Objectives To evaluate efficacy and safety of abatacept in adults with active primary Sjögren’s syndrome (pSS) in a phase III, randomised, double-blind, placebo-controlled trial.
Methods Eligible patients (moderate-to-severe pSS [2016 ACR/European League Against Rheumatism (EULAR) criteria], EULAR Sjögren’s Syndrome Disease Activity Index [ESSDAI] ≥5, anti-SS-related antigen A/anti-Ro antibody positive) received weekly subcutaneous abatacept 125 mg or placebo for 169 days followed by an open-label extension to day 365. Primary endpoint was mean change from baseline in ESSDAI at day 169. Key secondary endpoints were mean change from baseline in EULAR Sjögren’s Syndrome Patient Reported Index (ESSPRI) and stimulated whole salivary flow (SWSF) at day 169. Other secondary clinical endpoints included glandular functions and patient-reported outcomes. Selected biomarkers and immune cell phenotypes were examined. Safety was monitored.
Results Of 187 patients randomised, 168 completed double-blind period and 165 continued into open-label period. Mean (SD) baseline ESSDAI and ESSPRI total scores were 9.4 (4.3) and 6.5 (2.0), respectively. Statistical significance was not reached for primary (ESSDAI −3.2 abatacept vs −3.7 placebo, p=0.442) or key secondary endpoints (ESSPRI, p=0.337; SWSF, p=0.584). No clinical benefit of abatacept over placebo at day 169 was seen with other clinical and PRO endpoints. Relative to baseline, abatacept was associated with significant differences vs placebo in some disease-relevant biomarkers (including IgG, IgA, IgM-rheumatoid factor) and pathogenic cell subpopulations (post hoc analyses). No new safety signals were identified.
Conclusions Abatacept treatment did not result in significant clinical efficacy compared with placebo in patients with moderate-to-severe pSS, despite evidence of biological activity.
- autoimmune diseases
- Sjogren's syndrome
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What is already known about this subject?
In patients with primary Sjögren’s syndrome (pSS), open-label uncontrolled studies of various therapeutic agents with efficacy in other autoimmune diseases have shown some promising results based on different outcome measures, but large controlled studies have so far been unable to demonstrate a meaningful treatment benefit.
What does this study add?
Abatacept treatment did not result in significant clinical efficacy versus placebo in this randomised controlled trial, but it showed evidence of disease-relevant biological activity.
The lack of clinical benefit of abatacept treatment for patients with pSS in the face of an apparent biological effect is not understood.
How might this impact on clinical practice or future developments?
Although this study does not support the use of abatacept in pSS, further studies would be needed to assess the impact of factors such as the heterogeneity of pSS.
In highlighting the clinical heterogeneity of pSS and the major challenges in designing efficacy studies of novel therapies targeting systemic disease, the results from this study can be used to inform the development of new composite endpoints—which are sensitive to change and reflect clinical and biological effects—to aid future clinical development in pSS.
Primary Sjögren’s syndrome (pSS) is a chronic, systemic autoimmune disease typically affecting the salivary and lacrimal glands and producing symptoms of dry mouth, dry eyes, fatigue and pain.1 The estimated prevalence of pSS in the general population is 0.01%–0.1%; pSS is associated with a high burden of disease and diminished quality of life.2 3
Treatment recommendations for patients with pSS focus mainly on symptomatic agents.4 Available symptomatic therapies include artificial tears and saliva, cholinergic agonists such as pilocarpine5 and cevimeline,6 cyclosporine7 and lifitegrast eye drops.8 There are currently no approved disease-modifying treatments for pSS. Small, open-label, uncontrolled and controlled clinical efficacy studies of methotrexate,9 leflunomide,10 hydroxychloroquine,11 rituximab,12–14 epratuzumab (B-cell-targeted agents),15 belimumab (B-cell-activating factor-blocking agent)16 and infliximab (tumour necrosis factor-α-blocking agent)17 have shown mixed results using a variety of outcome measures. Additionally, randomised placebo-controlled trials of hydroxychloroquine18 and rituximab12 13 for pSS have been negative.
