estudio LEMVIDA fue dise&#241;ado para evaluar la calidad de vida &#40;CdV&#41; percibida por los pacientes con EMRR tratados con alemtuzumab&#46; El objetivo de este an&#225;lisis intermedio fue describir las caracter&#237;sticas cl&#237;nicas basales de los pacientes con EMRR que reciben alemtuzumab en Espa&#241;a&#46; Consideramos importante analizar la forma en que se est&#225; utilizando alemtuzumab en la pr&#225;ctica habitual en Espa&#241;a antes de las nuevas restricciones de uso&#44; mostrar si hay un cambio a lo largo del tiempo en el perfil cl&#237;nico del paciente candidato a recibir el f&#225;rmaco y analizar datos en relaci&#243;n con la seguridad&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">En el momento de la modificaci&#243;n de la FT&#44; la inclusi&#243;n de pacientes en el estudio se hab&#237;a completado y la mayor&#237;a hab&#237;a recibido los dos cursos de tratamiento inicial&#46; Este trabajo presenta los resultados de un an&#225;lisis intermedio del estudio LEMVIDA en el que se describe el cambio en las caracter&#237;sticas basales de los pacientes incluidos a lo largo del periodo de reclutamiento&#44; y c&#243;mo se modifica el paradigma de indicaci&#243;n de alemtuzumab en la pr&#225;ctica cl&#237;nica&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">M&#233;todos</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Dise&#241;o y poblaci&#243;n del estudio</span><p id="par0020" class="elsevierStylePara elsevierViewall">LEMVIDA es un estudio nacional&#44; en curso a la fecha del presente an&#225;lisis&#44; multic&#233;ntrico&#44; observacional y prospectivo de tres a&#241;os de seguimiento&#46; Se han incluido pacientes adultos con EMRR que iniciaron alemtuzumab durante la pr&#225;ctica cl&#237;nica habitual seg&#250;n las indicaciones de la FT&#44; bien como primera opci&#243;n de tratamiento o por respuesta sub&#243;ptima a otro TME&#46; El tiempo m&#225;ximo desde la administraci&#243;n de alemtuzumab hasta la inclusi&#243;n fue de ocho semanas&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">La variable principal del estudio es la CdV&#44; evaluada mediante la Escala de Impacto de la Esclerosis M&#250;ltiple &#40;MSIS-29&#44; <span class="elsevierStyleItalic">Multiple Sclerosis Impact Scale</span>&#41;&#46; Como variables secundarias se incluyen los niveles de fatiga y depresi&#243;n&#44; estado cognitivo&#44; disfunci&#243;n vesical&#44; discapacidad&#44; tasa de brotes&#44; hallazgos en RM y datos de seguridad&#46; En este an&#225;lisis inicial se evaluaron todos los pacientes participantes en el estudio LEMVIDA que hab&#237;an completado la visita basal entre octubre de 2016 y septiembre de 2018&#46; En el momento del presente an&#225;lisis&#44; los pacientes continuaban en seguimiento cada seis meses&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">En cumplimiento de la Declaraci&#243;n de Helsinki&#44; el estudio fue aprobado por el comit&#233; &#233;tico de cada centro participante y todos los pacientes otorgaron su consentimiento informado por escrito&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Variables y recogida de datos</span><p id="par0035" class="elsevierStylePara elsevierViewall">Este an&#225;lisis describe las siguientes caracter&#237;sticas basales&#58; edad&#44; sexo&#44; tiempo desde el diagn&#243;stico de EM hasta el inicio de alemtuzumab&#44; tiempo desde el &#250;ltimo brote&#44; puntuaci&#243;n EDSS &#40;<span class="elsevierStyleItalic">Expanded Disability Status Scale</span>&#41; al inicio de alemtuzumab&#44; n&#250;mero de brotes en los dos a&#241;os anteriores&#44; n&#250;mero y tipo de TME previo&#44; n&#250;mero y localizaci&#243;n de lesiones en la &#250;ltima RM &#40;en secuencia T2 y realzadas con gadolinio en secuencia T1&#41;&#46; La definici&#243;n de brote fue la aparici&#243;n de nuevos s&#237;ntomas neurol&#243;gicos o empeoramiento de previos atribuibles a la EM&#44; de al menos 24 horas de duraci&#243;n en ausencia de fiebre&#44; transcurridos al menos 30 d&#237;as desde el episodio anterior<span class="elsevierStyleBold">&#46;</span></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">An&#225;lisis de los datos</span><p id="par0040" class="elsevierStylePara elsevierViewall">Se realiz&#243; un an&#225;lisis estad&#237;stico descriptivo&#46; Las variables cuantitativas se describen con medidas de tendencia central y dispersi&#243;n &#91;media &#40;desviaci&#243;n est&#225;ndar&#41; o mediana &#40;rango intercuart&#237;lico&#41;&#93;&#44; y las cualitativas con frecuencias absolutas &#40;n&#41; y relativas &#40;&#37;&#41;&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Se realizaron tres suban&#225;lisis en funci&#243;n de&#58; &#40;1&#41; puntuaci&#243;n EDSS al inicio de alemtuzumab &#40;EDSS 0-3&#59; 3&#44;5-4&#59; &#8805; 4&#44;5&#41;&#59; &#40;2&#41; periodo de reclutamiento &#40;cohorte 1&#58; octubre de 2016 a marzo de 2017&#59; cohorte 2&#58; abril a septiembre de 2017&#59; cohorte 3&#58; octubre de 2017 a marzo de 