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Prospective study of the effect of rituximab on kidney function in membranous nephropathy.
Kanigicherla, Durga A K; Kehagia, Angie A; Jamshidi, Babak; Manounah, Lina; Barnes, Anna; Patrick, Hannah; Powell, Helen; Austin, Catrin; Norton, Stephen; Willcocks, Lisa; Griffith, Megan; Braddon, Fiona; Steenkamp, Retha; McKane, William S; Khwaja, Arif.
Afiliação
  • Kanigicherla DAK; Manchester Institute of Nephrology and Transplantation, Manchester, UK.
  • Kehagia AA; King's College Technology Evaluation Centre (KiTEC), UK.
  • Jamshidi B; King's College Technology Evaluation Centre (KiTEC), UK.
  • Manounah L; King's College Technology Evaluation Centre (KiTEC), UK.
  • Barnes A; King's College Technology Evaluation Centre (KiTEC), UK.
  • Patrick H; National Institute for Health and Care Excellence, UK.
  • Powell H; National Institute for Health and Care Excellence, UK.
  • Austin C; National Institute for Health and Care Excellence, UK.
  • Norton S; National Institute for Health and Care Excellence, UK.
  • Willcocks L; Cambridge University Hospital NHS Trust, UK.
  • Griffith M; Imperial College Healthcare NHS Trust Renal Unit, UK.
  • Braddon F; UK Kidney Association & UK National Registry of Rare Kidney Diseases, UK.
  • Steenkamp R; UK Kidney Association & UK National Registry of Rare Kidney Diseases, UK.
  • McKane WS; Sheffield Kidney Institute, UK.
  • Khwaja A; Sheffield Kidney Institute, UK.
Clin Kidney J ; 17(8): sfae179, 2024 Aug.
Article em En | MEDLINE | ID: mdl-39104870
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Kidney J Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Kidney J Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Reino Unido