For rheumatoid arthritis (RA), the treat-to-target concept  suggests attaining remission or at least low disease activity (LDA) after 12  weeks.
    This German, prospective, multicenter, non-interventional  study aimed to determine the proportion of patients with RA who achieved their  treat-to-target aim after 12 and 24 weeks of etanercept (ETN) treatment in a  real-life setting, as opposed to patients achieving their therapeutic target at  a later timepoint (week 36 or 52).
    A total of 824 adults with a confirmed diagnosis of RA  without prior ETN treatment were included. Remission and LDA were defined as  DAS28 < 2.6 and DAS28 ≤ 3.2, respectively.
    Results: 
    The proportion of patients achieving remission was 24% at  week 12 and 31% at week 24. The proportion of patients achieving LDA was 39% at  week 12 and 45% at week 24. The proportion of patients achieving remission or  LDA further increased beyond week 24 up to week 52. Improvement in pain and  reduction in concomitant glucocorticoid treatment were observed. Improvements  in patient-reported outcomes were also seen in patients who did not reach  remission or LDA. No new safety signals were detected. The people in this study  experienced side effects that were similar to those reported by people who took  etanercept in previous studies. The researchers concluded that a considerable  proportion of people responded to treatment with etanercept after 12 weeks.  This proportion increased when treatment was continued for longer than 12  weeks.
    Thus, the researchers concluded that considerable proportion  of patients with RA attained the target of remission or LDA after 12 weeks of  ETN treatment. Even beyond that timepoint, the proportion of patients achieving  treatment targets continued to increase up to week 52.
    Reference:
    Effectiveness of Etanercept in Rheumatoid Arthritis:  Real-World Data from the German Non-interventional Study ADEQUATE with Focus on  Treat-to-Target and Patient-Reported Outcomes by Eugen Feist et al. published  in the Springer. 
    https://pubmed.ncbi.nlm.nih.gov/35113363/
     
 
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