Objective To update the 2012 EULAR/ERA–EDTA recommendations for the management of lupus nephritis (LN).
Methods Following the EULAR standardised operating procedures, a systematic literature review was performed. Members of a multidisciplinary Task Force voted independently on their level of agreeement with the formed statements.
Results The changes include recommendations for treatment targets, use of glucocorticoids and calcineurin inhibitors (CNIs) and management of end-stage kidney disease (ESKD). The target of therapy is complete response (proteinuria <0.5–0.7 g/24 hours with (near-)normal glomerular filtration rate) by 12 months, but this can be extended in patients with baseline nephrotic-range proteinuria. Hydroxychloroquine is recommended with regular ophthalmological monitoring. In active proliferative LN, initial (induction) treatment with mycophenolate mofetil (MMF 2–3 g/day or mycophenolic acid (MPA) at equivalent dose) or low-dose intravenous cyclophosphamide (CY; 500 mg × 6 biweekly doses), both combined with glucocorticoids (pulses of intravenous methylprednisolone, then oral prednisone 0.3–0.5 mg/kg/day) is recommended. MMF/CNI (especially tacrolimus) combination and high-dose CY are alternatives, for patients with nephrotic-range proteinuria and adverse prognostic factors. Subsequent long-term maintenance treatment with MMF or azathioprine should follow, with no or low-dose (<7.5 mg/day) glucocorticoids. The choice of agent depends on the initial regimen and plans for pregnancy. In non-responding disease, switch of induction regimens or rituximab are recommended. In pure membranous LN with nephrotic-range proteinuria or proteinuria >1 g/24 hours despite renin–angiotensin–aldosterone blockade, MMF in combination with glucocorticoids is preferred. Assessment for kidney and extra-renal disease activity, and management of comorbidities is lifelong with repeat kidney biopsy in cases of incomplete response or nephritic flares. In ESKD, transplantation is the preferred kidney replacement option with immunosuppression guided by transplant protocols and/or extra-renal manifestations. Treatment of LN in children follows the same principles as adult disease.
Conclusions We have updated the EULAR recommendations for the management of LN to facilitate homogenization of patient care.
- systemic lupus erythematosus
- lupus nephritis
Statistics from Altmetric.com
Up to 40% of patients with systemic lupus erythematosus (SLE) develop kidney disease, which represents a major cause of morbidity.1–3 In 2012, the European League Against Rheumatism–European Renal Association–European Dialysis and Transplant Association (EULAR/ERA–EDTA) developed joint recommendations for lupus nephritis (LN),4 involving a panel of rheumatologists, nephrologists, renal pathologists and paediatricians. Since then, new evidence has emerged, which includes the use of calcineurin inhibitors (CNIs) and ‘multitarget’ therapy, disease monitoring and treatment targets. We therefore sought to update the recommendations for the management of LN.
Following approval by the EULAR and ERA/EDTA Executive Committees, the convenors (DTB, DJ) invited a multidisciplinary panel of 11 rheumatologists, 11 nephrologists, 1 nephropathologist, 1 paediatric rheumatologist, 1 paediatric nephrologist, 1 allied health professional and 2 patient representatives. The EULAR standardised operating procedures5 were followed and the Appraisal of Guidelines Research and Evaluation instrument was employed.6 Delphi-based methodology led to 15 questions for systematic literature review (SLR), which was undertaken by three fellows (AF, MK, KC; table 1). PubMed was searched using specific index terms and retrieved items were evaluated based on the title, abstract and/or full text. Since this is an update of the 2012 recommendations, we considered all English-language publications between January 2012 and December 2018. The total number of articles included are shown in table 1.
The results of the literature search were summarised, distributed to all members, presented and discussed on, during the meeting of the panel in May 2019. The previous recommendations4 were reappraised and revised accordingly. The final level of evidence (LoE; scale: 1–4) and grading of recommendations (GoRs; scale: A (highest) to D (lowest)), according to the Oxford Centre for Evidence Based Medicine definitions,7 (online supplementary table 1) considered the total body of evidence. Each member of the panel was then asked to rate their level of agreement (LoA) for each statement on a 0–10 rating scale (10 being full agreement), based on both the research evidence presented and their own clinical expertise. For the final voting, Task Force members had the ‘opportunity’ to express their potential disagreement for a particular statement, however omission of statements with less consensus was not considered necessary. The methods and results of the SLR will be published separately.
