Qin Jiayuan, Bi Hongxia, Tang Guangmin, Liu Xinyao, Qu Junyan, Lv Xiaoju, Liu Yanbin
Center of Infectious Diseases, West China Hospital, Sichuan University, Guoxuexiang 37, Chengdu 610041, China.
State Key Laboratory of Biotherapy, Division of Infectious Diseases, Chengdu 610041, China.
Microorganisms. 2025 Jan 1;13(1):55. doi: 10.3390/microorganisms13010055.
Invasive mucormycosis (IM) poses a substantial morbidity and mortality burden among immunocompromised patients.
We aim to compare the real-world effectiveness and safety of isavuconazole with those of amphotericin B in patients with IM.
In this observational cohort study, we enrolled patients who were diagnosed with IM and treated with either isavuconazole or amphotericin B.
A total of 106 patients met the study criteria. Of these, 47 received isavuconazole, and 59 received amphotericin B as the primary treatment. The two cohorts had similar baseline characteristics, including a history of malignancy, use of immunosuppressants, infection sites, and pathogens. The amphotericin B group demonstrated a significantly greater incidence of renal disorders ( < 0.001) and hypokalemia ( < 0.001) than the isavuconazole group. The proportion of patients who received salvage therapy was greater in the amphotericin B group than in the isavuconazole group (42% vs. 6%, < 0.001). Eighteen patients in the amphotericin B group discontinued treatment because of adverse events, whereas no patients in the isavuconazole group discontinued treatment because of adverse events. A significant difference in the primary therapeutic response between the isavuconazole and amphotericin B groups was noted ( = 0.013), with a higher treatment failure rate in the amphotericin B group (68% vs. 36%, = 0.001). However, there were no significant differences in all-cause mortality or mucormycosis-attributable mortality rates between the two groups.
Isavuconazole outperformed amphotericin B as a first-line treatment option for IM in terms of its clinical effectiveness and safety.
侵袭性毛霉病(IM)在免疫功能低下患者中造成了相当大的发病和死亡负担。
我们旨在比较艾沙康唑与两性霉素B在IM患者中的实际疗效和安全性。
在这项观察性队列研究中,我们纳入了被诊断为IM并接受艾沙康唑或两性霉素B治疗的患者。
共有106例患者符合研究标准。其中,47例接受艾沙康唑治疗,59例接受两性霉素B作为主要治疗。两组患者的基线特征相似,包括恶性肿瘤病史、免疫抑制剂的使用、感染部位和病原体。两性霉素B组的肾脏疾病(<0.001)和低钾血症(<0.001)发生率显著高于艾沙康唑组。接受挽救治疗的患者比例在两性霉素B组高于艾沙康唑组(42%对6%,<0.001)。两性霉素B组有18例患者因不良事件停药,而艾沙康唑组无患者因不良事件停药。艾沙康唑组和两性霉素B组在主要治疗反应上存在显著差异(=0.013),两性霉素B组的治疗失败率更高(68%对36%,=0.001)。然而,两组在全因死亡率或毛霉病归因死亡率方面没有显著差异。
在临床疗效和安全性方面,艾沙康唑作为IM的一线治疗选择优于两性霉素B。