Department of Rheumatology, Clinical Research Center for Rheumatic Diseases, National Hospital Organization Kumamoto Saishun Medical Center, 2659 Suya, Kohshi, Kumamoto 861-1196, Japan.
Divsion of Cardiology, Japanese Red Cross Kumamoto Hospital, Kumamoto, Japan.
Clin Rheumatol. 2021 Nov;40(11):4457-4471. doi: 10.1007/s10067-021-05911-4. Epub 2021 Sep 23.
Janus kinase (JAK) inhibitors have been developed as disease-modifying antirheumatic drugs. Despite the positive therapeutic impacts of JAK inhibitors, concerns have been raised regarding the risk of venous thromboembolism (VTE), such as deep vein thrombosis (DVT) and pulmonary embolism (PE). A recent post hoc safety analysis of placebo-controlled trials of JAK inhibitors in rheumatoid arthritis (RA) reported an imbalance in the incidence of VTE for a 4-mg daily dose of baricitinib versus placebo. In a recent postmarketing surveillance trial for RA, a significantly higher incidence of PE was reported in treatment with tofacitinib (10 mg twice daily) compared with tofacitinib 5 mg or tumor necrosis factor inhibitors. We also experienced a case of massive PE occurring 3 months after starting baricitinib (4 mg once daily) for multiple biologic-resistant RA. Nevertheless, the evidence to support the role of JAK inhibitors in VTE risk remains insufficient. There are a number of predisposing conditions and risk factors for VTE. In addition to the known risk factors that can provoke VTE, advanced age, obesity, diabetes mellitus, hypertension, hyperlipidemia, and smoking can also contribute to its development. Greater VTE risk is noted in patients with chronic inflammatory conditions, particularly RA patients with uncontrolled disease activity and any comorbidity. Prior to the initiation of JAK inhibitors, clinicians should consider both the number and strength of VTE risk factors for each patient. In addition, clinicians should advise patients to seek prompt medical help if they develop clinical signs and symptoms that suggest VTE/PE. Key Points • Patients with rheumatoid arthritis (RA) are at increased risk of venous thromboembolism (VTE), especially those with uncontrolled, high disease activity and those with comorbidities. • In addition to the well-known risk factors that provoke VTE events, advanced age and cardiovascular risk factors, such as obesity, diabetes mellitus, hypertension, hyperlipidemia, and smoking, should be considered risk factors for VTE. • Although a signal of VTE/pulmonary embolism (PE) risk with JAK inhibitors has been noted in RA patients who are already at high risk, the evidence is currently insufficient to support the increased risk of VTE during RA treatment with JAK inhibitors. • If there are no suitable alternatives, clinicians should prescribe JAK inhibitors with caution, considering both the strength of individual risk factors and the cumulative weight of all risk factors for each patient.
Janus 激酶 (JAK) 抑制剂已被开发为治疗风湿性疾病的药物。尽管 JAK 抑制剂具有积极的治疗作用,但人们对静脉血栓栓塞症 (VTE) 的风险表示担忧,如深静脉血栓形成 (DVT) 和肺栓塞 (PE)。最近一项针对 JAK 抑制剂治疗类风湿关节炎 (RA) 的安慰剂对照试验的事后安全性分析报告称,与安慰剂相比,巴瑞替尼每日 4 毫克剂量组 VTE 的发生率存在不平衡。在最近一项针对 RA 的上市后监测试验中,与托法替尼 5 毫克或肿瘤坏死因子抑制剂相比,托法替尼 (10 毫克,每日两次) 治疗组报告的 PE 发生率显著更高。我们还遇到了一例多发性生物耐药性 RA 患者开始接受巴瑞替尼 (4 毫克,每日一次) 治疗 3 个月后发生巨大 PE 的病例。然而,支持 JAK 抑制剂在 VTE 风险中作用的证据仍然不足。VTE 存在多种易患条件和危险因素。除了已知可引发 VTE 的危险因素外,高龄、肥胖、糖尿病、高血压、高血脂和吸烟也可导致 VTE 的发生。患有慢性炎症性疾病的患者,尤其是疾病活动度未得到控制且存在任何合并症的 RA 患者,VTE 风险更高。在开始使用 JAK 抑制剂之前,临床医生应考虑每位患者 VTE 危险因素的数量和强度。此外,临床医生应告知患者,如果出现提示 VTE/PE 的临床症状和体征,应立即寻求医疗帮助。关键点 • 类风湿关节炎 (RA) 患者发生静脉血栓栓塞症 (VTE) 的风险增加,尤其是疾病活动度未得到控制且存在合并症的患者。 • 除了引发 VTE 事件的已知危险因素外,高龄和心血管危险因素,如肥胖、糖尿病、高血压、高血脂和吸烟,也应被视为 VTE 的危险因素。 • 尽管在已经处于高风险的 RA 患者中注意到 JAK 抑制剂与 VTE/PE 风险相关的信号,但目前的证据不足以支持在 RA 治疗中使用 JAK 抑制剂会增加 VTE 的风险。 • 如果没有合适的替代药物,临床医生应谨慎使用 JAK 抑制剂,既要考虑每个个体危险因素的强度,也要考虑每位患者所有危险因素的累积权重。