Abatacept is a selective costimulation modulator that blocks the interaction between CD80/CD86 on antigen-presenting cells and CD28 on T cells,19 20 thereby disrupting T-cell activation, a likely key step in pSS pathogenesis.21 Proven efficacy of abatacept for treatment of patients with rheumatoid arthritis (RA),22 23 a T-cell-driven systemic autoimmune disease,19 24–27 supports the rationale that blocking this co-stimulatory pathway can produce clinical efficacy in an autoimmune disease.
Early studies of abatacept in pSS showed promising results. In two small, open-label pilot studies with pSS, a 24-week course of intravenous abatacept treatment was associated with a beneficial effect on disease activity and an acceptable safety profile.28 29 Additionally, a small, prospective observational study of 11 patients with pSS from Brazil recently reported a significant reduction in European League Against Rheumatism (EULAR) Sjögren’s Syndrome Disease Activity Index (ESSDAI) and improved salivary flow following treatment with intravenous abatacept.30 An open-label study of secondary SS (associated with RA) in Japanese patients demonstrated efficacy of intravenous abatacept for RA-related and SS-related manifestations.31
Here, we present the results of a double-blind (day 169) phase III, randomised, placebo-controlled trial with an extended open-label (day 365) treatment period to assess efficacy and safety of subcutaneous (SC) abatacept in patients with moderate-to-severe pSS.
In this phase III, double-blind, placebo-controlled trial (ClinicalTrials.gov: NCT02915159), eligible patients with active pSS were randomised 1:1 to receive either weekly SC abatacept 125 mg or SC matching placebo for 169 days. A subsequent 197-day (365-day in Japan) open-label extension followed the initial double-blind period, when all eligible patients received SC abatacept 125 mg/week (those receiving placebo switched to abatacept). Post-treatment safety follow-up lasted an additional 168 days.
Patients were recruited from December 2016 to January 2018 from 60 centres in 13 countries. Random assignment of study treatment was performed by a central system. Randomisation schedules were generated by the Randomisation Group within Drug Supply Management of Bristol Myers Squibb Company. Randomisation was stratified globally by current corticosteroid use, current hydroxychloroquine use, enrolment in Japan (yes/no) and level of stimulated whole salivary flow (SWSF; </≥0.1 mL/min). A block size of 2 was applied.
This study was conducted in accordance with the Declaration of Helsinki32 and the International Conference on Harmonisation Good Clinical Practice guidelines.33 All patients enrolled provided written informed consent in accordance with local laws.
Patients aged ≥18 years with pSS defined by 2016 American College of Rheumatology/EULAR criteria34 and moderate-to-severe disease activity with an ESSDAI score ≥5,35 who were refractory to symptomatic or local therapy (eg, non-steroidal anti-inflammatory drugs) and anti-SS-related antigen A/anti-Ro antibody positive, were included. Patients were excluded if: they had another systemic autoimmune disease, inflammatory conditions, severe fibromyalgia or other medical conditions associated with clinical features of pSS that could interfere with assessment of treatment response; or they had received intravenous, intramuscular, SC or intra-articular corticosteroids within 4 weeks prior to randomisation, rituximab within 12 months or belimumab, other biological therapy or methotrexate within 12 weeks. Additional information regarding exclusion criteria can be found in the online supplemental appendix.
Primary and key secondary endpoints
The primary endpoint was mean change from baseline (day 1) in ESSDAI at day 169 for abatacept versus placebo. The two key secondary endpoints were mean changes from baseline in EULAR Sjögren’s Syndrome Patient Reported Index (ESSPRI) and in SWSF (among patients with SWSF ≥0.1 mL/min at screening and baseline) of abatacept versus placebo at day 169. ESSDAI includes 12 domains (cutaneous, respiratory, renal, articular, muscular, peripheral nervous system, central nervous system, haematological, glandular, constitutional, lymphadenopathy and lymphoma, and biological)36 37 and ESSPRI is a patient-reported symptom index for dryness, fatigue and limb (joint/muscular) pain.38 SWSF was determined by vigorously chewing (one chew/second) a piece of preweighed sterile gauze for 2 min and determining difference in weight.
