Korean J Med.
1998 Apr;54(4):467-472.
Alterations of Coagulation and Fibrinolysis System in Lung Cancer
- Affiliations
-
- 1Department of Internal Medicine, Yonsei University, College of Medicine, Seoul, Korea.
- 2Department of Clinical Pathology, Yonsei University, College of Medicine, Seoul, Korea.
- 3Department of Internal Medicine, Ajou University, College of Medicine, Suwon, Korea.
Abstract
OBJECTIVES
It is well known that malignant diseases
exhibit an increased propensity to clotting and fibrinolytic
aberrations and early detection of these hemostatic
alterations is very important for the rapid institution of
appropriate treatment of thromboembolic and hemor
rhagic complications in patients with malignant disease.
The incidence of these abnormalities in lung cancer was
reported from 20% up to 95% according to various
investigators using different hemostatic parameters. We
measured the concentrations of plasma thrombin
antithrombin III complex(TAT) and plasmin-alpha2-plasmin
inhibitor complex(PIC), which are newly developed sen
sitive molecular markers of coagulation and fibrinolysis
system respectively in patients with lung cancer and
determined the degree of these hemostatic abnormalities
according to the histologic types and different clinical
stages in patients with lung cancer.
METHODS
We measured the concentrations of plasma
TAT and PIC in 62 patients with histologically confirmed
lung cancer, and we determined stage radiologically in
non-surgical patients and pathologically in surgical pa
tients. The plasma TAT and PIC levels were assayed using
a solid phase enzyme immunoassay with Enzygnost-TAT
kit(Behringwerke, Marburg, Germany) and Enzygnost-PAP
kit(Behringwerke, Marburg, Germany), respectively.
RESULTS
The concentrations of plasma TAT(6.8+/-4.8
ng/mL) and PIC(644.3+/-330.5 ng/mL) in patients with
lung cancer were significantly increased compared to
those of plasma TAT(2.8+/-1.2 ng/mL) and PIC(240.4+/-
69.7 ng/mL) in control subjects(p<0.05). The concen
trations of plasma TAT and PIC in patients with lung
cancer were not different according to histologic types,
clinical stage and distant metastasis. There was no
correlations between TAT and PIC(r=0.11, p > 0.05).
CONCLUSIONS
There was a subclinical activation of
coagulation and fibrinolysis system in patients with lung
cancer although they don't have overt clinical evidences
of thromboembolism or hemorrhage. But there were no
different activation of coagulation and fibrinolysis system
according to histologic types and clinical stages.