Belimumab: a technological advance for systemic lupus erythematosus patients? Report of a systematic review and meta-analysis

被引:12
作者
Kandala, Ngianga-Bakwin [1 ,2 ]
Connock, Martin [1 ]
Grove, Amy [1 ]
Sutcliffe, Paul [1 ]
Mohiuddin, Syed [3 ]
Hartley, Louise [1 ]
Court, Rachel [1 ]
Cummins, Ewen [4 ]
Gordon, Caroline [5 ]
Clarke, Aileen [1 ]
机构
[1] Univ Warwick, Warwick Med Sch, Div Hlth Sci, Coventry CV4 7AL, W Midlands, England
[2] KEMRI Univ Oxford Wellcome Trust Collaborat Progr, Ctr Geog Med, Malaria Publ Hlth & Epidemiol Grp, Nairobi, Kenya
[3] Univ Manchester, Manchester, Lancs, England
[4] McMaster Dev Consultants, McMDC Ltd, Glasgow, Lanark, Scotland
[5] Univ Birmingham, Coll Med & Dent Sci, Sch Immun & Infect, Birmingham, W Midlands, England
关键词
Clinical Pharmacology; Epidemiology; Preventive Medicine; Public Health; ELEVATION MYOCARDIAL-INFARCTION; INTERNATIONAL DIFFERENCES; REVISED CRITERIA; UNSTABLE ANGINA; DOUBLE-BLIND; DISEASE; COUNTRIES; CLASSIFICATION; OUTCOMES; TRIALS;
D O I
10.1136/bmjopen-2013-002852
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To undertake a systematic review and meta-analysis to investigate clinical effectiveness of belimumab for patients with systemic lupus erythematosus (SLE) and antinuclear and/or anti-double-stranded DNA (dsDNA) autoantibodies. Methods We searched eight electronic databases and reference lists for randomised controlled trials (RCTs) of belimumab against placebo or best supportive care. Quality assessment and random effects meta-analysis were undertaken. Design A meta-analysis of RCTs. Participants 2133 SLE patients. Primary and secondary outcome measures SLE Responder Index (SRI) at week 52. Results Three double-blind placebo-controlled RCTs (L02, BLISS-52 BLISS-76) investigated 2133 SLE patients. BLISS-52 and BLISS-76 trials recruited patients with antinuclear and/or anti-dsDNA autoantibodies and demonstrated belimumab effectiveness for the SRI at week 52. Ethnicity and geographical location of participants varied considerably between BLISS trials. Although tests for statistical heterogeneity were negative, BLISS-52 results were systematically more favourable for all measured outcomes. Meta-analysis of pooled 52-week SRI BLISS results showed benefit for belimumab (OR 1.63, 95% CI 1.27 to 2.09). By week 76, the primary SRI outcome in BLISS-76 was not statistically significant (OR 1.31, 95% CI 0.919 to 1.855).
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页数:12
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