Neutralizing antibodies to interferon beta-1b multiple sclerosis: a clinico-radiographic paradox in the BEYOND trial

被引:27
作者
Goodin, Douglas S. [1 ]
Hartung, Hans-Peter [2 ]
O'Connor, Paul [3 ]
Filippi, Massimo [4 ,5 ]
Arnason, Barry [6 ]
Comi, Giancarlo [7 ]
Cook, Stuart [8 ]
Jeffery, Douglas [8 ]
Kappos, Ludwig [9 ]
Bogumil, Timon
Knappertz, Volker [2 ]
Sandbrink, Rupert [2 ,10 ]
Beckmann, Karola [10 ]
White, Rick [11 ]
Petkau, John [11 ]
Pohl, Christoph [10 ,12 ]
机构
[1] Univ Calif San Francisco, San Francisco, CA 94143 USA
[2] Univ Dusseldorf, D-40225 Dusseldorf, Germany
[3] St Michaels Hosp, Toronto, ON M5B 1W8, Canada
[4] Inst Sci, Neuroimaging Res Unit, Milan, Italy
[5] Univ Milan, Osped San Raffaele, I-20127 Milan, Italy
[6] Surg Brain Res Inst, Chicago, IL USA
[7] Univ Vita Salute San Raffaele, Dept Neurol & Clin Neurophysiol, Milan, Italy
[8] UMD New Jersey Med Sch, Newark, NJ USA
[9] Univ Basel Hosp, Basel, Switzerland
[10] Bayer HealthCare Pharmaceut, Montville, NJ USA
[11] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[12] Univ Hosp Bonn, Bonn, Germany
关键词
BEYOND study; interferon beta-1b; multiple sclerosis; neutralizing antibodies; SECONDARY PROGRESSIVE MS; TECHNOLOGY-ASSESSMENT SUBCOMMITTEE; RELAPSING-REMITTING MS; TERM-FOLLOW-UP; IFN-BETA; AMERICAN-ACADEMY; DOUBLE-BLIND; SURROGATE; DISABILITY; IMPACT;
D O I
10.1177/1352458511418629
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The frequency and impact of neutralizing antibodies (NAbs) to interferon beta-1b (IFN beta-1b) on clinical and radiographic outcomes is controversial. Objective: To assess NAb impact in the BEYOND study. Methods: 2244 patients were randomized (2:2:1) to receive IFN beta-1b, either 250 or 500 mu g, or glatiramer acetate, 20 mg, and observed for 2-3.5 years. NAb titers were determined every 6 months. A titer >= 20 NU/ml was considered NAb positive. Efficacy was compared between NAb-positive and NAb-negative patients, using comprehensive statistical analyses, taking into account the delayed appearance of NAbs, the time-dependent changes in the relapse rate, spontaneous reversions to NAb-negative status, NAb-titer level, and also adjusting for baseline factors. Results: In the IFN beta-1b 250 mu g group, NAb-positive titers were detected (>= once) in 319 patients (37.0%); of these, 112 (35.1%) reverted to NAb-negative status. In the IFN beta-1b 500 mu g group, 340 patients (40.7%) became NAb-positive and 119 (35.0%) reverted to NAb-negative status. In both IFN beta groups, especially the 250 mu g arm, NAb-positive status was not associated with a convincing impact on any clinical outcome measure by any statistical analysis. By contrast, in both IFN beta groups, NAbs were associated with a very consistent deleterious impact on most MRI outcomes. Conclusion: There was a notable dissociation between the impact of NAbs on MRI and clinical outcomes. On MRI measures, the impact was consistent and convincing, whereas on clinical measures a negative impact of NAbs was not found. The basis for this clinico-radiographic paradox is unknown but it suggests that the relationship between NAbs and the therapeutic effects of IFN beta-1b is complex.
引用
收藏
页码:181 / 195
页数:15
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