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血液系统恶性肿瘤中的侵袭性真菌感染与靶向治疗

Invasive Fungal Infections and Targeted Therapies in Hematological Malignancies.

作者信息

Little Jessica S, Weiss Zoe F, Hammond Sarah P

机构信息

Division of Infectious Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

出版信息

J Fungi (Basel). 2021 Dec 10;7(12):1058. doi: 10.3390/jof7121058.

Abstract

The use of targeted biologic therapies for hematological malignancies has greatly expanded in recent years. These agents act upon specific molecular pathways in order to target malignant cells but frequently have broader effects involving both innate and adaptive immunity. Patients with hematological malignancies have unique risk factors for infection, including immune dysregulation related to their underlying disease and sequelae of prior treatment regimens. Determining the individual risk of infection related to any novel agent is challenging in this setting. Invasive fungal infections (IFIs) represent one of the most morbid infectious complications observed in hematological malignancy. In recent years, growing evidence suggests that certain small molecule inhibitors, such as BTK inhibitors and PI3K inhibitors, may cause an increased risk of IFI in certain patients. It is imperative to better understand the impact that novel targeted therapies might have on the development of IFIs in this high-risk patient population.

摘要

近年来,靶向生物疗法在血液系统恶性肿瘤治疗中的应用有了极大的扩展。这些药物作用于特定的分子途径以靶向恶性细胞,但通常会产生更广泛的影响,涉及固有免疫和适应性免疫。血液系统恶性肿瘤患者具有独特的感染危险因素,包括与其基础疾病相关的免疫失调以及既往治疗方案的后遗症。在这种情况下,确定与任何新型药物相关的个体感染风险具有挑战性。侵袭性真菌感染(IFI)是血液系统恶性肿瘤中观察到的最具致死性的感染并发症之一。近年来,越来越多的证据表明,某些小分子抑制剂,如BTK抑制剂和PI3K抑制剂,可能会使某些患者发生IFI的风险增加。更好地了解新型靶向疗法对这一高危患者群体中IFI发生发展的影响势在必行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3544/8706272/0908c9b5b9dd/jof-07-01058-g001.jpg

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