AI Article Synopsis

  • The study aimed to compare the retention rates of tumor necrosis factor inhibitors (TNFi) and tofacitinib (TOFA) for rheumatoid arthritis patients using combined data from two Canadian registries, addressing previous findings that were limited by small sample sizes.
  • A total of 1,318 patients starting either TNFi (825) or TOFA (493) were analyzed, revealing similar overall discontinuation rates between the two groups; however, TNFi users were significantly less likely to discontinue treatment due to adverse events.
  • The findings suggest that while discontinuation for any reason was comparable between TNFi and TOFA, TNFi had a better profile for patients regarding treatment-related side effects.

Article Abstract

Objectives: The similarity in retention of tumour necrosis factor inhibitors (TNFi) and tofacitinib (TOFA) was previously reported separately by the Ontario Best Practices Research Initiative and the Quebec cohort Rhumadata. However, because of small sample sizes in each registry, we aimed to confirm the findings by repeating the analysis of discontinuation of TNFi compared with TOFA, using pooled data from both these registries.

Design: Retrospective cohort study.

Setting: Pooled data from two rheumatoid arthritis (RA) registries in Canada.

Participants: Patients with RA starting TOFA or TNFi between June 2014 and December 2019 were included. A total of 1318 patients were included TNFi (n=825) or TOFA (n=493).

Outcome Measures: Time to discontinuation was assessed using Kaplan-Meier survival and Cox proportional hazards regression analysis. Propensity score (PS) stratification (deciles) and PS weighting were used to estimate treatment effects.

Results: The mean disease duration in the TNFi group was shorter (8.9 years vs 13 years, p<0.001). Prior biological use (33.9% vs 66.9%, p<0.001) and clinical disease activity index (20.0 vs 22.1, p=0.02) were lower in the TNFi group.Discontinuation was reported in 309 (37.5%) and 181 (36.7%) TNFi and TOFA patients, respectively. After covariate adjustment using PS, there was no statistically significant difference between the two groups in discontinuation due to any reason HR=0.96 (95% CI 0.78 to 1.19, p=0.74)) as well as discontinuation due to ineffectiveness only HR=1.08 (95% CI 0.81 to 1.43, p=0.61)).TNFi users were less likely to discontinue due to adverse events (AEs) (adjusted HRs: 0.46, 95% CI 0.29 to 0.74; p=0.001). Results remained consistent for firstline users.

Conclusions: In this pooled real-world data study, the discontinuation rates overall were similar. However, discontinuation due to AEs was higher in TOFA compared with TNFi users.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990670PMC
http://dx.doi.org/10.1136/bmjopen-2022-063198DOI Listing

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