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高危 MDS 和 AML 患者接受低甲基化药物治疗后的侵袭性真菌感染风险。

Risk of invasive fungal infections in patients with high-risk MDS and AML receiving hypomethylating agents.

机构信息

Department of Pharmacy and Clinical Services, Hackensack University Medical Center, Hackensack, New Jersey, USA.

Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.

出版信息

Am J Hematol. 2020 Jul;95(7):792-798. doi: 10.1002/ajh.25808. Epub 2020 May 4.

Abstract

Invasive fungal infections (IFI) are a significant source of morbidity and mortality for patients with acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS). Given the heterogeneity of the population receiving hypomethylating agents (HMA), it is difficult for clinicians to accurately assess their patients' risk of infection. Literature on the incidence of IFI following HMA is limited to several studies of azacitidine. The primary objective of this retrospective study was to establish the incidence of IFI in HMA treated AML/MDS patients at a large U.S. comprehensive cancer center. Secondary objectives included comparing incidence of IFI among pre-specified subgroups to identify potential risk factors for IFI. Two hundred three patients with AML, intermediate to very high risk MDS or chronic myelomonocytic leukemia who received at least two cycles of HMA were included. The incidence of IFI, as defined by the European Organization for Research and Treatment of Cancer / Invasive Fungal Infections Cooperative Group criteria, was 9.6%, with 20 IFI diagnosed following HMA (three proven, four probable, 13 possible). Among the proven cases of IFI, molds included Scedosporium and Fusarium spp. Eleven patients who developed IFIs were neutropenic upon initiating HMA. The majority (17/20) of infections occurred during the first four cycles. Given this incidence, mold-active prophylaxis can be considered in patients who are neutropenic at the start of therapy.

摘要

侵袭性真菌感染(IFI)是急性髓系白血病(AML)和骨髓增生异常综合征(MDS)患者发病率和死亡率的重要原因。由于接受低甲基化药物(HMA)治疗的患者人群存在异质性,临床医生难以准确评估其患者的感染风险。关于 HMA 后 IFI 发生率的文献仅限于几项阿扎胞苷研究。本回顾性研究的主要目的是在美国一家大型综合性癌症中心确定接受 HMA 治疗的 AML/MDS 患者中 IFI 的发生率。次要目标包括比较特定亚组中 IFI 的发生率,以确定 IFI 的潜在危险因素。该研究纳入了 203 例接受至少两个周期 HMA 治疗的 AML、中高危 MDS 或慢性粒单核细胞白血病患者。IFI 的发生率根据欧洲癌症研究与治疗组织/侵袭性真菌病合作组标准定义为 9.6%,在接受 HMA 后诊断出 20 例 IFI(3 例确诊,4 例可能,13 例可能)。IFI 确诊病例中,霉菌包括枝孢菌属和镰刀菌属。在发生 IFI 的 11 例患者中,有 11 例在开始接受 HMA 时存在中性粒细胞减少症。大多数(17/20)感染发生在头四个周期内。鉴于这种发生率,在开始治疗时中性粒细胞减少的患者可以考虑使用防霉药物进行预防。

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