Abstract | OBJECTIVE: To determine the prognostic value of K-ras mutations in plasma DNA of unresectable pancreatic cancer patients. METHODS: Blood samples were collected from 91 patients with unresectable pancreatic cancer prior to treatment. K-ras gene was amplified from the circulating plasma DNA. Mutations were detected by direct sequencing. The relationship between the types of K-ras gene and prognosis of unresectable pancreatic cancer was evaluated. RESULTS: K-Ras codon 12 mutations were found in 30 of 91(33%) plasma DNA samples, 17mutations were c.35G>A (p.G12D), 11 were c.35G>T (p.G12V) and only 2 were c.34G>C (p.G12R)). K-ras codon 12 mutations could significantly reflect the clinical parameters, including TNM tumor staging (P=0.033) and liver metastasis (P=0.014). The median survival time of patients with K-ras mutations was shorter than that of patients with wild-type K-ras gene (3.9 months vs. 10.2 months, P<0.001). K-ras codon 12 mutation from plasma DNA was an independent negative prognostic factor for survival (hazard ratio, 7.39; 95% confidence interval, 3.69-14.89). CONCLUSION:
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Authors | H Chen, H Tu, Z Q Meng, Z Chen, P Wang, L M Liu |
Journal | European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
(Eur J Surg Oncol)
Vol. 36
Issue 7
Pg. 657-62
(Jul 2010)
ISSN: 1532-2157 [Electronic] England |
PMID | 20542658
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adult
- Aged
- Asian People
(genetics)
- China
- Codon
- DNA, Neoplasm
(genetics)
- Female
- Genes, ras
- Humans
- Kaplan-Meier Estimate
- Liver Neoplasms
(secondary)
- Male
- Middle Aged
- Multivariate Analysis
- Mutation
- Neoplasm Staging
- Pancreatic Neoplasms
(genetics, pathology, therapy)
- Predictive Value of Tests
- Prognosis
- Risk Assessment
- Risk Factors
- Treatment Outcome
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