We performed a multi-centre randomized controlled trial to compare the efficacy of mycophenolate mofetil (MMF) to that of cyclosporine A (CsA) in treating children with frequently relapsing nephrotic syndrome and biopsy-proven minimal change disease. Of the 31 randomized initially selected patients, seven were excluded. The remaining 24 children received either MMF 1200 mg/m2 per day (n = 12) or CsA 4–5 mg/kg per day (n = 12) during a 12-month period. Of the 12 patients in the MMF group, two discontinued the study medication. Evaluation of the changes from the baseline glomerular filtration rate showed an overall significant difference in favour of MMF over the treatment period (p = 0.03). Seven of the 12 patients in the MMF group and 11 of the 12 patients in the CsA group remained in complete remission during the entire study period. Relapse rate in the MMF group was 0.83/year compared to 0.08/year in the CsA group (p = 0.08). None of the patients reported diarrhea. Pharmacokinetic profiles of mycophenolic acid were performed in seven patients. The patient with the lowest area under the curve had three relapses within 6 months. In children with frequently relapsing minimal change nephrotic syndrome, MMF has a favourable side effect profile compared to CsA; however, there is a tendency towards a higher relapse risk in patients treated with MMF.
Introduction
Nephrotic syndrome in children is primarily (77%) caused by minimal change disease [1]. The vast majority (92%) of these patients will respond well to corticosteroids. However, as many as 70% of children with nephrotic syndrome experience at least one relapse, and 30% will develop a more complicated course with frequent relapses (≥2 relapses/6 months) with or without steroid dependency (relapse during tapering or within 2 weeks after discontinuation of corticosteroids) [2, 3]. A short course of cyclophosphamide (2–3 months 2–3 mg/kg per day) will lead to prolonged remission in 25–60% of children with frequently relapsing nephrotic syndrome [4, 5]. Most patients (80%) who do not respond to cyclophosphamide can achieve prolonged remission with cyclosporine A (CsA), but long-term treatment can have harmful side-effects of which nephrotoxicity and hypertension are the most critical [6‐11].
The results from several uncontrolled studies have recently suggested a positive effect of the relatively new immunosuppressive drug mycophenolate mofetil (MMF) in preventing relapses in children with frequently relapsing nephrotic syndrome due to minimal changes and various other nephropathies [12‐21]. Mycophenolate mofetil inhibits inosine monophosphate dehydrogenase, an enzyme required for the de novo pathway of purine synthesis which, in turn, is essential for the proliferation of B and T lymphocytes. In contrast with CsA, MMF has no known nephrotoxic side effects. To the best of our knowledge, there are currently no randomized controlled studies comparing the efficacy of MMF and CsA in treating nephrotic syndrome in children or adults. Furthermore, pharmacokinetic profiles of MMF in children are scarce and mainly concern renal transplant recipients using multiple drugs [22, 23].
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We performed a randomized controlled trial to study the efficacy and side effects of MMF compared to CsA in children with frequently relapsing nephrotic syndrome and biopsy proven minimal change disease.
Methods
General outline of the study
This was a multi-centre randomized controlled trial aimed at studying the efficacy and side effects of MMF compared to CsA in children with frequently relapsing nephrotic syndrome. We also performed a pharmacokinetic study of MMF. Patients were enrolled between January 2003 and June 2005 in six University Hospitals in the Netherlands and Belgium. The ethics committees of the hospitals approved the study protocol. Informed consent was obtained after written and oral information was given.
Inclusion and exclusion criteria
Children (<18 years) with frequently relapsing nephrotic syndrome with or without steroid dependency, despite cyclophosphamide therapy, were asked to participate in the study. Inclusion requirements were glomerular filtration rate (GFR) >80 ml/min per 1.73 m2 and biopsy-proven minimal change disease. Patients already on CsA medication were still eligible for the study. The children had to be in remission at study entry (trace or nil proteinuria, as determined by the dipstick test or <100 mg/dl for at least 3 days). Patients with severe leucopenia (leucocytes <3.0 × 1000 cells/mm3), severe anemia (haemoglobin <8.9 g/dl) or active infection were excluded from the study.
