Objectives To review the evidence for the efficacy and safety of biological agents in patients with rheumatoid arthritis (RA) to provide data to develop treatment recommendations by the European League Against Rheumatism (EULAR) Task Force.
Methods Medline, Embase and Cochrane databases were searched for relevant articles on infliximab (IFX), etanercept (ETN), adalimumab (ADA), certolizumab-pegol (CZP), golimumab (GLM), anakinra (ANA), abatacept (ABT), rituximab (RTX) and tocilizumab (TCZ) published between 1962 and February 2009; published abstracts from the 2007–2008 American College of Rheumatology (ACR) and EULAR conference were obtained.
Results 87 articles and 40 abstracts were identified. In methotrexate (MTX) naïve patients, biological therapy with IFX, ETN, ADA, GLM or ABT has been shown to improve clinical outcomes (level of evidence 1B). In MTX/other synthetic disease-modifying antirheumatic drug (DMARD) failures all nine biological agents confer benefit (1B), with lower efficacy noted for ANA. RTX, ABT, TCZ and GLM demonstrate efficacy in tumour necrosis factor inhibitor (TNFi) failures (1B). Less evidence exists for switching between IFX, ETN and ADA (3B). Biological and MTX combination therapy is more efficacious than a biological agent alone (1B). A safety review shows no increased malignancy risk compared with conventional DMARDs (3B). TNFi are generally associated with an increased risk of serious bacterial infection, particularly within the first 6 months of treatment initiation; increased tuberculosis (TB) rates with TNFi are highest with the monoclonal antibodies (3B).
Conclusions There is good evidence for the efficacy of biological agents in patients with RA. Safety data confirm an increased risk of bacterial infection and TB with TNFi compared with conventional DMARDs.
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Biological disease-modifying antirheumatic drugs (DMARDs) for the treatment of rheumatoid arthritis (RA) have led to remarkable patient benefits. Initial development of cytokine-blocking treatments, tumour necrosis factor inhibitor (TNFi) agents and an interleukin 1 (IL-1) receptor antagonist, has been followed by drugs targeting alternative molecules and pathways, including B-cell depletion and T-cell costimulation agents. More recently, drugs targeting the IL-6 receptor and another two TNFi have been approved in the USA or Europe, or both.
The aim of this systematic literature review (SLR) was to assess the efficacy and safety of these biological DMARDs to provide data to inform a European League Against Rheumatism (EULAR) Task Force charged with developing EULAR recommendations for the management of RA with DMARDs.1
The scope of the literature search was outlined by the EULAR Task Force. A subgroup of this committee (see author list) focused on the role of biological DMARDs in the treatment of RA.
A systematic literature search was performed from 1962 to February 2009 using Medline, Embase and Cochrane databases. Studies evaluating nine biological DMARDs: infliximab (IFX), etanercept (ETN), adalimumab (ADA), certolizumab-pegol (CZP), golimumab (GLM), anakinra (ANA), abatacept (ABT), rituximab (RTX) and tocilizumab (TCZ) were included. Abstracts were also obtained from the 2007–8 American College of Rheumatology (ACR) and EULAR conferences. Where full papers of these abstracts were published online during this period, the latter were obtained and used for data extraction. Details of the search terms and search strategy can be found in the online supplementary material.
Study eligibility criteria
Existing meta-analyses and SLRs were obtained. Where research questions were not covered by systematic reviews, original studies were found.
The criteria for study selection for efficacy analysis were (1) double-blind randomised controlled trials (RCTs); (2) patients with RA; (3) studies evaluating one of the nine biological DMARDs mentioned above; (4) trials of ≥6 months' duration; (5) studies with ≥50 patients; (6) publications in English.
Safety aspects were evaluated using information from large cohorts with long-term follow-up data rather than those from RCTs. Criteria used for study selection to evaluate toxicity were (1) registries and observational studies; (2) inclusion of a control group; (3) report of incidence of events in the context of population-based expected incidences.
