Lu Yi-An, Liu Hsi-Che, Hou Jen-Yin, Chiu Nan-Chang, Huang Ting-Huan, Yeh Ting-Chi
Division of Pediatric Infectious Diseases, Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan.
Division of Pediatric Hematology-Oncology, Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medicine, MacKay Medical College, New Taipei City, Taiwan.
J Microbiol Immunol Infect. 2024 Dec;57(6):879-886. doi: 10.1016/j.jmii.2024.08.004. Epub 2024 Aug 20.
Data describing the risk factors for the occurrence of severe infections in acute lymphoblastic leukemia (ALL) patients following induction chemotherapy and the role of prophylactic granulocyte-colony stimulating factor (G-CSF) in the era of antimicrobials prophylaxis are limited.
This study enrolled 188 children aged ≤18 years with newly diagnosed ALL who received Taiwan Pediatric Oncology Group ALL-2002 and 2013 treatments between January 1, 2010 and June 30, 2021. Prophylactic G-CSF was administered when a patient continues neutropenia after achieving the first bone marrow remission since June 1, 2015. Clinical factors were assessed for their association with severe infections.
From January 2010 to May 2015, 80 children experienced a total of 11 (13.5%) episodes of severe infections; while 10 (9.2%) episodes were reported to occur in 108 patients who received prophylactic G-CSF. Reduction of severe infections occurrence did not achieve statistical significance during prophylactic G-CSF administration in ALL patients. Compared with ALL-high risk (HR) and very high risk patients with no G-CSF prophylaxis, the use of G-CSF prophylaxis significantly reduced episodes of febrile neutropenia. Occurrence of grade III-IV intestinal ileus, grade II-III oral mucositis, prolonged neutropenia, central venous catheter (CVC) placement, or the requirement insulin therapy for hyperglycemia were associated with higher risk of bloodstream infections.
ALL-HR patients with G-CSF prophylaxis were associated with reduction of febrile neutropenia episodes. Occurrence of severe ileus, oral mucositis, hyperglycemia, CVC placement, or prolonged neutropenia were associated with severe infections in ALL patients receiving induction chemotherapy.
关于急性淋巴细胞白血病(ALL)患者诱导化疗后发生严重感染的危险因素以及预防性粒细胞集落刺激因子(G-CSF)在抗菌药物预防时代作用的数据有限。
本研究纳入了188名年龄≤18岁的新诊断ALL儿童,他们在2010年1月1日至2021年6月30日期间接受了台湾儿科肿瘤学组ALL-2002和2013治疗方案。自2015年6月1日起,当患者首次骨髓缓解后持续出现中性粒细胞减少时,给予预防性G-CSF。评估临床因素与严重感染的相关性。
2010年1月至2015年5月,80名儿童共发生11次(13.5%)严重感染;而在接受预防性G-CSF的108名患者中报告发生了10次(9.2%)。在ALL患者预防性使用G-CSF期间,严重感染发生率的降低未达到统计学意义。与未接受G-CSF预防的ALL高危(HR)和极高危患者相比,使用G-CSF预防显著减少了发热性中性粒细胞减少的发作次数。III-IV级肠梗阻、II-III级口腔黏膜炎、中性粒细胞减少持续时间延长、中心静脉导管(CVC)置入或因高血糖需要胰岛素治疗与血流感染风险较高相关。
接受G-CSF预防的ALL-HR患者发热性中性粒细胞减少发作次数减少。严重肠梗阻、口腔黏膜炎、高血糖、CVC置入或中性粒细胞减少持续时间延长与接受诱导化疗的ALL患者发生严重感染相关。