New clinical scoring system for prognosis of early recurrence of colorectal liver metastases after surgical treatment
Language English Country Greece Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
21937396
DOI
10.5754/hge10045
Knihovny.cz E-resources
- MeSH
- Adult MeSH
- Carcinoembryonic Antigen genetics MeSH
- Colorectal Neoplasms pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Matrix Metalloproteinase 2 genetics MeSH
- Matrix Metalloproteinase 9 genetics MeSH
- RNA, Messenger analysis MeSH
- Liver Neoplasms metabolism mortality secondary surgery MeSH
- Prognosis MeSH
- Recurrence MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Tissue Inhibitor of Metalloproteinase-1 genetics MeSH
- Tissue Inhibitor of Metalloproteinase-2 genetics MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Carcinoembryonic Antigen MeSH
- Matrix Metalloproteinase 2 MeSH
- Matrix Metalloproteinase 9 MeSH
- RNA, Messenger MeSH
- Tissue Inhibitor of Metalloproteinase-1 MeSH
- Tissue Inhibitor of Metalloproteinase-2 MeSH
BACKGROUND/AIMS: To determine the relationship between the mRNA expression of MMP-2, MMP-9, TIMP-1, TIMP-2 and CEA in tumour tissue and preoperative serum levels of these tumour markers in patients with colorectal liver metastases (CLM). Additionally, to establish a new scoring system based upon these results in combination with the volume of the metastatic process to identify patients with a high risk of early recurrence of CLM. METHODOLOGY: The correlation between the mRNA expression of CEA, TIMP-1, TIMP-2, MMP-2 and MMP-9 in tissue samples and preoperative serum levels of the named tumour markers was performed on 27 patients. The scoring system was proposed as a combination of all the independent parameters (mRNA expression of TIMP-1, MMP-9 and CEA in tumour tissue samples and preoperative serum levels of CEA and TIMP-1) in combination with the volume of the metastatic process. The evaluation was conducted in relation to the disease free interval (DFI). RESULTS: We observed a statistically significant relationship between the volume of liver metastases and DFI (p<0.0337). The scoring system divided the patients into groups with a tendency of early recurrence (p<0.0126). CONCLUSIONS: The high stages in our scoring systems augment the risk of recurrence. The proposed scoring system was shown to be an efficient instrument helpful in complex surgical and oncological access to patients after radical surgical treatment of CLM.
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