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Sirolimus and mirabegron interaction in a hematopoietic cell transplant patient

机译:造血细胞移植患者的西罗莫司和M拉萨比克相互作用

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Purpose Hematopoietic cell transplant patients are exposed to numerous classes of medications. Transplant practitioners must vigilantly monitor for drug interactions especially involving immunosuppressants. We report a hematopoietic cell transplant patient receiving sirolimus who developed supratherapeutic serum concentrations after initiating mirabegron. Summary A 31-year-old, 98?kg female received a second umbilical cord blood transplant four years after the first transplant for relapsed acute myeloid leukemia. Mycophenolate mofetil and sirolimus were utilized for graft versus host disease prophylaxis. The patient was receiving sirolimus 2?mg daily and the serum concentration on day 26 post-transplant (day?+?26) was within therapeutic range (6.7?μg/L, goal range 3–12?μg/L). Her post-transplant course was complicated by BK viruria-associated cystitis for which she was started on mirabegron. Six days after starting the new medication (day?+?33), the sirolimus serum concentration increased to 19.2?μg/L. Thus mirabegron was discontinued and sirolimus was held. Sirolimus was restarted once the serum concentration was within goal and subsequently stabilized with a combination of 1?mg and 2?mg daily for a total weekly dose of 10?mg. The proposed mechanisms of interaction include: (1) sirolimus inhibition of organic anion transporting polypeptide leading to increased mirabegron in the intestinal lumen; (2) mirabegron inhibition of P-glycoprotein leading to increased absorption of sirolimus and; (3) increased sirolimus absorption leading to increased sirolimus serum concentrations. Conclusion To our knowledge, this is the first report of a potential drug interaction between sirolimus and mirabegron. Transplant specialists should be aware of this potential interaction when considering the concurrent use of these medications.
机译:目的造血细胞移植患者暴露于许多类药物。移植从业者必须耳垂监测尤其涉及免疫抑制剂的药物相互作用。我们报告了在发起Mirabegron后,接受造血细胞移植患者接受Sirolimus的西罗莫司。概述了31岁,98岁的女性在第一次移植到复发急性髓性白血病后4年后,每次接受第二次脐带血液移植。霉酚酸酯和西罗莫司用于移植物与宿主疾病预防。患者每天接受西罗莫司2毫克2毫克,并且在移植后第26天(日?+β26)的第26天血清浓度在治疗范围内(6.7ΩΩ·μg/ L,目标范围3-12Ω·μg/ L)。 BK Viruria相关的膀胱炎,她的移植后课程复杂化,她在M拉萨比顿开始。开始新药物后六天(日?+?33),西罗莫血清血清浓度增加至19.2μg/升。因此,麦比格隆被停产,并举行西罗莫司。一旦血清浓度在目标内并随后用1·mg和2·mg的组合稳定,每天稳定一旦每周剂量为10×mg,则重新启动西罗莫司。所提出的相互作用机制包括:(1)西罗莫司抑制有机阴离子输送多肽,所述多肽导致肠内腔内的米拉巴群增加; (2)甲苯克朗抑制对糖蛋白的抑制导致西罗莫司的吸收增加和; (3)增加西罗莫司吸收,导致西罗莫司血清浓度增加。结论据我们所知,这是西罗莫司和米拉巴克之间潜在药物相互作用的第一个报告。在考虑同时使用这些药物时,移植专家应该意识到这种潜在的相互作用。

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