Department of Rheumatology and Medical Sciences, ASST Gaetano Pini-CTO, Milan, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy.
Front Immunol. 2023 Aug 31;14:1225160. doi: 10.3389/fimmu.2023.1225160. eCollection 2023.
To evaluate in patients with rheumatoid arthritis (RA) the impact of EMA recommendations on the real-life prescription of JAK inhibitors (JAKis) and the use of the Expanded Risk Score in RA (ERS-RA) to quantify the risk of major adverse cardiac events (MACE).
We conducted a retrospective analysis of real-life RA patients treated with JAKis. Patients were classified as ineligible for JAKis if they fulfilled EMA criteria (>65 years-old, history of malignancy, or increased risk of venous thromboembolic events [VTE] or MACE including smoking). Risk of MACE was defined according to ORAL Surveillance trial inclusion criteria (ORALSURV) or by using the ERS-RA.
Of 194 patients enrolled, 57.9% were classified as ineligible according to EMA definition (ORALSURV criteria). The most frequent reason for ineligibility was increased MACE risk (70.2%), followed by age>65 (34.2%), smoking (30.7%), and increased risk of VTE (20.2%) or malignancy (7%). The use of the ERS-RA reduced the rate of patients carrying an increased CV risk to 18.6% (p<0.001 versus ORALSURV), leading to 46.4% overall ineligible patients. Over a drug-exposure of 337 patient/years, we observed 2 VTE, one MACE (non-fatal stroke), and one solid malignancy (all in the group of patients classified as ineligible according to both the definitions).
Rigorous application of EMA indications in clinical practice could result in the exclusion of a large proportion of RA patients from treatment with JAKis. A proper quantification of the risk for MACE by dedicated tools as ERS-RA is advocated to better tailor the management of RA.
评估 EMA 建议对类风湿关节炎(RA)患者真实世界中 JAK 抑制剂(JAKi)处方的影响,以及使用 RA 扩展风险评分(ERS-RA)来量化主要不良心脏事件(MACE)风险。
我们对接受 JAKi 治疗的真实世界 RA 患者进行了回顾性分析。如果患者符合 EMA 标准(>65 岁、恶性肿瘤史或静脉血栓栓塞事件[VTE]或 MACE 风险增加,包括吸烟),则认为不适合使用 JAKi。MACE 风险根据 ORAL Surveillance 试验纳入标准(ORALSURV)或使用 ERS-RA 定义。
在纳入的 194 名患者中,57.9%根据 EMA 定义被归类为不适合(ORALSURV 标准)。不适合的最常见原因是 MACE 风险增加(70.2%),其次是年龄>65 岁(34.2%)、吸烟(30.7%)、VTE 风险增加(20.2%)或恶性肿瘤(7%)。使用 ERS-RA 将携带 CV 风险增加的患者比例降低至 18.6%(p<0.001 与 ORALSURV 相比),导致总体不适合的患者为 46.4%。在 337 名患者/年的药物暴露期间,我们观察到 2 例 VTE、1 例 MACE(非致命性中风)和 1 例实体恶性肿瘤(均在根据两种定义均归类为不适合的患者组中)。
在临床实践中严格应用 EMA 适应证可能会导致很大一部分 RA 患者被排除在 JAKi 治疗之外。建议使用专用工具(如 ERS-RA)对 MACE 风险进行适当量化,以更好地调整 RA 的管理。