Study medication
Group A patients were treated for 12 months with MMF, 1200 mg/m2 per day b.i.d. (two doses per day, maximum dose 1 g twice daily). In the case of severe leucopenia, severe anemia, diarrhea (see Follow-up) or serious infection, the dose was decreased by 25%. If side effects persisted, the dose was reduced by an additional 25% of the initial dose. Dose adjustment was not based on mycophenolate trough levels.
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Group B patients were treated for 12 months with the conventional treatment, which consists of CsA 4–5 mg/kg per day b.i.d. The dose was adjusted aiming at trough levels of 50–150 µg/l. In total, four different assays were used [six patients, EMIT (enzyme multiplied immunoassay technique); three, FPIA (fluorescence polarization immunoassay); two, ACMIA (antibody conjugated magnetic immunoassay ); one, AxSYM (human chorionic gonadotropin test)]; however, all participating centres standardly aim at a trough level of 50–150 µg/l for their nephrotic patients irrespective of the method used. In patients already on CsA medication at study entry, the CsA was tapered and stopped within 2 weeks after starting MMF therapy (group A) or continued (group B).
Nephrotic syndrome relapses, defined as proteinuria of 3+ or more by the dipstick test or >40 mg/m2 per hour for more than 3 days after a period of remission, were treated with prednisolone 60 mg/m2 once daily until remission was achieved, followed by 4 weeks of 40 mg/m2 every other day or other tapering regimes at the discretion of the treating pediatrician.
Follow-up
Every 3 months during the study-period of 12 months, the number of relapses, (gastro-intestinal) side effects and additional medication were noted. Diarrhea was defined as an unusually frequent passage of loose stools that required intervention. The mean dose of prednisolone (mg/kg per day) over the 12-month study period was calculated. Blood pressure was also measured, and the patient was checked for gingival hyperplasia and hypertrichosis. An automatic device was used to measure blood pressure, which was then compared to that of healthy children of the same gender, age and height [24]. Hypertension was defined as a systolic and/or diastolic blood pressure >1.64 SDS (95th percentile) or when antihypertensive medication was prescribed (excluding indications such as proteinuria or headache).
In addition, blood count, serum creatinine, serum albumen, CsA or MMF trough levels and urine protein/creatinine were determined. The GFR was calculated using an adapted Schwartz formula [25, 26]. Serum lipids [cholesterol, triglycerides, low-density lipoprotein-cholesterol (LDL) and high-density lipoprotein cholesterol (HDL)] were measured at study entry and after 1 year.
Pharmacokinetic study of mycophenolic acid
Mycophenolic acid (MPA) area under the curve (AUC) was determined after 3–6 months of treatment, while patients were in remission, by the limited sampling method according to Schütz [27]. Blood samples were taken predose and 75 and 360 min after the morning dose. The AUC was calculated using the formula \({\text{AUC}} = {\text{5}}{\text{.2}} + {\text{7}}{\text{.1}} \times {\text{C}}_{{\text{0min}}} + {\text{1}} \times {\text{C}}_{{\text{75min}}} + {\text{5}}{\text{.4}} \times {\text{C}}_{{\text{360min}}} \). To measure the levels of MPA, we used an immunoassay for ten patients (EMIT–MPA Assay; Behring Diagnostics, San Jose, CA) and a high-pressure liquid chromatography system with a UV detector (HPLC-UV; Merck-Hitachi, Stuttgart, Germany) for two patients.
Statistics
Patients were stratified for both recent use of CsA and treatment centre and subsequently randomized, based on a computer-generated randomization list, using opaque sealed envelopes prepared by the trial statistician. Study-patients and investigators were not blinded to treatment group. Patients who did not complete the 12-month study period were included in the analysis according to the intention-to-treat-principle.
The primary end point in this study was GFR. Secondary end points were relapse-free survival time, occurrence of diarrhea, blood pressure and blood count parameters. Assuming a standard deviation for GFR of 20 ml/min per 1.73 m2, we calculated that 20 patients in each group was sufficient to detect a difference in GFR of 18 ml/min per 1.73 m2 between both groups (p < 0.05, power = 80%). We had aimed at 20 patients in each group, but failed to enrol these, among other reasons due to the growing preference of MMF treatment in this group of patients.
