Long-term efficacy, tolerability and retention rate of azathioprine in 103 aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder patients: a multicentre retrospective observational study from the UK

被引:98
作者
Elsone, Liene [1 ]
Kitley, Joanna [2 ]
Luppe, Sebastian [3 ]
Lythgoe, Daniel [4 ]
Mutch, Kerry [1 ]
Jacob, Saiju [5 ]
Brown, Rachel [2 ]
Moss, Kathryn [6 ]
McNeillis, Benjamin [2 ]
Goh, Yee Yen [1 ]
Leite, M. Isabel [2 ]
Robertson, Neil [3 ]
Palace, Jackie [2 ]
Jacob, Anu [1 ]
机构
[1] Walton Ctr NHS Fdn Trust, Liverpool L9 7LJ, Merseyside, England
[2] John Radcliffe Hosp, Nuffield Dept Clin Neurosci, Oxford, England
[3] Univ Wales Hosp, Cardiff & Vale Univ Hlth Board, Cardiff, S Glam, Wales
[4] Univ Liverpool, CRUK Liverpool Canc Trials Unit, Liverpool L69 3BX, Merseyside, England
[5] Univ Hosp Birmingham, Queen Elizabeth Neurosci Ctr, Birmingham, W Midlands, England
[6] Royal Liverpool Univ Hosp, Liverpool, Merseyside, England
关键词
Neuromyelitis optica; NMO; azathioprine; tolerability; retention; aquaporin-4; CLINICAL-PHARMACOLOGY; IGG PREDICTS; OPEN-LABEL; FOLLOW-UP; RITUXIMAB; SAFETY; MYCOPHENOLATE; MITOXANTRONE; THERAPY; RELAPSE;
D O I
10.1177/1352458514525870
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Azathioprine (AZA) is a common immunosuppressive drug used for relapse prevention in neuromyelitis optica (NMO). Objectives: The objective of this paper is to assess efficacy, tolerability and retention of AZA in a large NMO cohort. Methods: We conducted a retrospective review of medical records of 103 aquaporin-4 antibody-positive NMO and NMO spectrum disorder (NMOSD) patients treated with AZA. Results: This is the largest reported cohort of AQP4-Ab positive patients treated with AZA. Eighty-nine per cent (n = 92) had reduction in median annualised relapse rates from 1.5 (IQR 0.6-4.0) to 0 (IQR 0-0.27, p < 0.00005) with treatment. Sixty-one per cent (n = 63) remained relapse free at a median follow-up of 18 months. Neurological function improved or stabilised in 78%. At last follow-up, treatment was discontinued in 46% (n = 47). Of these, 62% (n = 29) were because of side effects, 19% (n = 9) because of death, 15% (n = 7) because of ongoing disease activity, and 2% (n = I) because of pregnancy. Using Kaplan-Meyer curves, we estimate that 73%, 58%, 47% and 33% of patients will remain on AZA for longer than one, three, five and 10 years, respectively, after initiation of treatment. Conclusions: AZA is a modestly effective treatment for NMO. However, many patients discontinue AZA over time and this seems to reflect poor tolerability more than lack of efficacy.
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收藏
页码:1533 / 1540
页数:8
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