Session Information
Session Type: Abstract Submissions (ACR)
Background/Purpose: The results from RCTs may not be generalizable to clinical practice because of their inclusion and exclusion criteria. Instead, observational cohorts and registries might provide complement information for each treatment strategies in the real world. This study aimed to compare the clinical effectiveness of treatment strategies for active RA patients refractory to non-biologic DMARDs using independent biologic registry and disease specific cohort for Korean RA patients.
Methods: One year follow-up data on drug uses and clinical outcomes were compared between Korean biologics registry (BIOlogics Pharmacoepidemiologic StudY, BIOPSY) and established RA cohort (KORONA). Since all the BIOPSY patients had moderate to high disease activity (DAS28>3.2) and have started TNF inhibitors, we selected patients from KORONA with inclusion criteria at baseline: 1) DAS 28>3.2, 2) changing DMARDs within 3 months, and 3) non-biologic DMARD user. A total of 528 subjects (208 from BIOPSY and 320 from KORONA) were included in this study. Propensity score matching was used to equalize patient characteristics between TNF inhibitor user and non-biologic DMARD user groups. The one year remission rates with DAS 28 and HAQ scores were compared between two treatment strategies for active RA patients: starting TNF inhibitors vs. changing non-biologic DMARDs.
Results: Of the 208 TNF inhibitor users and 320 non-biologic DMARDs users identified from each registry and cohort, 184 patients (92 in BIOPSY and 92 in KORONA) were included in this analysis after the propensity score matching. Their baseline characteristics were comparable with age (46.5 vs. 46.6, P=0.97), female (89.1% vs. 91.3%, p=0.81), RF positivity (83.7% vs. 84.8%, p=1.0), disease duration (6.0 years vs. 5.2 years, p=0.39), DAS 28 (5.58 vs. 5.60, p=0.63) and HAQ scores (1.20 vs. 1.20, P=0.97). Remission rates after 1 year follow up with sustaining baseline treatment were 16.3% in TNF inhibitor users and 13.0% in non-biologic DMARDs users (P=0.68). For the patients with continuing initial treatment for 1 year, TNF inhibitor users had lower HAQ score than non-biologic DMARDs users (0.59 vs. 0.77, P<0.01).
Conclusion: We compared clinical effectiveness of TNF inhibitors and non-biologic DMARDs in active RA patients using independent biologics registry and RA cohort. Although the use of TNF inhibitors did not increase the one year remission rate compared to the use of non-biologic DMARDs, it decreased the one year functional disability in active RA patients.
Disclosure:
Y. K. Sung,
None;
S. K. Cho,
None;
C. B. Choi,
None;
S. Won,
None;
S. Y. Bang,
None;
H. S. Cha,
None;
J. Y. Choe,
None;
W. T. Chung,
None;
S. J. Hong,
None;
J. B. Jun,
None;
H. A. Kim,
None;
J. Kim,
None;
S. K. Kim,
None;
T. H. Kim,
None;
H. S. Lee,
None;
J. Lee,
None;
J. Lee,
None;
S. S. Lee,
None;
S. W. Lee,
None;
Y. A. Lee,
None;
S. S. Nah,
None;
C. H. Suh,
None;
D. H. Yoo,
None;
B. Y. Yoon,
None;
S. C. Bae,
None.
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ACR Meeting Abstracts - https://acrabstracts.org/abstract/a-comparison-of-the-clinical-effectiveness-of-treatment-strategies-for-active-ra-patients-using-a-prospective-biologic-registry-biopsy-and-an-ra-specific-cohort-korona/