» Articles » PMID: 37720218

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
Journal Front Immunol
Date 2023 Sep 18
PMID 37720218
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Efficacy and Safety of Filgotinib in Rheumatoid Arthritis Patients Aged over and under 65 Years (ENANTIA-65).

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.

References
1.
Visseren F, Mach F, Smulders Y, Carballo D, Koskinas K, Back M . 2021 ESC Guidelines on cardiovascular disease prevention in clinical practice. Eur Heart J. 2021; 42(34):3227-3337. DOI: 10.1093/eurheartj/ehab484. View

2.
Ytterberg S, Bhatt D, Mikuls T, Koch G, Fleischmann R, Rivas J . Cardiovascular and Cancer Risk with Tofacitinib in Rheumatoid Arthritis. N Engl J Med. 2022; 386(4):316-326. DOI: 10.1056/NEJMoa2109927. View

3.
Au K, Reed G, Curtis J, Kremer J, Greenberg J, Strand V . High disease activity is associated with an increased risk of infection in patients with rheumatoid arthritis. Ann Rheum Dis. 2011; 70(5):785-91. DOI: 10.1136/ard.2010.128637. View

4.
Baecklund E, Iliadou A, Askling J, Ekbom A, Backlin C, Granath F . Association of chronic inflammation, not its treatment, with increased lymphoma risk in rheumatoid arthritis. Arthritis Rheum. 2006; 54(3):692-701. DOI: 10.1002/art.21675. View

5.
Tanaka Y, Luo Y, OShea J, Nakayamada S . Janus kinase-targeting therapies in rheumatology: a mechanisms-based approach. Nat Rev Rheumatol. 2022; 18(3):133-145. PMC: 8730299. DOI: 10.1038/s41584-021-00726-8. View