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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Generic immunosuppression in solid organ transplantation: A canadian perspective
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Generic immunosuppression in solid organ transplantation: A canadian perspective

机译:实体器官移植中的通用免疫抑制:加拿大的观点

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The introduction of generic immunosuppressant medications may present an opportunity for cost savings in solid organ transplantation if equivalent clinical outcomes to the branded counterparts can be achieved. An interprofessional working group of the Canadian Society of Transplantation was established to develop recommendations on the use of generic immunosuppression in solid organ transplant recipients (SOTR) based on a review of the available data. Under current Health Canada licensing requirements, a demonstration of bioequivalence with the branded formulation in healthy volunteers allows for bridging of clinical data. Cyclosporine, tacrolimus, and sirolimus are designated as "critical dose drugs" and are held to stricter criteria. However, whether this provides sufficient guarantee of therapeutic equivalence in SOTR remains controversial, and failure to maintain an appropriate balance of immunosuppression may have serious consequences, including rejection, graft loss, and death. Published evidence supporting therapeutic equivalence of generic formulations in SOTR is lacking. Moreover, in the setting of multiple generic formulations the potential for uncontrolled product switching is a major concern, since generic preparations are not required to demonstrate bioequivalence with each other. Although close monitoring is recommended with any change in formulation, drug product switches are likely to occur without prescriber knowledge and may pose a significant patient safety risk. The advent of generic immunosuppression will require new practices including more frequent therapeutic drug and clinical monitoring, and increased patient education. The additional workload placed on transplant centers without additional funding will create challenges and could ultimately jeopardize patient outcomes. Until more robust clinical data are available and adequate regulatory safeguards are instituted, caution in the use of generic immunosuppressive drugs in solid organ transplantation is warranted.
机译:如果可以实现与品牌对应产品相同的临床结果,则通用免疫抑制剂药物的引入可能为实体器官移植节省成本。建立了加拿大移植学会的跨专业工作组,以基于对现有数据的回顾,提出有关在实体器官移植接受者(SOTR)中使用仿制免疫抑制的建议。根据加拿大卫生部当前的许可要求,在健康志愿者中证明该品牌制剂具有生物等效性,可以桥接临床数据。环孢菌素,他克莫司和西罗莫司被指定为“关键剂量药物”,并遵守更严格的标准。但是,这是否能为SOTR的治疗等效性提供足够的保证仍存在争议,并且无法维持适当的免疫抑制平衡可能会产生严重的后果,包括排斥,移植物丢失和死亡。缺乏支持SOTR中通用制剂治疗等效性的公开证据。此外,在多种通用制剂的设置中,不受控制的产品转换的可能性是主要关注的问题,因为不需要通用制剂来证明彼此具有生物等效性。尽管建议对制剂进行任何更改时都应进行密切监视,但在没有开处方者知识的情况下,很可能会发生药品转换的情况,并且可能会带来重大的患者安全风险。通用免疫抑制的出现将需要新的实践,包括更频繁的治疗药物和临床监测,以及更多的患者教育。如果没有额外的资金,移植中心的额外工作量将带来挑战,最终可能危及患者的治疗效果。在可获得更可靠的临床数据并建立足够的监管保障措施之前,应在实体器官移植中使用通用免疫抑制药物时保持谨慎。

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