2018&#59; cohorte 4&#58; abril a septiembre de 2018&#44; y &#40;3&#41; enfermedad muy activa&#44; definida como &#40;a&#41; &#8805; 1 brote en el &#250;ltimo a&#241;o a pesar del TME&#44; y &#8805; 1 lesi&#243;n Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>en T1 o &#8805; 9 lesiones en T2<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">8</span></a>&#59; o &#40;b&#41; pacientes sin tratamiento previo con &#8805;2 brotes en el &#250;ltimo a&#241;o y &#8805;1 lesi&#243;n Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>en T1<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">9&#44;10</span></a>&#46; El segundo suban&#225;lisis se realiz&#243; para evaluar si el perfil de los pacientes candidatos a recibir alemtuzumab ha variado con el tiempo a medida que los neur&#243;logos adquieren experiencia con el f&#225;rmaco&#46; El suban&#225;lisis de los pacientes con EM muy activa servir&#225; para valorar si la restricci&#243;n actual de utilizaci&#243;n de alemtuzumab impuesto por la Agencia Europea de Medicamentos &#40;EMA&#41; influye en la elecci&#243;n de alemtuzumab en poblaci&#243;n con EM de alta actividad&#46; Por &#250;ltimo&#44; y aunque no fue objetivo de este an&#225;lisis intermedio&#44; consideramos que la revisi&#243;n de los hallazgos de seguridad podr&#237;a ser de inter&#233;s en relaci&#243;n con la alerta de seguridad que llev&#243; a la evaluaci&#243;n del riesgo-beneficio por parte de la EMA&#46; Este an&#225;lisis de la seguridad se realiz&#243; en el conjunto de pacientes con al menos una valoraci&#243;n de seguridad tras la inclusi&#243;n en el estudio&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Los an&#225;lisis se basaron en los datos disponibles&#59; es decir&#44; no se imputaron los datos perdidos&#44; y el valor de significaci&#243;n estad&#237;stica se estableci&#243; en 0&#44;05&#46; Todos los an&#225;lisis se realizaron con el programa estad&#237;stico SPSS 22&#46;0 &#40;SPSS Inc&#44; Chicago&#44; USA&#41;&#46;</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Resultados</span><p id="par0055" class="elsevierStylePara elsevierViewall">A 28 de septiembre de 2018&#44; se hab&#237;an incluido un total de 167 pacientes&#44; dos de los cuales no cumplieron con los criterios de selecci&#243;n&#46; De los 165 pacientes evaluables&#44; 161 hab&#237;an completado la visita basal y se incluyeron en este an&#225;lisis&#46; La edad media fue 38&#44;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&#44;4 a&#241;os&#59; el 67&#44;1&#37; eran mujeres y el 94&#44;4&#37; hab&#237;an recibido TMEs previo&#46; La media de TMEs previos fue 2&#44;1<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;1 &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">tabla 1</a>&#41; y los &#250;ltimos TMEs recibidos antes de alemtuzumab fueron fingolimod y natalizumab en el 43&#44;4&#37; y 19&#44;7&#37; de los pacientes&#44; respectivamente &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">tabla 1</a>&#44; <a class="elsevierStyleCrossRef" href="#fig0005">fig&#46; 1</a>&#41;&#46; Al inicio de alemtuzumab la duraci&#243;n media de la enfermedad era de 8&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>6&#44;0 a&#241;os&#44; la puntuaci&#243;n EDSS 3&#44;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;7 y el n&#250;mero medio de brotes en los dos a&#241;os anteriores 1&#44;8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;3 &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">tabla 1</a>&#41;&#46; El 55&#44;4&#37; de los pacientes presentaban una puntuaci&#243;n EDSS basal entre 0-3&#44; y el 56&#37; hab&#237;a tenido &#8805; 2 brotes en los dos a&#241;os anteriores&#46; La &#250;ltima RM se realiz&#243; una media de 3&#44;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#44;1 meses antes de iniciar alemtuzumab&#44; mostrando lesiones Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>en el 48&#44;3&#37; de los pacientes y un n&#250;mero de lesiones en secuencia T2 entre 10-50&#44; en el 73&#37;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><elsevierMultimedia ident="fig0005"></elsevierMultimedia><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Perfil del paciente que inicia alemtuzumab durante los dos a&#241;os de reclutamiento</span><p id="par0060" class="elsevierStylePara elsevierViewall">El porcentaje de pacientes que inici&#243; alemtuzumab result&#243; homog&#233;neo en los cuatro semestres del periodo de reclutamiento&#58; un 21&#37; de los pacientes se incluyeron entre octubre de 2016 y marzo de 2017&#59; 21&#37; entre abril y septiembre de 2017&#59; 27&#37; entre octubre de 2017 y marzo de 2018&#59; 30&#37; entre abril y septiembre de 2018&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Se observaron cambios significativos en la EDSS basal y n&#250;mero de lesiones Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>en T1 entre las cuatro cohortes de reclutamiento &#40;<a class="elsevierStyleCrossRef" href="#tbl0010">tabla 2</a>&#41;&#46; Los pacientes