The overarching principles and specific recommendations, with the respective LoE, GoR and LoA, are listed in table 2.
Despite an improved prognosis over the last decades,8 LN poses therapeutic challenges and is linked to increased morbidity, mortality and healthcare costs. The nature of the disease (involvement of the kidneys in the context of a systemic autoimmune disease) mandates a multidisciplinary approach by rheumatologists and nephrologists, following histological confirmation and assessment of LN by a nephropathologist. In this regard, management or periodic evaluation of these patients in centres with expertise is recommended. Decision-making requires that the patient is adequately informed about the nature and natural course of the disease and the therapeutic options.
Investigation of the patient with suspected LN
Patients with SLE with any sign of kidney involvement (glomerular haematuria and/or cellular casts, proteinuria >0.5 g/24 hours (or spot urine protein-to-creatine ratio (UPCR) >500 mg/g), unexplained decrease in glomerular filtration rate (GFR)) are candidates for kidney biopsy. Mild clinical presentations (eg, subnephrotic proteinuria) can nonetheless be associated with active histological lesions.9–11 In a review of kidney biopsies performed during 1970–2016, earlier use of biopsy based on urinary abnormalities, as done from 2001 to 2016, was associated with improved outcomes, despite similar rates of severe histology.12 The benefits of histological evaluation should be balanced against increased bleeding risk in selected patients such as those receiving anticoagulation. All patients with SLE, especially those with suspected kidney involvement, should be tested for antiphospholipid antibodies (aPL), since renal manifestations of antiphospholipid syndrome, such as thrombotic microangiopathy (TMA), may carry prognostic implications. Testing for anti-dsDNA and anti-C1q (whenever available) autoantibodies should be considered in patients with suspected LN, along with complement levels (C3 and C4).13
Pathological assessment of kidney biopsy
The 2003 International Society of Nephrology/Renal Pathology Society (ISN/RPS) classification still represents the gold standard for assessment of kidney biopsy in LN (online supplementary table 2).14 TMA lesions, although not pathognomonic, should raise suspicion of antiphospholipid syndrome nephropathy and thus, prompt aPL (re-)testing. Although TMA has been reported in up to 25% of LN biopsies,15 16 its prognostic implications remain unclear.17 18 Tubulointerstitial lesions, such as interstitial fibrosis and tubular atrophy, are associated with poor outcome.19–21 A revision of the 2003 ISN/RPS classification has recently been proposed and awaits endorsement.22
Indications of immunosuppressive treatment in LN
Immunosuppressive treatment is recommended in active class III or IV LN, with or without coexisting histological chronicity. For pure class V LN, the recommendation for immunosuppression pertains to patients with nephrotic-range proteinuria, which is associated with worse prognosis, in addition to cases with proteinuria >1 g/24 hours despite optimal use of renin–angiotensin–aldosterone system blockers for a reasonable time period (eg, at least 3 months). Class II LN usually does not need specific immunosuppressive therapy, but may be prone to histological transformation to more aggressive disease on repeat biopsy. The presence of significant proteinuria should prompt histological reassessment for detection of proliferative changes that may have been overlooked.
