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首页> 外文期刊>Infectious Diseases and Therapy >Effectiveness and Safety of Micafungin in Managing Invasive Fungal Infections among Patients in Greece with Hematologic Disorders: The ASPIRE Study
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Effectiveness and Safety of Micafungin in Managing Invasive Fungal Infections among Patients in Greece with Hematologic Disorders: The ASPIRE Study

机译:米卡芬净在治疗希腊血液系统疾病患者中侵袭性真菌感染的有效性和安全性:ASPIRE研究

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IntroductionInvasive 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. MethodsASPIRE 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. ResultsOne 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. ConclusionMicafungin 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. FundingAstellas Pharma Inc.
机译:简介侵染性念珠菌病(IC)在免疫受损的患者中可能是威胁生命的感染,尤其是患有癌症,血液病和/或造血干细胞移植(HSCT)的患者。这项研究的目的是在希腊的实际生活中,评估米卡芬净在血液恶性肿瘤或HSCT接受者中与IC临床表现相关的有效性。方法ASPIRE是一项在希腊的十家三级医院针对患有血液病的成年人进行的IV期,多中心,非干预,前瞻性队列研究。按照标准临床实践进行米卡芬净治疗IC或预防念珠菌感染,直至达到临床结果(成功或失败)。治疗成功由侵袭性真菌感染(IFI)的EORTC / MSG标准定义,并由研究者评估。还评估了治疗中止和安全性。结果共招募143例患者。中位年龄为62岁。男性为85位(59.4%),希腊族为133位(93.0%)。血液恶性肿瘤126例(占88.1%),HSCT患者21例(占14.7%)。对74名(51.7%)无IFI征象的患者[中位(范围)剂量:50(50–150)mg /天]进行了预防。总体而言,基线时有52个(36.4%)可能存在IFI的患者接受了米卡芬净治疗[100(50–125)mg /天],而12天(17.2%)可能接受的[100(75–150)mg /天]和5(3.5 %)和确定的[125(100–150)mg /天] IFI。总的来说,治疗成功率为91.6%(95%CI 85.80-95.59; n = 131),接受预防的患者为90.5%(n = 67)。中位治疗时间为13天。中止治疗(n = 26; 18.2%)与不良事件无关。没有报道与治疗有关的严重不良事件。结论在希腊的临床实践中,米卡芬净治疗IC或预防念珠菌感染有效且耐受性良好。这些结果表明米卡芬净可以更广泛地用于预防。需要进一步的工作来确定米卡芬净在血液学环境中治疗IFI的功效和安全性。资金Astellas Pharma Inc.

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