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Levamisole for corticosteroid-dependent nephrotic syndrome in childhood. British Association for Paediatric
Insights
Levamisole effectively maintains remission in children with frequently relapsing nephrotic syndrome, offering a safer alternative to long-term immunosuppression. This immunostimulant treatment showed significant benefits with minimal side effects.
Area of Science:
- Pediatric Nephrology
- Immunology
- Pharmacology
Background:
- Children with nephrotic syndrome often require high-dose corticosteroids, leading to dependence and potential long-term toxicity.
- Conventional alkylating therapies may fail to maintain remission and carry significant risks with prolonged use.
Purpose of the Study:
- To evaluate the efficacy and safety of levamisole as an alternative immunostimulant for maintaining steroid-free remission in children with frequently relapsing nephrotic syndrome.
Main Methods:
- A randomized controlled trial involving 61 children with corticosteroid-dependent nephrotic syndrome.
- Patients received either levamisole (2.5 mg/kg on alternate days) or a placebo for up to 112 days, with a planned reduction and cessation of prednisolone by day 56.
Main Results:
- Significantly more patients in the levamisole group (14/31) remained in remission at 112 days compared to the placebo group (4/30) (p < 0.01).
- No significant adverse events were reported in either group.
Conclusions:
- Levamisole is an effective and safe option for maintaining steroid-free remission in children with frequently relapsing nephrotic syndrome.
- It presents a promising alternative to prolonged immunosuppression or less effective therapies.
Abstract:
In children with corticosteroid-responsive nephrotic syndrome who are dependent on high-dose prednisolone, alkylating therapy often fails to maintain a remission, and long-term immunosuppression may be hazardous. An alternative approach to treatment is to use an immunostimulant such as levamisole. 61 children with frequently relapsing corticosteroid sensitive and dependent nephrotic syndrome were randomly allocated to receive levamisole, 2.5 mg/kg on alternate days (31 patients) or placebo (30 patients) for a maximum of 112 days. After entry to the trial, prednisolone was progressively reduced and was stopped by 56 days. The two groups were well matched for age and sex distribution, indices of corticosteroid toxicity, and previous alkylating therapy. 14 patients in the levamisole group and 4 in the placebo group remained in remission at 112 days (log rank analysis p less than 0.01). No significant adverse events were recorded. Levamisole is effective in maintaining a steroid-free remission in this condition and has few side-effects.
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