Clinical and radiological dissociation of anti-TNF plus methotrexate treatment in early rheumatoid arthritis in routine care: Results from the ABRAB study

Rheumatoid arthritis (RA) is a chronic systemic inflammatory musculoskeletal disease that represents a significant health burden both with regard to comorbidities as well as to the mortality of patients [1, 2]. The chronic inflammation and destruction of synovial joints leads to functional impairment, work loss and progressive disability [3]. In the past deeper insights into the pathogenesis of RA has led to the introduction of biologic agents and subsequently to considerable changes in the management of RA with respect to preventing and controlling disease progression [4]. The in-depth understanding of the disease course and the increasing data of treatment strategies supported the development of widely accepted recommendations on the management and therapy of the disease [5, 6]. Clinical remission, prevention of joint destruction and long-term disability have emerged as the primary goals of modern treatment for RA [5].

The concept of the ‘window of opportunity’ supports that early agressive treatment can significantly change the long-term course of the disease, resulting in higher clinical response rates, less disability and less erosive damage [7, 8]. Biological agents have proven to be effective in patients responding insufficiently to MTX in randomised controlled trials (RCTs), not only in reducing disease activity and improving functional status, but in slowing radiological progression [9–15]. Monoclonal antibodies against TNF including adalimumab, etanercept and infliximab, and lately the interleukin-6 receptor inhibitor tocilizumab and anti-CD20 rituximab prevented joint destruction even in patients failing to show a clinical response to MTX monotherapy [16–20]. Such “dissociation” between disease activity and radiological progression appears to be an additional advantage of biologics.

To the best of our knowledge as of yet the phenomenon of dissociation was evaluated only in RCTs, with selected patient populations and not in routine clinical care. Our aim was to examine how anti-TNF + MTX therapy affect clinical, functional and radiological outcomes – primarily focusing on dissociation - compared with MTX monotherapy in early RA patients in routine care.

As part of the ABRAB (Assessment of Biologics in Rheumatoid Arthritis in Budapest) study, a retrospective analysis of an observational cohort, adult (≥18 years) early RA patients (diagnosed ≤2 years) from the observational cohort of the outpatient clinic of the National Institute of Rheumatology and Physiotherapy, Budapest was performed. All patients were diagnosed according to the 1987 American College of Rheumatology criteria [21]. Patients were selected randomly based on the availability of baseline and 12 month radiographs of hands and feet in order to calculate radiological progression after 12 month. High baseline disease activity (DAS28 ≥ 5.1) was also among the selection criteria. Approval of the Ethics Committee of National Institute of Rheumatology and Physiotherapy in Budapest was given prior to the study, and informed consent was obtained from all patients.

We grouped selected patients into two groups: patients in group A (n = 49) received first-line MTX monotherapy (10–20 mg weekly) with no previous DMARDs, while those in group B (n = 35) received anti-TNF + MTX (10–20 mg weekly) treatment. Patients in group B were treated with the following agents: infliximab (20%), etanercept (22,9%), adalimumab (40%), golimumab (14,2%) and certolizumab (2,9%). All anti-TNFs were administrated according to the method of administration indicated in the summary of product characteristics. All patients in group B failed one or two prior DMARDs according to local guidelines on the use of biologics in RA.

Clinical data was recorded at five timepoints during the first 12 months of treatment in both groups (at 0, 3, 6, 9 and 12 month). Disease activity was measured by DAS28 based on the erythrocyte sedimentation rate and by CDAI (clinical disease activity index), functional status was determined using HAQ-DI score. We evaluated the efficacy of anti-TNF + MTX treatment and MTX monotherapy in reducing disease activity and improving functional status in both groups in the first 12 month of their investigated treatment period, and also compared the differences between their data. The ratio of patients reaching the state of remission or low disease activity was also determined in both groups. Remission was defined as DAS28 < 2.6 or CDAI ≤2,8 and low disease activity was defined as DAS28 ≤ 3.2 and ≥2.6 or CDAI ≤10 and ≥2.9. [5].

