Observations during an elective interruption of natalizumab treatment: a post-marketing study

被引:30
|
作者
Borriello, Giovanna [1 ]
Prosperini, Luca [1 ]
Marinelli, Fabiana [1 ]
Fubelli, Federica [1 ]
Pozzilli, Carlo [1 ]
机构
[1] Univ Roma La Sapienza, Multiple Sclerosis Ctr, S Andrea Hosp, Dept Neurol Sci, I-00185 Rome, Italy
关键词
magnetic resonance imaging; multiple sclerosis; natalizumab; observational study; progressive multifocal leukoencephalopathy; rebound; TRIAL;
D O I
10.1177/1352458510392098
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In this prospective post-marketing study, 21 patients with multiple sclerosis treated with natalizumab for 24 consecutive months elected a trial of treatment interruption (90-180 days). During a mean duration of treatment interruption of 111.5 days 4 patients (19.0%) experienced a relapse and 9 out of 19 (47.4%) had MRI activity. Number of contrast-enhancing lesions at baseline was lower than during treatment interruption, but the difference was not significant. These findings suggest that disease activity may return after the last infusion of natalizumab. Patients should have regular MRI assessment during treatment interruption to rapidly identify any return of disease activity. The aim of this study was to determine the optimal duration for temporary interruption of natalizumab therapy in patients who have received continuous therapy with natalizumab for 24 months.
引用
收藏
页码:372 / 375
页数:4
相关论文
共 50 条
  • [41] Risperidone in the treatment of affective spectrum disorders and schizophrenia: a large, multicenter post-marketing surveillance study
    Park, JI
    Kim, CY
    Lee, JY
    Hong, JP
    PRIMARY CARE PSYCHIATRY, 2004, 9 (04): : 131 - 136
  • [42] Safety and efficacy of idursulfase in the treatment of mucopolysaccharidosis II (Hunter syndrome): a post-marketing study in Japan
    Ueda, Kazuo
    Hokugo, Jiro
    EXPERT OPINION ON DRUG SAFETY, 2020, 19 (07) : 891 - 901
  • [43] A retrospective pharmacovigilance study of post-marketing safety concerns with cefuroxime
    Jiang, Cheng
    Zheng, Xiaoxiao
    Li, Ping
    Qian, Jiancheng
    Li, Qin
    THERAPEUTIC ADVANCES IN DRUG SAFETY, 2024, 15
  • [44] A post-marketing observational monocentric study of efficacy and tolerability of dimetilfumarate
    Moiola, L.
    Di Cristinzi, M.
    Pisa, M.
    Sangalli, F.
    Costa, G. Dalla
    Radaelli, M.
    Preziosa, P.
    Romeo, M.
    Colombo, B.
    Esposito, F.
    Martinelli, V.
    Comi, G.
    MULTIPLE SCLEROSIS JOURNAL, 2017, 23 : 667 - 667
  • [45] The effects of Valette® on skin and hair:: A post-marketing surveillance study
    Zimmermann, T
    Wisser, KH
    Dietrich, H
    INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2000, 54 (02) : 85 - +
  • [46] Post-marketing safety concerns with rimegepant based on a pharmacovigilance study
    Jia-Ling Hu
    Jing-Ying Wu
    Shan Xu
    Shi-Yan Qian
    Cheng Jiang
    Guo-Qing Zheng
    The Journal of Headache and Pain, 25 (1)
  • [47] Experience with paroxetine in the treatment of depressions. Results of a post-marketing surveillance study in 1242 patients
    Simhandl, C
    Leitner, B
    NEUROPSYCHIATRIE, 1998, 12 (02) : 110 - 115
  • [48] Itopride in the Treatment of Functional Dyspepsia in Chinese PatientsA Prospective, Multicentre, Post-Marketing Observational Study
    Jing Sun
    Yao-Zong Yuan
    Gerald Holtmann
    Clinical Drug Investigation, 2011, 31 : 865 - 875
  • [49] Prospective Observational Post-Marketing Study of Tafluprost for Glaucoma and Ocular Hypertension: Effectiveness and Treatment Persistence
    Yasuaki Kuwayama
    Masako Hashimoto
    Reiko Kakegawa
    Akio Nomura
    Fumiki Shimada
    Advances in Therapy, 2017, 34 : 1411 - 1425
  • [50] Itopride in the Treatment of Functional Dyspepsia in Chinese Patients A Prospective, Multicentre, Post-Marketing Observational Study
    Sun, Jing
    Yuan, Yao-Zong
    Holtmann, Gerald
    CLINICAL DRUG INVESTIGATION, 2011, 31 (12) : 865 - 875