Prospective study of the effect of rituximab on kidney function in membranous nephropathy

Author:

Kanigicherla Durga A K1ORCID,Kehagia Angie A2,Jamshidi Babak2,Manounah Lina2,Barnes Anna2,Patrick Hannah3ORCID,Powell Helen3,Austin Catrin3,Norton Stephen3,Willcocks Lisa4,Griffith Megan5,Braddon Fiona6,Steenkamp Retha6,McKane William S7,Khwaja Arif7

Affiliation:

1. Manchester Institute of Nephrology and Transplantation, Manchester , UK

2. King's College Technology Evaluation Centre (KiTEC) , UK

3. National Institute for Health and Care Excellence , UK

4. Cambridge University Hospital NHS Trust , UK

5. Imperial College Healthcare NHS Trust Renal Unit , UK

6. UK Kidney Association & UK National Registry of Rare Kidney Diseases , UK

7. Sheffield Kidney Institute , UK

Abstract

ABSTRACT Background Patients with membranous nephropathy (MN) and poor kidney function or active disease despite previous immunosuppression are underrepresented in clinical trials. It is unknown how effective rituximab is in this population. Methods This prospective, multi-centre, single-arm, real-world study of patients with active MN [urine protein-creatinine ratio (uPCR) >350 mg/mmol and serum albumin <30 g/L, or a fall in estimated glomerular filtration rate (eGFR) of at least 20% or more over at least 3 months] evaluated rituximab in those with contraindications to calcineurin inhibitors and cytotoxic therapy. The primary outcome was change in rate of eGFR decline before and after rituximab. Complete or partial remission were defined as uPCR <30 mg/mmol or uPCR <350 mg/mmol with a ≥50% fall from baseline, respectively. Results A total of 180 patients [median age 59 years, interquartile range (IQR) 48–68] received rituximab and were followed up for a median duration of 17 months. Seventy-seven percent had prior immunosuppression. Median eGFR and uPCR at baseline were 49.2 mL/min/1.73 m2 (IQR 34.4–80.6) and 766 mg/mmol (IQR 487–1057), respectively. The annual rate of decline of eGFR fell from 13.9 to 1.7 mL/min/1.73 m2/year following rituximab (Z score = 2.48, P < .0066). At 18 months 12% and 42% of patients were in complete or partial remission, respectively. Rituximab was well tolerated; patient survival was 95.6% at 2 years and in patients in whom eGFR was available, kidney survival was 93% at 2 years. Conclusion Rituximab significantly reduced the rate of eGFR decline in active MN including those who had received prior immunosuppression or with poor baseline kidney function.

Funder

NHS England

Publisher

Oxford University Press (OUP)

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