Abstract
Objective
The aim of this study was to evaluate the association between the methylenetetrahydrofolate reductase (MTHFR) C677T excision repair cross-complementation group 1 (ERCC1) genetic polymorphisms and the clinical efficacy of gemcitabine-based chemotherapy in advanced non-small cell lung cancer (NSCLC).
Methods
A total of 135 chemonaive patients with unresectable advanced NSCLC were treated with gemcitabine/platinum regimens. The polymorphisms of MTHFR C677T, ERCC1 C8092A, and ERCC1 C118T were genotyped using the TaqMan methods.
Results
The overall response rate was 28.9%. Patients with MTHFR CC genotype had a higher rate of objective response than patients with variant genotype (TT or CT) (41.2% versus 19.1%, P=0.01). Median time to progression (TTP) of patients with MTHFR CC genotype was longer than that of patients with variant genotype (7.6 months versus 5.0 months, P=0.003). No significant associations were obtained between ERCC1 C118T and C8092A polymorphisms and both response and survival.
Conclusions
Our data suggest the value of MTHFR C677T polymorphism as a possible predictive marker of response and TTP in advanced NSCLC patients treated with gemcitabine/platinum.
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Project supported by the National Natural Science Foundation of China (No. 30900654), the Medical Scientific Research Foundation of Zhejiang Province (Nos. 2007B025, 2010KYA036, and 2010KYA 032), the Science and Technology Department of Zhejiang Province (Nos. 2011c23017 and 2012c23081), and the Zhejiang Major Science and Technology Special Project (No. 2009C13018), China
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Hong, W., Wang, K., Zhang, Yp. et al. Methylenetetrahydrofolate reductase C677T polymorphism predicts response and time to progression to gemcitabine-based chemotherapy for advanced non-small cell lung cancer in a Chinese Han population. J. Zhejiang Univ. Sci. B 14, 207–215 (2013). https://doi.org/10.1631/jzus.B1200101
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DOI: https://doi.org/10.1631/jzus.B1200101
Key words
- Non-small cell lung cancer
- Single nucleotide polymorphism
- Methylenetetrahydrofolate reductase
- Gemcitabine
- Excision repair cross-complementation group 1