Table 5.
Study | Study design | Population | Rituximab protocol | Selected outcomes | Results |
---|---|---|---|---|---|
Kong et al35 | Retrospective case review | 24 patients with primary glomerular disease | One patient received a single infusion of rituximab 375 mg/m2 | CR: UPCR <30 mg/mmol and serum albumin ≥35 g/L | One patient achieved CR after 19 months |
Included two patients with idiopathic MPGN | The other received two rituximab infusions at 375 mg/m2 | PR: UPCR between 30 and 300 mg/mmol and serum albumin ≥30 g/L | One patient achieved PR after 29 months | ||
Adverse events | No serious adverse events during follow-up | ||||
Sugiura et al32 | Prospective, single-arm trial | 24 patients with primary glomerular disease | Single dose of 375 mg/m2 | Proteinuria at 6 months | In one patient with MPGN, proteinuria decreased from 9.8 g/day at baseline to 1.8 g/day at 6 months |
Included one patient with idiopathic MPGN | |||||
Dillon et al36 | Prospective, single-arm trial | Six patients with MPGN (four idiopathic, two with cryoglobulinemia) | 1 g on days 1 and 15 | CR: proteinuria ≤0.3 g/day without doubling of serum creatinine | The two patients with MPGN and cryoglobulinemia achieved CR at 12 months |
PR: proteinuria between 0.3 and 3.5 g/day without doubling of serum creatinine | The four patients with idiopathic MPGN achieved PR at 12 months | ||||
Adverse events | No adverse events during follow-up |
Abbreviations: CR, complete remission; MPGN, membranoproliferative glomerulonephritis; PR, partial remission; UPCR, urine protein over creatinine ratio.