Objectives To identify factors that predict response to belimumab treatment in the phase 3 BLISS trials of autoantibody-positive systemic lupus erythematosus (SLE) and further analyse clinical efficacy in various patient subsets.
Methods The BLISS trials compared belimumab 1 and 10 mg/kg versus placebo, all plus standard SLE therapy, over 52 or 76 weeks. Pooled subgroup analyses of week 52 SLE responder index rates (the primary endpoint in both trials) were performed based on demographic characteristics and baseline disease activity indicators. Pooled multivariate analysis was performed to determine predictors of response and treatment effect.
Results Pooled univariate and multivariate analyses (N=1684) identified baseline factors associated with an increased benefit of belimumab versus placebo. These factors included the Safety Of Estrogens In Lupus Erythematosus National Assessment–Systemic Lupus Erythematosus Disease Activity Index (SELENA–SLEDAI) ≥10, low complement, anti-dsDNA positivity and corticosteroid use. Efficacy outcomes were assessed in the low complement/anti-dsDNA-positive and SELENA–SLEDAI ≥10 subgroups. Week 52 SLE Responder Index rates in the low complement/anti-dsDNA-positive subgroup were 31.7%, 41.5% (p=0.002) and 51.5% (p<0.001) with placebo and belimumab 1 mg/kg and 10 mg/kg, respectively; corresponding rates in the SELENA–SLEDAI ≥10 subgroup were 44.3%, 58.0% (p<0.001) and 63.2% (p<0.001). Further analysis of secondary endpoints in the low complement/anti-dsDNA-positive subgroup showed that compared with placebo, belimumab produced greater benefits regarding severe flares, corticosteroid use and health-related quality of life.
Conclusions These findings suggest that belimumab has greater therapeutic benefit than standard therapy alone in patients with higher disease activity, anti-dsDNA positivity, low complement or corticosteroid treatment at baseline.
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Systemic lupus erythematosus (SLE) is a chronic, heterogeneous autoimmune disease associated with considerable morbidity, increased mortality and poor health-related quality of life (HRQoL).1 ,2 Anti-double-stranded DNA antibodies and low complement (C) levels are associated with more severe disease;3,–,8 the European League Against Rheumatism (EULAR) Task Force recommends that serum C3/C4 and anti-dsDNA be considered for monitoring patients with SLE because these markers may provide prognostic information on general outcome and the involvement of major organs, and have diagnostic utility in assessing SLE activity and flares.9
In the phase 3 BLISS trials over 52 (BLISS-52) or 76 (BLISS-76) weeks, treatment with belimumab—a soluble B lymphocyte stimulator-specific inhibitor—combined with current standard SLE therapy had superior responder rates (as assessed by the SLE Responder Index; SRI) compared with standard therapy alone in patients with autoantibody-positive SLE.10 ,11 The designs of these two trials were based on the results of a phase 2 study of belimumab, which showed evidence of efficacy in patients with autoantibody-positive SLE.12 Belimumab is currently indicated in the EU as ‘add-on therapy in adult patients with active, autoantibody-positive SLE with a high degree of disease activity (eg, low complement and anti-dsDNA positivity) despite standard therapy’. The present report describes analyses of baseline demographic and disease characteristics that were performed to identify factors that predicted response to belimumab treatment in the two BLISS studies. In addition, key efficacy findings are explored in the subgroup of patients who had low complement levels and were anti-dsDNA positive at baseline, a characteristic that was associated with both a high degree of disease activity at baseline and subsequent response to belimumab therapy.
BLISS-52 (N=865; ClinicalTrials.gov NCT00424476) and BLISS-76 (N=819; ClinicalTrials.gov NCT 00410384) were randomised, double-blind, placebo controlled, multicentre trials comparing belimumab 1 and 10 mg/kg plus standard therapy with placebo plus standard therapy in patients with active SLE. The trials had similar clinical designs that have been described in detail previously.10 ,11 All patients had a Safety Of Estrogens In Lupus Erythematosus National Assessment–Systemic Lupus Erythematosus Disease Activity Index (SELENA–SLEDAI) score of 6 or greater at screening, were autoantibody positive (antinuclear antibody ≥1:80 or anti-dsDNA ≥30 IU/ml), and had received stable standard therapy for 30 days or more before the study. Patients received standard therapy plus belimumab or placebo by intravenous infusion on days 0, 14 and 28, and then every 28 days to week 48 (BLISS-52) or 72 (BLISS-76). Patients had progressive restrictions on concurrent immunosuppressive and antimalarial medications and corticosteroids during the trials.