Other efficacy and exploratory endpoints
Other secondary clinical endpoints included mean change from baseline in 28-joint Disease Activity Score based on C reactive protein (DAS28 [CRP]) at day 169, ESSDAI score according to hydroxychloroquine and corticosteroid use (both were stratification variables for randomisation), Physician Global Assessment score and proportion of patients with minimally clinically important improvement in both ESSDAI score (decrease ≥3)35 and in ESSPRI score (decrease ≥1).35 Secondary patient-reported outcome endpoints included mean changes from baseline in Patient Global Assessment score, Patient-Reported Outcomes Measurement Information System fatigue score and Female Sexual Function Index score, which measures sexual function in six subdomains. Other glandular function endpoints were also evaluated and included mean changes from baseline in SWSF, unstimulated WSF (UWSF; expectorated unstimulated saliva for 15 min), numeric rating scale for eye and mouth dryness, Schirmer’s test (measure of aqueous tear production over 5 min), tear break-up time (TBUT; seconds between patient’s last blink and first appearance of a random dry spot on the cornea) and ocular staining scores39 (OSS; cornea and conjunctiva staining pattern). All ocular assessments were performed by a trained ophthalmologist. Exploratory endpoints included mean changes from baseline in biomarkers of B-cell hyperactivity and immune cell phenotypes.
Patient demographics and disease characteristics were assessed at baseline; clinical disease activity and safety were assessed regularly during the double-blind and open-label periods. The endpoint assessments were conducted at various intervals throughout the study along with tender and swollen joint counts.
For the post hoc analysis of biomarkers and laboratory parameters, changes from baseline were determined for erythrocyte sedimentation rate, high-sensitivity CRP, CH50 complement, C3 complement, C4 complement, IgG, IgA, IgM, IgM-rheumatoid factor (RF), kappa light chain, lambda light chain and beta-2 microglobulin. Serum biomarker chemokine ligand 13 (CXCL13) analyte was measured using the SIMOA assay from Myriad RBM. Immune cell phenotyping of whole blood samples was assessed in a subpopulation of patients from sites that participated in the flow cytometry analysis with data analysed using BD FACSDiva software.
Adverse events (AEs) were monitored throughout the study.
A hierarchical testing procedure was applied to the primary and key secondary endpoints to preserve the overall type I error of 5%. The first key secondary endpoint would only be tested (at significance level 5%) if the test for the primary endpoint was statistically significant (significance level 5%). If both the test for the primary endpoint and the first key secondary endpoint were statistically significant (both at significance level 5%), the second key secondary endpoint would be tested (at significance level 5%). The primary and key secondary endpoints, along with selected biomarkers, were analysed by a longitudinal repeated measures model. Power and sample size calculations are included in the online supplemental appendix.
Baseline demographics and disease characteristics of the study population were summarised descriptively. All efficacy analyses used the modified intent-to-treat (mITT) population, which comprised all randomised patients who received ≥1 dose of study medication. Missing data for responders were imputed as non-responders. Estimates of adjusted mean change were derived from a repeated measures mixed model; model analysis details are included in the online supplemental appendix.
Safety was summarised descriptively throughout the trial up to 56 days after last study drug dose.
Patient and public involvement
In addition to implementation of the intervention, patient-reported outcomes were key components of the study clinical efficacy outcomes. Independently of the study and through a patient engagement network, patients with pSS provided input towards key aspects of the final study design (such as the desired concomitant use of stable-dose hydroxychloroquine). Patients and patient advocacy groups were not involved in the data interpretation, writing or editing of this manuscript.
Patient disposition and baseline characteristics
Of 187 patients randomised (abatacept n=92; placebo n=95), 168 completed the double-blind period and 165 continued into the open-label period (online supplemental figure S1). A total of 19 patients discontinued treatment during the double-blind period; reasons for discontinuation were generally balanced between treatment arms (online supplemental figure S1). Patient baseline characteristics were similar between treatment groups (table 1). For the overall study population, mean age was 52 years, 95% of patients were female and 64% were white; mean disease duration was 5 years. Mean baseline ESSDAI and ESSPRI total scores were 9.4 and 6.5 and were similar between treatment groups. At baseline, 39% of patients received concomitant stable-dose hydroxychloroquine and 24% received oral corticosteroids (≤10 mg/day prednisone equivalent). Mean baseline SWSF (mL/min) was 1.0 and similar between treatment groups.
