ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Abstract: SA-PO0798

Double Trouble for Lupus Nephritis: Belimumab Meets the Calcineurin Inhibitor

Session Information

Category: Glomerular Diseases

  • 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics

Authors

  • Turner, Sarah, Allegheny Health Network, Pittsburgh, Pennsylvania, United States
  • Ruiz, Brian, Allegheny Health Network, Pittsburgh, Pennsylvania, United States
  • Ike, Joanne, Allegheny Health Network, Pittsburgh, Pennsylvania, United States
  • Habbach, Amr, Allegheny Health Network, Pittsburgh, Pennsylvania, United States
  • Manocha, Sonia J., Allegheny Health Network, Pittsburgh, Pennsylvania, United States
  • Arora, Swati, Allegheny Health Network, Pittsburgh, Pennsylvania, United States
Introduction

Lupus nephritis (LN) remains a major cause of morbidity and mortality in systemic lupus erythematosus (SLE). Current guidelines recommend glucocorticoids with immunosuppressive therapy and support add-on use of either belimumab or calcineurin inhibitors (CNIs), such as voclosporin or tacrolimus. However, evidence for combined belimumab and CNI therapy remains limited. Here, we report the outcomes of five patients with biopsy-proven LN treated with combination belimumab and CNI therapy.

Case Description

We present a series of five female patients between the ages of 34 and 47 with SLE and biopsy-proven LN. All patients were treated with background standard-of-care therapy consisting of mycophenolate mofetil, prednisone taper, and hydroxychloroquine (HCQ). Therapy was upgraded to quadruple regimen in three patients due to worsening proteinuria and two patients due to worsening extrarenal symptoms. The treatment response is shown in the table below. On follow up, renal function stabilized and serologies improved. No serious infections, hospitalizations, or major treatment-related adverse events were documented during the observation period (mean of 15.2 months).

Discussion

The rate of progression of LN to ESRD with the current treatment guidelines necessitates innovative strategies in management. The evidence on combined use of Belimumab and CNIs has shown some promising results but remains limited to case reports/ case series. The utility and safety of using multitarget therapy in LN is not well established. We report our center’s experience in treating 5 LN patients with multitarget therapy showing improvement in proteinuria, extra-renal manifestations and stabilization of renal function without the need for infectious prophylaxis and without infection related hospitalizations. Trials are much needed to evaluate this approach.

Patient Demographics and Treatment Response
CaseAgeGenderLN ClassReason for Adding CNI/BelimumabMonths on CNI plus
Belimumab
Treatment ResponsePrednisone DoseAdverse Events
134FemaleIIICNI added due to worsening proteinuria22Proteinuria improved from 2 g/g → 0.15 g/gCompletely weaned offNone
247FemaleIV/VBelimumab added due to worsening extra renal symptoms24Proteinuria improved from 0.61 g/g → 0.08 g/g, extra renal symptoms improved6 mg dailyNone
339FemaleIIIBelimumab added due to worsening extra renal symptoms15Proteinuria remained negligible, extra-renal symptoms improvedCompletely weaned offNone
441FemaleVCNI added due to worsening nephrotic syndrome5Proteinuria improved from 5 g/g → 0.67 g/g15 mg daily; currently weaning offSerum Cr increased 0.89 mg/dL → 1.11 mg/dL and developed tremors with Voclosporin 23.7 mg BID, both improved with decreased dose to 15.8 mg BID
534FemaleIIICNI added due to worsening proteinuria10Proteinuria improved from 1.4 g/g → 0.18 g/g8 mg daily; currently weaning 1 mg/monthNone