Liu F, Wu T, Wang J B, Cao X Y, Yin Y M, Zhao Y L, Lu D P
Hematology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Transpl Infect Dis. 2013 Jun;15(3):243-50. doi: 10.1111/tid.12068. Epub 2013 Mar 17.
Invasive fungal infections (IFIs) are a major cause of mortality among allogeneic hematopoietic stem cell transplantation (allo-HSCT) patients. Thanks to the widespread use of secondary antifungal prophylaxis (SAP), a history of IFI is not an absolute contraindication to allo-HSCT. However, IFI recurrence remains a risk factor for transplant-related mortality.
To evaluate the risk factors for IFI recurrence in allo-HSCT patients receiving SAP, we performed a retrospective analysis of 90 individuals treated at our hospital. SAP antifungal agents included fluconazole (n = 28), voriconazole (n = 25), itraconazole (n = 23), caspofungin (n = 7), and micafungin (n = 7).
By day +100, recurrent IFI had occurred in 23 (25.5%) patients. Our multivariate analysis identified 4 factors significantly associated with a risk of IFI recurrence within 100 days of allo-HSCT: duration of neutropenia >18 days, presence of severe acute graft-versus-host disease (aGVHD), <70-day interval between previous infection and transplantation, and use of a narrow-spectrum SAP agent (P = 0.008, 0.010, 0.041, and 0.001, respectively). Of the 87 patients who remained in the study for the duration of the follow-up period (median length: 551 days), 26 (29.9%) died; only 7 (8.0%) of these deaths resulted from a severe fungal infection.
These results suggest that transplantation outcome can be improved by adequate antifungal treatment before transplantation, better prevention of, and therapy for, severe aGVHD, use of granulocyte colony-stimulating factor to reduce the duration of neutropenia, and use of broad-spectrum prophylaxis agents.
侵袭性真菌感染(IFI)是异基因造血干细胞移植(allo-HSCT)患者死亡的主要原因。由于二级抗真菌预防(SAP)的广泛应用,IFI病史已不是allo-HSCT的绝对禁忌证。然而,IFI复发仍然是移植相关死亡率的一个危险因素。
为了评估接受SAP的allo-HSCT患者IFI复发的危险因素,我们对我院治疗的90例患者进行了回顾性分析。SAP抗真菌药物包括氟康唑(n = 28)、伏立康唑(n = 25)、伊曲康唑(n = 23)、卡泊芬净(n = 7)和米卡芬净(n = 7)。
到第100天时,23例(25.5%)患者出现了IFI复发。我们的多因素分析确定了4个与allo-HSCT后100天内IFI复发风险显著相关的因素:中性粒细胞减少持续时间>18天、存在严重急性移植物抗宿主病(aGVHD)、上次感染与移植之间的间隔<70天以及使用窄谱SAP药物(P分别为0.008、0.010、0.041和0.001)。在随访期(中位时长:551天)内一直留在研究中的87例患者中,26例(29.9%)死亡;这些死亡中只有7例(8.0%)是由严重真菌感染导致的。
这些结果表明,通过移植前充分的抗真菌治疗、更好地预防和治疗严重aGVHD、使用粒细胞集落刺激因子缩短中性粒细胞减少持续时间以及使用广谱预防药物,可以改善移植结局。