Primary and key secondary endpoints
At day 169, adjusted mean change from baseline in ESSDAI score (primary endpoint) was not statistically different between treatment groups: −3.2 for abatacept vs −3.7 for placebo (p=0.442; figure 1A). At day 365 (end of open-label period), adjusted mean change from baseline in ESSDAI score was −3.8 for abatacept vs −4.4 for placebo (switched to abatacept at day 169; figure 1A). At days 169 and 365, proportions of patients with minimally clinically important improvements from baseline in ESSDAI total score (decrease ≥3) were 55% and 48% for abatacept, and 58% and 56% for placebo (switched to abatacept at day 169), respectively. In the stratified subgroups, patients not receiving corticosteroids or hydroxychloroquine at baseline had similar mean changes in ESSDAI score in both treatment groups (adjusted mean differences from placebo [95% CI] 0.1 [−1.3 to 1.4] and 0.4 [−1.1 to 1.9], respectively). In patients who received concomitant stable-dose oral corticosteroids during the double-blind period, adjusted mean difference from placebo (95% CI) in ESSDAI at day 169 was 2.7 (0.2 to 5.1).
Due to non-statistically significant primary endpoint results, the two key secondary endpoints, ESSPRI and SWSF, could not be tested for significance; nominal p values are presented. For ESSPRI score, adjusted mean changes from baseline at day 169 were −1.3 and −1.5 in the abatacept and placebo groups, respectively (nominal p=0.337; figure 1B). At day 365, the adjusted mean change from baseline in ESSPRI score was −1.4 and −1.5 with abatacept and placebo (switched to abatacept at day 169), respectively (figure 1B). Proportions of patients with minimally clinically important improvement from baseline in ESSPRI total score (≥1) at days 169 and 365 were 41% and 41% for abatacept, and 53% and 51% for placebo (switched to abatacept at day 169), respectively. Among patients with SWSF ≥0.1 mL/min at screening and baseline, adjusted mean change from baseline at day 169 was 0.06 for abatacept vs 0.11 for placebo (p=0.5841).
The study was terminated prematurely by the sponsor after the primary analysis failed to show a statistically significant difference in the primary endpoint, and analyses of secondary endpoints failed to demonstrate clinically meaningful differences between abatacept and placebo groups.
Other efficacy endpoints
For SWSF score, adjusted mean changes from baseline at days 169 and 365 were 0.05 and 0.12 for abatacept vs 0.11 and 0.10 for placebo (switched to abatacept at day 169), respectively (figure 1C) in the overall mITT population. The adjusted mean treatment difference (95% CI) for UWSF at day 169 was –0.004 (−0.03, 0.03) (table 2). We observed no significant differences between treatment groups in mean change in DAS28 (CRP) from baseline (table 2). Mean changes from baseline in Schirmer’s test, TBUT and OSS were all similar between treatment groups (figure 1D–F).
Changes from baseline in other clinical, glandular and patient-reported outcome measures at days 169 and 365 are summarised in table 2.
Post hoc analyses
Numerical differences between ESSDAI domains were observed. For example, in patients with an ESSDAI biological domain involvement at baseline, the proportion of those with improvements (moderate to low/no activity and low to no activity) in this domain was higher (statistical significance was not tested) with abatacept (12/40; 30%) vs placebo (6/41; 15%) at day 169; this was maintained up to day 365 (data not shown). Additionally, proportions of patients with improvements in haematological and pulmonary domains of ESSDAI were numerically higher with abatacept (7/16; 44% and 3/6; 50%) vs placebo (6/29; 21% and 1/14; 7%) at day 169, respectively, among those with involvement of the corresponding domain at baseline (data not shown). Proportions of patients by ESSDAI domain activity at baseline and day 169 are shown (online supplemental figure S2). A high placebo effect was seen in several ESSDAI domains such as lymphadenopathy and articular.
