The Impact of EMA Recommendations on the Real-life Use of Janus Kinases Inhibitors for Rheumatoid Arthritis: the Expanded Risk Score in RA As a Tool to Quantify the Risk of Cardiovascular Events
Overview
Authors
Affiliations
Objective: 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).
Methods: 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.
Results: 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).
Conclusions: 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.
Benucci M, Bardelli M, Cazzato M, Bartoli F, Damiani A, Li Gobbi F J Pers Med. 2024; 14(7).
PMID: 39063966 PMC: 11278154. DOI: 10.3390/jpm14070712.
PIM Kinases as Potential Biomarkers and Therapeutic Targets in Inflammatory Arthritides.
Assirelli E, Ciaffi J, Scorcu V, Naldi S, Brusi V, Mancarella L Int J Mol Sci. 2024; 25(6).
PMID: 38542097 PMC: 10969826. DOI: 10.3390/ijms25063123.