de la cohorte 1 ten&#237;an una puntuaci&#243;n EDSS significativamente m&#225;s elevada que los pacientes de la cohorte 4 &#40;4&#44;1<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;8 vs&#46; 3&#44;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;7&#59; p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;040&#41;&#46; La media de lesiones Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>en T1 fue significativamente superior en los pacientes de la cohorte 1 &#40;que iniciaron alemtuzumab en una fecha m&#225;s cercana a su aprobaci&#243;n en el a&#241;o 2015&#41;&#44; que en la cohorte 4 &#40;10&#44;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>11&#44;9 vs&#46; 4&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#44;7&#59; p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;020&#41;&#46; El n&#250;mero de brotes fue similar en todas las cohortes &#40;p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;702&#41;&#44; pero el porcentaje de pacientes que iniciaron alemtuzumab tras fingolimod o natalizumab fue inferior en la cohorte 4 &#40;60&#44;6&#37;&#41; que en la cohorte 1 &#40;70&#44;6&#37;&#41;&#44; aunque la comparaci&#243;n estad&#237;stica entre grupos no se analiz&#243; &#40;<a class="elsevierStyleCrossRef" href="#tbl0010">tabla 2</a>&#41;&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Caracter&#237;sticas basales en funci&#243;n de la puntuaci&#243;n EDSS al inicio de alemtuzumab</span><p id="par0070" class="elsevierStylePara elsevierViewall">El 55&#44;4&#37; de los pacientes ten&#237;an una puntuaci&#243;n EDSS basal entre 0-3 y el 23&#44;5&#37; &#8805;<span class="elsevierStyleHsp" style=""></span>4&#44;5 &#40;<a class="elsevierStyleCrossRef" href="#tbl0015">tabla 3</a>&#41;&#46; Aunque los pacientes con mayor puntuaci&#243;n EDSS eran de mayor edad &#40;41&#44;4<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8&#44;2 a&#241;os en pacientes con EDSS entre 3&#44;5-4&#44; y 41&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8&#44;9 a&#241;os con EDSS &#8805;<span class="elsevierStyleHsp" style=""></span>4&#44;5&#41; y ten&#237;an una mayor duraci&#243;n de la EM &#40;9&#44;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#44;0 a&#241;os en pacientes con EDSS entre 3&#44;5-4&#59; 10&#44;4<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&#44;0 a&#241;os en pacientes con EDSS &#8805;<span class="elsevierStyleHsp" style=""></span>4&#44;5&#41;&#44; no se observaron diferencias significativas en el n&#250;mero de brotes en funci&#243;n de la EDSS&#46; El n&#250;mero basal de lesiones Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>en T1 fue significativamente diferente en funci&#243;n de la puntuaci&#243;n EDSS &#40;<a class="elsevierStyleCrossRef" href="#tbl0015">tabla 3</a>&#41;&#46;</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Alemtuzumab en esclerosis m&#250;ltiple muy activa</span><p id="par0075" class="elsevierStylePara elsevierViewall">Ochenta y seis &#40;86&#41; pacientes presentaban una enfermedad muy activa&#46; Este grupo ten&#237;a una edad media de 38<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&#44;5 a&#241;os&#44; una duraci&#243;n de la EM de 8&#44;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#44;7 a&#241;os&#44; una media de brotes en los dos a&#241;os previos de 2&#44;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;1 y un tiempo medio desde el &#250;ltimo brote de 4&#44;4<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3 meses&#46; La puntuaci&#243;n EDSS al inicio de alemtuzumab era 3&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;5 y el n&#250;mero medio de lesiones Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>5&#44;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&#44;9&#46;</p><p id="par0080" class="elsevierStylePara elsevierViewall">Los pacientes muy activos hab&#237;an recibido una media de 2&#44;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#44;8 TMEs antes de alemtuzumab&#44; siendo fingolimod y natalizumab los TMEs previos en el 50&#37; y el 11&#44;6&#37; de los casos&#44; respectivamente&#46;</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Resultados de seguridad</span><p id="par0085" class="elsevierStylePara elsevierViewall">A 5 de diciembre de 2019&#44; 148 pacientes continuaban en el estudio y 147 hab&#237;an recibido los dos cursos de tratamiento inicial&#46; Diecisiete pacientes interrumpieron el tratamiento con alemtuzumab por diversas razones&#44; incluidas falta de eficacia &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>5&#41;&#44; p&#233;rdida de seguimiento &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>5&#41;&#44; retirada del consentimiento &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>3&#41;&#44; decisi&#243;n del investigador &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>2&#41;&#44; cambio de tratamiento &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>1&#41; y fallecimiento &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>1&#41;&#46; Se