Δημοσίευση

Lack of association between KRAS mutations and 18F-FDG PET/CT in Caucasian metastatic colorectal cancer patients.

ΤίτλοςLack of association between KRAS mutations and 18F-FDG PET/CT in Caucasian metastatic colorectal cancer patients.
Publication TypeJournal Article
Year of Publication2014
AuthorsKrikelis, D., Skoura E., Kotoula V., Rondogianni P., Pianou N., Samartzis A., Xanthakis I., Fountzilas G., & Datseris I. E.
JournalAnticancer Res
Volume34
Issue5
Pagination2571-9
Date Published2014 May
ISSN1791-7530
Λέξεις κλειδιάAdult, Aged, Colorectal Neoplasms, DNA Mutational Analysis, Female, Fluorodeoxyglucose F18, Humans, Male, Middle Aged, Multimodal Imaging, Mutation, Positron-Emission Tomography, Proto-Oncogene Proteins, Radiopharmaceuticals, ras Proteins, Real-Time Polymerase Chain Reaction, Retrospective Studies, Tomography, X-Ray Computed
Abstract

BACKGROUND: Although Kirsten rat sarcoma (KRAS) gene mutational testing is essential for the optimal design of therapeutic strategies for colorectal cancer, it is not always feasible or reliable. In this retrospective study, we examined whether (18)F-Fluorodeoxyglucose positron-emission tomography/computed tomography ((18)F-FDG PET/CT) scans can serve as a surrogate examination for KRAS mutational testing.PATIENTS AND METHODS: KRAS codon 12 and 13 mutational status was tested in 44 colorectal primary tumors and was compared with the (18)F-FDG PET/CT maximum standardized uptake value (SUVmax) values of the respective metastatic lesions. Glucose transporter-1 (GLUT1) mRNA levels were also measured in colorectal primary tumors.RESULTS: No statistically significant correlation between (18)F-FDG PET/CT SUVmax values and KRAS mutation status was found (parametric t-test: p=0.4753; non-parametric Kruskal-Wallis test: p=0.51). This result cannot be attributed to the effect of differing GLUT1 mRNA levels, as shown by multivariate analysis.CONCLUSION: Our study failed to promote (18)F-FDG PET/CT uptake as a surrogate examination for KRAS mutation testing.

Alternate JournalAnticancer Res.
PubMed ID24778079

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