Background The effectiveness of therapeutic drug monitoring (TDM) of mycophenolic acid (MPA) trough levels in children with steroid-dependent nephrotic syndrome (SDNS)/frequently relapsing nephrotic syndrome (FRNS) treated with mycophenolate mofetil (MMF) has not been adequately assessed. Methods We performed an international, retrospective study including children with SDNS/FRNS treated with MMF as the first-line steroid-sparing agent and a follow-up of more than 6 months. Patients were categorized into two groups: TDM, if MPA trough levels were monitored, and no-TDM, if not. In the TDM group, MMF doses were adjusted to maintain MPA trough levels of more than 3 mu g/ml, unless toxicity occurred. The primary outcome was relapse-free survival. Results A total of 167 patients were observed, 90 in the TDM group and 77 in the no-TDM group. Relapse-free survival over the total follow-up was significantly longer in the TDM group (P = 0.001, log-rank test) with an estimated relapse-free survival at 6 months of 73% for the TDM group and 55% for the no-TDM group. After correcting for potential confounders, the association remained statistically significant (P < 0.001). TDM patients also received lower doses of prednisone after MMF introduction. In the TDM group, children were more likely to modify their initial dose (90% versus 9%; P < 0.001). Although MMF dose was not associated with relapse (median 1186 versus 1298 mg/m(2); P = 0.14), MPA trough levels were significantly higher in children who did not relapse (4.0 versus 2.7 mu g/ml, P = 0.001). Among children maintaining mean MPA levels more than 2.9 mu g/ml, relapse-free survival at 6 months was 86%. Reported side effects were similar in both groups. Conclusions Monitoring MPA trough levels was associated with an approximately 20% higher MMF effectiveness in maintaining remission at 6 months in children with SDNS/FRNS. Personalized MMF dosing, adjusted to maintain MPA levels more than 2.9 mu g/ml, was both safe and effective. We recommend including MPA trough level monitoring in future studies comparing MMF with other steroid-sparing agents in children with SDNS/FRNS.
Effectiveness of Mycophenolate Mofetil Trough Level Monitoring in Children with Relapsing Nephrotic Syndrome / W. Morello, S. Bernardi, G. Puccio, A.S. Bellotti, E. Preka, M. Grapin, M. Prévot, M. Charbit, T. Nittoli, M. Gallieni, L. Ghio, A. Edefonti, O. Boyer, G. Montini. - In: CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY. - ISSN 1555-9041. - (2025), pp. 1-9. [10.2215/cjn.0000000824]
Effectiveness of Mycophenolate Mofetil Trough Level Monitoring in Children with Relapsing Nephrotic Syndrome
W. Morello
Primo
;A.S. Bellotti;T. Nittoli;M. Gallieni;G. MontiniUltimo
2025
Abstract
Background The effectiveness of therapeutic drug monitoring (TDM) of mycophenolic acid (MPA) trough levels in children with steroid-dependent nephrotic syndrome (SDNS)/frequently relapsing nephrotic syndrome (FRNS) treated with mycophenolate mofetil (MMF) has not been adequately assessed. Methods We performed an international, retrospective study including children with SDNS/FRNS treated with MMF as the first-line steroid-sparing agent and a follow-up of more than 6 months. Patients were categorized into two groups: TDM, if MPA trough levels were monitored, and no-TDM, if not. In the TDM group, MMF doses were adjusted to maintain MPA trough levels of more than 3 mu g/ml, unless toxicity occurred. The primary outcome was relapse-free survival. Results A total of 167 patients were observed, 90 in the TDM group and 77 in the no-TDM group. Relapse-free survival over the total follow-up was significantly longer in the TDM group (P = 0.001, log-rank test) with an estimated relapse-free survival at 6 months of 73% for the TDM group and 55% for the no-TDM group. After correcting for potential confounders, the association remained statistically significant (P < 0.001). TDM patients also received lower doses of prednisone after MMF introduction. In the TDM group, children were more likely to modify their initial dose (90% versus 9%; P < 0.001). Although MMF dose was not associated with relapse (median 1186 versus 1298 mg/m(2); P = 0.14), MPA trough levels were significantly higher in children who did not relapse (4.0 versus 2.7 mu g/ml, P = 0.001). Among children maintaining mean MPA levels more than 2.9 mu g/ml, relapse-free survival at 6 months was 86%. Reported side effects were similar in both groups. Conclusions Monitoring MPA trough levels was associated with an approximately 20% higher MMF effectiveness in maintaining remission at 6 months in children with SDNS/FRNS. Personalized MMF dosing, adjusted to maintain MPA levels more than 2.9 mu g/ml, was both safe and effective. We recommend including MPA trough level monitoring in future studies comparing MMF with other steroid-sparing agents in children with SDNS/FRNS.| File | Dimensione | Formato | |
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