reportaron 33 acontecimientos adversos &#40;AAs&#41; graves&#44; 9 de los cuales se consideraron relacionados con alemtuzumab&#58; 1 rash maculopapular&#44; 1 trombocitopenia&#44; 1 reacci&#243;n cut&#225;nea&#44; 2 pirexias&#44; 1 linfohistiocitosis hemofagoc&#237;tica con desenlace fatal&#44; 1 elevaci&#243;n de transaminasas&#44; 1 reacci&#243;n a la perfusi&#243;n y 1 linfopenia&#46;</p><p id="par0090" class="elsevierStylePara elsevierViewall">La <a class="elsevierStyleCrossRef" href="#tbl0020">tabla 4</a> recoge otros AAs relacionados con alemtuzumab de intensidad leve o moderada en l&#237;nea con los nuevos informes de reacciones inmunomediadas y cardiovasculares&#46; La mayor&#237;a de las reacciones cardiacas&#47;vasculares se notificaron durante la perfusi&#243;n&#46; No se observaron episodios de accidente cerebrovascular hemorr&#225;gico&#44; disecci&#243;n de las arterias cervicocef&#225;licas&#44; hemorragia alveolopulmonar&#44; ni casos de hepatitis autoinmune&#46;</p><elsevierMultimedia ident="tbl0020"></elsevierMultimedia></span></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Discusi&#243;n</span><p id="par0095" class="elsevierStylePara elsevierViewall">La poblaci&#243;n del estudio LEMVIDA&#44; con una duraci&#243;n media de la enfermedad de unos ocho a&#241;os&#44; una puntuaci&#243;n media EDSS de 3&#44;3 y una media de dos TMEs previos&#44; presenta una peor situaci&#243;n cl&#237;nica basal que la incluida en los ensayos cl&#237;nicos del programa cl&#237;nico de alemtuzumab<a class="elsevierStyleCrossRefs" href="#bib0115"><span class="elsevierStyleSup">2&#8211;5</span></a>&#44; donde los pacientes eran m&#225;s j&#243;venes &#40;34&#44;8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8&#44;4 a&#241;os en CARE-MS II<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">5</span></a>&#41;&#44; con menor duraci&#243;n de la EM &#40;4&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>2&#44;7 a&#241;os en CARE-MS II<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">5</span></a>&#41;&#44; menor discapacidad &#40;EDSS entre 2-2&#44;7 seg&#250;n el estudio&#41; y menor exposici&#243;n previa a TMEs &#40;1 TME en el estudio CARE-MS II<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">5</span></a>&#41; &#40;<a class="elsevierStyleCrossRef" href="#tbl0025">tabla 5</a>&#41;&#46; M&#225;s de la mitad de los pacientes del estudio LEMVIDA presentaban actividad cl&#237;nica y radiol&#243;gica a pesar de haber recibido al menos dos TMEs&#46; Por todo ello&#44; <span class="elsevierStyleItalic">a priori</span>&#44; se trata de una poblaci&#243;n con un peor pron&#243;stico en cuanto al riesgo de progresi&#243;n de la discapacidad<a class="elsevierStyleCrossRefs" href="#bib0160"><span class="elsevierStyleSup">11&#8211;13</span></a> y una mayor posibilidad de presentar menor respuesta a alemtuzumab en comparaci&#243;n con la poblaci&#243;n de los estudios fase 3 CARE-MS<a class="elsevierStyleCrossRefs" href="#bib0115"><span class="elsevierStyleSup">2&#44;14&#8211;16</span></a>&#46; La pr&#225;ctica cl&#237;nica entre los neur&#243;logos que participaron en el estudio LEMVIDA muestra c&#243;mo en general se pospone el inicio de alemtuzumab hasta una fase m&#225;s tard&#237;a de la enfermedad despu&#233;s de la falta de respuesta a otros TMEs&#46; Aunque este hallazgo no diverge de las &#250;ltimas recomendaciones de expertos europeos<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">17</span></a>&#44; es contrario al concepto de inducir con alemtuzumab un cambio tolerog&#233;nico precoz en el sistema inmune&#46; Otras grandes cohortes prospectivas similares a nuestra serie&#44; como el estudio alem&#225;n TREAT-MS &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>779&#41;<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">18</span></a> o el programa canadiense MS One-to-One &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>494&#41;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">19</span></a> &#40;<a class="elsevierStyleCrossRef" href="#tbl0025">tabla 5</a>&#41;&#44; revelan la misma tendencia en las decisiones del tratamiento a medida que progresa la enfermedad &#40;resultados no publicados&#41;&#46;</p><elsevierMultimedia ident="tbl0025"></elsevierMultimedia><p id="par0100" class="elsevierStylePara elsevierViewall">La falta de un perfil de paciente candidato a tratamiento claramente definido&#44; de biomarcadores validados para la predicci&#243;n de la respuesta e incluso la falta de una definici&#243;n clara de actividad radiol&#243;gica en la indicaci&#243;n de alemtuzumab&#44; pueden haber supuesto condicionantes para la elecci&#243;n del momento m&#225;s adecuado en la indicaci&#243;n del f&#225;rmaco&#46; El hecho de que en la actualidad muchos de los pacientes que inician alemtuzumab han estado previamente expuestos a TMEs no disponibles ni comercializados durante el desarrollo cl&#237;nico del f&#225;rmaco &#40;como por ejemplo&#44; fingolimod&#41; y la ausencia