Prognostic value of ERCC1 and RRM1 in NSCLC patients with smoking history or not

被引:0
作者
Sun, Jiangtao [1 ,2 ]
Song, Kaifang [2 ]
Yuan, Xiang [3 ]
Gao, Shegan [2 ]
Feng, Xiaoshan [2 ]
Yang, Bo [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Neurosurg, Zhengzhou, Henan, Peoples R China
[2] Henan Univ Sci & Technol, Canc Inst, Affiliated Hosp 1, Coll Clin Med, Luoyang, Henan Province, Peoples R China
[3] Henan Univ Sci & Technol, Coll Clin Med, Affiliated Hosp 1, Henan Key Lab Canc Epigenet,Canc Inst, Luoyang, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2017年 / 10卷 / 05期
关键词
Smoking; NSCLC; ERCC1; RRM1; clinical outcome and therapeutic effect; CELL LUNG-CANCER; MESSENGER-RNA EXPRESSION; BIOMARKER EXPRESSION; NEVER-SMOKERS; DNA-REPAIR; CHEMOTHERAPY; SURVIVAL; IMMUNOHISTOCHEMISTRY; ADENOCARCINOMA; ENTITY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: We aimed to assess the expression of ERCC1 and RRM1 in NSCLC patients with smoking history or not and investigate the therapeutic effect of biomarker-guided chemotherapy in those patients. Patients and methods: A total of 131 NSCLC patients at stage IIIb or IV were enrolled and divided into two groups based on their smoking history. Group A were smokers (n=67); Group B were non-smokers (n=64). The expression of ERCC1 and RRM1 were determined by real-time polymerase chain reaction analysis (RT-PCR). Clinicopathological characteristics, tumor response and patient survival were monitored for both groups. Results: In our study, the expression of ERCC1 was significantly higher in smoking patients as compared with non-smoking group (P=0.028). Patients' characteristics in both groups were compared and there were no significant difference in patients age, tumor size or pathological types, but more male patients were occurred in Group A (P=0.001). Notably, the patients with low mRNA expression of ERCC1 (X-2=6.194, P=0.013) and RRM1 (X-2=5.012, P=0.025) were more sensitive to chemotherapy than patients with high expression levels. Compared with Group A, the patients in Group B displayed a higher response rate (59.3% vs. 32.8%; P=0.045), a lower 1-year recurrent rate (25.0% vs. 52.2%; P=0.001), a longer median progression-free survival (PFS) time (12.0 months vs. 14.1 months, P=0.008) and median overall survival (OS) time (22.9 months vs. 27.6 months; P=0.005). Conclusion: In summary, the expression levels of ERCC1 and RRM1 are mediated by smoking and correlated with the sensitivity to chemotherapy together with the clinical outcome of NSCLC patients. Our study suggests the adverse effect of smoking on the prognosis of NSCLC patients.
引用
收藏
页码:5889 / 5894
页数:6
相关论文
共 21 条
[1]   DNA repair and survival in lung cancer - The two faces of Janus [J].
Gazdar, Adi F. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (08) :771-773
[2]   RRM1 expression and clinical outcome of gemcitabine-containing chemotherapy for advanced non-small-cell lung cancer: A meta-analysis [J].
Gong, Weiyi ;
Zhang, Xinmin ;
Wu, Jinfeng ;
Chen, Lili ;
Li, Lulu ;
Sun, Jing ;
Lv, Yubao ;
Wei, Xiaobai ;
Du, Yijie ;
Jin, Hualiang ;
Dong, Jingcheng .
LUNG CANCER, 2012, 75 (03) :374-380
[3]   A randomized phase II trial of ERCC1 and RRM1 mRNA expression-based chemotherapy versus docetaxel/carboplatin in advanced non-small cell lung cancer [J].
Heo, Su Jin ;
Jung, Inkyung ;
Lee, Choong-kun ;
Kim, Jee Hung ;
Lim, Sun Min ;
Moon, Yong Wha ;
Shim, Hyo Sup ;
Jeong, Jaeheon ;
Kim, Joo-Hang ;
Kim, Hye Ryun ;
Cho, Byoung Chul .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2016, 77 (03) :539-548
[4]   Intratumour variation of biomarker expression by immunohistochemistry in resectable non-small cell lung cancer [J].
Jakobsen, Jan Nyrop ;
Santoni-Rugiu, Eric ;
Ravn, Jesper ;
Sorensen, Jens Benn .
EUROPEAN JOURNAL OF CANCER, 2013, 49 (11) :2494-2503
[5]   Assessment of XPD Lys751Gln and XRCC1 T-77C polymorphisms in advanced non-small-cell lung cancer patients treated with platinum-based chemotherapy [J].
Liu, Li ;
Yuan, Peng ;
Wu, Chen ;
Zhang, Xiaomin ;
Wang, Feng ;
Guo, Huan ;
Zhong, Rong ;
Xu, Yihua ;
Wu, Jing ;
Yu, Dianke ;
Wu, Tangchun ;
Zhang, Xuemei ;
Nie, Shaofa ;
Miao, Xiaoping ;
Lin, Dongxin .
LUNG CANCER, 2011, 73 (01) :110-115
[6]  
Lord RVN, 2002, CLIN CANCER RES, V8, P2286
[7]   Prognostic value of smoking status in operated non-small cell lung cancer [J].
Nia, PS ;
Weyler, J ;
Colpaert, C ;
Vermeulen, P ;
Van Marck, E ;
Van Schil, P .
LUNG CANCER, 2005, 47 (03) :351-359
[8]   Improved survival in never-smokers vs current smokers with primary adenocarcinoma of the lung [J].
Nordquist, LT ;
Simon, GR ;
Cantor, A ;
Alberts, WM ;
Bepler, G .
CHEST, 2004, 126 (02) :347-351
[9]   Clinical benefit in oncology trials: Is this a patient-centred or tumour-centred end-point? [J].
Ohorodnyk, Paulo ;
Eisenhauer, Elizabeth A. ;
Booth, Christopher M. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (13) :2249-2252
[10]   DNA repair by ERCC1 in non-small-cell lung cancer and cisplatin-based adjuvant chemotherapy [J].
Olaussen, Ken A. ;
Dunant, Ariane ;
Fouret, Pierre ;
Brambilla, Elisabeth ;
Andre, Fabrice ;
Haddad, Vincent ;
Taranchon, Estelle ;
Filipits, Martin ;
Pirker, Robert ;
Popper, Helmut H. ;
Stahel, Rolf ;
Sabatier, Laure ;
Pignon, Jean-Pierre ;
Tursz, Thomas ;
Le Chevalier, Thierry ;
Soria, Jean-Charles .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (10) :983-991