Position statement of the Brazilian society of Rheumatology on mesna use as a preventive therapy for bladder disease in patients with systemic autoimmune diseases and systemic vasculitis under cyclophosphamide treatment.

IF 2 4区 医学 Q3 RHEUMATOLOGY Advances in Rheumatology Pub Date : 2024-05-21 DOI:10.1186/s42358-024-00380-0
Alexandre Wagner S de Souza, João Gabriel Dantas, Ana Carolina de Oliveira E Silva Montandon, Ana Luísa Calich, Andrea Rocha de Saboia Mont' Alverne, Andrese Aline Gasparin, Dante Bianchi, Emily Figueiredo Neves Yuki, Nathalia Sacilotto, Edgard Torres Dos Reis Neto, Odirlei André Monticielo, Ivanio Alves Pereira
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Abstract

Objective: To review current literature to support the use of mesna as a preventive therapy for hemorrhagic cystitis and bladder cancer in patients with systemic autoimmune diseases and systemic vasculitis treated with cyclophosphamide.

Materials and methods: The search for articles was conducted systematically through MEDLINE, LILACS, Cochrane Library, and Embase databases. Only articles in English were selected. For available records, titles and abstracts were selected independently by two investigators.

Results: Eighteen studies were selected for analysis. The known adverse effects of cyclophosphamide were hematological toxicity, infections, gonadal toxicity, teratogenicity, increased risk for malignancy and hemorrhagic cystitis. Long-term toxicity was highly dependent on cyclophosphamide cumulative dose. The risk of bladder cancer is especially higher in long-term exposure and with cumulative doses above 36 g. The risk remains high for years after drug discontinuation. Hemorrhagic cystitis is highly correlated with cumulative dose and its incidence ranges between 12 and 41%, but it seems to be lower with new regimens with reduced cyclophosphamide dose. No randomized controlled trials were found to analyze the use of mesna in systemic autoimmune rheumatic diseases and systemic vasculitis. Retrospective studies yielded conflicting results. Uncontrolled prospective studies with positive results were considered at high risk of bias. No evidence was found to support the use of mesna during the treatment with cyclophosphamide for autoimmune diseases or systemic vasculitis to prevent hemorrhagic cystitis and bladder cancer. In the scenarios of high cumulative cyclophosphamide dose (i.e., > 30 g), patients with restricted fluid intake, neurogenic bladder, therapy with oral anticoagulants, and chronic kidney disease, mesna could be considered.

Conclusion: The current evidence was found to be insufficient to support the routine use of mesna for the prophylaxis of hemorrhagic cystitis and bladder cancer in patients being treated for systemic autoimmune diseases and systemic vasculitis with cyclophosphamide. The use may be considered for selected cases.

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巴西风湿病学会关于将美司那作为环磷酰胺治疗下的系统性自身免疫性疾病和系统性血管炎患者膀胱疾病预防疗法的立场声明。
目的回顾现有文献,以支持使用美斯那作为环磷酰胺治疗系统性自身免疫性疾病和系统性血管炎患者出血性膀胱炎和膀胱癌的预防疗法:通过 MEDLINE、LILACS、Cochrane Library 和 Embase 数据库系统地检索文章。只选择英文文章。对于现有记录,由两名研究人员独立选择标题和摘要:结果:共选取了 18 项研究进行分析。已知环磷酰胺的不良反应包括血液学毒性、感染、性腺毒性、致畸性、增加恶性肿瘤风险和出血性膀胱炎。长期毒性在很大程度上取决于环磷酰胺的累积剂量。长期接触和累积剂量超过 36 克时,罹患膀胱癌的风险尤其高。出血性膀胱炎与累积剂量高度相关,发生率在 12% 至 41% 之间,但在减少环磷酰胺剂量的新方案中,发生率似乎较低。目前还没有发现随机对照试验来分析美斯那在系统性自身免疫性风湿病和系统性血管炎中的应用。回顾性研究的结果相互矛盾。结果呈阳性的无对照前瞻性研究被认为存在较高的偏倚风险。没有证据支持在使用环磷酰胺治疗自身免疫性疾病或系统性血管炎期间使用美司那来预防出血性膀胱炎和膀胱癌。在高累积环磷酰胺剂量(即大于 30 克)、限制液体摄入、神经源性膀胱、口服抗凝剂和慢性肾病患者的情况下,可考虑使用美司纳:目前的证据不足以支持在使用环磷酰胺治疗系统性自身免疫性疾病和系统性血管炎的患者中常规使用美司那来预防出血性膀胱炎和膀胱癌。可考虑在特定病例中使用。
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来源期刊
Advances in Rheumatology
Advances in Rheumatology Medicine-Rheumatology
CiteScore
4.00
自引率
4.30%
发文量
41
审稿时长
53 weeks
期刊介绍: Formerly named Revista Brasileira de Reumatologia, the journal is celebrating its 60th year of publication. Advances in Rheumatology is an international, open access journal publishing pre-clinical, translational and clinical studies on all aspects of paediatric and adult rheumatic diseases, including degenerative, inflammatory and autoimmune conditions. The journal is the official publication of the Brazilian Society of Rheumatology and welcomes original research (including systematic reviews and meta-analyses), literature reviews, guidelines and letters arising from published material.
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