Differences between the groups at baseline were tested with the Mann–Whitney U test for continuous data and the chi-square test for categorical data. Kaplan–Meier curves were used to compare relapse-free survival time between the two groups. Relapse rate, prednisolone dose and MPA trough levels were analysed by the Mann-Whitney U test. The longitudinal measurements of GFR, blood pressure and blood count parameters were analyzed using repeated measurements analysis of variance (ANOVA) with baseline values as covariates. The GFR was logarithmically transformed in this analysis to approximate normal distributions. Serum lipids were analysed by ANOVA. A p value < 0.05 was considered to be significant. All computations were carried out in SPSS ver. 11.5 (SPSS, Chicago, IL).
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Results
Of the 31 randomized patients with frequently relapsing nephrotic syndrome who were originally selected for the study, seven were excluded (Fig. 1). The remaining 24 children were evaluated during the study, and their patient characteristics at baseline are summarized in Table 1. Renal biopsy was performed 20 months (median, range 0–110 months) prior to the onset of the study. Cyclophosphamide was given in 23 of the 24 patients at a dosage of 2–3 mg/kg per day for 8 weeks. The study medication was discontinued during the study-period in two patients receiving MMF (see Efficacy).
Fig. 1
Flow chart of the study comparing mycophenolate mofetil (MMF) and cyclosporine (CsA) for remission maintenance in nephrotic syndrome. Asterisk indicates frequent relapses. There was one request for withdrawal from the study
Table 1
Patient characteristics and previous treatment for nephrotic syndrome
Patient characteristics
MMF
CsA
p
Number of patients
12
12
Male
10
11
1.00
Age (years)
10.9 (4.0–15.2)
9.2 (3.7–17.5)
0.81
Duration of nephrotic syndrome (years)
5.3 (1.1–11.4)
5.2 (1.1–12.3)
0.99
Steroid dependency
8
8
1.00
Previous treatment
Cyclophosphamide
12
11
1.00
Months before study entry
22 (5–103)
47 (5–153)
0.65
Levamisole
0
1
CsA
5
6
1.00
Duration of CsA medication (years)
2.2 (1.4–3.2)
4.0 (1–10)
0.51
Data are given as number of patients or as the median, with the range in parenthesis
MMF Mycophenolate mofetil; CsA cyclosporine A
×
Glomerular filtration rate
Mean estimated GFR in the MMF group increased by 6 ml/min per 1.73 m2 in 1 year; during the same period, the estimated GFR in the CsA group declined by 14 ml/min per 1.73 m2 (Table 2). The use of CsA medication prior to randomization did not cause a significant difference in GFR between both groups (mean change in GFR with or without prior CsA medication in the MMF group was 5 ml versus 7 ml/min per 1.73 m2; in the CsA group, this was −10 vs. −16 ml/min per 1.73 m2, respectively). Follow-up values for GFR were on average 13% lower (95% confidence interval: 1–23%, p = 0.03) in patients treated with CsA. After 3, 6 and 12 months of drug therapy, the mean GFR of the CsA group was significantly lower than the baseline value (p = 0.048, 0.041, 0.013, respectively); this is in contrast to the MMF group, where no significant changes from baseline were found (Fig. 2). One patient with CsA had slightly impaired renal function (GFR 77 ml/min per 1.73 m2) at the end of the study period, while none of the patients in the MMF group showed any sign of renal impairment.
