Gan to kagaku ryoho. Cancer & chemotherapy · 2011
[Prediction of the efficacy of modified FOLFOX6 therapy according to the mRNA levels of thymidylate synthase (TS), excision repair cross-complementing-1 and -2( ERCC-1 and ERCC-2) and methylenetetrahydrofolate dehydrogenase( MTHFD) in the primary lesion of colorectal cancer].
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Ishibashi Keiichiro, Okada Norimichi, Tajima Yusuke, Ishiguro Toru, Kuwabara Kouki, Ohsawa Tomonori, Kumamoto Kensuke, Tsuji Yoshitaka, Haga Norihiro, Iwama Takeo, Ishida Hideyuki, Onouchi Tsuneko, Yakabi Koji
Аннотация
The aim of this study was to determine whether mRNA levels of thymidylate synthase (TS), excision repair cross-complementing -1 (ERCC-1), excision repair cross-complementing-2 (ERCC-2) and methylenetetrahydrofolate dehydrogenase( MTHFD) mRNA in the primary tumor could predict a tumor response in patients with unresectable liver metastasis from colorectal cancer treated with mFOLFOX6 therapy as a first-line treatment. Eighteen patients with unresectable liver metastasis from colorectal cancer treated with mFOLFOX6 therapy as a first-line treatment were enrolled in this study. There were no significant differences between the response rate and these enzymes mRNA levels. In ERCC-1 and MTHFD mRNA expression, the progression-free survival time tended to be longer in patients with low levels than in patients with high levels( ERCC-1: p=0.08, MTHFD: p=0.07). The progression-free survival time was significantly longer in patients with both ERCC-1 and MTHFD mRNA were low levels than in patients with other( p=0.03). The levels of ERCC-1 and MTHFD were low in patients who could perform a conversion therapy. There were no significant differences between an overall survival time and these enzymes mRNA levels. In this study, the ERCC-1 and MTHFD mRNA expression may be useful for the prediction of progression-free survival time in patients with unresectable liver metastasis from colorectal cancer treated with mFOLFOX6 therapy.
Предметные рубрики MeSH
AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsColorectal NeoplasmsDNA-Binding ProteinsEndonucleasesFemaleFluorouracilGene Expression Regulation, NeoplasticHumansLeucovorinLiver NeoplasmsMaleMethylenetetrahydrofolate Dehydrogenase (NADP)Middle AgedOrganoplatinum CompoundsRNA, MessengerThymidylate SynthaseXeroderma Pigmentosum Group D Protein