Bochennek K, Hassler A, Perner C, Gilfert J, Schöning S, Klingebiel T, Reinhardt D, Creutzig U, Lehrnbecher T
Division of Pediatric Hematology and Oncology, Hospital for Children and Adolescents, Johann Wolfgang Goethe-University, Frankfurt, Germany.
Paediatric Hematology and Oncology, Medical Center, University of Essen, Essen, Germany.
Blood Cancer J. 2016 Jan 15;6(1):e382. doi: 10.1038/bcj.2015.110.
Infections are an important cause for morbidity and mortality in pediatric acute myeloid leukemia (AML). We therefore characterized infectious complications in children treated according to the trial AML-BFM 2004. Patients with Down syndrome were excluded from the analysis. Data were gathered from the medical records in the hospital where the patients were treated. A total of 405 patients (203 girls; median age 8.4 years) experienced 1326 infections. Fever without identifiable source occurred in 56.1% of the patients and clinically and microbiologically documented infections in 17.5% and 32.4% of the patients, respectively. In all, 240 Gram-positive (112 viridans group streptococci) and 90 Gram-negative isolates were recovered from the bloodstream. Invasive fungal infection was diagnosed in 3% of the patients. Three children each died of Gram-negative bacteremia and invasive aspergillosis, respectively. As compared with the results of AML-BFM 93 with lower dose intensity, infection-related morbidity was slightly higher in AML-BFM 2004 (3.3. versus 2.8 infections per patient), whereas infection-related mortality significantly decreased (1.5% versus 5.4%; P=0.003). Specific anti-infective recommendations included in the treatment protocol, regular training courses for pediatric hematologists and increasing experience may be the reason for reduced infection-related mortality in children with AML. Further studies are needed to decrease infection-related morbidity.
感染是小儿急性髓系白血病(AML)发病和死亡的重要原因。因此,我们对按照AML-BFM 2004试验进行治疗的儿童的感染并发症进行了特征描述。分析中排除了唐氏综合征患者。数据收集自患者接受治疗的医院的病历。共有405例患者(203名女孩;中位年龄8.4岁)发生了1326次感染。56.1%的患者出现不明原因发热,17.5%和32.4%的患者分别有临床和微生物学记录的感染。总共从血流中分离出240株革兰氏阳性菌(112株草绿色链球菌)和90株革兰氏阴性菌。3%的患者被诊断为侵袭性真菌感染。分别有3名儿童死于革兰氏阴性菌血症和侵袭性曲霉病。与剂量强度较低的AML-BFM 93的结果相比,AML-BFM 2004中与感染相关的发病率略高(每名患者3.3次感染对2.8次感染),而与感染相关的死亡率显著降低(1.5%对5.4%;P=0.003)。治疗方案中包含的特定抗感染建议、为儿科血液学家举办的定期培训课程以及经验的增加可能是AML患儿感染相关死亡率降低的原因。需要进一步研究以降低与感染相关的发病率。