Of 12 selected disease-relevant laboratory parameters and biomarkers, mean change in IgG, IgA, IgM-RF, kappa light chain and C4 complement serum levels was significantly different between the abatacept and placebo treatment groups at day 169 (figure 2A–E; Benjamini–Hochberg procedure). At baseline, based on patients with data available at day 85, mean serum CXCL13 levels were similar between treatment arms (abatacept 90.4; placebo 97.0); however, by day 169, these levels were significantly reduced in the abatacept vs placebo group (nominal p<0.0001; figure 2F). At day 365, adjusted mean changes from baseline in IgG, IgA, IgM-RF, kappa light chain, C4 complement and CXCL13 serum levels were similar for the abatacept and placebo (switched to abatacept at day 169) treatment groups (figure 2). The numbers (%) of patients at baseline and day 169 with abnormally elevated IgG levels were 38 (41.3) and 31 (33.7) with abatacept, and 45 (47.4) and 50 (52.6) with placebo; those with elevated kappa light chains were 54 (58.7) and 41 (44.6) with abatacept, and 68 (71.6) and 61 (64.2) with placebo, respectively.
The subset of patients included for the immune cell phenotyping analysis (n=78) had similar baseline demographics and disease characteristics to the study population. In this subset, abatacept-treated patients had numerically greater decreases at day 169 (year 1 analysis) in the proportions of blood CD4+ effector memory T cells (TEM) (adjusted mean difference [95% CI] –9.1 [–14.2 to –4.0]), T helper type 1 cells (Th1) (adjusted mean difference [95% CI]–2.6 [–4.2 to –1.0]), regulatory T cells (Treg) (adjusted mean difference [95% CI] –1.8 [–3.0 to –0.6]), T follicular helper cells (Tfh) (adjusted mean difference [95% CI] –1.4 [–2.2 to –0.5]) and ICOS-positive Tfh (ICOS+ Tfh) (adjusted mean difference [95% CI] –14.4 [–19.3 to –9.5]) cells vs placebo (figure 3A–E). After switch to abatacept at day 169, mean changes from baseline in Treg, Tfh and ICOS+ Tfh cellular subsets were similar for abatacept and placebo treatment groups (figure 3C–E); for CD4+TEM and Th1, mean differences seen at day 169 were less pronounced by day 365 (figure 3A,B).
A summary of AEs in the double-blind and open-label treatment periods is shown in table 3. In the double-blind period, serious AEs (SAEs) were reported in 12 patients. Among patients treated with abatacept, 20 had SAEs: 9 in the double-blind period and 11 in the open-label period with follow-up to 56 days after the last treatment. Reported SAEs included two deaths (one placebo-treated patient [septic shock] and one abatacept-treated patient [cardiac event; patient had a history of pulmonary embolism]) and one neoplasm (plasma cell myeloma) in one abatacept-treated patient. SAEs related to study drug occurred during the double-blind treatment period in 3% (pneumonia bacterial, anaphylactoid reaction and drug hypersensitivity) of abatacept-treated and 1% (septic shock) of placebo-treated patients. Related AEs occurred during the double-blind treatment period in 46% and 25% of abatacept-treated and placebo-treated patients, respectively, but this difference was not driven by any specific AE. No new safety signals were identified compared with the known abatacept safety profile.
This large, randomised, double-blind study evaluated efficacy and safety of treatment with abatacept versus placebo in patients with active, moderate-to-severe pSS. The treatment effect did not reach statistical significance for the primary or two key secondary endpoints, and showed no clinical benefit of abatacept over placebo in other clinical efficacy and patient-reported outcome endpoints at the end of the double-blind period at day 169, or at the end of the open-label extended follow-up period at day 365. The safety profile of abatacept in patients with pSS was similar to that in other diseases treated with abatacept.40 Notably, abatacept therapy did have a clear impact on selected disease-relevant markers of biological activity likely related to central mechanisms of pSS pathogenesis.
