Jiang Lucan, Liu Yi, Zhang Lingli, Santoro Cristina, Rodriguez Armando
Department of Pharmacy, West China Second University Hospital, Sichuan University, No. 17, Section Three, Ren Min Nan Lu AvenueRoad, Chengdu, Sichuan, China, 610041.
Cochrane Database Syst Rev. 2017 Jul 7;7(7):CD010810. doi: 10.1002/14651858.CD010810.pub3.
Hemophilia A and B are inherited coagulation disorders characterized by a reduced or absent level of factor VIII or factor IX respectively. The severe form is characterized by a factor level less than 0.01 international units (IU) per milliliter. The development of inhibitors in hemophilia is the main complication of treatment, because the presence of these antibodies, reduces or even nullifies the efficacy of replacement therapy, making it very difficult to control the bleeding. People with inhibitors continue to have significantly higher risks of morbidity and mortality, with considerable treatment costs. Given the wide 'off-label' use of rituximab for treating people with hemophilia and inhibitors, its efficacy and safety need to be evaluated. This is an update of a previously published Cochrane Review.
To assess the efficacy and safety of rituximab for treating inhibitors in people with inherited severe hemophilia A or B.
We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group's Coagulopathies Trials Register, complied from electronic database searches and handsearching of journals and conference abstract books. We searched the reference lists of relevant articles and reviews and also searched for ongoing or unpublished studies. We also undertook further searches of other bibliographic databases and trial registries.Date of last search of the Cochrane Cystic Fibrosis and Genetic Disorders Group's Coagulopathies Trials Register: 16 February 2017.
Randomized controlled trials and controlled clinical trials investigating the efficacy and safety of rituximab for treating inhibitors in people with hemophilia.
No randomized controlled trials matching the selection criteria were eligible for inclusion.
No randomized controlled trials on rituximab for treating inhibitors in people with hemophilia were identified.
AUTHORS' CONCLUSIONS: We were unable to identify any relevant trials on the efficacy and safety of rituximab for treating inhibitors in people with hemophilia. The research evidence available is from case reports and case series. Randomized controlled trials are needed to evaluate the efficacy and safety of rituximab for this condition. However, prior to the publication of any possible future randomized controlled trials, meta-analysis of case reports and case series may provide some evidence.
甲型和乙型血友病是遗传性凝血障碍疾病,分别表现为凝血因子 VIII 或凝血因子 IX 水平降低或缺乏。重型血友病的特征是因子水平低于每毫升 0.01 国际单位(IU)。血友病患者体内产生抑制物是治疗的主要并发症,因为这些抗体的存在会降低甚至抵消替代疗法的疗效,使得控制出血变得非常困难。有抑制物的患者发病和死亡风险仍然显著更高,治疗成本也相当高。鉴于利妥昔单抗在治疗血友病及有抑制物患者方面广泛的“超说明书”使用情况,需要对其疗效和安全性进行评估。这是对先前发表的 Cochrane 系统评价的更新。
评估利妥昔单抗治疗遗传性重度甲型或乙型血友病患者体内抑制物的疗效和安全性。
我们检索了 Cochrane 囊性纤维化和遗传疾病小组的凝血障碍试验注册库,该注册库通过电子数据库检索以及对期刊和会议摘要集的手工检索整理而成。我们检索了相关文章和综述的参考文献列表,还检索了正在进行或未发表的研究。我们还对其他文献数据库和试验注册库进行了进一步检索。Cochrane 囊性纤维化和遗传疾病小组凝血障碍试验注册库的最后检索日期:2017 年 2 月 16 日。
调查利妥昔单抗治疗血友病患者体内抑制物疗效和安全性的随机对照试验和对照临床试验。
没有符合选择标准的随机对照试验 eligible 纳入。
未识别到关于利妥昔单抗治疗血友病患者体内抑制物的随机对照试验。
我们无法识别任何关于利妥昔单抗治疗血友病患者体内抑制物疗效和安全性的相关试验。现有研究证据来自病例报告和病例系列。需要进行随机对照试验来评估利妥昔单抗治疗这种情况的疗效和安全性。然而,在未来任何可能的随机对照试验发表之前,对病例报告和病例系列的荟萃分析可能会提供一些证据。