Fig. 2
Change in the glomerular filtration rate (GFR) from baseline for patients receiving mycophenolate mofetil (MMF, n = 12) and cyclosporine A (CsA, n = 12) medication. The change in the GFR is expressed as ratio compared to baseline. Data are given as ANOVA estimates with standard errors. *p < 0.05 compared to baseline
Table 2
Results from the clinical and laboratory tests throughout the study
Clinical and laboratory parameters
Therapeutic drug programme
0 months
3 months
6 months
9 months
12 months
pa
GFR (ml/min per 1.73 m2)
MMF
125 (34)
123 (33)
126 (26)
125 (31)
131 (40)
0.03
CsA
123 (22)
112 (26)
107 (16)
114 (18)
109 (16)
Systolic blood pressure (SDS)
MMF
1.04 (0.89)
0.87 (0.84)
0.61 (0.83)
0.89 (0.68)
0.62 (0.71)
0.17
CsA
1.35 (0.93)
1.19 (0.56)
1.13 (0.78)
1.17 (1.05)
0.88 (1.16)
Diastolic blood pressure (SDS)
MMF
0.36 (0.77)
0.44 (0.80)
0.22 (0.63)
0.27 (0.71)
0.05 (0.68)
0.57
CsA
0.21 (0.83)
−0.05 (0.77)
0.00 (0.72)
0.12 (0.89)
0.30 (0.91)
Haemoglobin (g/dl)
MMF
13.5 (1.1)
13.2 (1.0)
13.0 (1.4)
13.0 (1.0)
13.5 (1.1)
0.005
CsA
13.0 (1.3)
12.2 (0.6)
12.0 (0.3)
11.9 (0.8)
12.0 (1.0)
Leucocytes (×1000 cells/mm3)
MMF
7.3 (2.6)
6.7 (1.9)
7.4 (3.9)
6.5 (2.1)
6.1 (1.7)
0.43
CsA
8.1 (2.8)
7.0 (1.7)
7.7 (2.2)
7.7 (2.6)
8.1 (3.0)
Lymphocytes (×1000 cells/mm3)
MMF
2.5 (1.3)
2.5 (0.9)
2.0 (0.9)
2.0 (0.9)
2.0 (0.7)
0.99
CsA
2.8 (1.2)
2.3 (0.6)
2.3 (0.8)
2.0 (0.8)
2.3 (0.5)
Cholesterol (mg/dl)
MMF
196 (81)
181 (89)
0.59
CsA
181 (42)
177 (31)
Triglycerides (mg/dl)
MMF
114 (50)
84 (30)
0.59
CsA
114 (50)
85 (40)
LDL-cholesterol (mg/dl)
MMF
104 (23)
85 (19)
0.10
CsA
112 (46)
116 (35)
HDL-cholesterol (mg/dl)
MMF
58 (15)
54 (8)
0.60
CsA
54 (12)
58 (12)
All values are means, with the standard deviation given in parenthesis
aThe p value compares the overall change from baseline between the two groups
×
Efficacy
The relapse-free survival curve is shown in Fig. 3. An overview of the number of relapses during the study-period is given in Table 3. Although the relapse rate in the MMF group (0.83/year ± 1.27 SD) appears to be higher than that in the CsA group (0.08/year ± 0.29 SD), the difference did not reach significance (p = 0.08). One patient with MMF experienced treatment failure, with three relapses within 6 months, which was reason to switch to CsA. While on CsA for the remaining 6 months of the study, this patient had one more relapse. Of the two patients in the MMF group with two relapses each, one patient admitted to be non-compliant and switched after 6 months to CsA therapy at his own request because of a loss of appetite and recurrence of eczema; the other patient had two dose reductions (see Side effects). Two of five patients with relapses in the MMF group had previous treatment with CsA, versus three of the seven without relapses. The mean prednisolone dose during the 12-month study period was not significantly different between the two groups (Table 3). Steroids were only given for the treatment of relapses, with the exception of one patient in the CsA group, who received low dose prednisolone (5 mg) on alternate days as maintenance therapy.