In a recent randomised, placebo-controlled, investigator-initiated, single-centre study of SC abatacept in patients with early active pSS in the Netherlands (ASAP III NCT02067910; n=80), results for the primary endpoint (ESSDAI at 24 weeks) were similar to the present study.41 In contrast to the current study, the secondary ESSPRI endpoint (ESSPRI responders at weeks 12 and 24) was significantly different, in favour of abatacept versus placebo. Differences in results between ASAP III and the current study may be due to variations between study populations and designs, including the single-centre versus multiple-centre nature of the two studies. For instance, in ASAP III the use of hydroxychloroquine was not allowed and corticosteroids were used by fewer patients than in the current study. Additionally, at study entry all patients in ASAP III had positive biopsies, a ≤7 year disease duration and higher baseline activity (mean ESSDAI baseline score 13.5) than the current study.
Despite no detectable clinical effect in the current study, favourable improvements were observed in disease-relevant laboratory parameters and biomarkers. Some of these findings suggested an effect of therapy on T-cell-induced, B-cell hyperactivity. For example, CXCL13, the serum levels of which were significantly reduced by abatacept treatment,21 is a chemokine secreted by Tfh cells, which play a pivotal role in the migration and activation of B cells in salivary gland ectopic lymphoid structures42 43; in pSS, its serum levels correlate with disease activity and histomorphological parameters.21 44 45 In previous open-label pilot studies,28 29 24 week intravenous abatacept treatment reduced glandular inflammation, induced cellular changes (lymphocytic foci and B and T cell subtypes) and increased salivary production in 11 patients with pSS.29 Additionally, a study of 15 patients with early pSS found that 24-week intravenous abatacept treatment significantly reduced ESSDAI, ESSPRI, RF and IgG at 24 weeks.28 More recently, it has been reported that 24-week intravenous abatacept treatment decreased the number of germinal centres in parotid glands of patients with pSS.46 While abatacept has been proven effective for treatment of RA, polyarticular juvenile idiopathic arthritis and psoriatic arthritis, it has not shown significant therapeutic efficacy in systemic lupus erythematosus and multiple sclerosis.47 48 The mechanistic underpinnings across the autoimmune spectrum are complex and incompletely understood. A partial overlap in the clinical and serological features of different autoimmune diseases does not necessarily extrapolate to mutually shared treatment efficacy. Further explanation for why a detectable clinical effect was not observed with abatacept in this study, despite evidence of biological activity, may be due to limitations in the design of pSS studies. The variable characteristics and heterogeneity seen within the pSS patient population raise major challenges for study design.49 In addition, some pSS outcome measures can be subjective or difficult to standardise (eg, salivary flow has high intervariability and intravariability). Furthermore, there is a need for the development of composite study endpoints with improved cut-off and assessment time points. For example, although ESSDAI score reflects all domains of disease activity, its value in detecting small changes has been debated; as a result, there is a minimum ESSDAI score threshold required for trial entry, effectively excluding a large proportion of patients.13 50
The current trial did not confirm the promising early results from open-label studies of abatacept in pSS; this disparity has also been seen in the development of other biologics for treatment of pSS.12 13 In the TEARS13 and TRACTISS12 randomised controlled trials, rituximab demonstrated no significant improvement in ESSDAI score,12 13 despite promising early results from a previous smaller study.14 Potential explanations for the disparate findings in these rituximab trials include lack of patient stratification, insufficient tissue depletion of B cells, and the choice and timing of primary outcome evaluation.50 A study of leniolisib (a P13Kδ inhibitor), which had outcome measures and a patient population similar to the current study, showed no significant improvement in clinical outcome measures despite a significant decrease in CXCL13 serum levels, similar to our study.51 Other randomised controlled trials in pSS, like the current study, show evidence of a strong placebo effect.12 13 Considering the large placebo effect seen in this study, a reduction of at least –6.7 in ESSDAI score (placebo effect +≥3) from a baseline value of 8.7 would have been required to demonstrate therapeutic benefit over placebo.
