Hong Junshik, Woo Hyun Seon, Ahn Hee Kyung, Sym Sun Jin, Park Jinny, Cho Eun Kyung, Shin Dong Bok, Lee Jae Hoon
Division of Hematology and Medical Oncology, Department of Internal Medicine, Gachon University Gil Medical Center, Incheon Regional Cancer Center, Gachon University School of Medicine, 21 Namdongdae-ro 774-gil, Namdong-gu, Incheon, 405-760, Republic of Korea.
Support Care Cancer. 2016 Jan;24(1):187-194. doi: 10.1007/s00520-015-2762-1. Epub 2015 May 19.
The purpose of this study is to evaluate the role of C-reactive protein (CRP) and ferritin blood levels in predicting the incidence of systemic infection among adult patients with acute myeloid leukemia (AML) treated with induction chemotherapy.
Adult patients with newly diagnosed AML who were initially treated with conventional 3 + 7 induction chemotherapy within 5 days of their diagnosis were included. Patients with previous cytotoxic chemotherapy <3 years, acute promyelocytic leukemia diagnosis, human immunodeficiency virus infection, or significant systemic infection at the time of diagnosis were excluded. Patients were treated with an institutional policy of substantial identity with negligible differences regarding supportive care.
Among 110 patients (median age 54.5 years), 39 infectious events in 38 patients were reported, along with 21 episodes of infectious treatment-related mortality (TRM; 19.1%). Elevated pre-treatment CRP (p = 0.032) and ferritin (p = 0.002) were related to the incidence of systemic infection. The degree of increase of blood CRP and ferritin level was correlated with the extent of leukocytosis. However, patients with elevated inflammatory markers above normal range had increased risk of infection irrespective of whether they had leukocytosis or not, suggesting that expansion of leukemic blast is another factor affecting the elevation of the markers independent to infection propensity and therefore the magnitude of the elevation does not quantitatively predict the risk of infection.
Modest elevation of baseline blood inflammatory markers above the normal range could be an indicator for predicting the incidence of systemic infection in patients with AML.
本研究旨在评估C反应蛋白(CRP)和铁蛋白血水平在预测接受诱导化疗的成年急性髓系白血病(AML)患者发生全身感染中的作用。
纳入新诊断为AML且在诊断后5天内开始接受传统3+7诱导化疗的成年患者。排除既往接受细胞毒性化疗<3年、急性早幼粒细胞白血病诊断、人类免疫缺陷病毒感染或诊断时存在严重全身感染的患者。患者接受机构制定的在支持治疗方面基本一致且差异可忽略不计的治疗方案。
在110例患者(中位年龄54.5岁)中,报告了38例患者发生的39次感染事件,以及21例感染相关治疗死亡(TRM;19.1%)。治疗前CRP升高(p=0.032)和铁蛋白升高(p=0.002)与全身感染的发生率相关。血CRP和铁蛋白水平的升高程度与白细胞增多的程度相关。然而,炎症标志物高于正常范围的患者无论是否存在白细胞增多,感染风险均增加,这表明白血病原始细胞的扩增是影响标志物升高的另一个因素,独立于感染倾向,因此升高幅度并不能定量预测感染风险。
基线血炎症标志物适度高于正常范围可能是预测AML患者全身感染发生率的一个指标。