The Glasgow Prognostic Score, an inflammation based prognostic score, predicts survival in patients with hepatocellular carcinoma
Creators
- 1. Division of Gastroenterology and Hepatology, The Jikei University Daisan Hospital, 4-11-1 Izumihon-cho, Komae- shi, Tokyo, 201-8601 (Japan)
- 2. Division of Clinical Epidemiology, The Jikei University School of Medicine, 3-25-8 Nishishinbashi, Minato-ku, Tokyo, 105-8461 (Japan)
- 3. Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishishinbashi, Minato-ku, Tokyo, 105-8461 (Japan)
Description
Elevated Glasgow Prognostic Score (GPS) has been related to poor prognosis in patients with hepatocellular carcinoma (HCC) undergoing surgical resection or receiving sorafenib. The aim of this study was to investigate the prognostic value of GPS in patients with various stages of the disease and with different liver functional status. One hundred and fifty patients with newly diagnosed HCC were prospectively evaluated. Patients were divided according to their GPS scores. Univariate and multivariate analyses were performed to identify clinicopathological variables associated with overall survival; the identified variables were then compared with those of other validated staging systems. Elevated GPS were associated with increased asparate aminotransferase (P<0.0001), total bilirubin (P<0.0001), decreased albumin (P<0.0001), α-fetoprotein (P=0.008), larger tumor diameter (P=0.003), tumor number (P=0.041), vascular invasion (P=0.0002), extra hepatic metastasis (P=0.02), higher Child-Pugh scores (P<0.0001), and higher Cancer Liver Italian Program scores (P<0.0001). On multivariate analysis, the elevated GPS was independently associated with worse overall survival. Our results demonstrate that the GPS can serve as an independent marker of poor prognosis in patients with HCC in various stages of disease and different liver functional status
Availability note (English)
Available from http://dx.doi.org/10.1186/1471-2407-13-52; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3571892Additional details
Identifiers
Publishing Information
- Journal Title
- BMC cancer (Online)
- Journal Volume
- 13
- Journal Page Range
- p. 52
- ISSN
- 1471-2407
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46111927
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ALBUMINS; BILIRUBIN; CHILDREN; GLOBAL POSITIONING SYSTEM; HEPATOMAS; INFLAMMATION; LIVER; MULTIVARIATE ANALYSIS; PATIENTS
- Descriptors DEC
- AGE GROUPS; ANIMALS; AZOLES; BODY; CARBOXYLIC ACIDS; CARCINOMAS; DIGESTIVE SYSTEM; DISEASES; GLANDS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; MAMMALS; MAN; MATHEMATICS; NEOPLASMS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANS; PATHOLOGICAL CHANGES; PIGMENTS; PRIMATES; PROTEINS; PYRROLES; STATISTICS; SYMPTOMS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c)2013 Kinoshita et al.
- Notes
- PMCID: PMC3571892; PUBLISHER-ID: 1471-2407-13-52; PMID: 23374755; OAI: oai:pubmedcentral.nih.gov:3571892; licensee BioMed Central Ltd.