Benefits of early RA diagnosis and treatment

National and International recommendations address the importance of starting DMARD therapy as soon as the diagnosis of RA is made.5 Data from multiple observational cohorts and clinical trials indicate that treatment initiation in the first 12 weeks since disease onset is particularly effective in controlling disease activity and results in better mid-term and long-term outcomes. The FinRaCo trial demonstrated that a delay in therapy (>4 months) was the only significant predictor of remission using a single-DMARD strategy.6 According to the ‘window of opportunity’ hypothesis, the time to intervention within a limited time frame is associated with a particularly effective response to therapy, resulting in long-term sustained outcomes. A recent study on two large cohorts of patients from early clinics (Leiden Early Arthritis Clinic and ESPOIR) set this critical time point for DMARD introduction to 11.4 weeks from symptoms onset for anticitrullinated protein antibodies (ACPA)-positive RA and 15 weeks for ACPA-negative subjects, supporting the concept of two different pathological subsets of disease.6 The primary outcome was conventional synthetic DMARD (csDMARD)-free sustained remission up to 5 years of follow-up, still possible for a minority of patients (11.5% and 5.4% in the 2 cohorts), but that is strictly related to the inflammatory load before treatment is started.7 Very ERA (VERA), defined as symptom duration ≤12 weeks, has also been demonstrated as a predictor of remission in a large multicentre real-life prospective study including 1795 patients. The follow-up analysis up to 12 months was restricted to 481 patients presenting with at least Disease Activity Score (DAS28) moderate disease activity at baseline. DAS28 remission was achieved in 34.3% (ranging 19.5–49%) of patients with RA and was significantly associated with a diagnosis of VERA and an intervention with csDMARDs in the first 12 weeks of disease duration as shown in table 1.8

The superiority of functional and structural outcomes is particularly evident not only compared with established RA, but also compared with late ERA characterised by a median symptom duration of 12 months, even if still classifiable within the relatively flexible definition of early arthritis.9 A delayed rheumatological referral (≥12 weeks) has been associated with a long-term impact, leading to an HR of 1.87 for not achieving DMARD-free remission and a 1.3 times higher rate of joint destruction over 6 years. Unfortunately, despite the robust-evidence supporting the relevance of a window of opportunity, only 31% of patients with RA were assessed <12 weeks in a real-life setting of 1674 patients with early arthritis.10 A meta-analysis of 18 available randomised controlled trials (RCT) also reported that prolonged symptom duration before DMARD treatment initiation is independently associated with radiographic progression and a lower chance on DMARD-free sustained remission.11 Data from the ESPOIR cohort including 661 patients with early arthritis have stressed the favourable effect of very early DMARD initiation, within 3 months from diagnosis, in reducing 12-month radiographic progression.12

Some authors argue that, when dealing with such precocious disease, there might be some degree of overdiagnosis for patients whose disease would eventually resolve without DMARDs; however, this risk has been demonstrated to be very low: 8% with 2010 European League Against Rheumatism–American College of Rheumatology (EULAR/ACR) criteria for RA compared to 2% with 1987 criteria.13 In 2013, erosive disease, highly specific of RA, has been finally defined as a radiographic erosion involving at least three separate joints in the hands, wrists and feet, allowing a better diagnostic confidence.13 Moreover, among patients with ERA/undifferentiated arthritis, a score of the 2010 ACR/EULAR criteria sufficient to classify RA has been demonstrated to select patients with worse clinical outcome and more radiographic progression, therefore needing aggressive treatment.14 The risk of misclassifying other conditions such as palindromic rheumatism is also low as far as the diagnosis of RA is committed to an expert rheumatologist. Palindromic rheumatism is a recognised clinical entity that is typically monoarticular, with a very short duration of attacks (in the majority of cases less than 48 h and always shorter than a week). With such a presentation, it is quite unlikely that a patient would either fulfil RA classification criteria or be diagnosed with RA. The frequency of palindromic rheumatism is far lower than that of RA and has been estimated to be one-twentieth that of RA, making misclassification less probable. Moreover, the condition may preclude the onset of other rheumatic conditions, especially RA, in a significant proportion of patients, particularly when ACPA or rheumatoid factor is detected.15

