Predictive role of RRM1 and BRCA1 mRNA expression on the clinical outcome of advanced non-small cell lung cancer

被引:6
|
作者
Liang, J. G. [1 ,2 ]
Jin, Z. Y. [2 ]
Gao, X. D. [2 ]
Te, M. R. [2 ]
Ge, L. H. [3 ]
Wang, C. L. [1 ]
机构
[1] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Dept Pulm Tumor, Tianjin, Peoples R China
[2] Inner Mongolia Med Univ, Affiliated Hosp, Dept Chest Surg, Hohhot, Peoples R China
[3] Inner Mongolia Med Univ, Affiliated Hosp, Dept Radiol, Hohhot, Peoples R China
关键词
RRM1; BRCA1; Non-small cell lung cancer; Clinical outcome; PHASE-III TRIAL; CHEMOTHERAPY; GEMCITABINE; SURVIVAL; EFFICACY; CISPLATIN; ERCC1;
D O I
10.4238/2014.July.24.8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study aimed to evaluate the association between RRM1 and BRCA1 expressions and the therapeutic efficacy of platinum-based chemotherapy in non-small cell lung cancer patients in terms of their response and prognosis. In total, 377 patients agreed to participate in our study, and all of them received platinum-based combination chemotherapy between January 2008 and January 2009. The relative cDNA quantitation for RRM1 and BRCA1 was conducted using a fluorescence-based, real-time detection method, using beta-actin as a reference gene. The average age of the 377 patients was 64.6 years (range: 25.5-86.4 years), including 269 men and 108 women. Patients with high RRM1 expression benefited more from a platinum-containing regimen, and patients with high BRCA1 expression showed a high response rate to a platinum-containing regimen and reduced disease progression. Patients with high RRM1 expression were associated with a longer progression-free survival (PFS) and overall survival (OS) than those with low expression, and the hazard ratios (HRs) (95% confidence interval (CI)) were 0.67 (0.32-0.91) and 0.54 (0.30-0.95), respectively. Patients with high BRCA1 expression showed longer PFS and OS compared to those with low expression, and the HRs (95% CI) were 0.54 (0.30-0.95) and 0.62 (0.32-0.93), respectively. These results could be used in personalized chemotherapy decisions and to increase the response rate and prolonged survival, and could encourage exploration of the predictive value of other genes.
引用
收藏
页码:5292 / 5298
页数:7
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