Treatment of adult LN
Goals of treatment
Compared with the previous recommendations, the goals of treatment were further defined according to time since treatment initiation. Post hoc analyses from the MAINTAIN and Euro-Lupus Nephritis Trials suggest that proteinuria at 12 months represents the best single predictor for long-term renal outcome (ie, risk for end-stage kidney disease (ESKD) or doubling of serum creatine after 10 years).23–27 Accordingly, therapy should aim for proteinuria <0.5–0.7 g/24 hours by 12 months (complete clinical response), although up to 50% of patients not reaching this milestone may still have stable long-term kidney function.25 28 Evidence of improvement in proteinuria (with GFR normalisation/stabilisation) should be noted by 3 months,29 30 and at least 50% reduction in proteinuria (partial clinical response) by 6 months. For patients with nephrotic-range proteinuria at baseline, the aforementioned time frames may be extended by 6–12 months, due to slower proteinuria recovery.31 Thus, consideration of decreasing proteinuria can avoid premature treatment changes. Since SLE is a systemic disease, immunosuppressive therapy should also target remission or low disease activity from extra-renal domains.32
In class III-IV LN, an updated Cochrane systematic review suggested similar efficacy of mycophenolate mofetil/mycophenolate acid (MMF/MPA) compared with cyclophosphamide (CY),33 with possible ethnic/racial differences, that is, MMF potentially being more efficacious in African–Americans.34 The 10-year Euro-Lupus Nephritis Trial data showed equal efficacy of low-dose versus high-dose CY,24 and the low-dose regimen has been used in non-European populations.35–38 Consequently, both MMF/MPA and low-dose CY are recommended as first-line options for initial (induction) treatment. The recommended target dose of MMF is now changed to 2–3 g/day (MPA 1.44–2.16 g/day), based on evidence that therapeutic drug dosage may range between 1 and 3 g/day. Dose may be adjusted according to tolerance/adverse effects, efficacy and trough MPA blood levels. High-dose intravenous CY (0.5–0.75 g/m2 monthly for 6 months) can be considered in patients with adverse clinical (nephritic urine sediment and impaired renal function with GFR between 25 and 80 mL/min) or histological (crescents or necrosis in >25% of glomeruli) prognostic factors.39
The realisation of the adverse effects of long-term glucocorticoid treatment, together with emerging evidence that following initial pulse intravenous methylprednisolone, lower starting dose of glucocorticoids (≤0.5 mg/kg/day) may be as efficacious as higher dose,40–42 led the Task Force to recommend that total intravenous methylprednisolone dose may range from 500 to 2500 mg (allowing flexible dosing depending on disease severity), and starting oral prednisone dose may be 0.3–0.5 mg/kg/day, reducing to ≤7.5 mg/day by 3–6 months.
Focus has been placed on the use of calcineurin inhibitors (CNIs, tacrolimus (TAC) and cyclosporine A (CsA)), either as a monotherapy or in combination with MMF/MPA.43–46 A randomised controlled trial (RCT) in 362 Chinese patients found the combination of TAC/MMF to be superior to CY in the short-term.47 In a phase II RCT, a cyclosporine analogue, voclosporin when combined with MMF was associated with a higher frequency of complete response at 6 months as compared with MMF alone, although more side effects and deaths occurred in the former group.42 A number of meta-analyses suggest that CNI (alone or as part of multitarget regimen) may have favourable efficacy/toxicity ratio in LN,48 and thus, in a new statement (4.4), the combination of MMF with a CNI (especially TAC) is included as therapeutic option, particularly in cases with nephrotic-range proteinuria. Until more data in non-Asian populations and studies with longer follow-up and on renal outcomes such as prevention of kidney insufficiency/failure are available, CNI and the ‘multitarget’ regimen cannot be universally recommended as first-line treatment. Additionally, nephrotoxicity and other side effects of CNI use should be considered when opting for a CNI-based regimen.
In pure class V LN, no high-quality evidence has emerged over the last 7 years. MMF/MPA is recommended as first-choice at the same doses as in class III/IV disease. CY and CNI (especially TAC), the latter as monotherapy or combined with MMF, are alternative options.43 49 Similar to class III/IV LN, rituximab (RTX) is reserved for non-responders in class V LN (see below), although a recent RCT in idiopathic membranous nephropathy, which demonstrated short-term superiority over CsA, may justify a modification once similar data emerge in LN.50
Hydroxychloroquine (HCQ) is recommended for all patients with LN, in the absence of contraindications. HCQ use is linked to reduced risk of kidney flares, ESKD and death.51–55 In light of emerging data regarding ocular toxicity with more sensitive screening techniques, and in accordance to a revised statement by the American Academy of Ophthalmology, daily HCQ dose should not exceed 5 mg/kg actual body weight and should be continued indefinitely with regular ophthalmological screening (after 5 years on HCQ and yearly thereafter, or yearly from baseline in the presence of risk factors).32 56 Dose adjustments (50% reduction) and yearly eye monitoring from onset are recommended for patients with GFR <30 mL/min.
