在急性髓性白血病缓解诱导过程中评估预防性anidulafungin的影响-倾向评分匹配分析

IF 2.2 4区 医学 Q3 MYCOLOGY
Wellington Fernandes da Silva , Fernanda Rodrigues Mendes , Raphael da Costa Bandeira de Melo , Elvira Deolinda Rodrigues Pereira Velloso , Vanderson Rocha , Eduardo Magalhaes Rego
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引用次数: 0

摘要

侵袭性真菌感染(IFI)在成人急性髓性白血病(AML)治疗过程中占相当大的发病率。在强化化疗期间需要抗真菌预防(AP),泊沙康唑并不广泛使用。在这项研究中,我们的目的是检查预防性anidulafungin在急性髓性白血病(AML)强化缓解诱导中的影响。方法:这是一项回顾性队列研究,包括新诊断的AML成人患者。所有受试者均接受强化化疗,并分为三组:未接受任何AP治疗的患者和接受氟康唑(150 - 400mg /天)或阿尼哌宁(100mg /天)治疗的患者。结果在AML诱导过程中,82例患者未接受AP治疗,108例患者接受阿尼杜拉芬宁治疗,14例患者接受氟康唑治疗。IFI发生率为27%,分别为65%、2%和33%,分为可能、可能和已证实。多变量分析显示,中性粒细胞计数较低与IFI相关(OR = 2.8),而年龄、遗传分类和淋巴细胞计数与IFI无关。为了检查anidulafungin与“无AP”的影响,进行了倾向评分匹配分析。使用anidulafungin与诱导期间IFI减少无关,而中性粒细胞计数仍然显著。预防性阿尼哌宁组患者两性霉素B (p <0.001),伏立康唑没有(p = 0.49)。据我们所知,这是第一个关于anidulafungin在AML诱导中的作用的研究。在这里,霉菌感染的发病率并没有随着AP的降低而降低,这表明在IFI发病率高的环境中,广谱AP可能更合适。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing the impact of prophylactic anidulafungin during remission induction of acute myeloid leukemia – A propensity-score matching analysis

Introduction

Invasive fungal infection (IFI) accounts for substantial morbidity during the treatment of acute myeloid leukemia (AML) in adults. Antifungal prophylaxis (AP) is needed during intensive chemotherapy, and posaconazole is not widely available. In this study, we aimed to examine the impact of prophylactic anidulafungin during intensive AML remission induction.

Methods

This is a retrospective cohort encompassing newly diagnosed AML adult patients. All subjects received intensive chemotherapy and were divided into three groups: patients who did not receive any AP and patients who received fluconazole (150–400 mg/day) or anidulafungin (100 mg/day).

Results

During AML induction, 82 patients did not receive AP, 108 and 14 patients received anidulafungin and fluconazole, respectively. IFI incidence was 27%, classified as possible, probable, and proven in 65, 2 and 33%, respectively. Multivariable analysis showed that lower neutrophil counts are associated with IFI (OR = 2.8), whereas age, genetic classification, and lymphocyte counts were not. To examine the impact of anidulafungin in comparison with ‘no AP’, a propensity score matching analysis was performed. Use of anidulafungin was not related to less IFI during induction, while neutrophil counts remained significant. Patients under prophylactic anidulafungin received less amphotericin B (p < 0.001) but not voriconazole (p = 0.49).

Discussion

To our knowledge, this is the first study addressing the role of anidulafungin during AML induction. Here, the incidence of mold infections did not decrease with AP, suggesting that in a setting with a high incidence of IFI, broad spectrum AP might be more suitable.

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来源期刊
CiteScore
5.10
自引率
2.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: The Journal de Mycologie Medicale / Journal of Medical Mycology (JMM) publishes in English works dealing with human and animal mycology. The subjects treated are focused in particular on clinical, diagnostic, epidemiological, immunological, medical, pathological, preventive or therapeutic aspects of mycoses. Also covered are basic aspects linked primarily with morphology (electronic and photonic microscopy), physiology, biochemistry, cellular and molecular biology, immunochemistry, genetics, taxonomy or phylogeny of pathogenic or opportunistic fungi and actinomycetes in humans or animals. Studies of natural products showing inhibitory activity against pathogenic fungi cannot be considered without chemical characterization and identification of the compounds responsible for the inhibitory activity. JMM publishes (guest) editorials, original articles, reviews (and minireviews), case reports, technical notes, letters to the editor and information. Only clinical cases with real originality (new species, new clinical present action, new geographical localization, etc.), and fully documented (identification methods, results, etc.), will be considered. Under no circumstances does the journal guarantee publication before the editorial board makes its final decision. The journal is indexed in the main international databases and is accessible worldwide through the ScienceDirect and ClinicalKey platforms.
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