Benefits of achieving remission with a T2T and tight control strategy

Further evidence that the strategy is sometimes more important than the agent used to treat RA comes from a number of RCT supporting the T2T and tight control approach.12 ,13 The TICORA study analysed the differences between a sustained, tight control, DAS-driven approach to RA compared with clinical routine outpatient care, reporting an EULAR good response in 82% of patients in the intensive care group compared with 44% in the control group. An intensive management of RA also resulted in reduced radiographic progression (change in the total sharp radiographic score of 4.5 vs 8.5), physical function and quality of life, with no additional costs. The CAMERA trial also demonstrated the superiority of an intensive methotrexate (MTX) regimen with the T2T and tight control approach in ERA (<1 year disease duration) in reaching remission compared to usual care (DAS28-remission rate 50% vs 37%).16 The recently licensed EULAR guidelines state that treatment should be aimed at reaching a target of remission or low disease activity in every patient, following strict (every 1–3 months) clinical monitoring and adjusting therapy according to disease activity. Prognostic factors are important in adapting step-up treatment to bDMARDs. An overview of a large inception cohort from 1989 to 2009 investigating the improvement in outcomes related to the new treatment strategy reported significantly decreased disease activity and joint damage progression, increased functional ability (Health Assessment Questionnaire -HAQ) and fewer orthopaedic interventions.17 Real-life data on early arthritis cohorts have demonstrated remission rates as high as those achieved in RCT following a tight control protocol aiming at remission (DAS28-remission 55% vs 30% in usual care).18 Achieving clinical remission, regardless of the criterion used to define it (ACR/EULAR, Simplified Disease Activity Index (SDAI), DAS28), is indeed associated with a better control of disease, both in terms of functional disability and objectivable synovitis with power doppler positivity at sonographic evaluation, known to correlate with radiographic progression.19 A recent Italian rheumatologists’ survey on the acceptance of the T2T recommendations reported a high level of knowledge and agreement with the guidelines statements, confirming that this is becoming a consolidated standard of care also in everyday clinical practice.20

Benefits of reaching the target of remission early

As mentioned above, early diagnosis with prompt treatment initiation and a tight control follow-up aiming at remission should be regarded as the standard of care in the management of RA. Evidence has also demonstrated that the timing to achieve remission has a fundamental prognostic role: earlier time to remission predicts sustained clinical remission in ERA. Sustained remission represents the desired goal, being associated with long-term improvement of quality of life, physical function and reduced radiographic progression.21 Long-term persistence of remission is possible in about half of the patients meeting remission criteria.21 ,22 Predictive factors of reduced rates of sustained remission have been identified in female sex, greater pain, lack of initial DMARD therapy and older age.21 ,22 A shorter time to remission has been a consistent and strong determinant of sustained remission. Schipper et al demonstrated that earlier time to remission is the strongest predictor of sustainability over a 20-year period, regardless of the type of treatment.22 Disease duration is among the most relevant factors affecting the likelihood of patients’ response to treatment,19 ,20 even when bDMARDs are prescribed.23 ,24 In ERA (diagnosis of RA with symptoms duration <12 months), low-dose prednisone comedication has been reported to be associated with earlier disease activity control, higher rates of clinical remission and a more stable and sustained remission over time.25 Early remission significantly affects long-term outcomes. The 11-year results of the FIN-RACo trial showed that treating ERA with traditional DMARDs, targeting to remission and with tight clinical control results in low radiological progression in most patients; interestingly, long-term radiographic progression (Larsen score) up to 11 years of follow-up was significantly lower in patients reaching remission in the first year of treatment.26 Data from the CAMERA study also confirmed how early clinical response to MTX treatment can affect 5-year clinical and radiographic (Sharp-van der Heijde score) outcomes27 (figure 1). The same clinical, functional and structural outcomes, with a strict connection between time to treatment response and long-term benefits, have been reported for several bDMARDs.28–30 Real-life data from ERA patients recruited in the ESPOIR cohort (<6 months of disease duration with a certain of probable RA clinical diagnosis) and treated according to the standard of care with csDMARDs and/or bDMARDs, confirm the long-term detrimental effects of failing to reach good disease control during the first 12 months. Indeed, persistent moderate disease activity during the first year of disease is associated with greater radiographic progression at 3 years, increased HAQ up to 5 years, five-time increase in missed workdays and approximately a 10-fold smaller chance of achieving clinical remission in the long term24

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Figure 1

The effect of early response to treatment on 5-year follow-up of radiographic progression rate. Adapted from Bakker et al28 (EULAR, European League Against Rheumatism; SHS, Sharp van der Heijde score, median values).

Striving to early remission in RA also empowers further, more comprehensive implications. Rapid induction of remission is essential to maintain workability in patients with ERA; remission in the first year is an independent predictor of preserved working capacity and social productivity in the future.27 Studies investigating functional ability and health-related quality of life have also found the advantage of early remission in guaranteeing better or even normalised outcomes.31 Early treatment resulting in tight inflammation control and remission, also in the ERA setting, is strictly associated with improvement in cardiovascular risk and reduction of cardiovascular morbidity.32–34 Results from the Norfolk Arthritis Register demonstrated that early and sustained remission is associated with improved survival. Achievement of remission within the first 3 years of disease determined a fall of about 30% in the risk of all-cause mortality. Lowest risk of death was associated with the earliest and most persistent status of remission.35^–37