The primary endpoint in both trials was the SRI rate at week 52. The SRI is a composite responder index that includes one measure of disease activity improvement (≥4-point decrease in SELENA–SLEDAI score) and two measures to ensure that the improvement in disease activity is not offset by a worsening of disease in organ systems (ie, no new British Isles Lupus Assessment Group A and no more than one new B scores) or by a decline in overall health status (ie, <0.3-point increase from baseline in Physician's Global Assessment score).10,–,13 The SELENA–SLEDAI score reduction drives the SRI response as a score reduction generally requires normalisation of laboratory parameters or resolution, rather than only partial improvement, of a clinical manifestation. A 4-point reduction is, therefore, considered clinically meaningful.14 In addition, dose increases of concomitant medications, which would suggest disease worsening, were not allowed beyond protocol-specified limitations, thus further enhancing the clinical relevance of an SRI response in these studies. Patients who withdrew or required changes in background drugs for SLE other than those permitted by protocol were judged to be treatment failures.
Subgroup analyses of SRI rates at week 52 (also referred to as univariate analyses) were performed based on demographic characteristics (eg, age, sex, race, ethnicity, region) and baseline disease activity indicators (eg, SELENA–SLEDAI score, serological activity, corticosteroid and immunosuppressant use). Data from the phase 3 trials were pooled to allow for maximum sample size within subgroups. Analyses of categorical variables, including the primary endpoint, were performed using a logistic-regression model. Analysis of covariance was used for continuous variables, such as the change from baseline endpoints. Analyses of time to flares were performed using Cox regression. These analyses were adjusted for baseline stratification factors and were not subjected to any adjustments for multiple testing.
The analyses were performed in combined data from the two phase 3 studies to achieve a more stable estimate of belimumab's global treatment effect, as the studies were essentially identical in design and the effects of belimumab on the endpoints of interest were similar between the studies. In addition to the individual subgroup analyses, a multivariate analysis was performed based on pooled data to determine predictors of response and the effect of treatment adjusted for predictive factors. A main-effect logistic-regression model was developed using a stepwise forward selection process to identify baseline factors predictive of SRI response at week 52 irrespective of the treatment received. An interaction logistic-regression model, in which factors meeting a 0.05 significance level from the main-effect model were retained, was then used to determine how response to belimumab versus placebo varied across different categories within a baseline characteristic (ie, independent treatment-effect modifiers).
Multivariate analyses identified high disease activity—patients with both low complement levels and anti-dsDNA positivity, and those with SELENA–SLEDAI scores of 10 or greater—as being predictive of a response to belimumab treatment. Patients with low complement/anti-dsDNA positivity are immunologically active, at high risk of severe flares,6 and easily identifiable by laboratory studies readily available in the clinical setting. Furthermore, the presence of high disease activity in the low complement/anti-dsDNA-positive subgroup in the trials was supported by the high frequency of corticosteroid use (91.4%) (table 1). With regard to the SELENA–SLEDAI ≥10 subgroup, although SELENA–SLEDAI is a validated measure of disease activity, this assessment is not commonly used by physicians outside of the clinical trial setting. Results in the present report on the SELENA–SLEDAI ≥10 subgroup have, therefore, been limited to the primary efficacy endpoint.
Baseline characteristics of the pooled BLISS-52 and BLISS-76 population are shown in table 1. High disease activity was common, as indicated by SELENA–SLEDAI scores of 10 or greater in 52% of patients, corticosteroid use in 86% and anti-dsDNA positivity in 69%. In addition, 45% of patients had low C3 levels and 56% had low C4 levels. In the pooled analysis of BLISS-52 and BLISS-76 (N=1684), SRI rates at week 52 were 38.8% with placebo and 46.2% with belimumab 1 mg/kg and 50.6% with 10 mg/kg. Between-treatment differences for belimumab versus placebo were 7.4% (OR 1.4, 95% CI 1.1 to 1.8, p=0.006) with 1 mg/kg and 11.8% (OR 1.7, 95% CI 1.3 to 2.2, p<0.001) with 10 mg/kg.
