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FRI0331 Reasons and Risk Factors for Discontinuation of Biologic Agents in Rheumatoid Arthritis Patients
  1. K. Terabe1,
  2. T. Kojima1,
  3. N. Takahashi1,
  4. K. Funahashi1,
  5. A. Kaneko2,
  6. Y. Hirano3,
  7. N. Ishiguro1
  8. on behalf of TBCR Study Group
  1. 1Orthopedics, Nagoya University of Medical School
  2. 2Orthopedics, Nagoya Medical Center, Nagoya
  3. 3Orthopedics, Toyohashi Municipal Hospital, Toyohashi, Japan

Abstract

Background Rheumatoid arthritis (RA) patients who failed a first biologic agent due to any reasons have the option of switching to a second one along with the strategy of biologic agent treatment. Patients go over switching to the next one at failing their biologic agent. On the other hand, there are some patients who discontinue any biologic agent treatment due to various reasons such as tolerability concern, complications, economic issue, remission and so on. The impact of this concern has been less studied.

Objectives The objective of this study was to investigate the reasons and the risk factors for discontinuation any biologic agent in RA patients.

Methods In total patients (n=2179) who underwent biologic agent treatment between 2003 and 2011 at Nagoya University Hospital and 12 other institutes (Tsurumai Biologics Communication Study Group), 1966 patients who were confirmed continuation or discontinuation of biologic agent treatment were enrolled. We analyzed the retention rate of biologic agent treatment and the reasons for discontinuation. To identify the risks for discontinuation, baseline demographics were compared between the continuing group and the disc continuing group using cox hazard regression analysis.

Results In total 1966 patients, 1479 patients were administered biologics continuously, 487 patients were withdrew. Table 1 showed the demographic date in total patients. The retention rate was 72% (n=1563) at least 1 year from starting biologics treatment, 68.7% (n=866) at 3 years, 65.6% (n=360) at 5 years. In 327 patients who were confirmed the reasons of discontinuation, the reasons were adverse events in 191 patients, lack of effectiveness in 66 patients, others in 70 patients. Comparison of incidence for discontinuation using cumulative hazard function, the reason of adverse events was significantly higher than others reasons (Fig. 1). To identify o the risks of discontinuation, we used cox hazard model regression in patients who discontinued treatment due to adverse events and lack of effectiveness, the risk factors were over 70 years of age (OR 1.80 [1.31-2.46]), male (OR 1.79 [1.27-2.52]), over 3 of steinblocker class (OR 1.51 [1.12-2.04]). Non concomitant with methotrexate (OR 1.47 [1.06-2.04]) (Fig. 2).

Conclusions The most common reason for discontinuation was adverse events. In a numerically greater proportion of patients who discontinued any biologic agent treatment, timing of discontinuation was within a first year from starting treatment. In addition, the risk factors for discontinuation were similar with those of adverse events.

Disclosure of Interest None declared

DOI 10.1136/annrheumdis-2014-eular.5503

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