Department of Internal Medicine III, University Hospital, Bonn, Germany.
J Antimicrob Chemother. 2010 Apr;65(4):761-8. doi: 10.1093/jac/dkp507. Epub 2010 Jan 27.
Invasive fungal infections (IFIs) contribute significantly to mortality and morbidity in patients receiving myelosuppressive chemotherapy for haematological malignancies. The present study investigates the overall survival (OS), infection-related mortality and changes in treatment of IFIs in our department from 1995 until 2006.
Outcomes of all chemotherapy courses were retrospectively evaluated using a standard questionnaire. Modified EORTC/MSG criteria for IFIs were applied: a positive PCR result for Aspergillus spp. in bronchoalveolar lavage was also defined as probable IFI.
In total, 1693 chemotherapy courses in 592 patients were evaluated. Sixty-three percent of chemotherapy courses were given to treat acute myeloid leukaemia, with the rest for acute lymphoblastic leukaemia or aggressive lymphoma. IFIs were observed in 139/592 patients [23.5%, 95% confidence interval (CI) 20%-27%] and in 149/1693 courses (8.8%, 95% CI 8%-10%). IFI-related mortality was 56.9% in 1995-2001 and 28.6% in 2002-06, P < 0.001. Accordingly, median OS in patients with IFI increased: 54 days (95% CI 26-82 days) in 1995-2001 versus 229 days (95% CI 35-423 days) in 2002-06, P = 0.001. By multivariate analysis, factors predictive for better OS were controlled disease after chemotherapy [hazard ratio (HR) 0.228, P < 0.001], possible IFI (in contrast to proven/probable IFI, HR 0.537, P = 0.005), age <60 years (HR 0.583, P = 0.008), time period 2002-06 (HR 0.612, P = 0.021) and use of novel antifungals (HR 0.589, P = 0.033).
Compared with 1995-2001, IFI-related mortality decreased and OS in patients with IFI increased significantly in recent years. Improved OS was associated with controlled haematological disease, certainty of IFI diagnosis (possible), younger age, time period 2002-06 and the use of novel antifungals.
侵袭性真菌感染(IFI)会显著增加接受骨髓抑制化疗的血液恶性肿瘤患者的死亡率和发病率。本研究调查了 1995 年至 2006 年期间我们科室的总体生存率(OS)、与感染相关的死亡率以及 IFI 治疗的变化。
使用标准问卷回顾性评估所有化疗疗程的结果。应用改良的 EORTC/MSG IFI 诊断标准:支气管肺泡灌洗液中曲霉菌属 PCR 阳性结果也定义为可能的 IFI。
共评估了 592 名患者的 1693 个化疗疗程。63%的化疗疗程用于治疗急性髓细胞白血病,其余用于治疗急性淋巴细胞白血病或侵袭性淋巴瘤。592 名患者中有 139 名(23.5%,95%置信区间 [CI] 20%-27%)和 1693 个疗程中的 149 个(8.8%,95% CI 8%-10%)发生了 IFI。1995-2001 年 IFI 相关死亡率为 56.9%,2002-06 年为 28.6%,P<0.001。相应地,IFI 患者的中位 OS 增加:1995-2001 年为 54 天(95% CI 26-82 天),2002-06 年为 229 天(95% CI 35-423 天),P=0.001。多变量分析显示,与 OS 较好相关的因素包括化疗后疾病得到控制(风险比 [HR] 0.228,P<0.001)、可能的 IFI(与确诊/可能的 IFI 相比,HR 0.537,P=0.005)、年龄<60 岁(HR 0.583,P=0.008)、2002-06 时间段(HR 0.612,P=0.021)和新型抗真菌药物的使用(HR 0.589,P=0.033)。
与 1995-2001 年相比,近年来 IFI 相关死亡率下降,IFI 患者的 OS 显著提高。OS 的改善与血液学疾病得到控制、IFI 诊断的确定性(可能)、年龄较小、2002-06 时间段以及新型抗真菌药物的使用有关。