Fig. 3
Relapse-free survival curve for patients with mycophenolate mofetil (MMF, n = 12) and cyclosporine A (CsA, n = 12) medication. The p value is from the logrank test
Table 3
Efficacy of MMF compared to CsA
Parameter
MMF
CsA
p
Patient (n)
12
12
CsA (mg/kg per day)
-
5.1 (1.1)
MMF (mg/m2 per day)
1173 (114)
-
Prednisolone (n)a
9
5
0.21
Mean prednisolone dose (mg/kg/day)
0.13 (0.16)
0.08 (0.12)
0.21
Number of relapses (n)
Zero
7
11
One
2
1
Two
2
0
Four
1
0
Relapse rate (n/patient per year)
0.83
0.08
0.08
Data are given as mean, with the standard deviation given in parenthesis
aIncluding patients using prednisolone started just before study-entry as relapse treatment
×
Side effects
The side effects of MMF drug therapy were generally mild, and most patients tolerated MMF well. The MMF dose of one patient was reduced by 25% during a bout of pneumonia, and a few months later an additional 25% reduction was implemented because of unexplained fatigue; dose modification was not necessary in the other patients. None of the patients experienced diarrhea; however, one patient had a temporary slight increase in defecation frequency (one to three defecations per day), without other gastro-intestinal symptoms or weight loss.
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Blood pressure
Mean blood pressure did not change significantly in both groups during the study period (Table 2). After 12 months, one patient on MMF—compared to four patients on CsA—had hypertension, whereas at baseline four and three patients, respectively, were hypertensive (p = 0.32). One patient in the MMF group was treated for hypertension with angiotensin-converting enzyme (ACE) inhibition at study entry; this was withdrawn during the study period. Antihypertensive drugs were not prescribed for any other indications (e.g. proteinuria or headache).
Laboratory parameters
The laboratory results on the blood count and serum lipids are given in Table 2. At 12 months, the haemoglobin (Hb) level was significantly lower in the CsA group than in the MMF group (p = 0.005). None of the patients developed anemia (Hb <10.4 mmol/l in more than one measurement) or leucopenia (leucocytes <4.0 × 1000 cells/mm3 in more than one measurement). Two patients, one in each group, developed transient mild lymphopenia (lymphocytes 1.00–1.50 × 1000 cells/mm3). Two other patients in the MMF group, both with pre-existing lymphopenia (1.1 and 0.98 × 1000 cells/mm3, respectively), continued to have low lymphocyte counts (minimum 0.95 × 1000 cells/mm3) without infections.
Hypertrichosis and gingival hyperplasia
After 12 months, hypertrichosis occurred in three of eight patients on CsA drug therapy; in contrast none of the patients on MMF medication developed hypertrichosis. Gingival hyperplasia was observed in six of ten patients in the CsA group versus none in the MMF group.
Pharmacokinetic study
Pharmacokinetic profiles of MPA were determined in seven patients (Fig. 4). During AUC determination, all patients were in remission and using 1098–1315 mg/m2 per day MMF. One patient received co-medication with benazepril and cetirizine, and another patient received prednisolone, calcium and vitamin D; all other patients received MMF monotherapy. The patient with the lowest AUC had three relapses within 6 months while using MMF 1315 mg/m2 per day and showed no evidence of non-compliance
Fig. 4
Mycophenolic acid levels with area under the curve. Mycophenolic acid levels were measured using an immunoassay (filled symbols) or by high-performance liquid chromatography–ultraviolet test (open symbols). Unbroken line no relapses, broken line three relapses in 6 months
×
For ten patients on MPA drug therapy, four with relapses and six without, one or more MPA trough levels were available. Mean MPA trough level of patients with relapses was 3.4 (SD 2.4) mg/l compared to 3.6 (SD 1.0) mg/l of patients without relapses (p = 0.48).
Discussion
The current standard treatment of frequently relapsing nephrotic syndrome in children with long-term prednisolone is successful but eventually leads to unwanted side effects, such as osteopenia, growth failure and cataract. A switch of medication is then necessary to prevent further relapses of nephrotic syndrome. The long-term treatment of children with CsA is effective but also has unfavourable side effects, of which hypertension and nephrotoxicity are the most important [6‐11]. An alternative is welcome, and recent studies suggest a positive effect of MMF in children with nephrotic syndrome of various etiologies [12‐21]. Here we report the first randomized controlled trial comparing the side effects and efficacy of MMF and CsA in children with frequently relapsing nephrotic syndrome.