Data were extracted and checked independently by two of the authors (JLN and MHB). Discrepancies were resolved by discussion.
For efficacy analysis, studies were grouped according to the following patient categories consistent with current clinical practice and trial design: (1) no prior DMARD use (DMARD naïve); (2) no prior MTX use (MTX naïve); (3) inadequate response to MTX (MTX-IR); (4) incomplete response to any synthetic DMARD which may not necessarily include MTX (mixed DMARD-IR); (5) TNFi failure (TNF-IR).
Studies included and details of efficacy outcome measures extracted can be found in the online supplementary material.
Efficacy data were analysed using Review Manager (RevMan version 5.0, Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2008) software and expressed as relative risks (RRs) or standardised mean differences (SMDs). While these data were obtained and are depicted in the figures for each individual drug, for the majority of biological agents and most of the patient categories there were no major differences between the RR or SMD. Results of individual RCTs were therefore also pooled using a Dersimonian and Laird random-effects model; where appropriate, only these group results are mentioned in the ‘Results’ section and readers are referred to the figures for the results obtained for individual biological agents. The number needed to treat (NNT) was also calculated from the pooled results, which represent the number of patients who need to be treated with a drug to gain one additional positive outcome.2 Statistical heterogeneity was assessed using the I2 statistic. Toxicity data were not subject to formal statistical analysis.
Levels of evidence were assigned according to the Oxford Centre for Evidence-based Medicine levels of evidence (http://www.cebm.net/index.aspx?o=1025, accessed 29 March 2010).
Of 11 458 published articles that were screened, 87 articles and 40 abstracts met inclusion criteria.
The efficacy and safety data are summarised by addressing clinical questions posed by the task force. Efficacy outcomes included in the article relate to signs and symptoms, with figures for the ACR20 responses shown by way of example. Efficacy data for radiographic outcomes and physical function (Health Assessment Questionnaire (HAQ)) will be mentioned—details on these, other clinical outcomes and quality of life measures (Physical Component Score and Mental Component Score of the Short Form-36); fatigue (FACIT score) can be found in the online supplementary material.
(1.1) In patients who have received no prior DMARDs (DMARD naïve), what is the evidence for the efficacy of biological DMARD therapy?
There were no studies fulfilling inclusion criteria for analysis in this group. Although one RCT showed benefit using IFX and MTX versus MTX alone, fewer than 50 patients were studied.3 A larger open labelled strategy trial4 also assessed the use of biological DMARDs in DMARD-naïve patients—and is addressed in a SLR on the strategic approach to the management of RA with DMARDs.4a (ref – Rachel's SLR). Several studies in the MTX-naïve group however include a large proportion of DMARD-naïve patients and will be discussed here.
(1.2A) In patients who have received no prior MTX (MTX naïve), what is the evidence for the efficacy of biological DMARD+MTX combination therapy?
RCTs of five biological DMARDs (ABT, ADA, ETN, GLM and IFX) in MTX-naïve patients were included. Six-month ACR response from one trial on GLM,5 showed superior efficacy when starting treatment with a biological DMARD+MTX versus MTX alone with RR for the ACR20 and 50 responses of 1.25 (95% CI 1.04 to 1.49) and 1.31 (95% CI 0.99 to 1.72), respectively (figure 1A). The pooled RR for the 12-month ACR20 response from four studies on ADA,6 ,7 ETN8 and IFX9 was 1.24 (95% CI 1.15 to 1.34) (I2=18%) with a NNT of 7.1 (95% CI 5.0 to 11.1). The overall RR for the 12-month ACR50 and 70 responses for five studies on ABT,10 ADA,6 ,7 ETN8 ,11 and IFX9 were 1.43 (95% CI 1.30 to 1.56) (I2=0%) and 1.63 (95% CI 1.45 to 1.83) (I2=0%) with NNT of 7.1 (95% CI 4.8 to 12.5) and NNT of 6.3 (95% CI 5.0 to 7.7), respectively.