Univariate subgroup analysis
Patients with higher baseline disease activity—denoted by a higher SELENA–SLEDAI score, low complement levels, detectable anti-dsDNA, or treatment with corticosteroids—had a greater response to belimumab versus standard therapy alone than did those without these characteristics (figure 1). The greater benefit of belimumab treatment in patients with high disease activity was more marked with 10 mg/kg than with 1 mg/kg, suggesting a dose-related effect—eg, the week-52 SRI rate was higher with 10 mg/kg versus 1 mg/kg in those who had a SELENA–SLEDAI score of 10 or greater (63.2% vs 58.0%), were positive for anti-dsDNA antibodies (51.1% vs 45.4%), or had low C3 (50.8% vs 39.9%) or C4 (50.8% vs 41.7%) levels. Treatment by subgroup interactions (p<0.10) were observed for SELENA–SLEDAI (score ≥10 vs ≤9) with both belimumab 1 and 10 mg/kg, and for anti-dsDNA antibodies (≥ vs <30 IU/ml), C3 (low vs normal/high level), C4 (low vs normal/high) and corticosteroid use (yes vs no) with 10 mg/kg. No significant interaction was observed for corticosteroid dose (> vs ≤7.5 mg/day), antimalarial use (yes vs no) or immunosuppressive use (yes vs no). For demographic variables, the only significant interaction observed was for region with belimumab 10 mg/kg, an interaction driven by better SRI rates in the western Europe/Australia/Israel regions (24.3% with placebo, and 36.8% and 51.9% with belimumab 1 and 10 mg/kg, respectively; p<0.05; n=217) than in all other regions.
Analysis of factors associated with response irrespective of treatment group, while controlling for study and each of the significant predictors of response in the model, showed that belimumab significantly increased the odds of an SRI response at week 52 compared with standard therapy alone. A more marked effect was observed with belimumab 10 mg/kg (adjusted OR 1.5, 95% CI 1.2 to 1.9, p=0.002 with 1 mg/kg; adjusted OR 1.8, 95% CI 1.4 to 2.4, p<0.001 with 10 mg/kg). In addition, a multivariate analysis was performed to determine whether the response with belimumab versus standard therapy alone varied across different subgroups. This analysis generally supported the results of the individual subgroup analysis, again indicating that patients with greater baseline disease activity—as reflected by a SELENA–SLEDAI score of 10 or greater, corticosteroid use and low complement levels—benefited most from belimumab treatment (data not shown).
Outcomes in high disease activity subgroups
As the multivariate analyses identified indicators of high disease activity—either clinically or serologically, or both—as predictors of a response to belimumab treatment, efficacy outcomes were then assessed in the pooled BLISS trials in the two high disease activity subgroups noted previously: patients with both low complement levels and anti-dsDNA positivity, and patients with SELENA–SLEDAI scores of 10 or greater. Of the 1684 autoantibody-positive patients in the pooled dataset, 876 (52.0%) had low C3 or C4 levels and were anti-dsDNA positive, and 877 (52.1%) had SELENA–SLEDAI scores of 10 or greater. The two subgroups exhibited considerable overlap, with 574 patients (65.5%) in the low complement/anti-dsDNA-positive group having a SELENA–SLEDAI score of 10 or greater at baseline.
Primary efficacy endpoint in the low complement/anti-dsDNA-positive and SELENA–SLEDAI ≥10 subgroups
The SRI rates at week 52 in the low complement/anti-dsDNA-positive subgroup were 31.7% with standard therapy alone, 41.5% with belimumab 1 mg/kg (p=0.002) and 51.5% with belimumab 10 mg/kg (p<0.001; table 2, figure 2A). Corresponding rates in the SELENA–SLEDAI ≥10 subgroup were 44.3%, 58.0% (p<0.001) and 63.2% (p<0.001). Significant differences in SRI rates were observed between belimumab 10 mg/kg and placebo beginning at week 8 in both subgroups (except for week 20 in the SELENA–SLEDAI ≥10 subgroup, p=0.07), and between belimumab 1 mg/kg and placebo from week 28 in the low complement/anti-dsDNA-positive subgroup, and from week 36 in the SELENA–SLEDAI ≥10 subgroup (data not shown). To test the belimumab treatment effect in the low complement/anti-dsDNA-positive subgroup, a modified SRI analysis was performed excluding the complement and anti-dsDNA components from SELENA–SLEDAI scoring, as the 4-point reduction in the SELENA–SLEDAI score required for a SRI response can be achieved by normalisation of complement levels and anti-dsDNA antibodies. This analysis confirmed a treatment benefit with belimumab versus placebo at week 52 in the low complement/anti-dsDNA-positive subgroup (table 2, figure 2B).
