Department of Infectious Diseases, Infection Control, and Employee Health, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Transplantation. 2012 Aug 15;94(3):302-8. doi: 10.1097/TP.0b013e3182577485.
Antifungal prophylaxis is shown to decrease the risk of invasive fungal infection (IFI) after hematopoietic stem-cell transplantation (HSCT). Posaconazole has been approved for prophylaxis in HSCT. However, it is only available orally given three times per day. We evaluated once weekly intravenous amphotericin B lipid complex (ABLC), given its broad-spectrum antifungal activity and prolonged half-life (172 hr), as an alternative prophylaxis in HSCT.
We prospectively randomized allogeneic HSCT patients to receive 7.5 mg/kg of intravenous ABLC weekly or 200 mg of posaconazole orally three times per day as prophylaxis for up to 6 weeks. Endpoints were the incidence of IFI and drug-related toxicities. ABLC was discontinued if creatinine level increased to two times the baseline or greater.
A total of 46 patients were randomized; 40 received at least one dose of the drug and were included in the analysis: 19 received ABLC and 21 received posaconazole. All patients received tacrolimus. Apache II score, neutropenia, and creatinine, bilirubin, and alanine aminotransferase levels were similar in both groups at baseline. One patient in the ABLC arm and none in posaconazole arm developed IFI (5% vs. 0%, P=0.48). More patients in the ABLC arm doubled their serum creatinine (53% vs. 5%, P=0.001) necessitating discontinuation of the study drug.
High-dose prophylactic ABLC in HSCT was associated with nephrotoxicity that could be aggravated by the concomitant use of other nephrotoxic agents. Further studies are needed to evaluate the role of weekly high-dose ABLC as antifungal prophylaxis in patients at lower risk for nephrotoxicity.
抗真菌预防治疗可降低造血干细胞移植(HSCT)后侵袭性真菌感染(IFI)的风险。泊沙康唑已被批准用于 HSCT 的预防治疗。然而,它仅能每日口服三次。我们评估了每周一次静脉注射两性霉素 B 脂质复合物(ABLC),因为它具有广谱抗真菌活性和较长的半衰期(172 小时),作为 HSCT 的替代预防治疗。
我们前瞻性地将异基因 HSCT 患者随机分为两组,一组接受每周 7.5mg/kg 的静脉注射 ABLC,一组接受每日口服 200mg 的泊沙康唑,每日三次,预防治疗时间最长为 6 周。终点为 IFI 的发生率和药物相关毒性。如果肌酐水平增加到基线的两倍或更高,则停止使用 ABLC。
共有 46 名患者被随机分配;40 名患者至少接受了一剂药物治疗,并纳入分析:19 名患者接受 ABLC,21 名患者接受泊沙康唑。所有患者均接受了他克莫司治疗。两组患者的 Apache II 评分、中性粒细胞减少症以及肌酐、胆红素和丙氨酸氨基转移酶水平在基线时相似。ABLC 组中有 1 名患者(5%)和泊沙康唑组中无患者(0%)发生 IFI(P=0.48)。ABLC 组中更多的患者血清肌酐加倍(53%比 5%,P=0.001),需要停止使用研究药物。
HSCT 中高剂量预防性 ABLC 与肾毒性相关,同时使用其他肾毒性药物可能会加重肾毒性。需要进一步研究评估每周高剂量 ABLC 作为较低肾毒性风险患者的抗真菌预防治疗的作用。