Disease Activity Score 28 (DAS28) remission rates were also higher with the use of biological DMARD+MTX therapy in this group with a pooled RR for DAS28 remission at 12 months of 1.78 (95% CI 1.57 to 2.02) (I2=0%) and a NNT of 5.9 (95% CI 4.5 to 8.3).
Radiographic data at 12 months showed less progression for ABT,10 ADA,7 ETN8 and IFX9 in combination with MTX than for MTX monotherapy. Rates of radiographic non-progression were higher for ABT,10 ADA7 and ETN8 combination therapy.
(1.2B) In patients who have received no prior MTX (MTX naïve), what is the evidence for the efficacy of biological DMARD monotherapy?
Six-month ACR responses from one trial on GLM5 showed similar efficacy when starting treatment with a biological DMARD versus MTX alone with the RR for the ACR20 and 50 responses 1.04 (95% CI 0.84 to 1.3) and 1.1 (95% CI 0.8 to 1.55), respectively. Twelve-month ACR20 responses from two studies on ADA7 and ETN11 showed a RR=0.87 (95% CI 0.74 to 1.03) and 1.22 (95% CI 1.06 to 1.4), respectively; overall RR=0.98 (95% CI 0.76 to 1.26) (figure 1B). The RR for the ACR50 and 70 responses from one study on ADA7 were 0.89 (95% CI 0.78 to 1.08) and 0.92 (95% CI 0.7 to 1.22).
Remission rates were also similar for biological DMARD monotherapy compared with MTX in this group, with a RR for DAS28 remission for one study on GLM5 at 6 months of 0.89 (95% CI 0.62 to 1.29) and 1.09 (95% CI 0.79 to 1.51) for another on ADA at 12 months.7
Change in the modified Sharp score was lower for ADA7 than for MTX monotherapy at 12 months with greater numbers achieving radiographic non-progression. From one RCT12 the numbers of patients achieving non-progression were similar for ETN and MTX.
HAQ scores at 12 months were similar for ADA and MTX monotherapy.7
(1.3A) In patients who have had inadequate response to MTX (MTX-IR), what is the evidence for the efficacy of biological DMARD+MTX combination therapy?
Efficacy data exist for all nine biological DMARDs studied in the MTX-IR group (figure 2A). Six-month ACR responses pooled from 16 trials,13,–,28 comparing a biological DMARD with placebo in combination with background MTX showed overall RR for the ACR20, 50 and 70 at 6 months of 2.16 (95% CI 1.83 to 2.55) (I2=77%), 3.20 (95% CI 2.6 to 3.95) (I2=54%) and 4.82 (95% CI 2.43 to 9.57) (I2=33%), respectively. The corresponding NNT were 3.2 (95% CI 2.4 to 4.0), 4.2 (95% CI 3.6 to 4.8) and 7.7 (95% CI 6.7 to 10.0). The RR for the 12-month ACR20, 50 and 70 responses pooled from seven studies on ABT,15 ,29 ADA,17 CZP,21 IFX,30 RTX26 and TCZ31 were 2.47 (95% CI 1.99 to 3.07) (I2=72%), 3.64 (95% CI 2.74 to 4.83) (I2=52%) and 4.79 (95% CI 3.65 to 6.29) (I2=0%), respectively. The corresponding NNT were 3.0 (95% CI 2.6 to 3.6), 3.7 (95% CI 3.2 to 4.2) and 5.9 (95% CI 5.0 to 6.7).
The overall DAS28 remission rate at 6 months for four studies on ABT,29 CZP,22 GLM24 and RTX27 was 3.54 (95% CI 2.28 to 5.47) (I2=0%) with a NNT of 9.1 (95% CI 6.3 to 16.7). At 12 months DAS28 remission was also superior with biological DMARD use in three studies of ABT15 ,29 and TCZ.31
(1.3B) In patients who have had inadequate response to MTX (MTX-IR), what is the evidence for the efficacy of biological DMARD monotherapy?
