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Evidence for treating rheumatoid arthritis to target: results of a systematic literature search update
  1. Michaela A Stoffer1,2,
  2. Monika M Schoels3,
  3. Josef S Smolen1,3,
  4. Daniel Aletaha1,
  5. Ferdinand C Breedveld4,
  6. Gerd Burmester5,
  7. Vivian Bykerk6,
  8. Maxime Dougados7,
  9. Paul Emery8,
  10. Boulos Haraoui9,
  11. Juan Gomez-Reino10,
  12. Tore K Kvien11,
  13. Peter Nash12,
  14. Victoria Navarro-Compán4,13,
  15. Marieke Scholte-Voshaar14,
  16. Ronald van Vollenhoven15,
  17. Désirée van der Heijde4,
  18. Tanja A Stamm1
  1. 1Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria
  2. 2University of Applied Sciences for Health Professions Upper Austria, Linz, Austria
  3. 3Department of Internal Medicine, Centre for Rheumatic Diseases, Hietzing Hospital, Vienna, Austria
  4. 4Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands
  5. 5Department of Rheumatology and Clinical Immunology, Charité—University Medicine Berlin, Free University and Humboldt University Berlin, Berlin, Germany
  6. 6Division of Rheumatology, Weill Cornell Medical College, Cornell University, Hospital for Special Surgery, New York, USA
  7. 7Department of Rheumatology, Hôpital Cochin, Paris Descartes University, Assistance Publique—Hôpitaux de Paris; INSERM (U1153): Clinical Epidemiology and Biostatistics, PRES Sorbonne Paris-Cité, Paris, France
  8. 8Academic Unit of Musculoskeletal Disease, University of Leeds, Leeds, UK
  9. 9Rheumatic Disease Unit, University of Montreal, Montreal, Canada
  10. 10Rheumatology Service and Department of Medicine, Hospital Clinico Universitario, Universidad de Santiago, Spain
  11. 11Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway
  12. 12Department of Medicine, University of Queensland, Brisbane, Australia
  13. 13Department of Rheumatology, University Hospital La Paz, Madrid, Spain
  14. 14Department of Psychology, Health and Technology, University of Twente, Enschede, The Netherlands
  15. 15The Karolinska Institute, Stockholm, Sweden
  1. Correspondence to Dr Tanja A Stamm, Department of Medicine 3, Division of Rheumatology, Medical University of Vienna, Währinger Gürtel 18-20 A, Vienna 1090, Austria; tanja.stamm{at}meduniwien.ac.at

Abstract

Objective A systematic literature review (SLR; 2009–2014) to compare a target-oriented approach with routine management in the treatment of rheumatoid arthritis (RA) to allow an update of the treat-to-target recommendations.

Methods Two SLRs focused on clinical trials employing a treatment approach targeting a specific clinical outcome were performed. In addition to testing clinical, functional and/or structural changes as endpoints, comorbidities, cardiovascular risk, work productivity and education as well as patient self-assessment were investigated. The searches covered MEDLINE, EMBASE, Cochrane databases and Clinicaltrial.gov for the period between 2009 and 2012 and separately for the period of 2012 to May of 2014.

Results Of 8442 citations retrieved in the two SLRs, 176 articles underwent full-text review. According to predefined inclusion/exclusion criteria, six articles were included of which five showed superiority of a targeted treatment approach aiming at least at low-disease activity versus routine care; in addition, publications providing supportive evidence were also incorporated that aside from expanding the evidence provided by the above six publications allowed concluding that a target-oriented approach leads to less comorbidities and cardiovascular risk and better work productivity than conventional care.

Conclusions The current study expands the evidence that targeting low-disease activity or remission in the management of RA conveys better outcomes than routine care.

  • Rheumatoid Arthritis
  • Treatment
  • Disease Activity

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Introduction

New treatment options and new treatment strategies have changed the achievable outcomes in rheumatoid arthritis (RA) over the last 20 years.1–5 The treat-to-target (T2T) algorithm developed in 2010 consisted of 10 recommendations advocating the implementation of therapeutic principles, especially targeting remission or low-disease activity by adjusting therapy in the context of regular disease activity assessments. These recommendations were based on evidence obtained from a systematic literature review (SLR),6 but to a large extent also on expert opinion. The international task force of the T2T project assumed that the evidence base for the T2T recommendations may have expanded and further developed and that an update was needed especially to learn whether the expert-based statements were supported or contested by new evidence. Moreover, it was deemed interesting and important by the steering committee to not only focus on the traditional clinical, functional and structural endpoint but also on additional aspects related to quality of life and other outcomes important to patients.