To determine if responses in these subgroups persisted with longer treatment, outcomes by subgroup were assessed in the BLISS-76 trial, in which patients continued to receive belimumab or standard therapy alone to 76 weeks. In the low complement/anti-dsDNA-positive subgroup, SRI rates were higher with belimumab versus placebo, with significant differences observed with belimumab 10 mg/kg at weeks 52, 60, 68, 72 and 76 (figure 2C).
Secondary efficacy endpoints in the low complement/ anti-dsDNA-positive subgroup
Further analyses of corticosteroid use, flare occurrence and HRQoL secondary endpoints were performed in the low complement/anti-dsDNA-positive subgroup. Of patients receiving a prednisone dose greater than 7.5 mg/day at baseline, more receiving belimumab than standard therapy alone had dose reductions of 25% or greater to 7.5 mg/day or less during weeks 40–52 and any dose reductions to 7.5 mg/day or less at week 52 (table 2, figure 3A), and fewer patients receiving belimumab had dose increases (figure 3B). Belimumab treatment significantly reduced the risk of a first severe flare (figure 3C), and rates of both severe flares (per patient-year: placebo, 0.63; belimumab 1 mg/kg, 0.43 [p=0.015]; belimumab 10 mg/kg, 0.37 [p<0.001]) and any flares (placebo, 3.31; 1 mg/kg, 2.44 [p<0.001]; 10 mg/kg, 2.20 [p<0.001]). With regard to HRQoL measures, both belimumab doses were associated with significantly greater improvements in Functional Assessment Of Chronic Illness Therapy–Fatigue scale scores at week 52, with differences observed as early as week 8 (table 2, figure 3D), and in short form 36 health survey physical component summary scores (least-squares mean treatment difference vs placebo: belimumab 1 mg/kg, +1.38 [p=0.03]; belimumab 10 mg/kg, +1.56 [p=0.01]; table 2).
Safety in the low complement/anti-dsDNA-positive subgroup
In the low complement/anti-dsDNA-positive subgroup, the belimumab and placebo groups had similar rates of adverse events (AEs), AEs considered to be related to study treatment, severe AEs and AEs leading to dose interruption or discontinuation of study medication (table 3). Rates of serious AEs were somewhat higher with belimumab, but there was no excess of AEs within any individual system organ class. Furthermore, rates of serious infections were similar across treatment groups. The AE rates in the low complement/anti-dsDNA-positive subgroup were similar to those in the overall pooled population for the three treatment groups.
The BLISS-52 and BLISS-76 trials showed that belimumab plus standard SLE therapy resulted in significantly greater SRI rates than did placebo plus standard therapy at 52 weeks in antinuclear antibody-positive or anti-dsDNA-positive SLE patients.10 ,11 Univariate and multivariate analyses in the pooled population of the BLISS trials identified baseline factors associated with an increased benefit of belimumab treatment versus placebo. These factors consisted of SELENA–SLEDAI scores of 10 or greater, low complement levels, anti-dsDNA positivity and the requirement for corticosteroid treatment. Among these factors, SELENA–SLEDAI is a reliable index of SLE disease activity, although it is used primarily in clinical trials and in certain highly specialised centres. Although corticosteroid treatment is relatively subjective, dependent partly on physician experience and access to other treatments, it may be a sign of higher underlying disease activity. Complement and anti-dsDNA levels, however, are objective measures and routine laboratory tests that are widely available in clinical practice, and may be prognostic markers for major organ involvement. Monitoring of these serological markers is supported by EULAR recommendations for the management of SLE.9
In the multivariate analysis of SRI response, both belimumab doses plus standard therapy demonstrated a better treatment effect than standard therapy alone in all SELENA–SLEDAI score categories and corticosteroid dosing levels tested, and for patients with low C3 or C4 levels, with the 10 mg/kg dose appearing to provide greater benefit in all measures.
