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Poor prognostic factors independently impact remission and treatment escalation in rheumatoid arthritis regardless of disease activity: A nationwide prospective cohort study - 23/01/25

Doi : 10.1016/j.jbspin.2024.105798 
You-Jung Ha a, b, Seunghwan Shin c, Se Rim Choi a, b, Eun Ha Kang a, b, Yeong Wook Song d, Yun Jong Lee a, b, e,
a Division of Rheumatology, Department of Internal Medicine, Seoul National University Bundang Hospital, 82, Gumi-ro 173beon-gil, Bundang-gu, Seongnam, Gyeonggi, 13620, Republic of Korea 
b Department of Internal Medicine, Seoul National University College of Medicine, 103, Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea 
c Lunit Inc., 374, Gangnam-daero, Gangnam-gu, Seoul, 06241, Republic of Korea 
d Institute of Human-Environment Interface Biology, Medical Research Center, Seoul National University, 103, Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea 
e Department of Medical Device Development, Seoul National University College of Medicine, 103, Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea 

Corresponding author. Department of Internal Medicine, Seoul National University Bundang Hospital, 82 Gumi-ro, 173 Beongil, Bundang-gu, Seongnam-si, Gyeonggi-do 13620, South Korea.Department of Internal Medicine, Seoul National University Bundang Hospital82 Gumi-ro, 173 Beongil, Bundang-guSeongnam-siGyeonggi-do13620South Korea

Graphical abstract




Il testo completo di questo articolo è disponibile in PDF.

Highlights

Patients with rheumatoid arthritis (RA) and more ACR-defined poor prognostic factors (PPFs) had higher disease activity and poorer patients’ reported outcomes.
RA patients with3 PPFs were less likely to achieve remission during the 5-year follow-up period, regardless of disease activity.
RA patients with a higher number of PPFs were significantly associated with a greater likelihood of initiating biologic or targeted synthetic disease-modifying anti-rheumatic drugs.
Considering that the ACR-defined PPFs affect both patients’ long-term outcomes and clinician's decisions, the number of PPF should be integrated into the ‘treat-to-target strategy’ for RA.

Il testo completo di questo articolo è disponibile in PDF.

Abstract

Objective

To elucidate the impact of poor prognostic factors (PPFs) in daily practice on achieving remission and the requirement for biologic or targeted synthetic DMARDs (b/tsDMARDs) in a large Korean cohort of patients with rheumatoid arthritis (RA).

Methods

Using the KORean Observational study Network for Arthritis (KORONA) database, patients with RA were categorized into three groups based on the number of PPFs (0–1, 2, or3): the presence of functional limitation, extra-articular disease, seropositivity, and bone erosions. Factors related to achieving remission and to initiating b/tsDMARDs were evaluated using Cox proportional hazard regression analyses after adjusting confounders.

Results

Among 5076 patients with RA, group L (PPF1), group M (PPFs 2), and group H (PPFs3) were 1788 (35.2%), 2027 (39.9%), and 1261 (24.9%), respectively. Group H had higher disease activity and worse patient-reported outcomes than groups L and M. Among moderately-to-highly active patients at baseline, group H was significantly less likely to attain point (hazard ratio [HR]=0.55, 95% confidence interval [CI] 0.38–0.79) and sustained (HR=0.45, 95% CI 0.21–0.99) Boolean-based remission in 5-year. Groups M (HR=1.47, 95% CI 1.10–1.96) and H (HR=1.69, 95% CI 1.22–2.32) had an increased risk of escalation to b/tsDMARDs, compared to group L among b/tsDMARDs-naïve patients at baseline.

Conclusion

Achieving remission was particularly challenging for group H, and more patients in groups M and H initiated b/tsDMARDS during the 5-year observation period. Therefore, the presence of PPFs3 significantly influences both patients’ outcomes and clinician's treatment decisions regardless of disease activity.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Rheumatoid arthritis, Poor prognostic factors, Outcome measures, Targeted therapy


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© 2024  Sociýtý Franýaise de Rhumatologie. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 92 - N° 1

Articolo 105798- gennaio 2025 Ritorno al numero
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