MMF/MPA and azathioprine (AZA) remain the drugs of choice for subsequent immunosuppressive treatment, following adequate response during the initial phase. The two regimens did not differ in terms of kidney flares in the 10-year follow-up of the MAINTAIN Trial,24 in contrast to the Aspreva Lupus Management Study (ALMS) which showed superiority of MMF.56 Based on evidence showing increased relapses when MMF/MPA is followed by AZA,57 58 we recommend MMF/MPA induction to be followed by MMF/MPA maintenance. CY induction can be followed by either MMF/MPA or AZA; the latter agent is preferred if pregnancy is contemplated or the higher cost of MMF is an issue. CNI can be used in class V LN at the lowest effective dose, since chronic use of these agents may increase the risk of kidney side effects.
Most renal flares occur within the first 5–6 years following treatment initiation.24 59–62 Therefore, for most patients it is recommended not to discontinue immunosuppression prior to that time. Therapy deescalation should be contemplated in patients who have attained sustained complete renal response and glucocorticoids (GC) should be tapered first. Gradual immunosuppressive drug tapering is recommended prior to complete withdrawal. Both longer duration of treatment and longer duration of remission were associated with reduced risks of kidney flares in patients who discontinued immunosuppressive therapy after 6 years of treatment.53 63 To this end, duration of immunosuppressive therapy should be individualised according to the timing and magnitude of response, duration of flare-free maintenance, extra-renal SLE activity and patient preferences.64
Failure to achieve the treatment goals described above raises the possibility for non-responding or refractory disease. In this context, proteinuria kinetics are important as a decreasing proteinuria—to a level not yet meeting these targets—could justify further waiting prior to therapy switch, especially in patients with nephrotic-range proteinuria at baseline, provided that kidney function is stable. Thorough assessment, including adherence to treatment with measurement of drug levels, where available, is warranted prior to declaring non-responding/refractory disease (the role of repeat kidney biopsy is discussed below).
All first-line therapies, including MMF/MPA (2–3 g/day),65 CY and CNI (especially TAC) as monotherapy or ‘multitarget’ therapy,66–69 are recommended in non-responding disease. B-cell depleting therapies such as RTX, although off-label, are also indicated either as monotherapy or as add-on therapy to MMF/MPA or CY70–74; complete depletion of circulating B-cells predicted clinical remission at 76 weeks.75 This has recently been supported by a successful trial of obinutuzumab.76 Following a response to RTX, relapses are not uncommon, but occur after a variable length of time.77 78 Repeat dose can be considered to prevent or treat a relapse. Although belimumab is not formally indicated for treating LN, post hoc analyses from RCTs and observational studies suggest that, when added to standard-of-care (including MMF), it may gradually reduce proteinuria and the risk for kidney flares.79–83 Importantly, positive results from the phase III RCT of belimumab as an add-on therapy in LN have been released,84 and the results of this study are awaited. The combination of RTX and belimumab has recently been used in refractory disease.85 High-dose intravenous immunoglobulin (2 g/kg) could be considered when there are contraindications to increasing glucocorticoids or immunosuppressive drugs, such as infection,86 while plasma exchange is rarely indicated.
Adjunct treatment in patients with LN
Renin–angiotensin–aldosterone system blockade is recommended (in non-pregnant patients) due to its antiproteinuric and antihypertensive effects; judicious use and dose titration is warranted in cases of impaired renal function. Hypertension should be controlled to values below 130/80 mm Hg.87 General kidney-protective measures (eg, avoidance of nonsteroidal anti-inflammatory drugs) cannot be over-emphasised. Vaccination status should be reviewed and patients be vaccinated accordingly with non-live vaccines.88 Vaccination against influenza and Streptococcus pneumoniae are strongly recommended; regarding vaccination against herpes zoster, existing data suggest an acceptable safety profile of the live attenuated vaccine (available in most countries) in patients with lupus. The decision should be individualised, taking into account patient age and net state of immunosuppression. Patients under less intensive immunosuppression may be more appropriate for vaccination.
