Czyzewski Krzysztof, Galazka Przemyslaw, Zalas-Wiecek Patrycja, Gryniewicz-Kwiatkowska Olga, Gietka Agnieszka, Semczuk Katarzyna, Chelmecka-Wiktorczyk Liliana, Zak Iwona, Salamonowicz Malgorzata, Fraczkiewicz Jowita, Zajac-Spychala Olga, Bien Ewa, Plonowski Marcin, Wawrykow Pawel, Pierlejewski Filip, Gamrot Zuzanna, Malas Zofia, Stolpa Weronika, Musial Jakub, Styczynski Jan
Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
Department of General and Oncological Surgery for Children and Adolescents, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
Infect Drug Resist. 2019 May 30;12:1471-1480. doi: 10.2147/IDR.S199657. eCollection 2019.
The analysis of epidemiology, risk factors and outcome of infections in children with malignant bone tumors (MBT) undergoing chemotherapy. In this retrospective nationwide multicenter cross-sectional study, a total number of 126 children with MBT including 70 with Ewing sarcoma (ES) and 56 with osteosarcoma (OSA) were screened for infections over a period of 72 consecutive months. The risk of infection was 7.15-fold higher in patients with ES as compared to the OSA group, especially concerning bacterial infections (4.1-fold increase risk). Bacterial infections occurred in 74.3% patients with ES and in 41.1% with OSA. The median time from diagnosis to first infection was 4.9 months. 33.0% of bacterial episodes were diagnosed as bloodstream (BSI), 31.1% as gastrointestinal tract, 30.1% as urinary tract infection. Infection-related mortality (IRM) from bacterial infection was 6% and 15% in ES and OSA patients, respectively. Cumulative incidence was 7.1% for invasive fungal disease and 6.3% for viral infections. The only significant risk factor for IRM was time to infection ≥5 months since the beginning of chemotherapy. All patients who have died from infection had BSI and were in neutropenia. Infections in the children with MBT in our study occurred with high frequency, especially in patients with ES. The most frequent were bacterial infections, while fungal and viral infections were episodic. Among the bacterial infections, bloodstream, urinary tract and gastrointestinal tract infections occurred with similar frequency. All deceased patients died due to BSI. Bacterial infection occurring ≥5 months since the beginning of chemotherapy was a risk factor for death.
对接受化疗的儿童恶性骨肿瘤(MBT)感染的流行病学、危险因素及结局进行分析。在这项回顾性全国多中心横断面研究中,连续72个月对总共126例MBT患儿进行感染筛查,其中包括70例尤因肉瘤(ES)患儿和56例骨肉瘤(OSA)患儿。与OSA组相比,ES患儿的感染风险高7.15倍,尤其是细菌感染(风险增加4.1倍)。74.3%的ES患儿和41.1%的OSA患儿发生细菌感染。从诊断到首次感染的中位时间为4.9个月。33.0%的细菌感染发作被诊断为血流感染(BSI),31.1%为胃肠道感染,30.1%为尿路感染。ES和OSA患儿因细菌感染导致的感染相关死亡率(IRM)分别为6%和15%。侵袭性真菌病的累积发病率为7.1%,病毒感染为6.3%。IRM的唯一显著危险因素是自化疗开始后至感染的时间≥5个月。所有因感染死亡的患者均发生BSI且处于中性粒细胞减少状态。在我们的研究中,MBT患儿感染发生率高,尤其是ES患儿。最常见的是细菌感染,而真菌和病毒感染为偶发。在细菌感染中,血流、尿路和胃肠道感染的发生率相似。所有死亡患者均因BSI死亡。自化疗开始后≥5个月发生的细菌感染是死亡的危险因素。