Suppressed neutrophil function as a risk factor for severe infection aftercytotoxic chemotherapy in patients with acute nonlymphocytic leukemia

Citation
K. Hubel et al., Suppressed neutrophil function as a risk factor for severe infection aftercytotoxic chemotherapy in patients with acute nonlymphocytic leukemia, ANN HEMATOL, 78(2), 1999, pp. 73-77
Citations number
16
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
ANNALS OF HEMATOLOGY
ISSN journal
09395555 → ACNP
Volume
78
Issue
2
Year of publication
1999
Pages
73 - 77
Database
ISI
SICI code
0939-5555(199902)78:2<73:SNFAAR>2.0.ZU;2-M
Abstract
Severe infections are a major problem in patients suffering from acute nonl ymphocytic leukemia (ANLL) undergoing myeloablative chemotherapy. Possible factors leading to infectious complications in these patients are suppresse d immune defense mechanisms existing prior to therapy, including those invo lving the neutrophil granulocyte department. In this study we investigated whether neutrophil function as measured by oxidative burst and phagocytosis before the start of treatment correlates with the severity of infection af ter therapy. Forty-four patients were included, 27 men and 17 women. Their median age was 46 years (range 20-70 years). According to the development o f infectious complications the patients were assigned retrospectively to gr oup 1 (no or only mild infections, n=29) or to group 2 (severe infection or death due to infection, n=15). The phagocytic activity was significantly r educed in group 2 as compared with group 1 [113.7+/-13.7 (SEM) vs 170.0+/-1 9.2, mean channel fluorescence; p = 0.04]. In contrast, the oxidative burst as measured by FMLP stimulation was pronounced but not significantly enhan ced in group 2 (24.8+/-6.1 vs 14.5+/-3.4, mean channel fluorescence). In co nclusion, patients with severe infections after chemotherapy might already have preactivated neutrophils with suppressed function prior to treatment. Thus, evaluating function parameters could help to estimate the individual risk of infection for a patient with ANLL.