Efficacy and Baseline Predictors of Tofacitinib Response in Patients with Rheumatoid Arthritis at a Private Tertiary Care Hospital in Pakistan
DOI:
https://doi.org/10.51253/pafmj.v76iSUPPL-1.13219Keywords:
Tofacitinib, Efficacy, BMI, Serology, Inflammatory, Rheumatoid ArthritisAbstract
Objective: To analyze the efficacy of Tofacitinib and predictors of response in Rheumatoid Arthritis patients
Study Design: Prospective longitudinal study
Place and Duration of Study: Rheumatology Department, Fauji Foundation Hospital, Rawalpindi, Pakistan, from Mar to Sep 2024.
Methodology: The study included 76 adult RA patients (75 females and 1 male), who were advised to take Tofacitinib. We recorded the DAS-28 ESR at baseline and after 3 months and noted patient demographics, BMI, serology, and concomitant DMARD use. The primary outcome was remission/low disease activity (DAS-28≤3.2) at 3 months. DAS-28 levels were compared by Wilcoxon test. Treatment outcome was categorized as a good response and poor response. Predictors of treatment response were analyzed using univariate logistic regression analysis.
Results: The median age of patients was 50.50(IQR 57.00 - 45.25) years. Median RA duration was 9.00(IQR 15.00 – 6.00) years with 60(78.95%) patients being seropositive. Conventional DMARD was continued in combination with Tofacitinib in 55(72.4%) patients. Only 11(14.5%) patients achieved the treatment target. Tofacitinib therapy significantly reduced DAS-28 from baseline of 5.64 (IQR 5.99 - 5.08), to 3.99±0.76 at 3 months (p-value <0.001). Lower baseline DAS-28 predicted an effective treatment response (OR 4.13, 95%CI 1.07-16.03, p-value 0.03). Tofacitinib monotherapy predicted a good response in comparison to Tofacitinib combination with conventional DMARDs (OR 4.00, 95% CI1.06-14.96, p-value 0.03). Baseline BMI, inflammatory markers, and serology did not have an impact on treatment response.
Conclusion: Tofacitinib therapy significantly reduced DAS-28 ESR at 3 months with baseline predictive factors such as BMI and ....
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