de informaci&#243;n cl&#237;nica en este sentido&#44; refuerzan la importancia de disponer de cohortes de pacientes con este perfil&#46; Estos estudios en curso<a class="elsevierStyleCrossRefs" href="#bib0195"><span class="elsevierStyleSup">18&#44;19</span></a> junto con el estudio LEMVIDA&#44; aportar&#225;n informaci&#243;n sobre el uso de alemtuzumab en la pr&#225;ctica cl&#237;nica real&#46;</p><p id="par0105" class="elsevierStylePara elsevierViewall">Los pacientes que al iniciar alemtuzumab presentaban una EDSS &#8805; 3&#44;5 &#40;44&#44;8&#37;&#41; ten&#237;an una mayor edad&#44; duraci&#243;n la enfermedad y n&#250;mero de lesiones Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>en T1 que aquellos con EDSS &#60;<span class="elsevierStyleHsp" style=""></span>3&#44;5&#44; aunque la tasa de brotes y la actividad en RM &#40;secuencia T2&#41; fue similar&#46; Estos datos del estudio LEMVIDA muestran el considerable n&#250;mero de pacientes con una EM evolucionada tratados con alemtuzumab en la pr&#225;ctica cl&#237;nica real&#46; Aunque la proporci&#243;n de pacientes con EDSS 0-3 es notable &#40;55&#37;&#41;&#44; resulta inferior al estudio CARE-MS II &#40;69&#37;&#41;&#46; Sin embargo&#44; si nos fijamos en la forma en que han evolucionado a lo largo del tiempo las caracter&#237;sticas cl&#237;nicas basales de los pacientes que iniciaron alemtuzumab en LEMVIDA&#44; se observa un cambio en esta tendencia&#44; ya que en los &#250;ltimos a&#241;os el tratamiento se inici&#243; en una fase m&#225;s precoz y con menor grado de discapacidad y actividad de la EM debido&#44; probablemente&#44; a una mayor experiencia con el f&#225;rmaco y la constataci&#243;n de mayor efectividad cuando se utiliza en etapas m&#225;s tempranas&#46; Los pacientes que iniciaron alemtuzumab en 2016 presentaban una puntuaci&#243;n EDSS casi un punto mayor que aquellos que iniciaron tratamiento en 2018 &#40;4&#44;1 vs&#46; 3&#44;2&#41; y el doble de lesiones Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>en secuencia T1 &#40;10&#44;9 vs&#46; 4&#44;5&#41;&#46; La tasa de brotes y el n&#250;mero de TME previos resultaron similares&#44; pero la proporci&#243;n de pacientes que cambi&#243; a alemtuzumab desde inmunosupresores selectivos&#44; como fingolimod o natalizumab&#44; disminuy&#243; en la &#250;ltima cohorte &#40;70&#44;6&#37; vs&#46; 60&#44;6&#37;&#41;&#46; Esto sugiere un cambio en la pr&#225;ctica cl&#237;nica de los neur&#243;logos durante los dos a&#241;os de reclutamiento del estudio&#44; mostrando una tendencia a iniciar alemtuzumab de forma m&#225;s temprana y en pacientes con menor discapacidad&#44; en lugar de prescribirlo como tratamiento de tercera l&#237;nea tras natalizumab o fingolimod&#44; indicados en pacientes con EM muy activa o grave de evoluci&#243;n r&#225;pida<a class="elsevierStyleCrossRefs" href="#bib0205"><span class="elsevierStyleSup">20&#44;21</span></a>&#46;</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Conclusiones</span><p id="par0110" class="elsevierStylePara elsevierViewall">Este art&#237;culo publica los datos basales de una amplia cohorte de pacientes con EMRR tratados con alemtuzumab en la pr&#225;ctica real en Espa&#241;a&#46; Aunque el estudio LEMVIDA incluy&#243; una poblaci&#243;n principalmente caracterizada por una mayor duraci&#243;n de la enfermedad y discapacidad&#44; tambi&#233;n demuestra una tendencia creciente hacia un inicio temprano de alemtuzumab en pacientes previamente tratados&#46; Estos resultados se publican despu&#233;s del procedimiento del Art&#237;culo 20 para reevaluar el riesgo-beneficio de alemtuzumab&#44; por lo que tambi&#233;n resulta importante comunicar los hallazgos de seguridad con el f&#225;rmaco en una poblaci&#243;n que no coincide exactamente con la nueva indicaci&#243;n&#46; Esperamos que los datos finales del estudio LEMVIDA sirvan para mostrar el perfil de pacientes que se benefician del uso de alemtuzumab&#44; y para entender mejor el perfil de seguridad del f&#225;rmaco&#46; Mientras tanto&#44; en este an&#225;lisis intermedio no se encontraron problemas de seguridad inesperados asociados a alemtuzumab&#46;</p><p id="par0115" class="elsevierStylePara elsevierViewall">La interpretaci&#243;n de estos resultados puede verse limitada por el car&#225;cter observacional del estudio&#46; Tampoco debemos ignorar que la situaci&#243;n que refleja este an&#225;lisis probablemente est&#233; cambiando a medida que aparecen nuevos datos del f&#225;rmaco&#46;</p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Contribuci&#243;n de los autores</span><p id="par0120" class="elsevierStylePara elsevierViewall">JCAC&#44; BCS&#44; GIA&#44; ROC&#44; ARA contribuyeron a la concepci&#243;n y dise&#241;o del estudio&#46; JEML&#44; BCS&#44; ARA y CCH participaron en la recogida de datos&#46; JEML y ROC redactaron el borrador del art&#237;culo&#46; Todos los autores contribuyeron al an&#225;lisis e interpretaron de los datos&#44; revisaron de forma cr&#237;tica el manuscrito y aprobaron