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Pre-treatment blood inflammatory markers as predictors of systemic infection during induction chemotherapy: results of an exploratory study in patients with acute myeloid leukemia

Authors
Hong, JunshikWoo, Hyun SeonAhn, Hee KyungSym, Sun JinPark, JinnyCho, Eun KyungShin, Dong BokLee, Jae Hoon
Issue Date
Jan-2016
Publisher
SPRINGER
Keywords
Acute myeloid leukemia; Induction chemotherapy; C-reactive protein; Ferritin; Infection
Citation
SUPPORTIVE CARE IN CANCER, v.24, no.1, pp.187 - 194
Journal Title
SUPPORTIVE CARE IN CANCER
Volume
24
Number
1
Start Page
187
End Page
194
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/8684
DOI
10.1007/s00520-015-2762-1
ISSN
0941-4355
Abstract
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.
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