Statin therapy should be considered on the basis of lipid levels and presence of other cardiovascular risk factors; calculation of the 10-year cardiovascular disease risk using the Systematic Coronary Risk Evaluation, QRisk3, or other validated score is recommended to aid this decision, taking into account that such scores may underestimate the actual risk especially in young patients with SLE .32 89 Primary prevention of thrombosis with low-dose aspirin is recommended in the presence of high-risk aPL profile, balancing thrombotic versus bleeding risk.90 Bone protection and prevention of osteoporosis should follow non-pharmacological (exercise uptake, maintenance of normal body mass index) as well as pharmacological measures, according to fracture risk.
Monitoring and prognosis of LN
Patients should be assessed periodically in centres with experienced clinicians interpreting urine microscopy, serology and histology.91 Kinetics of proteinuria and serum creatinine within the first 6–12 months are more sensitive than haematuria in prred after balancing tedicting long-term prognosis. Quantification of proteinuria can be done by means of a spot UPCR, as its correlation with a 24-hour urine protein collection is high in most studies (although lower when urine protein is <1000 mg/24 hours).92–94 The 24-hour urine protein may be preferred prior to therapeutic decisions. Urinalysis should be included at each visit; reappearance of glomerular haematuria or cellular casts can be a predictor of impending kidney flare.95 Serum C3/C4 and anti-dsDNA should be monitored; although a rise in anti-dsDNA titres has been associated with a forthcoming flare, the specificity is modest.96–98 Anti-C1q antibodies have the highest correlation with active LN and may also predict relapse.99 100
Repeat kidney biopsy can be considered in cases of non-responsiveness to immunosuppressive treatment, to differentiate between ongoing activity and irreversible damage, or in cases of relapse. Following a LN flare, histological transition is found in 40%–76%, typically from class V to III–IV forms.95 101 Per protocol repeat biopsies following immunosuppressive treatment frequently show a discordance between clinical and histological response, as 30% of complete responders have ongoing histological activity.102 The value of protocol rebiopsy to determine the need for continuous treatment was examined in a prospective study of 36 patients with LN who were in complete remission for 12 months, following 3 years of immunosuppressive therapy. Ongoing histological activity was strongly predictive of a subsequent kidney flare when reducing immunosuppression.103
Management of ESKD in LN
Recent studies suggest that the risk for ESKD in LN has decreased to <10% in 15 years.8 12 Still, some patients will progress to irreversible kidney injury, which carries increased risks of morbidity and mortality.104–106 Once on kidney replacement therapy, the disease usually follows a quiescent course and flares (renal and extra-renal) are less frequent but still can occur. Among kidney replacement modalities, haemodialysis and continuous peritoneal dialysis are accompanied by similar patient survival rates in comparative retrospective studies.107 108 By contrast, kidney transplantation is associated with higher 10-year patient survival rates109 110; data from the United States Renal Data System showed 70% reduced mortality among patients with LN–ESKD who underwent transplantation as compared with non-transplanted counterparts.111 The updated statement now emphasises that ‘transplantation may be preferred over other kidney replacement options and should be considered when extra-renal lupus is clinically (and ideally, serologically) inactive for at least 6 months’. Currently, only a small fraction of patients undergo pre-emptive transplantation, although this strategy has the most favourable outcome (10-year patient survival rates 94%,vs 76% and 42%, for peritoneal dialysis and haemodialysis, respectively).105 112 Transplantation should not be delayed and can be safely performed in the presence of isolated serological activity. Recurrent LN in the transplanted kidney is rarely clinically significant. Patients with transplanted LN are at increased risk of opportunistic infections due to their previous drug exposures.
