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抗MDA5抗体阳性皮肌炎三联和四联疗法中的严重感染风险

Severe infection risk in triple and quadruple therapy for anti-MDA5 antibody-positive dermatomyositis.

作者信息

Ueda Yoshitaka, Chinen Naofumi, Shimada Kota, Yokogawa Naoto

机构信息

Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.

Department of Rheumatic Diseases, Tama-Nambu Chiiki Hospital, Tokyo, Japan.

出版信息

Clin Rheumatol. 2025 Apr 17. doi: 10.1007/s10067-025-07445-5.

Abstract

INTRODUCTION

Anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive dermatomyositis (MDA5-DM) can be refractory to treatment, and a triple combination therapy (TCT) consisting of a glucocorticoid, cyclophosphamide, and a calcineurin inhibitor is widely used in induction therapy. For progressive or severe disease despite TCT, another immunosuppressive agent, such as a Janus kinase (JAK) inhibitor, may be added to the induction regimen.

METHOD

A retrospective cohort study across two centers in Japan was undertaken between January 2016 and December 2024 evaluating patients with MDA5-DM receiving TCT or quadruple combination therapy (QCT) determining the presence of severe infection. The latter therapy consisted of the addition of a JAK inhibitor to the TCT. A severe infection was defined as Grade 3 or higher according to the Common Terminology Criteria for Adverse Events (CTCAE), version 5.0.

RESULTS

There were 24 patients were included; TCT: n = 19 and QCT: n = 5. In the former, three (3/19, 16%), two (2/19, 11%), and three (3/19, 16%) patients had a severe bacterial infection, invasive fungal infection, and a CMV infection, respectively. In the QCT group, two (2/5, 40%), two (2/5, 40%), and four (4/5: 80%) patients had a severe bacterial infection, invasive fungal infection, and a CMV infection, respectively. CMV infections were significantly more frequent in the QCT group (p = 0.014). Both TCT and QCT groups had five patients each with a severe infection (5/19, 26% and 5/5, 100%, respectively) (p = 0.006).

CONCLUSION

While both TCT and QCT have infection, the QCT group may be at a higher risk, hence highlighting the need for vigilance and adequate prophylaxis.

摘要

引言

抗黑色素瘤分化相关基因5(MDA5)抗体阳性皮肌炎(MDA5-DM)的治疗可能效果不佳,由糖皮质激素、环磷酰胺和钙调神经磷酸酶抑制剂组成的三联联合疗法(TCT)被广泛用于诱导治疗。对于尽管接受了TCT但仍进展或严重的疾病,可在诱导方案中添加另一种免疫抑制剂,如Janus激酶(JAK)抑制剂。

方法

2016年1月至2024年12月期间,在日本的两个中心进行了一项回顾性队列研究,评估接受TCT或四联联合疗法(QCT)的MDA5-DM患者,确定是否存在严重感染。后者的治疗方法是在TCT基础上加用JAK抑制剂。根据不良事件通用术语标准(CTCAE)第5.0版,严重感染定义为3级或更高等级。

结果

共纳入24例患者;TCT组:n = 19例;QCT组:n = 5例。在TCT组中,分别有3例(3/​19,16%)、2例(2/​19,11%)和3例(3/​19,16%)患者发生严重细菌感染、侵袭性真菌感染和巨细胞病毒(CMV)感染。在QCT组中,分别有2例(2/​5,40%)、2例(2/​5,40%)和4例(4/​5,80%)患者发生严重细菌感染、侵袭性真菌感染和CMV感染。QCT组中CMV感染明显更频繁(p = 0.014)。TCT组和QCT组各有5例患者发生严重感染(分别为5/​19,26%和5/​5,100%)(p = 0.006)。

结论

虽然TCT和QCT都有感染风险,但QCT组的风险可能更高,因此强调需要保持警惕并进行充分的预防。

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