Methods

In 2012 and 2014, systematic literature searches of available evidence regarding the effects of treating RA strategically were conducted. In addition to testing clinical, functional and/or structural changes as endpoints, comorbidities, cardiovascular (CV) risk, work productivity and education as well as patient self-assessment were investigated. In the opinion of the steering committee, an initial search of the 2009–2012 literature performed in 2012 did not provide sufficient new evidence to justify an amendment of the recommendations. A new search on the literature published between 2012 and 5/2014 was now performed; that latter SLR focuses also on the additional outcomes mentioned above.

SLR: update

The new SLRs are a follow-up to the SLR performed by Schoels et al in 2009.6 The search strategy developed then by the international steering committee of the T2T project and described in detail elsewhere6 was expanded by using additional keywords (see below). Two research fellows (MMS in 2012; MAS in 2014) performed the SLRs with support from their mentors.

The definitions of the 2009 SLR were generally also used for this update (with slight changes). These were:

  1. Strategy trial—clinical trial of any RA drug treatment, in which a clear outcome target was the primary endpoint and therapeutic consequences of failing to reach the target were predefined.

  2. Targets—a target could be formulated by clinical, serological, patient reported, functional or imaging-derived variables; individual measures (eg, joint counts or acute phase reactants), composite scores (eg, disease activity score (DAS) or simplified disease activity index (SDAI)), response criteria (eg, those defined by the American College of Rheumatology (ACR) or the European League Against Rheumatism (EULAR)), structural or ultrasound outcomes were considered alike.

  3. Outcomes—clinical, functional, serological, structural changes and comorbidity, as defined in the respective trials, were compared between treatment groups.6

Beyond those applied in 2009, several new keywords: “patient-self assessment”, “comorbidities”, “cardiovascular risk”, “work productivity” and “education” in a target-oriented study were used. Controlled trials and observational studies were included. The searches covered the databases MEDLINE, EMBASE, Cochrane and Clinicaltrial.gov for the period between 1/2009 and 5/2014. The PICOs (see online supplementary table S1) and the search strings are shown in the online supplementary material (see online supplementary table S2 for 2012, supplementary table S3 for 2014). Like in the previous work, the search was limited to human  RA, adults and the English language. Furthermore, we did not exclude studies based on quality in the initial searches.

Results

The first search performed in 2012 yielded 3256 hits. The search performed in 2014 arrived at 5186 records for further investigation (figure 1). Title and abstract review according to the inclusion/exclusion criteria led to assessment of eligibility of 91 and 85 full-text documents, respectively. The detailed review of the records in relation to the primary search objectives (comparison of primary endpoints in a priori strategy trials) resulted in the inclusion of four papers7–10 from the search in 2012 and two additional papers11 ,12 from the search performed in 2014. An overview of the six included studies is given in table 1A. From the identified references, we extracted information about the targets driving treatment decisions, the interval of control examinations, the numbers of patients included and the outcomes (table 1A).

Table 1

 (A) Publications comparing an a priori targeted treatment strategy with routine care; (B) supportive evidence

Figure 1

Flow chart of the systematic literature search. Diagrammed are the results of the initial and second search (2012 and 2014, respectively) and the selection process of abstract screening, full-text review and inclusion according to expert opinion.

Five of the six included studies dealt with early RA7–10 ,12 and one trial with established RA.11 All studies showed a superiority of a T2T strategy compared with routine care (RC)7 ,8 ,10–12 except for one study (Strategic Reperfusion Early After Myocardial Infarction).9 For the included studies, the risk of bias was assessed according to the scheme proposed by the ‘Cochrane risk of bias assessment’ (figure 2).

Figure 2

Rick of bias summary figure. +Low risk of bias, −High risk of bias, ?Unclear risk of bias, n.a. Not applicable. *In the study of Pope et al physicians were randomised. **Vermeer et al was comparing real life data from cohorts.

