J. Fujita et al., SERIAL MEASUREMENTS OF PLASMA ELASTASE ALPHA-1-PROTEINASE INHIBITOR COMPLEXES IN PATIENTS RECEIVING CANCER-CHEMOTHERAPY, Chest, 104(2), 1993, pp. 522-526
We monitored the plasma elastase:alpha1-proteinase inhibitor complexes
during chemotherapy for cancer and investigated the relationship betw
een the elastase burden and the onset of adult respiratory distress sy
ndrome (ARDS) in 20 patients with primary lung cancer who received com
bination chemotherapy; 15 normal nonsmokers served as controls. Of the
20 patients, 6 developed pneumonia, and 6 developed ARDS. We measured
peripheral WBCs, C-reactive protein (CRP), plasma elastase:alpha1-pro
teinase inhibitor complex (complex), and the ratio of complex/WBC duri
ng chemotherapy for cancer. In patients who did not experience complic
ations during combination chemotherapy, WBC counts changed, but levels
of complex were normal. In patients who developed pneumonia, levels o
f complex were abnormally high during the WBC nadir, and the complex/W
BC count increased along with the level of CRP. In patients who develo
ped ARDS during chemotherapy for cancer, levels of complex were abnorm
ally high immediately after chemotherapy and remained high after the o
nset of ARDS. In addition, complex/WBC counts and CRP levels increased
at the onset of ARDS. The maximum complex concentration was significa
ntly higher in patients with pneumonia (414.3 +/- 57.2 ng/ml) and ARDS
(683.2 +/- 72.8 ng/ml), compared with normal nonsmokers (130.2 +/- 5.
5 ng/ml; p<0.01) and patients who did not develop complications (211.5
+/- 23.3 ng/ml; p<0.01). The maximum complex/WBC count was also signi
ficantly higher in patients with pneumonia (0.56 +/- 0.12) and ARDS (1
.03 +/- 0.27), compared with normal nonsmokers (0.03 +/- 0.002; p<0.01
) and patients without complications (0.09 +/- 0.01; p<0.01). These fi
ndings suggested a possible correlation between increased levels of co
mplex and the onset of ARDS.