Department of Infectious Diseases, Peter MacCallum Cancer Centre, National Centre for Infections in Cancer, Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia.
Department of Internal Medicine, National Taiwan University Hospital and College of Medicine, No. 7, Chung-Shan South Road, Taipei, 100, Taiwan.
J Antimicrob Chemother. 2021 Dec 24;77(1):16-23. doi: 10.1093/jac/dkab317.
Invasive aspergillosis (IA) is an acute infection affecting patients who are immunocompromised, as a result of receiving chemotherapy for malignancy, or immunosuppressant agents for transplantation or autoimmune disease. Whilst criteria exist to define the probability of infection for clinical trials, there is little evidence in the literature or clinical guidelines on when to change antifungal treatment in patients who are receiving prophylaxis or treatment for IA. To try and address this significant gap, an advisory board of experts was convened to develop criteria for the management of IA for use in designing clinical trials, which could also be used in clinical practice. For primary treatment failure, a change in antifungal therapy should be made: (i) when mycological susceptibility testing identifies an organism from a confirmed site of infection, which is resistant to the antifungal given for primary therapy, or a resistance mutation is identified by molecular testing; (ii) at, or after, 8 days of primary antifungal treatment if there is increasing serum galactomannan, or galactomannan positivity in serum, or bronchoalveolar lavage fluid when the antigen was previously undetectable, or there is sudden clinical deterioration, or a new clearly distinct site of infection is detected; and (iii) at, or after, 15 days of primary antifungal treatment if the patient is clinically stable but with ≥2 serum galactomannan measurements persistently elevated compared with baseline or increasing, or if the original lesions on CT or other imaging, show progression by >25% in size in the context of no apparent change in immune status.
侵袭性曲霉病(IA)是一种影响免疫功能低下患者的急性感染,这些患者因接受恶性肿瘤化疗或移植或自身免疫性疾病的免疫抑制剂而免疫功能低下。虽然存在用于临床试验的感染可能性定义标准,但在文献或临床指南中,关于何时改变正在接受 IA 预防或治疗的患者的抗真菌治疗的证据很少。为了尝试解决这一重大差距,召集了一个专家顾问委员会,制定用于临床试验设计的 IA 管理标准,这些标准也可用于临床实践。对于原发性治疗失败,应改变抗真菌治疗:(i)当从确认的感染部位获得的微生物对原发性治疗中使用的抗真菌药物具有耐药性,或者通过分子检测鉴定出耐药突变时;(ii)在原发性抗真菌治疗 8 天内,如果血清半乳甘露聚糖不断增加,或血清半乳甘露聚糖呈阳性,或支气管肺泡灌洗液中的抗原以前无法检测到时,或出现突然的临床恶化,或检测到新的明显不同的感染部位;和(iii)在原发性抗真菌治疗 15 天内,如果患者临床稳定但与基线相比有≥2 次血清半乳甘露聚糖测量值持续升高或增加,或者如果 CT 或其他影像学上的原始病变在免疫状态无明显变化的情况下大小增加>25%。