All patients had hands and feet radiographs at baseline and at the end of the 12th month treatment period. Radiological progression was measured according to the van der Heijde modified Sharp method (vdHS; 0–448 points) on radiographs of the hands and feet. All radiographs were scored by three readers, a radiologist and two rheumatologists (AM, JB, PJ) blinded to patient identity, treatment and the date of the radiographs. Radiological values given by agreement of the three readers were used for the analysis. As a consequence of routine clinical care, the interval between the two different radiographic timepoints were for some patients less or more than 12 months (13 ± 2,4). In these cases radiological progression at 12 months (vdHS U/year) was calculated dividing the change in the radiological score with the ratio of the real time interval and the assumed 12 months. The impact on radiological progression was compared between the different treated groups, and in addition the ratio of patients with no radiological progression (vdHS = 0 U/year) and those showing rapid radiological progression (vdHS ≥ 5 U/year) was also compared between the two groups [22]. To investigate the dissociation between reduction of disease activity and impact on radiological progression in groups, radiological progression at 12 months as well as the ratio of radiological non-progression and that of rapid radiological progression was compared in patients who failed to show a clinical response. Clinical non-response was defined as a time-averaged DAS28 ≥ 3.2. The time-averaged DAS28 was calculated as the mean DAS28 of visits at month 3, 6, 9 and 12.

Statistical analysis was performed with Graphpad Prism 5.00 statistical software. The distribution of the variables is provided as mean ± SD. We used the independent two-tailed Student’s t-test and paired t-test to compare continuous variables between and in groups. We used either Mann–Whitney or Wilcoxon matched pairs test for non-parametric data, while one-way or repeated measures ANOVA with corresponding post-tests (Tukey’s or Dunnet’s multiple comparison) was used for comparing three or more variables. We used Fisher’s exact test to compare dichotomous variables between groups and considered p < 0.05 as statistically significant.

We evaluated early RA patients under different treatment in routine rheumatological outpatient care and showed comparable clinical efficacy of anti-TNF + MTX and MTX monotherapy in the first 12 month of treatment. Both groups had significant improvement in DAS28 reduction which was noticeable at the 3 months visit, and was sustained along the observed 12 months treatment period. The value of DAS28 reduction was higher at all visits in the anti-TNF + MTX treated group, and was significant at 3 months. The percentage of patients achieving DAS28 remission as the desirable therapeutic goal in RA [5], was comparable between the anti-TNF + MTX and MTX monotherapy treated groups, despite the higher DAS28 reduction in the former group. The rate of remission at month 12 was 31.4% in the anti-TNF + MTX treated group consistent with data found in the literature on patients treated in clinical practice [23, 24]. Similar rates of DAS28 remission in the MTX-treated group (30.6%) can be explained by the early, tight controlled design of the treatment.

Functional status (HAQ-DI) was significantly improved in both groups from month 3 and was sustained along the observed 12-month treatment period, with no clear differences between the two groups. Functional disability, as measured by HAQ-DI has been shown to have two components. The irreversible component correlates with radiological status, mainly cartilage destruction and subluxation, and worsens with time. The reversible domain is related to disease activity and can be therapeutically influenced [25, 26]. Our observed groups had comparable baseline radiological status as well as comparable improvement of clinical activity that explains the similar effect of anti-TNF + MTX and MTX monotherapy on functional status.

There is strong evidence on the efficacy of anti-TNF + MTX vs. MTX monotherapy in slowing/halting radiological progression [9–13]. Comparing the two groups, anti-TNF + MTX treated patients had significantly less radiological progression than those treated with MTX monotherapy. Our data confirms the superiority of anti-TNF + MTX treatment not only in decreasing radiological progression, but also in inhibiting rapid radiological progression and increasing the rate of radiological non-progression. The high percentage of radiological non-progression in the anti-TNF + MTX treated group indicates marked clinical success since the investigated patients had baseline radiographic damage and anti-CCP positivity in high percentage that are the main predictive factors of poor radiologic outcome [27].

