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March 6, 2026Frontiers in Nephrology0 citationsOpen Access

Successful use of obinutuzumab in focal segmental glomerulosclerosis with inadequate response to rituximab: a case report

AHAndreia Rita HenriquesJVJoão VendaEFEmanuel Ferreira

Key Points

  • This report investigates the effectiveness of obinutuzumab in a patient with focal segmental glomerulosclerosis who did not respond completely to rituximab.
  • Documented clinical history of a 33-year-old woman with nephrotic syndrome and primary FSGS.
  • Treated with corticosteroids, cyclosporine, and rituximab with only partial response.
  • Administered obinutuzumab (two doses) after persistence of symptoms.
  • Monitored proteinuria and serum albumin levels post-treatment.
  • Achieved complete remission with obinutuzumab after two months, with proteinuria reduced to 0.2 g/24 h.
  • Sustained B-cell depletion without adverse events noted.
  • Repeated administration of obinutuzumab successfully re-induced remission after initial response had diminished.

Abstract

Introduction Podocytopathies such as minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS) remain therapeutic challenges in adults. Although corticosteroids and rituximab (RTX), a chimeric anti-CD20 monoclonal antibody, are effective in most patients, up to 10% show resistance or relapse despite B-cell depletion. Obinutuzumab (OBZ), a humanized type II anti-CD20 monoclonal antibody, achieves deeper and more sustained B-cell depletion and may overcome RTX inadequate response. Case report A 33-year-old woman presented with nephrotic syndrome (proteinuria 7.1 g/24 h, serum albumin 2.6 g/dL, preserved renal function). Kidney biopsy revealed primary FSGS. She achieved only partial remission with corticosteroids and cyclosporine. RTX (1 g × 2 doses) induced transient peripheral B-cell depletion but no complete remission. A second biopsy excluded chronic changes, and genetic testing for hereditary podocytopathy was negative. Thus 67 weeks after diagnosis and initial treatment with persistent proteinuria 1g/24 h and hypoalbuminemia, the patient received OBZ (1 g × 2 doses, two weeks apart). Two months later, she achieved complete remission (proteinuria 0.2 g/24 h, serum albumin 3.7 g/dL), with sustained B-cell depletion and no adverse events. A repeat administration of OBZ (1 g) was performed 10 months later due to B-cell repopulation, rising proteinuria (0.6 g/24 h), and mild hypoalbuminemia (serum albumin 3.4 g/dL), successfully re-inducing complete remission (proteinuria 0.2 g/24 h, serum albumin 3.8 g/dL). Discussion This case illustrates the potential of OBZ as an effective therapeutic option in podocytopathies with RTX inadequate response. The superior efficacy of OBZ may result from enhanced antibody-dependent cellular cytotoxicity, depletion of tissue-resident B cells, and reduced immunogenicity compared with RTX. OBZ may thus offer an alternative in refractory MCD/FSGS.

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Cite This Study

Henriques et al. (2026) studied this question.

synapsesocial.com/papers/69aa6f0d531e4c4a9ff5938chttps://doi.org/10.3389/fneph.2026.1772736
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