Pooled RR from two trials on GLM24 and RTX26 for 6-month ACR20, 50 and 70 responses were 1.43 (95% CI 1.06 to 1.93) (I2=10%), 1.71 (95% CI 1.02 to 2.88) (I2=12%) and 2.32 (95% CI 1.09 to 4.54) (I2=0%), respectively, when starting treatment with a biological DMARD monotherapy versus continuing MTX (figure 2B). The corresponding NNT were 6.7 (95% CI 2.9 to not estimable), 9.1 (95% CI 4.2 to not estimable) and 14.3 (95% CI 7.7 to not estimable). RR for the 12-month ACR20, 50 and 70 responses from the study on RTX26 showed a RR=1.63 (95% CI 0.76 to 3.49), 2.5 (95% CI 0.51 to 12.14) and 7 (95% C1 0.37 to 131.28). Numbers for the study, however, were small and CI wide. ACR20, 50 and 70 responses at 24 months were 0.60 (95% CI 0.15 to 2.34), 0.75 (95% CI 0.18 to 3.14) and 0.33 (95% CI 0.04 to 3.07), respectively, showing similar efficacy between biological and synthetic DMARD monotherapy.
(1.4A) In patients who have had inadequate response to a synthetic DMARD, not necessarily MTX (mixed DMARD-IR), what is the evidence for the efficacy of biological+synthetic DMARD combination therapy?
Six-month ACR20, 50 and 70 responses from four trials on ADA,33 ETN,34 RTX35 and TCZ36 assessed the use of a biological DMARD compared with placebo in combination with background synthetic DMARD therapy (figure 3A). Pooled RR for ACR20, 50 and 70 responses were 2.06 (95% CI 1.52 to 2.78) (I2=82%), 3.19 (95% CI 2.38 to 4.27) (I2=43%) and 5.44 (95% CI 3.74 to 7.91) (I2=0%), respectively. The corresponding NNT were 3.2 (95% CI 0.2 to 5.3), 4.0 (95% CI 3.0 to 5.9) and 6.3 (95% CI 5.0 to 8.3). Twelve-month RR for ACR20, 50 and 70 responses from one study on ETN37 were 1.13 (95% CI 1.03 to 1.24), 1.60 (95% CI 1.35 to 1.90) and 2.27 (95% CI 1.67 to 3.09), respectively. DAS remission at 6 months from the same study showed a RR=2.2 (95% CI 1.50 to 3.22) for combination therapy with ETN versus MTX alone. The RR for DAS and DAS28 remission at 12 months were 2.65 (95% CI 1.85 to 3.81) and 2.23 (95% CI 1.65 to 3.06), respectively.
Radiographic progression at 12 months was lower and numbers achieving non-progression higher for combination therapy with ETN+MTX versus MTX alone.37
(1.4B) In patients who have had inadequate response to a synthetic DMARD, not necessarily MTX (mixed DMARD-IR), what is the evidence for the efficacy of biological DMARD monotherapy?
Six-month ACR20 responses from six trials on ADA,38 ANA,39 CZP40,ETN34 ,41 and TCZ42 showed a pooled RR=2.50 (95% CI 1.56 to 4.02) (I2=90%) and NNT of 3.2 (95% CI 2.4 to 5.3) comparing treatment with a biological DMARD with control; in three studies38 ,39 ,41 the control group received placebo alone with no synthetic DMARD (figure 3B). The overall RR for the 6-month ACR50 and 70 responses for ADA,38 CZP,40 ETN34 ,41 and TCZ42 were 3.51 (95% CI 1.57 to 7.84) (I2=88%) and 5.50 (95% CI 0.9 to 33.56) (I2=0%), respectively with corresponding NNT of 4.3 (95% CI 3.2 to 7.1) and 7.1 (95% CI 5.3 to 12.5). Twelve-month ACR20, 50 and 70 responses from 1 study on ETN37 showed a RR=1.01 (95% CI 0.91 to 1.12), 1.12 (95% CI 0.91 to 1.37) and 1.28 (95% CI 0.9 to 1.02).
