Auberger Jutta, Lass-Flörl Cornelia, Ulmer Hanno, Nogler-Semenitz Elisabeth, Clausen Johannes, Gunsilius Eberhard, Einsele Hermann, Gastl Günther, Nachbaur David
Department of Internal Medicine, Division of Hematology and Oncology, Innsbruck Medical University, Anichstrasse 35, 6020, Innsbruck, Austria.
Section Hygiene, Institute for Hygiene and Social Medicine, Innsbruck Medical University, Innsbruck, Austria.
Int J Hematol. 2008 Dec;88(5):508-515. doi: 10.1007/s12185-008-0184-2. Epub 2008 Nov 5.
Invasive fungal infections (IFI) remain a leading cause of morbidity and mortality in immunocompromised patients. This retrospective single-center study analyzed incidence, treatment and outcome of invasive fungal infections in 1,095 patients with hematological malignancies receiving either cytoreductive chemotherapy or autologous or allogeneic hematopoietic stem cell transplantation at our institution between 1995 and 2004. IFI occurred in 167/1,095 (15%) patients with a significant increase over time (12.7% between 1995 and 2000 vs. 18.1% in the later IFI cohort, P = 0.0134). Fifty-four (32%) patients had proven, 70 (42%) patients had probable, and 43 (26%) patients suffered from possible IFI according to EORTC/MSG criteria. In 108/124 (87%) cases with proven or probable IFI, moulds were the causative pathogens. Both, Aspergillus fumigatus (n = 46) and Aspergillus terreus (n = 41) were predominant. Yeast infections (Candida spp.) were documented in 16/124 (10%) cases with proven or probable IFI. Median overall survival of the entire IFI cohort was 7 (3-17) months. Overall survival was significantly better in patients with probable or possible IFI (37 and 38%, respectively) compared with patients with proven IFI (28%, P = 0.019). In 35% of patients, IFI was the principal cause of death with a significant decrease over time (44% in time cohort 1995-2000 vs. 28% in the later IFI cohort, P = 0.018) accompanied by an increased use of novel antifungals. By multivariate analysis, only proven IFI was significantly predictive for death (HR 1.7, P = 0.018). A significant decrease in fungus-related deaths was observed despite a significant increase of IFI over time, probably due to improved diagnostic and therapeutic approaches.
侵袭性真菌感染(IFI)仍然是免疫功能低下患者发病和死亡的主要原因。这项回顾性单中心研究分析了1995年至2004年间在我们机构接受减瘤化疗或自体或异基因造血干细胞移植的1095例血液系统恶性肿瘤患者的侵袭性真菌感染的发病率、治疗方法及预后情况。167/1095例(15%)患者发生了IFI,且随时间显著增加(1995年至2000年间为12.7%,而后期IFI队列中为18.1%,P = 0.0134)。根据欧洲癌症研究与治疗组织/美国国立医学研究院(EORTC/MSG)标准,54例(32%)患者确诊为IFI,70例(42%)患者可能患有IFI,43例(26%)患者疑似患有IFI。在108/124例(87%)确诊或可能患有IFI的病例中,霉菌是致病病原体。烟曲霉(n = 46)和土曲霉(n = 41)均占主导地位。在16/124例(10%)确诊或可能患有IFI的病例中记录到酵母感染(念珠菌属)。整个IFI队列的中位总生存期为7(3 - 17)个月。与确诊IFI的患者(28%)相比,可能或疑似IFI的患者的总生存期明显更好(分别为37%和38%,P = 0.019)。在35%的患者中,IFI是主要死亡原因,且随时间显著下降(1995年至2000年时间段为44%,而后期IFI队列中为28%,P = 0.018),同时新型抗真菌药物的使用增加。通过多变量分析,只有确诊IFI对死亡有显著预测性(风险比1.7,P = 0.018)。尽管IFI随时间显著增加,但真菌相关死亡显著减少,这可能是由于诊断和治疗方法的改进。