Introduction
Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease associated with progressive joint damage and disability. The prevalence of RA is 0.24 % globally and between 0.3 and 1 % in developed countries [
1,
2]. In Mainland China, the prevalence of RA has been reported to be 0.28 % [
3,
4]. As shown by recent studies, RA is becoming one of the most common disabling and costly disease in China [
5‐
7]. Chou et al. reported a significantly higher RA prevalence in urban areas than in rural areas of Taiwan [
8]. Socioeconomic and genetic factors might contribute to the lower prevalence in China compared with Western countries [
9].
Disease-modifying antirheumatic drugs (DMARDs) are the standard treatment for patients with RA [
10]. In addition to conventional synthetic DMARDs (csDMARDs), such as methotrexate, biological DMARDs (bDMARDs), including inhibitors targeting tumor necrosis factor (TNF)-α, T cells, B cells, and interleukin-6, have been increasingly used in recent years [
10,
11]. According to the 2013 European League Against Rheumatism (EULAR) and the 2012 American College of Rheumatology (ACR) recommendations, csDMARDs such as methotrexate should be chosen as the first-line treatment [
10,
11]. However, the recommendations suggest bDMARDs for patients who fail to achieve low disease activity (LDA) or remission after receiving csDMARDs [
10,
11]. Although a combination therapy of csDMARDs and bDMARDs is recommended and commonly practiced, real-life registry data show that approximately 30 % of patients receive bDMARDs as monotherapy in Western countries [
12]. In a double-blind randomized trial, Dougados et al. found that the efficacy of tocilizumab monotherapy was comparable to a combined therapy of tocilizumab plus methotrexate in patients who had insufficient responses to methotrexate [
13]. Emery et al. systematically reviewed trials evaluating bDMARD monotherapy and found that only tocilizumab monotherapy appeared to show efficacy equivalent to combination therapy with methotrexate [
12]. In a recent large observational study, Gabay et al. found that patients receiving tocilizumab with or without concomitant csDMARD showed comparable clinical response [
14].
Until the end of patient enrollment of this study, a total of six bDMARDs have been approved for use in RA in China, including the interleukin-6 receptor inhibitor, tocilizumab, and five TNF inhibitors (infliximab, adalimumab, and etanercept, including Enbrel® and local brand Yi Sai Pu® and Qiangke®). In recent years, bDMARDs have been increasingly prescribed in routine clinical practice in China. However, the “real-world” data on bDMARD usage patterns in China might be different from those in developed countries owing to socioeconomic factors. The objective of this cross-sectional study was to characterize the usage patterns of bDMARDs in Chinese patients with RA and examine the association between disease activity and clinical remission, and the duration and pattern of bDMARD therapy, with the goal to optimize the management of RA in China.
Discussion
This is the first large-scale multicenter study to characterize real-life bDMARD usage patterns and disease activity in routine practice in Chinese patients with RA receiving bDMARDs. The results show that combination therapy of bDMARDs and csDMARDs was substantially more common than bDMARD monotherapy in real-world clinical practice in China. Methotrexate was the predominant csDMARD administered to Chinese patients. The usage pattern of bDMARDs in China is in accordance with the guidelines for management of RA, in which methotrexate is recommended as the first-line agent and bDMARDs are used as secondary agents, mostly in combination with csDMARDs [
10].
This study found that the proportion of patients receiving bDMARD monotherapy in China was only 10.5 %, considerably lower than that in other countries. Yazici et al. investigated the RA patient cohort in the Thomson Healthcare MarketScan Research databases and found that 30 % of adults with RA received bDMARD monotherapy in the USA [
19]. Gabay et al. examined the data from the Swiss Clinical Quality Management in Rheumatic Diseases registry for RA patients and found that bDMARD monotherapy was prescribed for up to 39 % of treatment courses [
21]. Kaufmann et al. conducted a retrospective study of 254 German patients and found that between 18 % and 41 % of patients treated with bDMARDs received the agent as monotherapy [
22].
Overall, disease control in our patient cohort was not optimal despite the use of bDMARDs. The majority (75 %) of patients were classified as having moderate- or high-disease activity per DAS28 scores. The substantially shorter mean treatment duration of bDMARD therapy (4.7–34.5 weeks) in our study population versus that shown in other studies [
23,
24] may be responsible for the suboptimal remission rates that we observed. The mean duration of treatment with etanercept, adalimumab, and infliximab in Italian patients with RA from the Italian Group for the Study of Early Arthritis registry was 3.1, 2.6, and 2.7 years, respectively [
23]. Patients with RA from the Swiss Clinical Quality Management in Rheumatic Diseases registry received anti-TNF therapy for a median duration of 37 months [
24]. The possible reason for the short treatment duration in the Chinese patients in the current study may be associated with poor socioeconomic condition, poor patient compliance, and the limitation of cross-sectional study. bDMARDs are relatively expensive and are not covered by the national health insurance reimbursement policies in China.
