Efficacy and safety of mycophenolate mofetil versus cyclophosphamide therapy for Henoch schonlein purpura nephritis in children: A meta-analysis

Author:

Wang Di1,Liu Tongqiang1,Lu Jingkui23,Li Xianping4,Liu Xiaoming4,Xu Wei234ORCID

Affiliation:

1. Department of Nephrology, The Affiliated Changzhou NO.2 People’s Hospital of Nanjing Medical University, Jiangsu, China

2. Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, Jiangsu, China

3. Department of Nephrology, Wujin Hospital Affiliated with Jiangsu University, Changzhou, Jiangsu, China

4. Department of Nephrology, People’s Hospital of Hainan Tibetan Autonomous Prefecture, Hainan Tibetan Autonomous Prefecture, Qinghai, China.

Abstract

Objective: The objective of this meta-analysis was to compare the efficacy and safety between glucocorticoids combined with mycophenolate mofetil (MMF) versus glucocorticoids combined with cyclophosphamide (CTX) for henoch schonlein purpura nephritis (HSPN) in children. Methods: Databases including PubMed, EMbase, the Cochrane Library, China National Knowledge Infrastructure, and Wanfang database were searched from the inception to April 5th, 2024. Eligible studies comparing glucocorticoids combined with MMF versus glucocorticoids combined with CTX for HSPN in children were included. Data were analyzed using Review Manager Version 5.3. Results: Ten studies were included in the meta-analysis. Six randomized controlled trials (RCTs) and 4 non-randomized studies involving 675 patients were identified. Compared with CTX therapeutic schedule, MMF therapeutic schedule had a higher complete remission (CR) within the 6 months (OR 1.61, 95%CI 1.16–2.22, P = .004) and CR within the 12 months (OR 1.73, 95%CI 1.00–2.97, P = .05). However, there was no significant difference between MMF and CTX therapeutic schedule concerning total remission (TR) within the 6 months (OR 1.54, 95%CI 0.82–2.92, P = .18) and TR within the 12 months (OR 2.08, 95%CI 0.86–5.01, P = .10). In addition, incidences of gastrointestinal discomfort (OR 0.33, 95%CI 0.19–0.56, P < .0001), liver function injury (OR 0.28, 95%CI 0.09–0.87, P = .03), myelosuppression (OR 0.15, 95%CI 0.06–0.41, P = .0001), alopecia (OR 0.25, 95%CI 0.07–0.91, P = .03) in MMF therapeutic schedule were all lower than CTX therapeutic schedule. There was no statistically significant difference between the 2 therapeutic schedules concerning infection (OR 0.90, 95%CI 0.50–1.61, P = .72), rash (OR 0.38, 95%CI 0.07–2.04, P = .26). Conclusion: Glucocorticoids combined with MMF had a higher CR and lower incidence of adverse effects compared with glucocorticoids combined with CTX in the treatment of HSPN in children.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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