Kotsopoulou Maria, Papadaki Christina, Anargyrou Konstantinos, Spyridonidis Alexandros, Baltadakis Ioannis, Papadaki Helen A, Angelopoulou Maria, Pappa Vasiliki, Liakou Kleoniki, Tzanetakou Manto, Moustaka Marina, Vassilopoulos George
Metaxa Cancer Hospital, Piraeus, Greece.
General Hospital of Athens "G. Gennimatas", Athens, Greece.
Infect Dis Ther. 2019 Jun;8(2):255-268. doi: 10.1007/s40121-019-0236-3. Epub 2019 Feb 14.
Invasive candidiasis (IC) can be a life-threatening infection in immunocompromised patients, particularly those with cancer, hematologic diseases and/or hematopoietic stem cell transplantation (HSCT) recipients. The objective of this study was to evaluate the effectiveness of micafungin in patients with hematologic malignancies or HSCT recipients, relevant to clinical presentation of IC, in real-life practice in Greece.
ASPIRE was a phase IV, multicenter, non-interventional, prospective cohort study, conducted at ten tertiary hospitals in Greece, in adults with hematologic disease. Micafungin treatment for IC or prophylaxis for Candida infection was administered per standard clinical practice until a clinical outcome (success or failure) was reached. Treatment success was defined by the EORTC/MSG criteria for invasive fungal infections (IFI) and was assessed by the investigator. Treatment discontinuation and safety were also evaluated.
One hundred forty-three patients were enrolled. Median age was 62; 85 (59.4%) patients were male, and 133 (93.0%) had Greek ethnicity. One hundred twenty-six (88.1%) patients had hematologic malignancies, and 21 (14.7%) had received HSCT. Prophylaxis was administered to 74 (51.7%) patients [median (range) dose: 50 (50-150) mg/day] with no signs of IFI. Overall, 52 (36.4%) patients with possible IFI at baseline received micafungin treatment [100 (50-125) mg/day] versus 12 (17.2%) with probable [100 (75-150) mg/day] and 5 (3.5%) with confirmed [125 (100-150) mg/day] IFI. Treatment success was 91.6% (95% CI 85.80-95.59; n = 131) overall and 90.5% (n = 67) in patients receiving prophylaxis. Median time on treatment was 13 days. Treatment discontinuation (n = 26; 18.2%) was not related to adverse events. No treatment-related serious adverse events were reported.
Micafungin treatment for IC or prophylaxis for Candida infection was effective and well tolerated in patients with hematologic disorders in clinical practice in Greece. These results demonstrate that micafungin could be used more widely for prophylaxis. Further work is required to determine the efficacy and safety of micafungin for the management of IFIs in hematologic settings.
Astellas Pharma Inc.
侵袭性念珠菌病(IC)对于免疫功能低下的患者可能是一种危及生命的感染,尤其是癌症、血液系统疾病患者和/或造血干细胞移植(HSCT)受者。本研究的目的是评估米卡芬净在希腊实际临床实践中对血液系统恶性肿瘤患者或HSCT受者(与IC临床表现相关)的有效性。
ASPIRE是一项IV期、多中心、非干预性前瞻性队列研究,在希腊的十家三级医院对成年血液系统疾病患者进行。根据标准临床实践给予米卡芬净治疗IC或预防念珠菌感染,直至达到临床结局(成功或失败)。治疗成功根据欧洲癌症研究与治疗组织/侵袭性真菌感染协作组(EORTC/MSG)的侵袭性真菌感染(IFI)标准定义,并由研究者评估。还评估了治疗中断情况和安全性。
共纳入143例患者。中位年龄为62岁;85例(59.4%)为男性,133例(93.0%)为希腊族裔。126例(88.1%)患者患有血液系统恶性肿瘤,21例(14.7%)接受了HSCT。74例(51.7%)患者接受了预防治疗[中位(范围)剂量:50(50 - 150)mg/天],且无IFI迹象。总体而言,52例(36.4%)基线时可能患有IFI的患者接受了米卡芬净治疗[100(50 - 125)mg/天],12例(17.2%)可能患有IFI的患者[100(75 - 150)mg/天],5例(3.5%)确诊患有IFI的患者[125(100 - 150)mg/天]。总体治疗成功率为91.6%(95%CI 85.80 - 95.59;n = 131),接受预防治疗的患者中治疗成功率为90.5%(n = 67)。中位治疗时间为13天。治疗中断(n = 26;18.2%)与不良事件无关。未报告与治疗相关的严重不良事件。
在希腊的临床实践中,米卡芬净治疗IC或预防念珠菌感染对血液系统疾病患者有效且耐受性良好。这些结果表明米卡芬净可更广泛地用于预防。需要进一步开展工作以确定米卡芬净在血液系统疾病中管理IFI的疗效和安全性。
安斯泰来制药公司