Adverse reactions to Janus kinase inhibitors: Study of their incidence and predictive factors in patients with rheumatoid arthritis

Cristina Martinez-Molina , Jose Maria Guardiola Tey , Jesus Ruiz-Ramos , Anna Feliu , Mireia Puig-Campmany , Silvia Vidal , Hèctor Corominas
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Abstract

Background and objective

The safety profile of Janus kinase (JAK) inhibitors has acquired attention due to post-marketing observed adverse drug reactions. The study focuses on the analysis of adverse reactions related to tofacitinib, baricitinib, upadacitinib, and filgotinib in rheumatoid arthritis patients, including identifying predictive factors linked to their occurrence.

Patients and methods

Observational retrospective study. Adult patients with rheumatoid arthritis from a university hospital receiving JAK inhibitor treatment between September 2017 and January 2024 were included. The cumulative incidence of each adverse reaction was calculated using the Naranjo scale. Risk factors for developing adverse reactions were identified through logistic regression analyses.

Results

Two hundred twenty-three patients were included, with 28.7% presenting adverse reaction related to JAK inhibitor treatment. The adverse drug reactions with the highest cumulative incidence were infections and gastrointestinal disorders. Infections included: upper respiratory tract (4.5%), cellulitis (3.1%), urinary tract (2.7%), herpes zoster (1.8%). Gastrointestinal disorders comprised: abdominal pain (4.0%), diarrhea (3.6%), nausea and vomiting (3.6%), gastrointestinal perforation (1.3%), diverticulitis (0.9%). Classified at 0.5% were: headache, paresthesias, skin rash, severe neutropenia, insomnia, dyspnea, hypertensive crisis. As risk factors, were identified: the treatment with a non-selective JAK inhibitor (OR adjusted: 4.03; 95% CI: 1.15–14.10; P = 0.029) and older age (OR adjusted: 1.03; 95% CI: 1.00–1.05; P = 0.036).

Conclusions

Infections and gastrointestinal disorders represented the adverse reactions related to JAK inhibitor treatment with the highest cumulative incidence, with risk factors for their occurrence being non-selective JAK inhibitor treatment and older age of the patient.
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Janus 激酶抑制剂的不良反应:类风湿关节炎患者不良反应发生率及预测因素研究
背景和目的由于上市后观察到的药物不良反应,Janus 激酶(JAK)抑制剂的安全性备受关注。本研究的重点是分析类风湿性关节炎患者对法替尼、巴利昔尼、乌达替尼和非格替尼的不良反应,包括确定与不良反应发生相关的预测因素。纳入了一家大学医院在2017年9月至2024年1月期间接受JAK抑制剂治疗的成年类风湿关节炎患者。采用纳兰霍量表计算每种不良反应的累积发生率。通过逻辑回归分析确定了发生不良反应的风险因素。结果共纳入 223 例患者,其中 28.7% 出现与 JAK 抑制剂治疗相关的不良反应。累计发生率最高的药物不良反应是感染和胃肠功能紊乱。感染包括:上呼吸道感染(4.5%)、蜂窝织炎(3.1%)、泌尿道感染(2.7%)、带状疱疹(1.8%)。胃肠道疾病包括:腹痛(4.0%)、腹泻(3.6%)、恶心和呕吐(3.6%)、胃肠道穿孔(1.3%)、憩室炎(0.9%)。占 0.5%的病例包括:头痛、麻痹、皮疹、严重中性粒细胞减少症、失眠、呼吸困难、高血压危象。结论感染和胃肠道疾病是与JAK抑制剂治疗相关的不良反应中累积发生率最高的,其发生的风险因素是非选择性JAK抑制剂治疗和患者年龄较大。
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