la versi&#243;n final para su publicaci&#243;n&#46;</p></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Financiaci&#243;n</span><p id="par0125" class="elsevierStylePara elsevierViewall">El estudio LEMVIDA fue patrocinado por Sanofi&#46;</p></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Conflicto de intereses</span><p id="par0130" class="elsevierStylePara elsevierViewall">JEML ha recibido becas y honorarios por consultor&#237;a o conferencias de Almirall&#44; Biogen&#44; Celgene&#44; Genzyme&#44; Merck&#44; Novartis&#44; Roche y Teva&#46; JCAC ha recibido honorarios como miembro del consejo asesor de Sanofi&#46; BCS declara que la Unidad de Inmunolog&#237;a Cl&#237;nica ha recibido donaciones de&#58; Sanofi&#44; Roche&#44; Novartis&#44; Merck&#44; Biogen Idec&#44; Teva&#44; Almirall&#44; Celgene&#44; Mylan y Bayer&#44; as&#237; como honorarios por participaci&#243;n en reuniones y congresos de&#58; Sanofi&#44; Roche&#44; Novartis&#44; Merck y Celgene&#46; GIA ha recibido honorarios como conferenciante o miembro de consejos asesores de Bayer&#44; Biogen Idec&#44; Novartis&#44; Sanofi&#44; Merck Serono&#44; Almirall&#44; Roche&#44; Actelion&#44; Celgene y Teva&#46; ROC es empleado de Sanofi y puede tener acciones y&#47;o opciones sobre acciones de la empresa&#46; ARA ha recibido honorarios como conferenciante o miembro de comit&#233;s asesores de Biogen&#44; Sanofi&#44; Merck&#44; Novartis&#44; Roche y Teva&#46; CCH ha recibido honorarios como conferenciante o miembro de comit&#233;s asesores de Merck&#44; Sanofi&#44; Teva&#44; Novartis y Biogen Idec&#46;</p></span></span>"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Introducci&#243;n</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">LEMVIDA es un estudio de pr&#225;ctica cl&#237;nica&#44; prospectivo&#44; de tres a&#241;os de seguimiento sobre calidad de vida en pacientes con esclerosis m&#250;ltiple &#40;EM&#41; tratados con alemtuzumab en Espa&#241;a&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">M&#233;todos</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">An&#225;lisis intermedio de las caracter&#237;sticas basales de los pacientes que iniciaron alemtuzumab entre octubre de 2016 y septiembre de 2018&#46; Se realizaron tres suban&#225;lisis en funci&#243;n de&#58; puntuaci&#243;n EDSS basal&#59; periodo de inicio de alemtuzumab durante el reclutamiento &#40;cohorte 1&#58; octubre de 2016 a marzo de 2017&#44; cohorte 2&#58; abril a septiembre de 2017&#59; cohorte 3&#58; octubre de 2017 a marzo de 2018&#44; y cohorte 4&#58; abril a septiembre de 2018&#41;&#59; y criterios de EM muy activa&#46;</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Resultados</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Se analizaron a 161 pacientes&#58; 67&#44;1&#37; mujeres&#44; edad 38&#44;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&#44;4 a&#241;os&#44; duraci&#243;n EM 8&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>6&#44;0 a&#241;os&#44; EDSS 3&#44;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;7 y n&#250;mero de brotes en los dos a&#241;os previos 1&#44;8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;3&#46; El 48&#44;3&#37; presentaba lesiones realzadas con gadolinio &#40;Gd<span class="elsevierStyleHsp" style=""></span>&#43;&#41; &#40;media&#58; 5&#44;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>6&#44;9&#41; y el 63&#44;1&#37; hab&#237;a recibido tratamiento previo con fingolimod o natalizumab&#46; En el momento basal&#44; la puntuaci&#243;n EDSS y el n&#250;mero de lesiones Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>fue significativamente superior en la cohorte 1 que en la cohorte 4 &#40;4&#44;1<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;8 vs&#46; 3&#44;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;7&#59; p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;040 y 10&#44;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>11&#44;9 vs&#46; 4&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#44;7&#59; p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;020&#41;&#46; La frecuencia de tratamiento previo con fingolimod y natalizumab fue menor en la cohorte 4 &#40;60&#44;6&#37;&#41; que en la cohorte 1 &#40;70&#44;6&#37;&#41; &#40;comparaci&#243;n entre grupos no analizada&#41;&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusiones</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">A diferencia de los estudios fase 3 de alemtuzumab&#44; los pacientes incluidos en LEMVIDA tienen mayor edad&#44; duraci&#243;n de la EM y discapacidad&#44; y han recibido inmunosupresores previos&#46; Sin embargo&#44; a lo largo del reclutamiento se tiende a adelantar el inicio de alemtuzumab&#44; probablemente debido a la evidencia de una mayor efectividad en etapas tempranas&#46;</p></span>"
