Park Sun Hee, Choi Su-Mi, Lee Dong-Gun, Choi Jung-Hyun, Yoo Jin-Hong, Min Woo-Sung, Shin Wan-Shik
Department of Internal Medicine, The Catholic Hematopoietic Stem Cell Transplantation Center, The Catholic University of Korea College of Medicine, Seoul, Korea.
Korean J Intern Med. 2006 Sep;21(3):165-72. doi: 10.3904/kjim.2006.21.3.165.
Amphotericin B dexoycholate is currently the standard empirical antifungal therapy for neutropenic patients with hematologic malignancies and who also have persistent fever that does not respond to antibacterial therapy. The antifungal triazoles offer a potentially safer and effective treatment alternative to Amphotericin B dexoycholate.
We assessed the efficacy and safety of intravenous itraconazole, as compared with the efficacy and safety of amphotericin B deoxycholate, as an empirical antifungal therapeutic agent in a matched case-control clinical trial from June 2004 to August 2005.
Efficacy was evaluated in 96 patients (48 received itraconazole and 48 received amphotericin B deoxycholate) and all the patients who received the study drugs were evaluated for safety. The baseline demographic characteristics were well matched. The overall success rates were 47.9% for itraconazole and 43.8% for amphotericin B deoxycholate (% difference: 4.1% [95% confidence interval for the difference: -15.8 to 24]), which fulfilled the statistical criteria for the non-inferiority of itraconazole. The proportions of patients who survived for at least seven days after discontinuation of therapy or who were prematurely discontinued from the study were not significantly different between the two groups. The rates of breakthrough fungal infections and resolution of fever during neutropenia were similar in both groups. More patients who received amphotericin B deoxycholate developed nephrotoxicity, hypokalemia or infusion-related events than did those patients who received itraconazole (nephrotoxicity: 16.7% vs. 1.8%, hypokalemia: 66.7% vs. 24.6%, and infusion-related events: 41.7% vs. 3.5%, respectively).
Intravenous itraconazole is as effective as amphotericin B deoxycholate and it is generally better tolerated than amphotericin B deoxycholate when it is given as empirical antifungal therapy for Korean patients with persistent neutropenic fever.
两性霉素B去氧胆酸盐目前是血液系统恶性肿瘤中性粒细胞减少且持续发热对抗菌治疗无反应患者的标准经验性抗真菌治疗药物。抗真菌三唑类药物为两性霉素B去氧胆酸盐提供了一种潜在更安全有效的治疗选择。
在2004年6月至2005年8月的一项匹配病例对照临床试验中,我们评估了静脉注射伊曲康唑作为经验性抗真菌治疗药物的疗效和安全性,并与两性霉素B去氧胆酸盐的疗效和安全性进行比较。
对96例患者(48例接受伊曲康唑,48例接受两性霉素B去氧胆酸盐)进行了疗效评估,所有接受研究药物的患者均进行了安全性评估。基线人口统计学特征匹配良好。伊曲康唑的总体成功率为47.9%,两性霉素B去氧胆酸盐为43.8%(差异百分比:4.1%[差异的95%置信区间:-15.8至24]),满足伊曲康唑非劣效性的统计标准。两组在治疗停药后至少存活7天或提前退出研究的患者比例无显著差异。两组中性粒细胞减少期间突破性真菌感染率和发热缓解率相似。接受两性霉素B去氧胆酸盐的患者比接受伊曲康唑的患者发生肾毒性、低钾血症或输液相关事件的更多(肾毒性:16.7%对1.8%,低钾血症:66.7%对24.6%,输液相关事件:41.7%对3.5%)。
对于韩国持续性中性粒细胞减少发热患者,静脉注射伊曲康唑与两性霉素B去氧胆酸盐疗效相当,且作为经验性抗真菌治疗时,其耐受性通常优于两性霉素B去氧胆酸盐。