Antiphospholipid syndrome and LN
Antiphospholipid syndrome-associated nephropathy represents a rare yet distinct type of aPL-induced vascular nephropathy. Although considered a hallmark of antiphospholipid syndrome-associated nephropathy, TMA is not pathognomonic, because similar lesions are found in thrombotic thrombocytopenic purpura/haemolytic uraemic syndrome, malignant hypertension or complement-mediated TMA.113 114 There are no controlled studies to guide the treatment of antiphospholipid syndrome-associated nephropathy. Antiplatelet agents or anticoagulants (if criteria for antiphospholipid syndrome are fulfilled) are recommended, in addition to HCQ. Renin–angiotensin–aldosterone system blockade may delay disease progression.115
LN and pregnancy
The 2017 EULAR recommendations for the management of family planning in SLE and antiphospholipid syndrome fully cover the issue of pregnancy, including assisted reproduction, in the context of LN.116 In the absence of new evidence, the statements of the 2012 recommendations for pregnancy LN were kept unchanged. UPCR should be controlled (ideally, to <500 mg/g) without the use of renin–angiotensin–aldosterone system inhibitors, which are contraindicated in the first trimester due to teratogenicity. Compatible drugs include glucocorticoids, AZA and CNI, and HCQ, which should be continued at safe dosages throughout pregnancy and lactation.117 118 Withdrawal of MMF for longer period, for example, 6 months before attempts for conception, offers time to assess the tolerability and efficacy of an alternative immunosuppressive.119 Severe flares during pregnancy—not responding to drugs with an acceptable safety profile—merit multidisciplinary specialist referral; occasionally, termination of pregnancy and/or use of embryotoxic drugs may be considered after balancing the risk/benefit ratio.
Management of paediatric LN
Kidney involvement is more common in childhood compared with adult-onset SLE, often as a presenting manifestation, while renal flares are observed in more than 50% of patients.120 121 Since the 2012 EULAR/ERA—EDTA recommendations, American and European groups of experts in paediatric SLE and LN have published recommendations for the management of childhood-onset LN; both are largely based on data extrapolation from the studies in adults.122 123 Notwithstanding differences between children and adults, the respective statements from the 2012 recommendations remained unchanged; diagnosis, treatment (paediatric doses of drugs, online supplementary table 3) and monitoring should follow the same principles as in adult disease. For children in adolescence, a transition programme is recommended to ensure adherence and optimal outcomes.
Additional points to consider and the research agenda in LN are shown in box 1.
Research agenda in lupus nephritis
Clinical presentation, histopathological features, response to treatments, prognostic factors and genetic background (eg, APOL1) in various ethnicities.
Revision of the International Society of Nephrology/Renal Pathology Society classification criteria (under way).
Atypical lupus nephritis: podocytopathies and pauci-immune lupus nephritis, other forms.
Approach to non-lupus (or antinuclear antibody negative) full-house glomerulonephritis.
Validated definition of kidney flares.
Existing therapies and disease monitoring
Calcineurin inhibitor efficacy in non-Asian patients.
B-cell targeting therapies (eg, belimumab, combination of rituximab and belimumab, obinutuzumab) and cytokine inhibitors in lupus nephritis.
Imaging for kidney fibrosis.
Duration and withdrawal of therapy.
Damage accrual in long-term disease.
Protocolised repeat biopsies: value of early (vs late) repeat biopsy.
Non-immune mechanisms in progression of lupus nephritis, such as hypertension, obesity, dyslipidaemia.
Impact of patient education programs.
Role of eculizumab in antiphospholipid syndrome-associated nephropathy.
Pathophysiology and biomarkers
Risk stratification of subgroups based on molecular signatures or other biomarkers.
Explore non-invasive means to classify the types of lupus nephritis and activity status (urine cells, omics, etc).
Renal progenitor cells and their proliferation in lupus nephritis.
Kidney repair in lupus nephritis.
Biomarkers for liquid biopsy.
Lupus nephritis trial design
Risk stratification of subgroups based on molecular signatures or biomarkers.
Innovative trial designs.
Optimisation of ‘standard-of-care’ (background) treatments.
Better definition of clinical trial endpoints.
Recent insights in LN necessitated an update of the EULAR-ERA/EDTA recommendations, which were developed by a large group of physicians from different specialties and nurses caring for LN, with input from patients, and complement the recently updated recommendations for SLE.32 Inclusion of all involved medical disciplines is an advantage and accords to the multidisciplinary care that these patients need. These recommendations intend to inform rheumatologists, nephrologists, patients, national professional societies, hospital officials, social security agencies and regulators about the treatment of LN based on most recent evidence, to ensure optimal outcomes with existing therapies. In addition to the quality of evidence for risks and benefits, considerations were also given to the availability and costs of treatments.
