scholarly journals Comparative efficacy and safety of mycophenolate mofetil and cyclophosphamide in the induction treatment of lupus nephritis

Medicine ◽  
2020 ◽  
Vol 99 (38) ◽  
pp. e22328 ◽  
Author(s):  
Yue-Peng Jiang ◽  
Xiao-Xuan Zhao ◽  
Rong-Rong Chen ◽  
Zheng-Hao Xu ◽  
Cheng-Ping Wen ◽  
...  
2010 ◽  
Vol 38 (1) ◽  
pp. 69-78 ◽  
Author(s):  
ZAHI TOUMA ◽  
DAFNA D. GLADMAN ◽  
MURRAY B. UROWITZ ◽  
JOSEPH BEYENE ◽  
ELIZABETH M. ULERYK ◽  
...  

Objective.To systematically review the efficacy and safety of mycophenolic acid and mycophenolate mofetil (MMF) compared to cyclophosphamide (CYC) for the induction treatment of lupus nephritis (LN).Methods.Medline, Embase, the Cochrane Center Register of Controlled Trials, and abstracts presented in major international conferences were searched for randomized controlled trials. The primary outcome was renal remission (complete, partial, and overall) and secondary outcomes were adverse events during study period and longterm followup data. Data were compared between groups and relative risk (RR) and 95% CI were calculated.Results.Four trials of a total of 618 patients were included. MMF was not superior to CYC for renal remission (partial RR 0.94, 95% CI 0.80 to 1.12; complete RR 0.67, 95% CI 0.35 to 1.28, and overall RR 0.89, 95% CI 0.71 to 1.10). There was a significant reduction in alopecia (RR 5.77, 95% CI 1.56 to 21.38) and amenorrhea (RR 6.64, 95% CI 2.00 to 22.07) with the use of MMF compared to CYC. These results should be interpreted with caution given the width of the CI. There was no significant difference for infections, leukopenia, gastrointestinal symptoms, herpes zoster, endstage renal disease, and death among groups during study period and longterm followup data.Conclusion.We could not show that MMF is superior to CYC for the induction treatment of LN. Patients treated with MMF showed reduced risk of certain side effects. MMF can be used as an alternative to CYC for the induction treatment of LN.


Drugs ◽  
2012 ◽  
Vol 72 (11) ◽  
pp. 1521-1533 ◽  
Author(s):  
Lin-Lin Liu ◽  
Yi Jiang ◽  
Li-Ning Wang ◽  
Li Yao ◽  
Zi-Long Li

2020 ◽  
Vol 5 (3) ◽  
pp. S349-S350
Author(s):  
G. Aroca ◽  
W.A. PEÑA-VARGAS ◽  
H.J. Gonzalez-Torres ◽  
A. Iglesias-Gamarra ◽  
R. García-Toloza ◽  
...  

2021 ◽  
Author(s):  
Panagiotis Athanassiou ◽  
Lambros Athanassiou ◽  
Ifigenia Kostoglou-Athanassiou

Systemic lupus erythematosus (SLE) is a systemic autoimmune disease. It is characterized by a variable clinical course ranging from mild to fatal disease. It can affect the kidneys. The aim of treatment in SLE is the prevention of flares and the prevention of accumulation of damage to the main organs affected as well as the prevention of drug side effects. The cornerstone of SLE treatment is hydroxychloroquine. Corticosteroids are used both as induction treatment in disease flares as well as in small doses as maintenance treatment. Immunosuppressants, such as azathioprine, methotrexate and mycophenolate mofetil are used as steroid sparing agents. Calcineurin inhibitors, namely tacrolimus and cyclosporin A may also be used as immunosuppressants and steroid sparing agents. Pulse methylprednisolone, along with mycophenolate mofetil and cyclophosphamide are used as induction treatment in lupus nephritis. Rituximab, an anti-CD20 biologic agent may be used in non-renal SLE. In patients insufficiently controlled with hydroxychloroquine, low dose prednisone and/or immunosuppressive agents, belimumab may be used with beneficial effects in non-renal disease and lupus nephritis.


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