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我们如何治疗急性白血病患者的侵袭性真菌感染:个体化方法的重要性。

How we treat invasive fungal diseases in patients with acute leukemia: the importance of an individualized approach.

机构信息

University Hospital, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil; and.

Division of Hematology/Oncology, University of Cincinnati, Cincinnati, OH.

出版信息

Blood. 2014 Dec 18;124(26):3858-69. doi: 10.1182/blood-2014-04-516211. Epub 2014 Oct 22.

DOI:10.1182/blood-2014-04-516211
PMID:25339358
Abstract

Invasive fungal diseases (IFDs) represent an important cause of treatment failure in adults with acute leukemia. Because of leukemia's heterogeneity, the risk for IFDs is highly variable. We therefore apply a risk-adapted antifungal strategy with strong emphasis on pretreatment and day-15 posttreatment to allow earlier and more individualized interventions. We determine pretreatment risks for IFDs based on 4 factors: (1) host fitness for standard therapy (ie, fit, unfit, or frail); (2) leukemia resistance (high vs low probability of achieving complete remission [CR]); (3) anticipated treatment-related toxicity such as neutropenia, mucositis, and steroid-induced immunosuppression; and (4) patient exposure to opportunistic fungi. Accordingly, we stratify patients as high, intermediate, or low risk for IFDs and apply risk-adapted antifungal strategies, including primary or secondary prophylaxis and diagnostic-based preemptive or empiric therapy. Prevention of IFDs also relies on optimizing organ function, decreasing exposure to opportunistic fungi, and improving net state of immunosuppression with use of better-tolerated and investigational agents for unfit patients and those with adverse leukemia biology. Novel targeted and safe therapies that can achieve higher rates of sustained CR among patients with adverse genetics offer the best promise for reducing the burden of IFDs in these patients.

摘要

侵袭性真菌病(IFD)是成人急性白血病治疗失败的重要原因。由于白血病的异质性,IFD 的风险高度可变。因此,我们采用了一种风险适应的抗真菌策略,强调预处理和治疗后 15 天,以便更早和更个体化的干预。我们根据以下 4 个因素确定 IFD 的预处理风险:(1)宿主对标准治疗的适应能力(即适应、不适应或虚弱);(2)白血病耐药性(完全缓解[CR]的可能性高或低);(3)预计与治疗相关的毒性,如中性粒细胞减少症、粘膜炎和类固醇诱导的免疫抑制;(4)患者接触机会性真菌。因此,我们将患者分为 IFD 高、中、低风险,并采用风险适应的抗真菌策略,包括原发性或继发性预防以及基于诊断的先发制人或经验性治疗。IFD 的预防还依赖于优化器官功能、减少机会性真菌暴露以及通过使用耐受性更好和正在研究的药物来改善免疫抑制的净状态,以适应不适应患者和具有不良白血病生物学的患者。新型靶向和安全的治疗方法可以在具有不良遗传特征的患者中实现更高的持续 CR 率,为降低这些患者的 IFD 负担提供了最佳希望。

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