At baseline, 52% of the pooled BLISS trial population had low complement levels and were anti-dsDNA positive. The presence of high disease activity in this subgroup is supported by the observations that two-thirds of these patients had a SELENA–SLEDAI score of 10 or greater and nearly all required corticosteroid treatment at baseline. In addition, patients in this low complement/anti-dsDNA-positive subgroup were more difficult to treat with standard therapy alone as their SRI rate was 32% compared with 39% in the overall population and 44% in the SELENA–SLEDAI ≥10 subgroup. In this low complement/anti-dsDNA-positive subgroup, belimumab treatment was associated with significantly greater SRI rates at 52 weeks versus placebo, including when complement and anti-dsDNA changes were excluded from the calculation of the SELENA–SLEDAI score as a component of the SRI. For both these measures, the treatment differences for belimumab versus placebo in this subgroup were greater than those between belimumab and placebo in the total pooled BLISS population. In the BLISS-76 trial, SRI rates were numerically greater with belimumab 1 mg/kg and significantly greater with 10 mg/kg from weeks 52 to 76 in this subgroup, with the treatment differences also being greater than those in the total BLISS-76 population. Analysis of 52-week outcomes for BLISS trial secondary endpoints in this subgroup showed that belimumab treatment reduced the risk of a first severe flare, increased the proportion of patients with corticosteroid dose reductions, and decreased the proportion with corticosteroid dose increases, and improved HRQoL. In accordance with the phase 2 belimumab trial, these findings suggest that belimumab has a relatively greater benefit in patients with higher disease activity, or low complement levels or anti-dsDNA positivity, and are consistent with the mechanism of action of belimumab.12 ,15 ,16 Furthermore, the finding that these benefits were present when complement and anti-dsDNA changes were excluded from the SELENA–SLEDAI component of response demonstrates the benefits in clinical aspects and suggests that the benefits are not solely due to the resolution of serological activity.
The subgroup analysis comprises combined data from two separate clinical trials of patients from different international regions, and the retrospective nature of these analyses means the results need confirmation in a prospective study. As patients with severe active lupus nephritis or severe active central nervous system manifestations, as well as patients treated with other biological agents or intravenous cyclophosphamide, were excluded from the two trials, no conclusion can be drawn in these patients.
In summary, the subgroup data from the BLISS-52 and BLISS-76 clinical trials suggest that belimumab may be particularly effective in patients characterised by higher SLE disease activity at baseline, who are identified by anti-dsDNA positivity, hypocomplementaemia, or requiring treatment with corticosteroids. In these subgroups of patients, a range of clinical benefits with belimumab treatment was demonstrated, including improved disease activity, reduced risk of flares and an effect on steroid reduction. These findings may be of use to the practising clinician and may represent a first step towards identifying SLE disease characteristics in patients that can enhance the potential for a response to a given biological therapy.
Editorial support (writing assistance, assembling tables and figures, collating author comments, grammatical editing and referencing) was provided by Matt Stenger and Eleanore Gross of BioScience Communications, New York, NY, USA, and was funded by Human Genome Sciences, Inc, Rockville, Maryland, USA, and GlaxoSmithKline, Uxbridge, UK.
Correction notice This article has been corrected since it was published Online First. On page 2, in line 13, "no more than two new B scores)" was changed to "no more than one new B score)".
Funding This study was funded by Human Genome Sciences and GlaxoSmithKline.
Ethics approval Ethics approval was granted by the institutional review boards at every clinical study site.
Competing interests RFvV has received consultancy fees and honoraria from Human Genome Sciences and GlaxoSmithKline. MAP and RC have received payment for board membership and consultancy from Human Genome Sciences and GlaxoSmithKline. DAR, BNJ and CSK are employed by and own stock in GlaxoSmithKline. ZJZ and WF are employed by and own stock in Human Genome Sciences.
Provenance and peer review Not commissioned; externally peer reviewed.
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