Summary
Background
In rheumatoid arthritis and psoriasis female sex has been shown to be associated with discontinuation of anti‐tumour necrosis factor‐α (TNF‐α) therapy.
Aim
To retrospectively assess the association between sex and TNF‐α drug persistence in patients with inflammatory bowel disease (IBD).
Methods
All IBD patients on anti‐TNF‐α therapy with a minimum follow‐up of 12 months in a single tertiary centre were identified. Patient and treatment characteristics and reasons for anti‐TNF‐α discontinuation were recorded. Overall and cause‐specific drug persistence was analysed with Kaplan‐Meier followed by Cox proportional hazards regression models.
Results
We included 529 patients (49.9% male) with 631 treatment episodes (2280 anti‐TNF‐α treatment years) and 289 discontinuations of therapy. Female sex (adjusted hazard ratio [aHR] 1.42, 95% confidence interval [CI] 1.16‐1.74), greater age at start of therapy per decade (aHR 1.15, 95% CI 1.04‐1.27] and dose escalation (aHR 3.74, 95% CI 2.78‐5.02) were associated with TNF‐α inhibitor discontinuation. Total cohort cause‐specific analysis identified female sex to be associated with side effects (aHR 4.05, 95% CI 2.36‐6.98) but not to other discontinuation reasons. Adalimumab (aHR 1.70, 95% CI 1.11‐2.60) and golimumab (aHR 4.97, 95% CI 2.30‐10.74) use and dose‐escalation (aHR 7.71, 95% CI 5.28‐11.26) were associated with secondary loss of response.
Conclusion
Drug persistence of anti‐TNF‐α therapy is lower in females as compared to males, mainly because of higher rates of side effects in females. Understanding the sex specific differences in effectiveness and safety of anti‐TNF‐α compounds can aid physicians in clinical decision‐making.