The RR for DAS28 remission for one study on TCZ42 as monotherapy compared with MTX at 6 months was 2.81 (95% CI 1.92 to 4.12). At 12 months, the RR for DAS28 remission in 1 study, ETN44 was 1.02 (95% CI 0.68 to 1.53).
(1.5) In patients who have had inadequate response to a TNF inhibitor (TNF-IR), what is the evidence for the efficacy of combination therapy with an alternative biological DMARD+MTX?
In patients for whom ADA, ETN and IFX have failed, the search found no RCTs on switching between these three established TNFi. A literature review by Carmona et al47 documented 29 reports on switching from one TNFi to another in RA. Overall, the data indicated benefit of switching from a first TNFi to a second; with switching for secondary non-response likely to be more effective. A systematic review by Lopez-Olivo et al48 reported similar findings.
Several RCTs have evaluated non-TNF targeted biological DMARDs after TNFi failure, and most recently an alternative TNFi has also been assessed; ABT,49 GLM,39 RTX50 and TCZ51 have all shown efficacy. Overall RR for the ACR20, 50 and 70 responses at 6 months when comparing the addition of an alternative biological DMARD to an existing synthetic DMARD with continuing a synthetic DMARD alone were 2.78 (95% CI 2.28 to 3.38) (I2=10%), 5.00 (95% CI 3.45 to 7.24) (I2=0%) and 8.27 (95% CI 3.65 to 18.76) (I2=0%), respectively (figure 4). The corresponding NNTs were 3.4 (95% CI 2.4 to 4.2), 5.6 (95% CI 4.8 to 6.7) and 11.1 (95% CI 9.1 to 14.3). The RR for achieving low disease activity for ABT,49 RTX50 and TCZ51 at 6 months was 6.59 (95% CI 4.01 to 10.82) (I2=0%); RR for DAS28 remission for TCZ51 was 10.02 (95% CI 3.20 to 31.42).
Six-month radiographic progression was lower with RTX combination therapy than with control.50
(2) Is combination therapy with a biological agent plus MTX better than biological DMARD monotherapy?
Data from three studies on ADA,7 ETN37 and RTX26 showed pooled RR for 12-month ACR20, 50 and 70 responses of 1.31 (95% CI 1.05 to 1.64) (I2=81%), 1.49 (95% CI 1.32 to 1.68) (I2=4%) and 1.77 (95% CI 1.48 to 2.12) (I2=0%), respectively (figure 5). The corresponding NNT were 5.9 (95% CI 3.6 to 14.3), 4.8 (95% CI 3.7 to 6.7) and 6.3 (95% CI 4.2 to 14.3). Overall RR for DAS28 remission for two studies on ADA7 and ETN37 at 12 months was 1.98 (95% CI 1.62 to 2.42) (I2=0%) and the NNT was 5.0 (95% CI 3.8 to 6.7). These findings are further supported by long-term data on ETN54 and ADA55 showing higher DAS/DAS28 remission rates and less radiographic progression with initial biological and synthetic DMARD combination therapy than with monotherapy.54 One RCT on TCZ also showed benefit with combination with MTX compared with TCZ alone—however, as the study was less than 6 months' duration it did not fulfil inclusion criteria for formal analysis.56
Radiographic progression at 12 months was lower for combination therapy for ADA7 plus MTX versus ADA monotherapy and ETN plus MTX37 versus ETN alone. Improvements in HAQ was also greater with ADA7 and MTX combination therapy versus ADA alone.
(3) What are the safety concerns to consider when starting a biological DMARD?
Longer-term data evaluating the safety of biological DMARDs have become available with their increasing use. The majority of the evidence pertains to IFX, ETN and ADA.
A summary of the findings relating to specific safety aspects will be presented in this article. Further details with tables including reported standardised incidence ratios and RRs are available in the online supplementary material.