This study demonstrated that the proportion of remission + LDA was the highest in patients with ≥12 months of treatment, indicating that long-time treatment maximizes the benefits for patients. These results are in line with those of a previous 4-year follow-up study of infliximab therapy in refractory RA patients, which showed that longer duration of infliximab therapy resulted in lower DAS28 score [
25]. Nam et al. found that maintenance of clinical responses was higher with bDMARD continuation [
26]. Thus, our results suggest that, to achieve the best treatment outcome, patients with RA should continue bDMARD therapy for longer than 12 months. Furthermore, this study revealed that the remission rate in Chinese patients receiving bDMARDs was 12.6 % (DAS28), 5.4 % (CDAI), and 3.5 % (SDAI). In a multicenter cross-sectional study of RA in Chinese patients receiving csDMARDs, bDMARDs, and/or glucocorticoids, Wang et al. found the remission rate to be 8.6 % (DAS28), 8.2 % (CDAI), 8.4 % (SDAI), and 6.8 % (Boolean) [
27]. In Qatari, the remission rate of patients with RA receiving bDMARDs and/or csDMARDs was 49 % by DAS28 score [
28]. In the QUEST-RA study including patients with RA from 25 mostly European countries, remission rate was 13.8 % and 19.6 % by CDAI and DAS28, respectively [
29]. These results indicate that treatment for Chinese patients with RA is insufficient. Further, the inhibitory costs of biologics ($15,000–$25,000 per patient per year) [
30] present challenges in developing countries [
31] and may result in early treatment discontinuation or dose reduction, resulting in flaring of the disease. While the guidelines do not recommend treatment discontinuation, “step-down” or tapering strategies by careful dose reduction or injection spacing can maintain a disease-free status in patients who have achieved remission or low disease activity [
32]. Studies have shown that patients in remission after bDMARD mono or combination therapy continued to maintain their remission status after careful dose tapering or treatment discontinuation [
33,
34]. Further, in order to maintain the alleviating effect, the dose of traditional DMARDS may be increased or treatment options such as double and triple combination treatment may be prescribed. Therapy can be reinitiated when necessary, making this approach desirable from a safety viewpoint and curbing unnecessary healthcare expenditure. Careful patient selection based on clinical and practical considerations may also improve outcomes with continuous bDMARD use in the developing world.
The current RA management regimen in China should be optimized to allow patients to benefit from more aggressive treatment. Given the comparable efficacy and cost-effectiveness of triple DMARD combinations in comparison with bDMARDs and methotrexate [
35,
36], further studies are needed to assess the use of triple DMARD combination therapy in comparison with biologics in China.
Although the 2013 EULAR guidelines for RA management recommend bDMARDs to be used concomitantly with csDMARDs [
10], the 2015 ACR guidelines take monotherapy into consideration [
37] and bDMARDs monotherapy is also used in clinical practice as needed [
12]. In some studies, bDMARD monotherapy has been shown to be as effective as the combination therapy of csDMARDs and bDMARDs. In terms of DAS28 score, ACR responses, and swollen and tender joint counts, tocilizumab and methotrexate combination therapy was not superior to tocilizumab monotherapy [
13,
38]. Consistently, the current study also demonstrated that DAS28 score in patients receiving tocilizumab monotherapy was similar to that in patients receiving tocilizumab and csDMARD combination therapy. In the current study, although the average DAS28 score was significantly higher in patients receiving bDMARD monotherapy than in patients receiving combination therapy, the rate of reaching treatment target was similar in patients receiving monotherapy versus combination therapy. Interestingly, the current study found that patients with tocilizumab monotherapy showed significantly lower DAS28 score and higher proportion of reaching treatment target than patients receiving other types of bDMARD monotherapy. These findings suggest that tocilizumab monotherapy may be a promising option for patients with RA. Simplification and optimization of the treatment for RA are beneficial for both patients and physicians.
This cross-sectional study design presents a “snapshot” of bDMARD usage in Chinese patients with RA. It is difficult to infer causal relationships between bDMARD usage pattern and disease activity of RA, although longer duration of bDMARD therapy was associated with lower DAS28 score and higher rate of achievement of treatment goal through ad hoc analysis. Confounding factors that might affect the relationship between duration of bDMARD therapy and disease activity, such as the disease status prior to receiving bDMARD therapy and other concomitant therapies, were not considered in this study.
In conclusion, the usage of bDMARDs in Chinese patients with RA is in accordance with the global recommendations despite the short treatment duration. The bDMARDs are commonly used in combination with csDMARDs. Longer duration of bDMARD therapy appears to be associated with lower DAS28 scores and higher proportion of achievement of treatment target. These results should be kept in mind by the clinicians while treating patients with RA who do not achieve the treatment goal within 3 to 6 months of therapy. To achieve the best treatment outcome, patients with RA should continue bDMARD therapy for longer than 12 months. Our results provide a strong evidence base for the government to make decisions for the benefit of a greater number of patients with RA. Tocilizumab monotherapy may be a promising option for patients with RA. Further prospective studies are needed to assess the impact of bDMARD usage on RA remission among the Chinese population.