The use of the tyrosine kinase inhibitor Nilotinib in Spondyloarthritis: does targeting inflammatory pathways with a treatment lead to vascular toxicity?
Loukman OmarjeeVincent JaquinandiGuillaume MahePublished in: Journal of translational medicine (2017)
Spondylarthritis (SpA) is an inflammatory rheumatic disease associated with increased incidence of major adverse cardiovascular events (MACEs). Recently, Paramarta et al. proposed the use of the tyrosine kinase inhibitor Nilotinib in Spondyloarthritis to target certain inflammatory pathways. However, Nilotinib, which is highly effective for the treatment of patients with chronic myeloid leukaemia (CML), is also associated with an increased risk of MACEs. The authors suggest that Nilotinib may be effective in peripheral SpA by modulating inflammation, but not in axial SpA. Considering the vascular toxicity of Nilotinib and the acceleration of atherosclerosis in SpA patients, we suggest taking MACEs as an end-point in future trials.
Keyphrases
- chronic myeloid leukemia
- oxidative stress
- cardiovascular events
- cardiovascular disease
- end stage renal disease
- coronary artery disease
- ankylosing spondylitis
- disease activity
- rheumatoid arthritis
- newly diagnosed
- ejection fraction
- acute myeloid leukemia
- peritoneal dialysis
- emergency department
- cancer therapy
- systemic lupus erythematosus
- patient reported outcomes