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Off-label use of rituximab in a tertiary Queensland hospital.

机译:在昆士兰一家三级医院中非处方使用利妥昔单抗。

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BACKGROUND: Rituximab is a monoclonal antibody directed against CD20, a pan B lymphocyte marker. It is approved in Australia for treatment of CD20-positive B cell non-Hodgkin lymphoma and rheumatoid arthritis. There is increasing off-label use of rituximab in conditions where B cells and autoantibodies play a role in the pathophysiology. Rituximab is not only expensive, but its safety in unregistered indications is uncertain. METHODS: We performed a retrospective review of the off-label use of rituximab approved by the High Cost Drug Subcommittee at the Princess Alexandra Hospital between 2005 and 2008. Cases of post transplant lymphoproliferative disorder were excluded. RESULTS: A total of 28 patients received rituximab for a variety of off-label indications. There were no reported cases of serious infusion reactions or other notable adverse events. The most favourable outcomes were seen in myasthenia gravis, shrinking lung syndrome, thrombotic thrombocytopenic purpura, prevention and treatment of renal transplant rejection and lupus nephritis. No benefit was observed in cases of focal segmental glomerulosclerosis (primary or post-transplant recurrence) and post-transplant recurrence of haemolytic uremic syndrome. There was limited benefit in cryoglobulinaemic vasculitis. The cost of off-label use was in excess of Dollars 210,000. CONCLUSION: In the absence of formal clinical trials, decisions regarding off-label use of rituximab are difficult. Our cases contribute to the published literature and should help provide clinicians with greater insights into which conditions are likely to respond. As can be seen in our series, rituximab benefits people with certain conditions; longevity and cost-effectiveness are currently unknown.
机译:背景:利妥昔单抗是针对CD20(pan B淋巴细胞标志物)的单克隆抗体。它在澳大利亚被批准用于治疗CD20阳性B细胞非霍奇金淋巴瘤和类风湿关节炎。在B细胞和自身抗体在病理生理学中起作用的情况下,越来越多的利妥昔单抗的标签外使用。利妥昔单抗不仅昂贵,而且在未注册适应症中的安全性尚不确定。方法:我们对2005年至2008年间亚历山大公主医院高成本药物小组委员会批准的非处方利妥昔单抗的使用进行了回顾性研究。排除了移植后淋巴细胞增生性疾病的病例。结果:共有28例患者接受了利妥昔单抗治疗,这些适应症包括多种适应症。没有关于严重输液反应或其他明显不良事件的报道。重症肌无力,肺收缩综合征,血栓性血小板减少性紫癜,肾移植排斥反应和狼疮性肾炎的预防和治疗最为理想。在局灶性节段性肾小球硬化症(原发或移植后复发)和溶血性尿毒症综合征的移植后复发的病例中未观察到益处。冷冻球蛋白性血管炎的获益有限。标签外使用的成本超过210,000美元。结论:在没有正式的临床试验的情况下,关于非处方使用利妥昔单抗的决定是困难的。我们的病例有助于发表文献,并应帮助临床医生更深入地了解哪些疾病可能会缓解。从我们的系列文章中可以看出,利妥昔单抗使某些情况下的人受益。寿命和成本效益目前未知。

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