In early RA, the T2T strategy brought more patients into remission or low-disease activity and this was achieved more rapidly. Also, patients in the T2T group experienced larger improvements in patient assessments of pain, functional ability and disease activity (Dutch Rheumatoid Arthritis Monitoring (DREAM)).10 In one trial of recent-onset active RA, the tight control approach showed that more patients achieved remission without disability and radiographic progression (Guérir la Polyarthrite Rhumatoide Débutante (GUEPARD)/Etude et Suivi des Polyarthrites Indifférenciées Récentes (ESPOIR)).8 Another study showed similar findings: the DAS-driven treatment led to better clinical outcomes (health assessment questionnaire, DAS28 and median erythrocyte sedimentation rate) and numerically, but not statistically different suppression of joint damage in the T2T group.7

In a study dealing with established active RA,11 physicians were randomised into three groups (treating according to RC or targeting a DAS28<2.6 or a swollen joint count of 0). Although there was no difference in terms of therapeutic endpoint achievement, the time to reach a good/moderate EULAR response was significantly shorter and the dropout rates were significantly lower when using the targeted approaches.11 Furthermore, using real-life data from the DREAM registry and the Nijmegen early RA inception cohort, a T2T strategy was found to be cost-effective compared with RC.12

Only one study did not show superior effects of a T2T strategy; however, this study assessed only a small number of patients with low radiographic damage and presented good functional status in both treatment groups.9 Further studies are discussed in some more detail in the online supplement S4.

Regarding comorbidities, CV risk, work productivity or the role of (patient) education, none of the studies comparing T2T to RC had any of these outcomes as primary endpoint. However, these outcomes were addressed in observational data or registry studies comparing different strategic treatment approaches and endpoints, and therefore, these publications were regarded as further supporting evidence and are presented in table 1B.

Subanalysis of PREMIER (a multicenter, randomised, double-blind clinical trial of combination therapy with adalimumab plus methotrexate versus methotrexate alone or adalimumab alone in patients with early, aggressive rheumatoid arthritis who had not had previous methotrexate treatment) and Active-Controlled Study of Patients Receiving Infliximab for the Treatment of Rheumatoid Arthritis of Early Onset (ASPIRE) data showed that the level of disease activity, the duration of SDAI remission and latency to remission all affect radiographic progression.13 There is a direct relationship between disease activity and radiographic changes but a dissociation of the effect with tumour necrosis factor inhibitor use.14 Among these publications were studies showing that Clinical Activity Disease Index remission is associated with lower CV risk and improved CV outcomes,15 ,16 and the absence of swollen joints with improved overall survival.17

Additional studies that emerged during the SLR were categorised by topics and also presented to the task force. All these studies are listed in the online material (see online supplementary table S5).

Aside from the work of Pope et al,11 all of the above-described articles studied patients with early RA. However, Gullick et al18 investigated an observational cohort of patients with long-standing RA in a setting of usual care. In their study, the authors compared the outcomes of an RA centre routinely using goal-directed therapy aimed at DAS28<2.6 with an age-matched and sex-matched sample of consecutive patients from other RA clinics. Significantly more T2T patients achieved the target, irrespective of their disease duration, and T2T led to significantly improved functional outcomes compared with RC.

Discussion

Since the original search informing the T2T task force, six new studies have been published, five of which fully support that a treatment strategy using a defined target conveys superior clinical, functional and structural outcomes compared with RC. In contrast to the data available in 2010, now more studies have used clinical remission defined by DAS or DAS28 as a main endpoint, which is a more stringent target than low-disease activity. While trials directly comparing potential differences in targeting remission versus low-disease activity are not available, supportive evidence exists that reaching ACR–EULAR remission is superior in terms of physical function, quality of life and work productivity and significant differences ensue when moving from one of these desired states to the other.19

In 2010, studies evaluating target-steered versus non-steered treatment approaches were only available for early RA. The new search revealed additional investigations on early or even recent-onset RA, but also data on established RA. Indeed, information on target steered therapy in established RA was a point in the research agenda in 2010; the data reveal that also in long-standing RA a T2T strategy is superior to RC.11 ,18

Finally, some new aspects were evaluated here, namely work productivity, comorbidities and effect of education on treatment outcomes. While trials comparing different therapeutic strategies using these outcomes as primary endpoints are not yet available, secondary analyses reveal that lower disease activity is associated with better work productivity, less comorbidity and CV risk and that better education is likewise related to better clinical outcomes.11 ,15 ,16 ,19–25 The task force was informed about these data as supportive evidence.