Six published papers and two abstracts from registries and retrospective studies regarding infection were reviewed (table 7, online supplementary section).
Several registries and databases have documented an increased risk of serious bacterial infections with the use of biological DMARDs compared with patients not treated with these drugs57 ,58; in particular, increased rates of pneumonia were seen, greatest within first 6 months of treatment initiation.57 ,58 HAQ, older age, comorbidity and past hospitalisation predicted subsequent hospitalisation for infection.58 Data published by Wolfe et al59 suggested a greater hospitalisation risk for pneumonia in patients with RA receiving prednisolone rather than with the use of TNFi and MTX.
UK registry data60 have shown increased rates of serious skin and soft tissue infections with TNFi, and when limiting analysis to the first 90 days after the start of biological agents, found significantly increased risks for all serious infections when compared with synthetic DMARDs.61 No difference in infection rates between ADA, ETN or IFX was reported. From French registry data62 an increase in the risk of Legionella has been reported in patients receiving TNFi compared with the general population.
Long-term, open-label studies with ETN showed no difference in rates of serious infections when compared with patients receiving MTX/placebo.63
Four published papers and three abstracts from registries and retrospective studies regarding TB were reviewed (table 8, online supplementary section).
Spanish,64 US,65 Swedish66 and Korean67 registry data have shown an increased incidence of tuberculosis (TB) with TNFi compared with the general population and with patients with RA not receiving TNFi. Incidence rates were also reported to be higher for IFX and ADA compared with ETN in several cohorts68,–,70 TB risks decreased with the introduction of screening measures and prophylaxis for those with latent TB infection before the start of TNFi therapy.68
Five published papers and seven abstracts on malignancy were reviewed (table 9, online supplementary section).
Data from US, Canadian, Swedish, German, Spanish and UK registries71,–,79 and long-term, open-label extension data on ADA80 and ETN63 have shown no overall increased risk of malignancy. Although an increased occurrence of non-melanoma skin cancer, central nervous system tumours and colorectal cancer was suggested in the Swedish cohort, numbers were small and not found to be statistically significant.73
Within the group of non-TNFi biological DMARDs, the risk of malignancy for patients receiving ABT has been reported to be no greater than for the general population or patients with RA receiving non-biological DMARDs.81 (Details on lymphoma can be found on the online supplementary section including table 14.)
Interstitial lung disease
One published paper and one abstract from registries on interstitial lung disease (ILD) were reviewed (table 11, online supplementary section).
Analysis of data by Wolfe et al82 showed no increase in the risk of development of new ILD on treatment; HR were 0.7 (0.4; 1.3) for IFX and 0.9 (0.4; 1.7) for ETN. From UK registry data83 baseline RA-ILD, irrespective of TNFi therapy, was a predictor of increased all-cause mortality. In patients with baseline RA-ILD, TNFi were associated with a worse all-cause and RA-ILD-specific mortality; standardised mortality ratio 2.93 (95% CI 2.14 to 3.99) compared with those receiving TNFi without ILD at baseline.
Optimal use of complex and effective biological agents warrants a systematic review of the literature. This analysis provided data to inform treatment recommendations for the EULAR Task Force. In essence, it demonstrates the benefits of biological DMARDs, confirming a favourable efficacy/safety profile and highlights areas in need of further evaluation.
In particular, it shows that few studies have formally evaluated the use of biological DMARDs in DMARD-naïve patients, with one pilot study showing benefit with combination IFX therapy.3 Further efficacy data, however, may be extrapolated from studies in the MTX-naïve group: MTX is often the first preferred synthetic DMARD and, where reported, between 50%11 and 97%10 of patients in these RCTs were also DMARD naïve. An Oxford based level of evidence 2B has therefore been assigned for efficacy of biological DMARDs in this group.
