Alemtuzumab: a review of efficacy and risks in the treatment of relapsing remitting multiple sclerosis

被引:55
作者
Guarnera, Cristina [1 ]
Bramanti, Placido [1 ]
Mazzon, Emanuela [1 ]
机构
[1] IRCCS Ctr Neurolesi Bonino Pulejo, Expt Neurol Lab, Via Prov Palermo, Messina, Italy
关键词
effectiveness; clinical studies; follow-up; adverse events; NECROTIZING LEUKOENCEPHALOPATHY; LYMPHOCYTE DEPLETION; INFUSION REACTIONS; INTERFERON-BETA; THERAPY; ANTIBODY; AUTOIMMUNITY; INFECTION; PATIENT; TRIAL;
D O I
10.2147/TCRM.S134398
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Alemtuzumab is a selective humanized monoclonal antibody directed against the CD52 antigen, and has been found to be a powerful treatment for relapsing remitting multiple sclerosis. Alemtuzumab demonstrated high efficacy in several clinical studies. The risk of relapse and sustained accumulation of disability showed significant reduction in the Phase II CAMMS223 and the Phase III clinical trials CARE MS I and CARE MS II. The data presented at the 32nd Congress of the European Committee for Treatment and Research in Multiple Sclerosis confirmed these results. After completion of a 1- year treatment cycle, alemtuzumab showed a sustained effect. Although the efficacy of alemtuzumab has been widely proven, several severe adverse effects have been reported with its use. Infusion- associated reactions, increased risk of infections, and secondary autoimmunity have been associated with alemtuzumab. Autoimmune disease - mainly of the thyroid - has been reported. Immune thrombocytopenic purpura and autoimmune nephropathies have been observed less frequently. These adverse effects, given the short period of alemtuzumab marketing for relapsing remitting multiple sclerosis, require strict monitoring.
引用
收藏
页码:871 / 879
页数:9
相关论文
共 49 条
[1]  
Achiron A, 2015, MULT SCLER J, V21, P581
[2]  
[Anonymous], 2013, LEMTR SUMM PROD CHAR
[3]  
Arnold D, 2015, NEUROLOGY
[4]   Predicting autoimmunity after alemtuzumab treatment of multiple sclerosis [J].
Azzopardi, Laura ;
Thompson, Sara A. J. ;
Harding, Katherine E. ;
Cossburn, Mark ;
Robertson, Neil ;
Compston, Alastair ;
Coles, Alasdair J. ;
Jones, Joanne L. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2014, 85 (07) :795-798
[5]  
Berkovich R, 2015, NEUROLOGY
[6]  
Breslin Sheila, 2007, Clin J Oncol Nurs, V11, P37, DOI 10.1188/07.CJON.S1.37-42
[7]  
Caon Christina, 2015, Int J MS Care, V17, P191, DOI 10.7224/1537-2073.2014-030
[8]   Active CMV infection in two patients with multiple sclerosis treated with alemtuzumab [J].
Clerico, Marinella ;
De Mercanti, Stefania ;
Artusi, Carlo Alberto ;
Durelli, Luca ;
Naismith, Robert T. .
MULTIPLE SCLEROSIS JOURNAL, 2017, 23 (06) :874-876
[9]   Alemtuzumab versus interferon beta 1a as first-line treatment for patients with relapsing-remitting multiple sclerosis: a randomised controlled phase 3 trial [J].
Cohen, Jeffrey A. ;
Coles, Alasdair J. ;
Arnold, Douglas L. ;
Confavreux, Christian ;
Fox, Edward J. ;
Hartung, Hans-Peter ;
Havrdova, Eva ;
Selmaj, Krzysztof W. ;
Weiner, Howard L. ;
Fisher, Elizabeth ;
Brinar, Vesna V. ;
Giovannoni, Gavin ;
Stojanovic, Miroslav ;
Ertik, Bella I. ;
Lake, Stephen L. ;
Margolin, David H. ;
Panzara, Michael A. ;
Compston, D. Alastair S. .
LANCET, 2012, 380 (9856) :1819-1828
[10]   Campath-1H treatment of multiple sclerosis: lessons from the bedside for the bench [J].
Coles, A ;
Deans, J ;
Compston, A .
CLINICAL NEUROLOGY AND NEUROSURGERY, 2004, 106 (03) :270-274