European Study of Cerebral Aspergillosis treated with Isavuconazole (ESCAI): A study by the ESCMID Fungal Infection Study Group.

IF 8.2 1区 医学 Q1 IMMUNOLOGY Clinical Infectious Diseases Pub Date : 2024-10-15 DOI:10.1093/cid/ciae371
Alexandra Serris, Riina Rautemaa-Richardson, Joana D Laranjinha, Anna Candoni, Carolina Garcia-Vidal, Ana Alastruey-Izquierdo, Helena Hammarström, Danila Seidel, Jan Styczynski, Raquel Sabino, Frederic Lamoth, Juergen Prattes, Adilia Warris, Raphaël Porcher, Fanny Lanternier
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Abstract

Background: Cerebral aspergillosis (CA) is associated with high mortality. According to the European Conference on Infections in Leukemia and the European Society of Clinical Microbiology and Infectious Diseases guidelines, the recommended first-line treatment for all forms of aspergillosis is voriconazole or isavuconazole. However, little is known about the efficacy and safety of isavuconazole in CA.

Methods: We conducted a European multicenter retrospective study of patients treated with isavuconazole for proven or probable CA between 2014 and 2022 and compared the outcomes with those of weighted control groups from the previously published French national cohort of CA, the Cerebral Aspergillosis Lesional Study (CEREALS).

Results: Forty patients from 10 countries were included. The main underlying conditions were hematological malignancies (53%) and solid-organ transplantation (20%). Isavuconazole was administered as a first-line treatment to 10 patients, primarily in combination therapy, resulting in control of CA in 70% of these cases. Thirty patients received isavuconazole after a median of 65 days on another therapy, mostly because of side effects (50%) or therapeutic failure (23%) of the previous treatment. Predominantly given as monotherapy, it achieved control of CA in 73% of the patients. Seventeen patients (43%) underwent neurosurgery. When measured, isavuconazole levels were low in cerebrospinal fluid but adequate in serum and brain tissue. Isavuconazole toxicity led to treatment interruption in 7.5% of the patients. Twelve-week mortality was 18%. Comparison with the CEREALS cohort showed comparable survival in patients receiving isavuconazole or voriconazole as a first-line treatment.

Conclusions: Isavuconazole appears to be a well-tolerated treatment. Mortality of CA treated with isavuconazole is similar to that reported with voriconazole.

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伊沙窝康唑治疗脑曲霉菌病的欧洲研究:EFISG 研究。
简介脑曲霉菌病(CA)死亡率很高。根据 ECIL-6 和 ESCMID 指南,所有曲霉菌病的一线治疗推荐使用伏立康唑或异武康唑。然而,人们对异唑康唑在 CA 中的疗效和安全性知之甚少:我们对 2014 年至 2022 年期间接受异武康唑治疗的已证实或可能患有 CA 的患者进行了一项欧洲多中心回顾性研究,并将其结果与之前发表的法国全国 CA 队列--脑曲霉菌病病变研究--中的加权对照组结果进行了比较:来自 10 个国家的 40 名患者被纳入研究。主要基础疾病为血液恶性肿瘤(53%)和实体器官移植(20%)。伊沙夫康唑作为一线治疗药物用于10例患者,主要是联合治疗,结果70%的患者CA得到控制。30名患者在接受另一种疗法治疗中位数65天后接受了伊沙夫康唑治疗,其中大部分是因为副作用(50%)或之前的治疗失败(23%)。该药主要作为单药治疗,73%的患者的CA得到了控制。17名患者(43%)接受了神经外科手术。经测定,脑脊液中的异武康唑含量较低,但血清和脑组织中的异武康唑含量充足。7.5%的患者因异武康唑毒性而中断治疗。12周的死亡率为18%。与CEREALS队列的比较显示,接受异武康唑或伏立康唑作为一线治疗的患者生存率相当:结论:异武康唑似乎是一种耐受性良好的治疗方法。结论:伊沙武康唑似乎是一种耐受性良好的治疗方法,接受伊沙武康唑治疗的CA患者的死亡率与接受伏立康唑治疗的患者的死亡率相似。
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来源期刊
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
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