A challenging issue is the absence of licenced medications for LN, in spite of high-quality evidence supporting the use of existing drugs. Again, in these recommendations, MMF and low-dose intravenous CY are recommended as drugs of first choice based on their better toxicity profile, while allowing room for the use of high-dose intravenous CY for selected patients with aggressive disease, especially if gonadal toxicity is not a consideration. CNI, especially TAC, in combination with glucocorticoids and MMF in the so called ‘multitarget’ therapy, have been included. The absence of robust evidence on CNI in non-Asian populations and their potential for renal toxicity with chronic use has led the committee to adopt a more cautious attitude, recommending them for patients with nephrotic-range proteinuria or not responding to initial therapy. Glucocorticoid usage, in view of their contribution to damage in SLE, received special attention in these recommendations with the committee recommending the use of pulse glucocorticoids, followed by lower doses of daily glucocorticoids to decrease cumulative dose. Glucocorticoid reduction is receiving increased attention in recent years, being used as an outcome measure in SLE trials.124
The development of new classification criteria for SLE with increased weighting for kidney disease will facilitate the inclusion of more patients in LN trials.125 New drugs in development for LN, including novel CNI, B-cell inhibiting and depleting agents, kinase inhibitors, inhibitors of costimulation, inhibitors of complement activation, in combination with improved trial designs, may provide additional agents in the near future.
The committee wishes to acknowledge the support of the EULAR Standing Committee on Clinical Affairs. The committee also expresses its sincere appreciation and gratitude to the EULAR Secretariat and especially to Patrizia Jud, executive assistant, for the outstanding organisation.
Disclaimer : This is a summary of a scientific article written by a medical professional (“the Original Article”). The Summary is written to assist non medically trained readers to understand general points of the Original Article. It is supplied “as is” without any warranty. You should note that the Original Article (and Summary) may not be fully relevant nor accurate as medical science is constantly changing and errors can occur. It is therefore very important that readers not rely on the content in the Summary and consult their medical professionals for all aspects of their health care and only rely on the Summary if directed to do so by their medical professional. Please view our full Website Terms and Conditions.
Copyright © 2020 BMJ Publishing Group Ltd & European League Against Rheumatism. Medical professionals may print copies for their and their patients and students non commercial use. Other individuals may print a single copy for their personal, non commercial use. For other uses please contact our Rights and Licensing Team.
Handling editor David S Pisetsky
GB, DJ and DTB contributed equally.
Contributors AF, MK and KC performed the systematic literature review and AF drafted the manuscript. GB supervised the methodology and edited the manuscript. DJ and DTB convened and supervised the project and edited the manuscript. All authors edited the manuscript and accepted its final form.
Funding This study was funded by European League against Rheumatism.
Competing interests AF reports personal fees from GSK, Abbvie, Amgen, Enorasis, Roche and Genesis Pharma, outside the submitted work. HJA reports personal fees from GSK, Astra Zeneca and Janssen, during the conduct of the study; personal fees from Secarna, Inositec, Previpharma and Noxxon, outside the submitted work. MA reports honoraria fees from GSK and Roche, outside the submitted work; FH reports honoraria fees from GSL, outside the submitted work. MP reports personal fees from Otsuka, grants and personal fees from Alexion, personal fees from Retrophin, outside the submitted work. YKOT reports grants from GSK, personal fees from Aurinia Pharmaceuticals, personal fees from Novartis, during the conduct of the study. MT reports grants from Abbvie, BMS, Novartis, Pfize and Roche and honoraria fees from Novartis, outside the submitted work. DJ reports personal fees from Astra-Zeneca, Aurinia, Boehringer-Ingelheim, grants and personal fees from Chemocentryx, GSK, Roche/Genentech, and Sanofi-Genzyme, personal fees and other from Vifor, outside the submitted work.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting or dissemination plans of this research.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Detailed data relating to this article will be published separately and are also available upon request.
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.