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        "resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Introduction</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">LEMVIDA is a real-world prospective study of 3-year follow-up on quality of life of patients with multiple sclerosis &#40;MS&#41; receiving alemtuzumab in Spain&#46;</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Methods</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">This is an interim analysis evaluating the baseline characteristics of patients who started alemtuzumab between October 2016-September 2018&#46; For 3 additional subanalysis patients were categorized by baseline EDSS score&#59; time of alemtuzumab initiation during the recruitment period &#40;cohort 1&#58; October 2016-March 2017&#44; cohort 2&#58; April-September 2017&#44; cohort 3&#58; October 2017-March 2018 and cohort 4&#58; April-September 2018&#41;&#59; and the presence of highly active MS criteria&#46;</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Results</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">161 patients were analyzed&#58; 67&#46;1&#37; female&#44; age 38&#46;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&#46;4 years&#44; MS duration 8&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>6&#46;0 years&#44; EDSS 3&#46;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#46;7 and number of relapses in the previous 2 years 1&#46;8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#46;3&#46; 48&#46;3&#37; of patients presented gadolinium-enhanced &#40;Gd<span class="elsevierStyleHsp" style=""></span>&#43;&#41; lesions &#40;mean&#58; 5&#46;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>6&#46;9&#41; and 63&#46;1&#37; had received prior treatment with fingolimod or natalizumab&#46; Baseline EDSS scores and number of Gd<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>lesions were higher in cohort 1 than in cohort 4 &#40;4&#46;1<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#46;8 <span class="elsevierStyleItalic">vs</span>&#46; 3&#46;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#46;7&#59; p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;040 and 10&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>11&#46;9 <span class="elsevierStyleItalic">vs</span> 4&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#46;7&#59; p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;020&#41;&#46; The frequency of prior treatment with fingolimod and natalizumab was lower in cohort 4 &#40;60&#46;6&#37;&#41; than in cohort 1 &#40;70&#46;6&#37;&#41; &#40;comparison between groups not analyzed&#41;&#46;</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclusions</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Unlike phase 3 studies of alemtuzumab&#44; the patients included in LEMVIDA are older&#44; have a longer duration of MS&#44; higher disability and have received previous immunosuppressants&#46; However&#44; throughout the recruitment period&#44; there is a tendency towards an early beginning of treatment with alemtuzumab&#44; probably due to the evidence of higher effectiveness in the early stages of MS&#46;</p></span>"
        "secciones" => array:4 [
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            "titulo" => "Introduction"
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            "identificador" => "abst0035"
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            "identificador" => "abst0040"
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    "multimedia" => array:6 [
      0 => array:7 [
        "identificador" => "fig0005"
        "etiqueta" => "Figura 1"
        "tipo" => "MULTIMEDIAFIGURA"
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          "es" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">&#218;ltimos f&#225;rmacos para la EM recibidos antes de alemtuzumab en la cohorte LEMVIDA&#46; Otros&#58; rituximab &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>3&#41; y daclizumab &#40;n<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>1&#41;&#46;</p>"
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        "etiqueta" => "Tabla 1"
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          "leyenda" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Los datos se expresan como media<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>DE&#44; n&#47;N disponible &#40;&#37;&#41;&#44; o mediana &#40;IQR&#41;&#46;</p><p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">DE&#58; desviaci&#243;n est&#225;ndar&#59; EM&#58; esclerosis m&#250;ltiple&#59; EDSS&#58; escala ampliada del estado de discapacidad &#40;<span class="elsevierStyleItalic">Expanded Disability Status Scale</span>&#41;&#59; Gd&#58; gadolinio&#59; IQR&#58; rango intercuart&#237;lico&#59; TMEs&#58; tratamientos modificadores de la enfermedad&#46;</p>"
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Cohorte LEMVIDA &#40;N<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>161&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Mediana&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