No significant clinical effect was seen with abatacept versus placebo in this randomised controlled trial in patients with active, moderate-to-severe pSS. However, abatacept therapy had a positive effect on disease-relevant biomarkers, providing evidence of biological activity. No new safety signals were identified for abatacept.
These data were presented in part at EULAR 2019 (OP0039) and ACR 2019 (1907). We thank the patients and all the investigators who participated in the study. We thank the contributions of Marianne Peluso as protocol manager of this study. Professional medical writing and editorial assistance was provided by Fiona Boswell, PhD, at Caudex, and was funded by Bristol Myers Squibb Company.
Handling editor Josef S Smolen
Contributors All authors were involved in drafting the article or revising it critically for important intellectual content, and all authors approved the final version to be published. All authors are accountable for all aspects of the work and will ensure questions related to the accuracy or integrity of any part of the work will be appropriately investigated and resolved. Study conception and design: ANB, J-EG, EWSC, TT, GF, MN, RW and NR. Acquisition of data: EWSC, TS, RS, GF, SM, RW and NR. Analysis and interpretation: ANB, J-EG, EWSC, TT, RS, GF, MN, SM, RW, NR and HB.
Funding This study was sponsored by Bristol Myers Squibb Company.
Competing interests ANB: Consultant: Bristol Myers Squibb Company, Sanofi, VielaBio; Fees: UpToDate; Clinical trials: VielaBio, Novartis. J-EG: Grant/research support: Bristol Myers Squibb Company; Consultant: Bristol Myers Squibb Company, Lilly, UCB, Sanofi-Genzyme, Pfizer. EWSC: Consulting fees and grant/research support: Bristol Myers Squibb Company; Consulting fees: AbbVie, VielaBio. TS: Grant/research support and Speakers’ bureau: Bristol Myers Squibb Company. TT: Grant/Research: AbbVie, Asahi Kasei, Astellas, AYUMI, Chugai, Daiichi Sankyo, Eisai, Mitsubishi Tanabe, Nipponkayaku, Novartis, Pfizer Japan, Takeda; Consultant: AbbVie, Astellas, Astra Zeneca, Chugai, Eli Lilly Japan, GlaxoSmithKline, Janssen, Mitsubishi Tanabe, Nipponkayaku, Novartis, Taiho, Taisho Toyama, UCB Japan; Speakers’ bureau: AbbVie, Astellas, Bristol Myers Squibb Company, Chugai, Daiichi Sankyo, Eisai, Mitsubishi Tanabe, Novartis, Pfizer Japan, Sanofi, Takeda, Teijin. RS: Grant/research support: Pfizer; Consultant: Amgen, Bristol Myers Squibb Company, Celgene, GlaxoSmithKline, Lilly, Pfizer, Roche. GF: Consultant: Aldeyra, Allysta, Aurinia, Bristol Myers Squibb Company, Clemencia, Hovione, Kala, Lexitas PharmaServices, Nicox, Noveome, Sight Sciences, Tarsus, Tear Solutions; Stock: TearLab. MN: Employee: Bristol Myers Squibb Company; Shareholder: Bristol Myers Squibb Company. SM: Employee: Bristol Myers Squibb Company; Shareholder: Bristol Myers Squibb Company. RW: Employee: Bristol Myers Squibb Company; Shareholder: Bristol Myers Squibb Company. NR: Employee: Bristol Myers Squibb Company; Shareholder: Bristol Myers Squibb Company. HB: Unrestricted grant: Bristol Myers Squibb Company, Roche; Consultant: Speakers bureau: Bristol Myers Squibb Company, Novartis.
Patient consent for publication Not required.
Ethics approval This study was conducted in accordance with the Declaration of Helsinki and the International Conference on Harmonisation Good Clinical Practice guidelines. The study protocol and patient enrolment materials were approved by local ethics committees and institutional review boards prior to study initiation.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement All data relevant to the study are included in the article or uploaded as online supplemental information. Bristol Myers Squibb policy on data sharing may be found at https://www.bms.com/researchers-and-partners/independent-research/data-sharing-request-process.html.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.
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