Long‐term safety profile of belimumab plus standard therapy in patients with systemic lupus erythematosus

贝里穆马布 医学 不利影响 安慰剂 入射(几何) 内科学 红斑狼疮 恶心 医学名词 外科 免疫学 B细胞激活因子 抗体 物理 替代医学 B细胞 病理 药物警戒 光学
作者
Joan T. Merrill,Ellen M. Ginzler,Daniel J. Wallace,James D. McKay,Jeffrey Lisse,Cynthia Aranow,Frank R. Wellborne,Michael Burnette,John J. Condemi,Z. John Zhong,Lilia Pineda,Jerry L. Klein,William W. Freimuth
出处
期刊:Arthritis & Rheumatism [Wiley]
卷期号:64 (10): 3364-3373 被引量:114
标识
DOI:10.1002/art.34564
摘要

Abstract Objective To evaluate the safety profile of long‐term belimumab therapy combined with standard therapy for systemic lupus erythematosus (SLE) in patients with active disease. Methods Patients who were randomized to receive intravenous placebo or belimumab 1, 4, or 10 mg/kg, plus standard therapy, and completed the initial 52‐week double‐blind treatment period were then allowed to enter a 24‐week open‐label extension phase. During the extension period, patients in the belimumab group either received the same dose or were switched to 10 mg/kg and patients in the placebo group were switched to belimumab 10 mg/kg. Patients who achieved a satisfactory response during the 24‐week extension period were allowed to participate in the long‐term continuation study of monthly belimumab 10 mg/kg. Adverse events (AEs) and abnormal laboratory results were analyzed per 100 patient‐years in 1‐year intervals. Results Of the 364 patients who completed the 52‐week double‐blind treatment period, 345 entered the 24‐week extension, and 296 continued treatment with belimumab in the long‐term continuation study. Safety data through 4 years of belimumab exposure (1,165 cumulative patient‐years) are reported. Incidence rates of AEs, severe/serious AEs, infusion reactions, infections, malignancies, grades 3/4 laboratory abnormalities, and discontinuations due to AEs were stable or declined during 4‐year belimumab exposure. The most common AEs included arthralgia, upper respiratory tract infection, headache, fatigue, and nausea. Serious infusion reactions were rare: only 1 occurred during the 4‐year followup period. Rates of serious infection decreased from 5.9/100 patient‐years to 3.4/100 patient‐years, and no specific type of infection predominated. Conclusion Belimumab added to standard therapy was generally well‐tolerated over the 4‐year treatment period in patients with SLE, which suggests that belimumab can be administered long term with an acceptable safety profile.

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