Tüfekçi Özlem, Yılmaz Bengoa Şebnem, Demir Yenigürbüz Fatma, Şimşek Erdem, Karapınar Tuba Hilkay, İrken Gülersu, Ören Hale
Dokuz Eylül University Faculty of Medicine, Department of Pediatric Hematology, İzmir, Turkey Phone: +90 532 666 90 50 E-mail:
Turk J Haematol. 2015 Dec;32(4):329-37. doi: 10.4274/tjh.2014.0035. Epub 2015 Apr 27.
Rapid and effective treatment of invasive fungal infection (IFI) in patients with leukemia is important for survival. In this study, we aimed to describe variations regarding clinical features, treatment modalities, time of restarting chemotherapy, and outcome in children with IFI and acute leukemia (AL).
The charts of all pediatric AL patients in our clinic between the years of 2001 and 2013 were retrospectively reviewed. All patients received prophylactic fluconazole during the chemotherapy period.
IFI was identified in 25 (14%) of 174 AL patients. Most of them were in the consolidation phase of chemotherapy and the patients had severe neutropenia. The median time between leukemia diagnosis and definition of IFI was 122 days. Twenty-four patients had pulmonary IFI. The most frequent finding on computed tomography was typical parenchymal nodules. The episodes were defined as proven in 4 (16%) patients, probable in 7 (28%) patients, and possible in 14 (56%) patients. The median time for discontinuation of chemotherapy was 27 days. IFI was treated successfully in all patients with voriconazole, amphotericin B, caspofungin, or posaconazole alone or in combination. Chemotherapy was restarted in 50% of the patients safely within 4 weeks and none of those patients experienced reactivation of IFI. All of them were given secondary prophylaxis. The median time for antifungal treatment and for secondary prophylaxis was 26 and 90 days, respectively. None of the patients died due to IFI.
Our data show that rapid and effective antifungal therapy with rational treatment modalities may decrease the incidence of death and that restarting chemotherapy within several weeks may be safe in children with AL and IFI.
快速有效地治疗白血病患者的侵袭性真菌感染(IFI)对其生存至关重要。在本研究中,我们旨在描述患有IFI和急性白血病(AL)的儿童在临床特征、治疗方式、重新开始化疗的时间及预后方面的差异。
回顾性分析了2001年至2013年间我院所有儿科AL患者的病历。所有患者在化疗期间均接受氟康唑预防治疗。
174例AL患者中有25例(14%)确诊为IFI。其中大多数处于化疗巩固期,且患者存在严重中性粒细胞减少。从白血病诊断到IFI确诊的中位时间为122天。24例患者患有肺部IFI。计算机断层扫描最常见的表现为典型的实质结节。4例(16%)患者的感染被定义为确诊,7例(28%)为很可能,14例(56%)为可能。化疗中断的中位时间为27天。所有患者单用或联合伏立康唑、两性霉素B、卡泊芬净或泊沙康唑治疗IFI均获成功。50%的患者在4周内安全地重新开始化疗,且这些患者均未出现IFI复发。所有患者均接受了二级预防。抗真菌治疗和二级预防的中位时间分别为26天和90天。无一例患者死于IFI。
我们的数据表明,采用合理的治疗方式进行快速有效的抗真菌治疗可降低死亡率,并且在患有AL和IFI的儿童中,数周内重新开始化疗可能是安全的。