The present SLR provided new evidence regarding several items of the 2010 T2T recommendations,26 which allowed to update the recommendations as presented in the paper by Smolen et al.27 Indeed, the evidence base of several items increased from D to B or A (for details, see main paper) and several items, such as the overarching principle B and points 1 and 3 (with respect to established RA), as well as point 7, could be amended or expanded based on this new SLR. In conclusion, new and expanded evidence has been identified confirming that treating RA to a target of low-disease activity or remission enables patients to reach better outcomes than when they are exposed to RC. This information was provided to and discussed in detail by the task force allowing to develop an update of the T2T recommendations with much higher levels of evidence.27

References

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Footnotes

  • Handling editor Francis Berenbaum

  • Contributors MAS and MMS are joint first author. Conception and design: MAS, MMS, JSS, DA, FCB, GB, VB, MD, PE, BH, JG-R, TKK, PN, VN-C, MS-V, RvV, DvdH, TAS. Analysis and interpretation of data: MAS, MMS, JSS, TAS, with all authors involved in the revision and final phases. Drafting the article and revising it critically for content: MAS, MMS, JSS, TAS, with all authors involved in the revision and final phases. Approval of the final version to be published: all authors were involved.

  • Funding This study was supported by an unrestricted educational grant from AbbVie. AbbVie had no influence on the selection of papers, extraction of data or writing of this manuscript.

  • Competing interests MAS has received speaker fees from MSD, none of them relates to this work. JSS has provided expert advice to AbbVie, Amgen, Astra-Zeneca, Astro, BMS, Celgene, Glaxo, Janssen, Novartis-Sandoz, Novo-Nordisk, Pfizer, Roche, Samsung, Sanofi and UCB. DA has provided expert advice to AbbVie, Astra-Zeneca, BMS, Celgene, Janssen, Lilly, Novo-Nordisk, Pfizer, Roche, and UCB. GB has provided expert advice to AbbVie, BMS, MSD/Merck, Novartis/Sandoz, Pfizer, Roche and UCB. VB has unrestricted grants or consulting agreements with Abbvie, Amgen, BMS, Roche, Medexus, Pfizer, Crescendo, UCB, Janssen, Regeneron. MD has received honorarium fees for participation at symposia and/or advisory boards organised by PFIZER, ABBVIE, UCB, MERCK, NOVARTIS, LILLY. His department has received research grants to conduct studies from PFIZER, ABBVIE, UCB, MERCK, NOVARTIS, LILLY. PE has received consulting fees from Abbvie, Bristol-Meyers Squibb, Merck, Pfizer, Roche, Lilly, Novartis and grant/research support from Abbvie, Merck, Pfizer, Roche. BH has received speaker fees from Abbvie, Amgen, BMS, Janssen, Pfizer, Roche and UCB but none in relation with this work. JG-R has received speaker fees from AbbVie, BMS, Celgene, Glaxo, Janssen, MSD, Pfizer, Roche, and UCB, and provided expert advice to AbbVie, BMS, Janssen, Pfizer, Roche, Sanofi and UCB. TKK has provided expert advice to AbbVie, BMS, Celgene, Celltrion, Eli Lilly, Hospira, Merck Serono, MSD, Novartis, Orion Pharma, Pfizer, Roche, UCB. PN received research grants for clinical trials and honoraria for advice and lectures on behalf of all pharma making targeted biological therapies. VN-C has received speaker fees from AbbVie, BMS and MSD, none of them relates to this work. RvV received research support and grants from AbbVie, BMS, GSK, Pfizer, Roche, UCB and consultancy honoraria from AbbVie, Biotest, BMS, Crescendo, GSK, Janssen, Lilly, Merck, Pfizer, Roche, UCB, Vertex. DvdH has received consulting fees from AbbVie, Amgen, AstraZeneca, Augurex, BMS, Boehringer Ingelheim, Celgene, Centocor, Chugai, Covagen, Daiichi, Eli-Lilly, Galapagos, GSK, Janssen Biologics, Merck, Novartis, Novo-Nordisk, Otsuka, Pfizer, Roche, Sanofi-Aventis, UCB, Vertex and is Director of Imaging Rheumatology bv. TAS has received speaker fees from UCB, AbbVie and MSD, none of them relates to this work.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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