Cerebral aspergillosis in a patient treated with acalabrutinib, a second generation Bruton's tyrosine kinase inhibitor

IF 2.4 4区 医学 Q3 MYCOLOGY
Journal de mycologie medicale Pub Date : 2025-12-01 Epub Date: 2025-10-20 DOI:10.1016/j.mycmed.2025.101586
Scheherazade Rezig , Jean-Philippe Talarmin , Solène Le Gal , Hussam Saad
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引用次数: 0

Abstract

Bruton’s tyrosine kinase (BTK) inhibitors are key drugs in the frontline therapy of chronic lymphocytic leukemia. Invasive fungal infection is a well-documented adverse event in patient treated with first-generation BTK inhibitors. This rare but severe adverse event has been described in several case-reports and series in patients receiving ibrutinib, particularly invasive aspergillosis, especially of cerebral location. Second-generation BTK inhibitors such as acalabrutinib are more selective for BTK and are as effective and better tolerated than ibrutinib. Only six case-reports have described an opportunistic fungal infection occurring with second-generation BTK inhibitors. Here, we report the case of a patient who developed fatal invasive pulmonary and cerebral aspergillosis while being treated with acalabrutinib.
阿卡拉布替尼治疗的脑曲霉病患者,第二代布鲁顿酪氨酸激酶抑制剂
布鲁顿酪氨酸激酶(BTK)抑制剂是慢性淋巴细胞白血病一线治疗的关键药物。侵袭性真菌感染是第一代BTK抑制剂治疗患者的不良事件。这种罕见但严重的不良事件已在接受伊鲁替尼的患者的几个病例报告和系列中描述,特别是侵袭性曲霉病,特别是大脑部位。第二代BTK抑制剂如阿卡拉布替尼对BTK具有更强的选择性,与依鲁替尼一样有效且耐受性更好。只有6个病例报告描述了第二代BTK抑制剂发生的机会性真菌感染。在这里,我们报告的情况下,患者谁发展致命的侵袭性肺和脑曲霉病,而接受阿卡拉布替尼治疗。
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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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