Division of Infectious Diseases, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
Biol Blood Marrow Transplant. 2012 Sep;18(9):1462-5. doi: 10.1016/j.bbmt.2012.04.015. Epub 2012 May 4.
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.
西罗莫司用于异基因造血干细胞移植(HSCT)以预防和治疗移植物抗宿主病(GVHD)。泊沙康唑用于该人群侵袭性真菌感染(IFD)的预防和治疗。由于泊沙康唑强烈抑制 CYP3A4,同时给予西罗莫司(CYP3A4 的底物)和泊沙康唑已被报道会大大增加西罗莫司的药物暴露量。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 名在我院接受 HSCT 的患者,他们在 2006 年 1 月至 2009 年 3 月期间接受了西罗莫司的稳态剂量,随后开始接受泊沙康唑治疗。我们记录了基线特征、药物管理细节以及与两种药物相关的潜在不良反应。所有患者均因血液系统恶性肿瘤而接受 HSCT。所有患者最初均因 GVHD 预防而开处方西罗莫司,并在发生 GVHD 后继续接受治疗。12 名患者(80%)因 GVHD 而接受泊沙康唑预防 IFD,3 名患者(20%)因 IFD 治疗而接受泊沙康唑。患者接受西罗莫司和泊沙康唑联合治疗的中位数时间为 78 天(四分位距 [IQR] 25-177;范围 6-503)。在开始使用泊沙康唑之前,西罗莫司的中位日剂量(2 毫克/天)减少了 50%,稳定状态时的中位日剂量为 1 毫克/天。6 名患者在联合治疗期间西罗莫司谷浓度大于 12 ng/mL,但只有 1 名患者在联合治疗的第一个月出现与西罗莫司暴露相关的不良反应。在开始使用泊沙康唑时,该患者的西罗莫司剂量仅经验性减少了 30%。同时使用西罗莫司和泊沙康唑似乎耐受性良好,在开始使用泊沙康唑时,西罗莫司的剂量需要减少 33%至 50%,并密切监测西罗莫司的血药谷浓度。