In contrast, biological DMARDs have been more systematically evaluated in patients who are either (1) MTX naïve; (2) MTX failures and (3) other synthetic DMARD failures, with RCT data providing evidence for each of these groups (Oxford level of evidence 1B). Several SLRs and meta-analyses provide further supportive evidence (level 1A) for IFX,84 ,85 ETN86 and ADA87 individually and as a group of established TNFi,88,–,96 for ANA,89 ,93,–,96 ABT97,–,99 and TCZ100 for the use of biological DMARDs in patients with RA. Less efficacy has been noted for ANA in several meta-analyses,89 ,93,–,96 than for the other biological DMARDs.
Although the RR for the use of biological DMARDs is generally higher in the groups for whom synthetic DMARDs have failed compared with those who were MTX naïve, different treatment comparisons are relevant; the former group compares the use of a new treatment—the biological DMARD—with an existing failed synthetic DMARD (therefore essentially, a placebo-controlled trial), whereas the latter group compares the start of two new treatment regimens—a biological DMARD in the treatment arm and a synthetic DMARD (usually MTX) in the comparator group.
Response to a TNFi is not universal30; there may be benefit from switching to an alternative TNFi, although the literature on this comprises smaller, non-controlled studies (level of evidence 3B). The newer biological DMARDs (ABT, RTX and TCZ) and, most recently, the newer TNFi GLM, have demonstrated efficacy compared with placebo in this TNFi-resistant group (level of evidence 1B). The decision on which agent to switch to after initial TNFi failure still remains unclear with no head-to-head comparisons undertaken to date.
Use of the biological DMARDs has been evaluated both as monotherapy and in combination with concomitant synthetic DMARDs. Review of the literature confirms the efficacy of combination therapy. In patients who may not tolerate MTX or another synthetic DMARD, however, biological DMARD monotherapy—with the exceptions of ABT (for which no RCT data were available) and IFX—has demonstrated efficacy. It also substantiates the superiority of combination treatment over biological DMARD monotherapy with particular evidence for the TNFi7 and RTX26 (level of evidence 1B), supporting this approach wherever possible. Although a 20-week study56 has demonstrated efficacy of both TCZ monotherapy and combination therapy, further comparative studies assessing synergy of TCZ with a synthetic DMARD compared with TCZ monotherapy have not been undertaken to date.
The use of biological DMARDs has raised new problems and concerns, including those of safety. This review confirms an overall increased risk of serious bacterial infections with biological DMARDs compared with non-biological treated patients, appearing greatest within the first 6 months of treatment initiation. Increased TB risk with TNFi is higher for patients treated with monoclonal antibodies (level of evidence 3B). Minimal data exist on TB risk in patients treated with non-TNF biological therapies but to date this risk seems to be limited. The concerns of the increased risk of malignancy have not been borne out from registries or long-term follow-up of patients receiving biological DMARDs—a similar pattern of malignancy to those not taking biological DMARDs has been seen (level of evidence 3B). The risk of solid cancers including skin cancer is largely similar to the risk for other patients with RA.73,–,76
We acknowledge that there are several limitations to this literature review. To evaluate the efficacy of all the current biological DMARDs, data on outcomes were extracted and results pooled. Studies were grouped and statistical methods applied to minimise heterogeneity. Trials, however, differed to various degrees in their patient selection, study design, inclusion criteria and treatment regimens. Accordingly, the pooled risk estimates across studies should be interpreted with caution and direct head-to-head comparisons between the biological DMARDs cannot be made. Nevertheless, it is clear that there is good evidence for the overall benefit of biological DMARDs in RA.
In summary, review of the literature confirms the efficacy of biological DMARDs in the treatment of RA. Continued vigilance and recording of future safety signals is important as well as the collection of safety data on the more recently introduced non-TNF biological DMARDs. Future studies should provide additional guidance for the use of biological DMARDs in early RA as well as the management of those for whom TNFi fail.
The authors would like to thank Liz Neilly, University of Leeds Library Health Faculty Team librarian for her advice and help with the literature search.
Provenance and peer review Not commissioned; externally peer reviewed.
Competing interests None.
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