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                  \t\t\t\t" scope="col">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">Octubre de 2016-marzo de 2017&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">Abril-septiembre de 2017&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">Octubre de 2017-marzo de 2018&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">Abril-septiembre de 2018&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th></tr><tr title="table-row"><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&#40;N<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>34&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&#40;N<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>43&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&#40;N<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>50&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&#40;N<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>34&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Edad&#44; a&#241;os&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">37&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&#44;3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">38&#44;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>8&#44;1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">38&#44;1<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&#44;7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">41&#44;0<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>10&#44;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">0&#44;428&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleItalic">Tiempo desde el diagn&#243;stico de EM hasta inicio de alemtuzumab&#44; a&#241;os</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Media&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">10&#44;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#44;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">7&#44;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>6&#44;9&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">8&#44;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#44;5&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">8&#44;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>5&#44;7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t\ttop\n
                  \t\t\t\t">0&#44;154&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Mediana&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">6&#44;6 &#40;9&#44;4-14&#44;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">6&#44;9 &#40;2&#44;1-11&#44;7&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">8&#44;1 &#40;3&#44;9-12&#44;3&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">7&#44;5 &#40;2&#44;7-11&#44;4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleItalic">Puntuaci&#243;n en EDSS</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Media&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">4&#44;1<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;8&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
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                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">0&#44;034<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">&#182;</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Mediana&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">4&#44;0 &#40;2&#44;5 - 6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">2&#44;5 &#40;2-4&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">3&#44;0 &#40;2-3&#44;6&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">3&#44;0 &#40;2-3&#44;5&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleItalic">Brotes en los dos a&#241;os anteriores</span>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="" valign="\n
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                  \t\t\t\t">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Media&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">1&#44;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;5&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">1&#44;8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;2&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">1&#44;8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#44;3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">TMEs previos</span>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t">32&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Pacientes con lesiones&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">TME previos</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">Inmunosupresores previos a alemtuzumab</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n
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                  \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Natalizumab&nbsp;\t\t\t\t\t\t\n
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Información del artículo
ISSN: 02134853
Idioma original: Español
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