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Steroid-sensitive nephrotic syndrome: an evidence-based update of immunosuppressive treatment in children
Nicholas Larkins1, Siah Kim2, Jonathan Craig3
1Centre for Kidney Research, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
Insights
Corticosteroids treat childhood nephrotic syndrome, but relapses are common. Extended initial treatment doesn't prevent frequent relapses, and steroid-sparing agents are used for difficult cases.
Area of Science:
- Pediatric Nephrology
- Glomerular Diseases
Background:
- Nephrotic syndrome is a common pediatric kidney disease.
- Corticosteroids are the primary treatment, inducing remission in most children.
- Relapses are frequent, leading to frequently relapsing nephrotic syndrome (FRNS) or steroid-dependent nephrotic syndrome (SDNS) in many.
Purpose of the Study:
- To review recent randomized trial data on interventions for steroid-sensitive nephrotic syndrome (SSNS).
- To update pediatricians on current evidence for managing SSNS, including relapses.
Main Methods:
- Review of recent large, well-designed randomized control trials.
- Analysis of data on initial steroid regimens and management of relapses.
- Evaluation of evidence for non-corticosteroid immunosuppressive agents.
Main Results:
- Extended initial corticosteroid treatment (up to 6 months) did not significantly reduce relapse risk compared to shorter durations (2-3 months).
- Evidence suggests short corticosteroid courses during infections may prevent relapses.
- Several steroid-sparing agents (e.g., cyclophosphamide, rituximab) reduce relapse risk in FRNS/SDNS, but head-to-head comparisons are limited.
Conclusions:
- Initial treatment duration for SSNS may not need to exceed 2-3 months.
- Management of relapses and choice of steroid-sparing agents require further research.
- Current evidence supports a shift towards shorter initial steroid courses and judicious use of steroid-sparing agents for refractory cases.
Abstract:
Nephrotic syndrome is one of the most common paediatric glomerular diseases, with an incidence of around two per 100,000 children per year. Corticosteroids are the mainstay of treatment, with 85%-90% of children going into remission with an 8-week course of treatment. Unfortunately, nephrotic syndrome follows a relapsing and remitting course in the majority, with 90% relapsing at least once. About half will progress to frequently relapsing nephrotic syndrome (FRNS) or steroid-dependent nephrotic syndrome (SDNS). Different initial steroid regimens have been evaluated since the first trials in Europe and America in the 1960s. Most trials have been designed to evaluate the optimal duration of the initial therapy, rather than different cumulative doses of corticosteroid, or the management of relapses. Until recently, these data suggested that an initial treatment duration of up to 6 months reduced the number of children developing a relapse, without evidence of increased steroid toxicity. Recently, three large, well-designed randomised control trials were published, which demonstrated no significant reduction in risk of relapse or of developing FRNS by extended treatment compared with 2 or 3 months. While there are few trial data to guide the treatment of individual relapses in steroid-sensitive nephrotic syndrome (SSNS), there is some evidence that a short course of corticosteroid therapy during upper respiratory tract infection may prevent relapse. In patients with FRNS or SDNS who continue to relapse despite low-dose alternate-day steroids a number of non-corticosteroid, steroid-sparing immunosuppressive agents (cyclophosphamide, ciclosporin, tacrolimus, mycophenolate mofetil, levamisole, rituximab) have been shown to reduce the risk of relapse and of FRNS. However, there are limited head-to-head data to inform which agent should be preferred. In this article, we review recent data from randomised trials to update paediatricians on the current evidence supporting interventions in SSNS.
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