The side-effect profile of MMF in our patients was more favourable than that of CsA. The mean estimated GFR in the MMF group increased with 6 ml/min per 1.73 m2 during 1 year of treatment compared to a decline of 14 ml/min per 1.73 m2 in the CsA group. This finding is in line with previous studies in which no nephrotoxicity of MMF was reported [28]. The reduction in the GFR in the CsA-treated patients may be related to the vasoconstrictive effects of CsA [7, 8]. Although this haemodynamic effect can be reversible following the cessation of therapy, long-term treatment is often needed for remission maintenance in these children. In addition, it is well known that even after only 1 year of treatment with CsA, tubulointerstitial lesions can be found [29].
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As expected, hypertrichosis and gingival hypertrophy were only seen in patients treated with CsA. Although diarrhea occurs in up to 43% of transplant recipients treated with MMF, we found only mild gastrointestinal symptoms, which is in agreement with recent studies on MMF in nephrotic children [14, 19]. Surprisingly, our analysis of haematological parameters revealed that patients in the MMF group had a significantly higher haemoglobin level at 12 months than those in the CsA group. This finding is in contrast with studies reporting a negative effect of MMF on erythropoiesis in renal transplant recipients [30, 31]. However, none of our patients developed anemia, nor did any of the patients suffer from significant leucopenia or lymphopenia.
Our data suggest that CsA is more effective in preventing relapses than MMF, but the number of patients in our study is too small to draw definite conclusions on this endpoint. Despite the lack of previous randomized controlled trials proving the efficacy of MMF in nephrotic syndrome, pediatric nephrologists already feel that MMF is effective in these children. This made recruitment for our study difficult and explains the small number of children enrolled.
However, taking into account that all patients had a history of frequently relapsing nephrotic syndrome, the current relapse rate of <1 /patient per year even in the MMF group is a positive finding. One patient on MMF medication experienced treatment failure, with three relapses within 6 months, and needed alternative treatment. This patient had the lowest AUC of MPA. We hypothesize that dose adjustment in this patient might have improved the efficacy of the MMF drug therapy. An AUC was not available for the two patients with two relapses. One of these appeared to be non-compliant; in the second patient, the MMF was tapered to 50% of the original dose. As such, these patients may have had suboptimal MPA levels. Based on these anecdotal observations as well as on reports by others, we suggest that the issue of dose dependency should be further addressed in any prospective MMF trial in the future [13, 20, 23].
We used two methods for therapeutic drug monitoring: EMIT and HPLC. Westley et al. showed a good correlation between both methods (r2 = 0.851), with a small overestimation of MPA plasma concentration with the EMIT in the therapeutic range \(\left( {{\text{EMIT}} = {\text{0}}{\text{.973 HPLC}} + {\text{0}}{\text{.55}}} \right)\) [32]. The pharmacokinetic profiles of MPA depict a lower level in six of seven patients after 6 h compared to predose level; this is due to the enterohepatic circulation of MPA glucuronide, which undergoes deglucuronidation and reabsorption as MPA [33, 34]. In renal transplant children, a secondary increase in MPA levels was observed, occurring 6–12 h after ingestion, which was compatible with enterohepatic recirculation [34, 35].
The preponderance of males in our study differs from the male:female ratio of 1.5 in children with first episode nephrotic syndrome, but it is in concert with a higher relapse frequency found in boys [1, 36, 37].
In conclusion, this study suggests a beneficial effect of MMF in children with frequently relapsing minimal change nephrotic syndrome. However, although MMF may not be as efficacious as CsA, the side-effect profile of MMF is much more benign. We postulate that there is a role for MMF in the treatment of frequently relapsing nephrotic syndrome in children; however, larger randomized controlled trials with therapeutic drug monitoring and individual dose adjustment are warranted.
Acknowledgements
We are very grateful to the physicians who participated in the study and provided the follow up data: K.J.M van Hoeck, L.J.W.M. Pierik, J.G.J. Vande Walle and P. Vos. Roche provided the mycophenolate mofetil.
Open Access
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License (https://creativecommons.org/licenses/by-nc/2.0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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