Greater Tofacitinib Persistence in Patients With Psoriatic Arthritis, Enthesitis

By Rebecca Araujo - Last Updated: April 17, 2024

According to a retrospective study in The Journal of Rheumatology, patients with psoriatic arthritis (PsA) who have enthesitis are more likely to persist on treatment with the Janus kinase (JAK) inhibitor tofacitinib.

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The study was a longitudinal, observational study of all patients with PsA at a single center who received at least 1 dose of tofacitinib. “Information on the persistence of tofacitinib in PsA is scarce in real-life conditions,” the authors wrote. “Our objective was to analyze persistence and safety of tofacitinib under these conditions.”

The primary end points were adverse events (AEs) and drug survival. Seventy-two patients were included, of whom 54 were women. The mean age was 51.9 ± 11.1 years.

The mean disease duration was 10.40 ± 6.99 years. For more than 70% of patients, tofacitinib was the third or higher line of therapy they received. Median treatment survival was 13 months (interquartile range [IQR], 5.3-29.0). The 1-year retention rate on tofacitinib was 52.7% (95% CI, 42.4-65.6).

Sex, disease duration, comorbidities, or line of treatment were not associated with tofacitinib survival. Younger patients were less likely to discontinue tofacitinib compared with older patients (hazard ratio [HR], 0.96; P<.05). Patients with enthesitis were also less likely to discontinue treatment (HR, 0.37; P<0.05).

Regarding AEs, the overall rate was 52.9 events per 100 person-years (95% CI, 38.5-70.6). Most AEs occurred during the first 6 months of tofacitinib exposure.

In this real-life study, tofacitinib showed a reasonably good retention rate in a PsA population mostly refractory to biologic and oral targeted-synthetic [disease-modifying antirheumatic drugs],” the authors summarized. “Patients with refractory PsA and enthesitis might be a specific target population for this drug. No new alarm signals emerged.”

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