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The biomarkers and potential pathogenesis of lung cancer related cerebral hemorrhage
Kemin Qin1, Yicong Chen2, Haiyin Long1
1Department of Neurology, The First Affiliated Hospital of Guangxi Medical University, Nanning City, Guangxi.
Insights
Lung cancer patients experiencing cerebral hemorrhage show distinct biomarkers. Lengthened prothrombin time, elevated CEA, and CA199 levels are key indicators for lung cancer-related cerebral hemorrhage (LCRCH).
Area of Science:
- Oncology
- Neurology
- Biochemistry
Background:
- Cerebral hemorrhage is a known complication in lung cancer (LC) patients.
- The pathogenesis and specific biomarkers for lung cancer-related cerebral hemorrhage (LCRCH) are not well understood.
Purpose of the Study:
- To investigate the pathogenesis and identify plasma biomarkers for LCRCH.
Main Methods:
- Retrospective review of 56 acute cerebral hemorrhage patients with active LC and no conventional vascular risks (LCRCH group).
- Comparison with 112 age, gender, and cancer subtype-matched active LC patients without hemorrhage (control group).
- Analysis included prothrombin time (PT), plasma carcinoembryonic antigen (CEA), cancer antigen 125 (CA125), cancer antigen 199 (CA199), and platelet (PLT) levels.
Main Results:
- LCRCH patients often presented with lobar hemorrhages, typically in advanced-stage adenocarcinoma with poor short-term prognosis.
- LCRCH patients exhibited significantly lengthened PT, elevated plasma CEA, CA125, and CA199, and decreased PLT levels compared to controls.
- Multivariate analysis identified lengthened PT, elevated plasma CEA, and CA199 as independent risk factors for LCRCH.
Conclusions:
- Lengthened PT, elevated plasma CEA, and CA199 levels are associated with the pathogenesis of LCRCH.
- An index derived from these independent risk factors could serve as a specific biomarker for LCRCH.
Abstract:
Cerebral hemorrhage is one of the common complications in patients with lung cancer (LC). Although cancer related cerebral hemorrhage was aware, the pathogenesis and biomarkers of lung cancer related cerebral hemorrhage (LCRCH) remained not well known. The aim of this study was to investigate the pathogenesis and plasma biomarkers of LCRCH.A retrospective review was conducted on acute cerebral hemorrhage patients with active LC who was admitted to the hospital between January 2007 and December 2017. A total of 56 patients with LCRCH (active LC patients with acute cerebral hemorrhage but without conventional vascular risks) was recruited. Meanwhile, 112 patients with active LC alone and gender, age, and subtype of cancer cell matched were recruited as control group.In LCRCH patients, most of the hemorrhagic lesions were located in lobes. And most of them with adenocarcinoma were in medium to terminal stage with poor prognosis short-term. Moreover, LCRCH patients had a lengthened prothrombin time (PT), elevated plasma carcinoembryonic antigen (CEA), cancer antigen 125 (CA125) and cancer antigen 199 (CA199) levels and decreased platelet (PLT) level than did the patients with LC. Multivariate logistic regression analysis showed that lengthened PT, elevated plasm CEA, and CA199 levels were independent risk factors for LCRCH.It was suggested that lengthened PT, elevated plasm CEA and CA199 levels associated with the pathogenesis of LCRCH, and that the Index derived from independent risks should be serve as a specific biomarker of LCRCH.
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