首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Safety of Posaconazole and Sirolimus Coadministration in Allogeneic Hematopoietic Stem Cell Transplants
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Safety of Posaconazole and Sirolimus Coadministration in Allogeneic Hematopoietic Stem Cell Transplants

机译:异源造血干细胞移植中泊沙康唑和西罗莫司联合给药的安全性

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Sirolimus is used in allogeneic hematopoietic stem cell transplants (HSCTs) for prevention and treatment of graft-versus-host disease (GVHD). Posaconazole is used in this population for invasive fungal disease (IFD) prophylaxis and treatment. As posaconazole strongly inhibits CYP3A4, concurrent administration of sirolimus, a CYP3A4 substrate, and posaconazole has been reported to increase sirolimus drug exposure substantially. Coadministration of posaconazole and sirolimus is contraindicated by the manufacturer of posaconazole. We identified 15 patients who underwent HSCTs at our institution receiving a steady-state dose of sirolimus who subsequently started posaconazole therapy from January 2006 to March 2009. We recorded baseline characteristics, drug administration details, and potential adverse effects related to either drug. All patients underwent HSCTs for treatment of hematologic malignancy. All patients were initially prescribed sirolimus for GVHD prophylaxis and continued therapy after developing GVHD. Twelve patients (80%) received posaconazole for IFD prophylaxis in the setting of GVHD and 3 (20%) for IFD treatment. Patients received sirolimus and posaconazole concurrently for a median of 78 days (interquartile range [IQR] 25-177; range, 6-503). The median daily dose of sirolimus (2 mg/day) before initiation of posaconazole was reduced 50% to a median daily dose of 1 mg/day at steady state. Six patients experienced sirolimus trough levels greater than 12 ng/mL during coadministration, but only 1 patient experienced an adverse event potentially associated with sirolimus exposure during the first month of coadministration. This patient's sirolimus dose was empirically reduced by only 30% on posaconazole initiation. Concurrent sirolimus and posaconazole use seems to be well tolerated with a 33% to 50% empiric sirolimus dose reduction and close monitoring of serum sirolimus trough levels at the time of posaconazole initiation.
机译:西罗莫司用于同种异体造血干细胞移植(HSCT)中,用于预防和治疗移植物抗宿主病(GVHD)。泊沙康唑用于该人群中以预防和治疗侵袭性真菌病(IFD)。由于泊沙康唑强烈抑制CYP3A4,已报道同时给药CYP3A4底物西罗莫司和泊沙康唑可显着增加西罗莫司药物的暴露量。泊沙康唑的制造商禁止同时使用泊沙康唑和西罗莫司。我们确定了15例在我们机构接受HSCT的患者,他们接受了稳定剂量的西罗莫司治疗,随后于2006年1月至2009年3月开始进行泊沙康唑治疗。所有患者均接受HSCT治疗以治疗血液恶性肿瘤。最初所有患者均接受西罗莫司的GVHD预防治疗,并在发展GVHD后继续治疗。 12名患者(80%)在GVHD的情况下接受了泊沙康唑预防IFD,3名患者(20%)进行了IFD治疗。患者同时接受西罗莫司和泊沙康唑的中位数为78天(四分位间距[IQR] 25-177;范围6-503)。西沙莫司开始服用泊沙康唑之前的中位日剂量(2 mg /天)减少了50%,稳定状态下的中位日剂量为1 mg /天。在联合用药期间,有6名患者的西罗莫司谷水平超过12 ng / mL,但是在联合用药的第一个月中,只有1名患者经历了与西罗莫司暴露有关的不良事件。泊沙康唑开始后,根据经验,该患者的西罗莫司剂量仅降低了30%。西罗莫司和泊沙康唑的同时使用似乎可以耐受33%至50%的经验性西罗莫司剂量,并在开始泊沙康唑时密切监测血清西罗莫司谷水平。

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