首页> 外文期刊>Yonsei Medical Journal >Clinical Outcomes and Prognostic Factors of Empirical Antifungal Therapy with Itraconazole in the Patients with Hematological Malignancies: A Prospective Multicenter Observational Study in Korea
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Clinical Outcomes and Prognostic Factors of Empirical Antifungal Therapy with Itraconazole in the Patients with Hematological Malignancies: A Prospective Multicenter Observational Study in Korea

机译:伊曲康唑对血液恶性肿瘤患者进行经验性抗真菌治疗的临床结果和预后因素:韩国一项前瞻性多中心观察性研究

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Purpose To identify prognostic factors for the outcomes of empirical antifungal therapy, we performed a multicenter, prospective, observational study in immunocompromised patients with hematological malignancies. Materials and Methods Three hundred seventy-six patients (median age of 48) who had neutropenic fever and who received intravenous (IV) itraconazole as an empirical antifungal therapy for 3 or more days were analyzed. The patients with possible or probable categories of invasive fungal disease (IFD) were enrolled. Results The overall success rate was 51.3% (196/376). Age >50 years, underlying lung disease (co-morbidity), poor performance status [Eastern Cooperative Oncology Group (ECOG) ≥2], radiologic evidence of IFD, longer duration of baseline neutropenic fever (≥4 days), no antifungal prophylaxis or prophylactic use of antifungal agents other than itraconazole, and high tumor burden were associated with decreased success rate in univariate analysis. In multivariate analysis, age >50 years ( p =0.009) and poor ECOG performance status ( p =0.005) were significantly associated with poor outcomes of empirical antifungal therapy. Twenty-two patients (5.9%) discontinued itraconazole therapy due to toxicity. Conclusion We concluded that empirical antifungal therapy with IV itraconazole in immunocompromised patients is effective and safe. Additionally, age over 50 years and poor performance status were poor prognostic factors for the outcomes of empirical antifungal therapy with IV itraconazole.
机译:目的为了确定经验性抗真菌治疗结果的预后因素,我们对免疫功能低下的血液系统恶性肿瘤患者进行了多中心,前瞻性和观察性研究。材料与方法分析了376例中性粒细胞减少的患者(中位年龄为48岁)并接受伊曲康唑静脉(IV)作为经验性抗真菌治疗3天或更长时间的患者。纳入具有侵袭性真菌病(IFD)可能或可能类别的患者。结果总体成功率为51.3%(196/376)。年龄> 50岁,潜在的肺部疾病(合并症),表现不佳[东部合作肿瘤小组(ECOG)≥2],IFD的放射学证据,基线中性白细胞减少症持续时间较长(≥4天),无抗真菌药物预防或预防性使用伊曲康唑以外的抗真菌药以及高肿瘤负荷与单因素分析成功率降低相关。在多变量分析中,年龄> 50岁(p = 0.009)和不良ECOG表现状态(p = 0.005)与经验性抗真菌治疗的不良结局显着相关。 22名患者(5.9%)由于毒性而终止伊曲康唑治疗。结论我们得出结论,静脉使用伊曲康唑的经验性抗真菌治疗对免疫功能低下的患者有效且安全。此外,年龄超过50岁和表现不佳是静脉使用伊曲康唑进行经验性抗真菌治疗的不良预后因素。

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