托珠单抗治疗类风湿性关节炎以外全身性疾病患者的严重感染:一项回顾性多中心观察性研究

IF 1.3 Q4 RHEUMATOLOGY
Florent Broca, Odile Souchaud-Debouverie, Evelyne Liuu, Pascal Roblot, Mickaël Martin
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引用次数: 1

摘要

目的:本研究旨在描述tocilizumab治疗除类风湿关节炎以外的全身性疾病患者的严重感染。方法:回顾性收集2012年1月1日至2020年7月1日在法国普瓦图-夏朗德地区接受至少2剂tocilizumab治疗类风湿性关节炎以外全身性疾病的患者的医疗记录。银屑病关节炎和系统性青少年特发性关节炎也被排除在外,因为它们通常采用与类风湿关节炎相似的治疗方式。结果:37例以巨细胞动脉炎为主的患者中,25例(68%)至少发生1次感染事件,6例(3.2/100患者-年)发生15次严重感染,以细菌性感染为主。下呼吸道和皮肤是主要部位。严重的细菌感染与明显的生物炎症综合征相关,即使在托珠单抗给药周期下也是如此。严重带状疱疹2例,严重憩室炎1例。没有观察到结核病或病毒性肝炎的再激活。结论:严重感染发生率为3.2/100患者-年,似乎低于类风湿关节炎的报道。c -反应蛋白剂量可能有助于托珠单抗患者细菌感染性不良事件的诊断。需要进一步进行更大规模的研究来证实这些结果,以评估严重感染的潜在危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Severe Infections in Patients Treated with Tocilizumab for Systemic Diseases Other Than Rheumatoid Arthritis: A Retrospective Multicenter Observational Study.

Severe Infections in Patients Treated with Tocilizumab for Systemic Diseases Other Than Rheumatoid Arthritis: A Retrospective Multicenter Observational Study.

Severe Infections in Patients Treated with Tocilizumab for Systemic Diseases Other Than Rheumatoid Arthritis: A Retrospective Multicenter Observational Study.

Objective: This study aimed to describe severe infections in patients treated with tocilizumab for systemic diseases other than rheumatoid arthritis.

Methods: Data from patients receiving at least 2 doses of tocilizumab for systemic diseases other than rheumatoid arthritis between January 1, 2012, and July 1, 2020, in the region Poitou-Charentes (France) were retrospectively collected from medical records. Psoriatic arthritis and systemic juvenile idiopathic arthritis were also excluded as usually treated with similar modalities to rheumatoid arthritis.

Results: Of 37 patients, mainly suffering from giant cell arteritis, 25 patients (68%) had at least 1 infectious event and 15 severe infections occurred in 6 patients (3.2/100 patient-years), mainly bacterial. Lower respiratory tract and skin were the main sites. Severe bacterial infections were associated with a marked biological inflammatory syndrome, even under a cycle of administration of tocilizumab. Two severe zonas and 1 severe diverticulitis occurred. No tuberculosis or viral hepatitis reactivation was observed.

Conclusion: The incidence rate of severe infections was 3.2/100 patient-years and seems lower than that reported in rheumatoid arthritis. C-reactive protein dosage could be helpful for the diagnosis of bacterial infectious adverse events in patients on tocilizumab. Further larger studies are needed to confirm these results to assess potential risk factors for severe infections.

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