Erosions of the joints and cartilage destruction are hallmarks of RA. Formerly, it was conceptualized that in RA inflammation leads directly to the destruction of bone and cartilage. Recently we have learned that bone destruction is intricately linked to the RANKL (receptor activator of nuclear factor kB ligand)-OPG (osteoprotegerin) system which is strongly, but not exclusively connected to the inflammatory processes occurring within the joint [28]. The disbalance between RANKL and OPG mainly determines the degree of proliferation and activity of osteoclasts in RA. Osteoblasts produce both RANKL and OPG, the ratio of which is influenced by hormones, growth factors and many cytokines, among them TNF-alpha [28]. The strong inhibitory effect of anti-TNFs on radiological progression may be explained by their direct inhibitory effects on osteoclast activity, in addition to their overall anti-inflammatory effect [16].

RCTs (randomized controlled trials) comparing anti-TNFs + MTX to MTX support the phenomenon of dissociation between inflammation and radiological progression, which may explain the slowing/halting of radiological progression in the absence of a clinical response [16–18]. Dissociation may potentially be explained by the threshold hypothesis, which assumes that TNF-driven osteoclast activation occurs only when the level of TNF reaches a putative threshold. In case of clinical and radiological dissociation anti-TNF therapy decreases the level of TNF below this threshold, but not low enough to cease the inflammatory activity as well [29]. This assumes that inflammation is sustained at lower levels of TNF than at levels at which osteoclast activation occurs. Recent analysis from the PREMIER trial showed that the dissociation between clinical and radiological outcomes (joint space narrowing and joint erosions) at week 52 and 104 occurred in patients treated with adalimumab (ADA) + MTX but only to a mild degree in patients on ADA monotherapy [30], which might indicate that MTX may enchance the dissociative potential of ADA treatment. Dissociation has also been shown for IL-6 inhibition with tocilizumab [19] and with anti-CD20 rituximab therapy [20], A recent meta-analysis of intensive DMARD combination therapy with step-down prednisolone study also suggested a similar phenomenon in patients [31].

Nevertheless, there are some limitations to our clinical study. Firstly the anti-TNF + MTX treated group received preliminary DMARDs that decreases comparability with the DMARD naїve MTX treated patients. Secondly the X-ray examinations for calculating radiological progression were made not exactly at the 12th month of treatment which could have minimally distorted the value of radiological progression at 12 months assumed as linear in the analysis. Thirdly the relatively low number of early RA cases with available X-rays, especially in a subanalysis may have reduced the statistical power of our calculations. All of these limitations stem from the fact that our analysed patients were treated in routine clinical care and according to the local guidelines, DMARD treatment is mandatory before starting anti-TNFs. Additionally the use of hands and feet X-rays for following radiological disease progression is not regular in routine care, especially not at exactly a time interval of 12 month: the fact that the availability of X-rays at two timepoints was an inclusion criteria may have indeed introduced a selection bias into our study.

Our results prove the superiority of anti-TNF + MTX therapy in dissociating inflammation and radiologic destruction. Anti-TNF + MTX treatment strongly inhibited radiological progression even in patients not reaching clinical remission or low disease activity. Not only therapeutic responders, but also non-responders of the combination group showed better radiologic results than patients on MTX monotherapy. Our data indicates that even if anti-TNF + MTX treatment is only partly successful in achieving remission or low disease activity, it can inhibit radiographic damage.

Anti-TNF + MTX treatment strongly inhibited radiological progression even in patients not reaching clinical remission or low disease activity. Further “real-life” investigations are needed in the future to evaluate the impact of anti-TNF + MTX treatment on clinical and radiological dissociation in routine clinical practice.