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首页> 外文期刊>Journal of Korean medical science. >Success Rate and Risk Factors for Failure of Empirical Antifungal Therapy with Itraconazole in Patients with Hematological Malignancies: A Multicenter, Prospective, Open-Label, Observational Study in Korea
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Success Rate and Risk Factors for Failure of Empirical Antifungal Therapy with Itraconazole in Patients with Hematological Malignancies: A Multicenter, Prospective, Open-Label, Observational Study in Korea

机译:血液恶性肿瘤患者伊唑康唑失效的成功率和风险因素:韩国多中心,前瞻性,开放标签,观测研究

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摘要

We assessed the success rate of empirical antifungal therapy with itraconazole and evaluated risk factors for predicting the failure of empirical antifungal therapy. A multicenter, prospective, observational study was performed in patients with hematological malignancies who had neutropenic fever and received empirical antifungal therapy with itraconazole at 22 centers. A total of 391 patients who had abnormal findings on chest imaging tests (31.0%) or a positive result of enzyme immunoassay for serum galactomannan (17.6%) showed a 56.5% overall success rate. Positive galactomannan tests before the initiation of the empirical antifungal therapy ( P =0.026, hazard ratio [HR], 2.28; 95% confidence interval [CI], 1.10-4.69) and abnormal findings on the chest imaging tests before initiation of the empirical antifungal therapy ( P =0.022, HR, 2.03; 95% CI, 1.11-3.71) were significantly associated with poor outcomes for the empirical antifungal therapy. Eight patients (2.0%) had premature discontinuation of itraconazole therapy due to toxicity. It is suggested that positive galactomannan tests and abnormal findings on the chest imaging tests at the time of initiation of the empirical antifungal therapy are risk factors for predicting the failure of the empirical antifungal therapy with itraconazole. (Clinical Trial Registration on National Cancer Institute website, NCT01060462)
机译:我们评估了用伊曲康唑的经验抗真菌疗法的成功率,并评估了预测经验抗真菌疗法失败的危险因素。在患有中性发烧的血液恶性肿瘤患者中进行多中心,前瞻性观察研究,并在22个中心接受伊丙胺的实证抗真菌治疗。共有391名在胸部成像试验中具有异常发现(31.0%)或酶免疫测定的阳性结果,血清半乳甘露聚糖(17.6%)显示总成功率为56.5%。阳性半乳甘露乳甘露乳甘油在发起经验抗真菌治疗之前(P = 0.026,危害比[HR],2.28; 95%置信区间[CI],1.10-4.69)和胸部成像试验的异常发现在发起经验抗真菌之前治疗(p = 0.022,HR,2.03; 95%CI,1.11-3.71)与经验抗真菌治疗的差异显着相关。八名患者(2.0%)由于毒性而过早停止伊拉昔氮唑治疗。建议在发起经验抗真菌治疗时胸膜成像试验的阳性半乳甘露乳甘油试验和异常发现是预测伊唑康唑的经验抗真菌疗法失败的危险因素。 (国家癌症学院网站上的临床试验登记,NCT01060462)

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