Positive expression of ERCC1 predicts a poorer platinum-based treatment outcome in Chinese patients with advanced non-small-cell lung cancer

被引:0
|
作者
Xin Wang
Jun Zhao
Lu Yang
Li Mao
Tongtong An
Hua Bai
Shuhang Wang
Xuyi Liu
Guoshuang Feng
Jie Wang
机构
[1] Beijing Cancer Hospital and Institute,Department of Thoracic Medical Oncology, Peking University School of Oncology
[2] The University of Texas M. D. Anderson Cancer Center,The Department of Thoracic/Head and Neck Medical Oncology
[3] Beijing Cancer Hospital and Institute,Department of Biostatistics, Peking University School of Oncology
来源
Medical Oncology | 2010年 / 27卷
关键词
ERCC1; RRM1; NSCLC; Platinum-based chemotherapy;
D O I
暂无
中图分类号
学科分类号
摘要
The goal of this study is to determine role of excision repair cross-complementing group 1 gene (ERCC1) and ribonucleotide reductase subunit M1 (RRM1) expression in predicting response and survival in Chinese patients with advanced stage non-small cell lung cancer (NSCLC) treated with platinum-based chemotherapy. Formalin-fixed, paraffin-embedded biopsy tissues were retrospectively obtained from 124 advanced NSCLC patients. Protein expression levels of ERCC1 and RRM1 were determined by immunohistochemistry (IHC). Associations between expression of ERCC1 and RRM1 and clinic-pathologic parameters were analyzed. The study shows that ERCC1 and RRM1 expression was detected in 43 (35%) and 50 (40%) of the 124 tumor samples, respectively. Expression of ERCC1 and RRM1 was negatively associated with tumor response. Fifty-four percent patients whose tumors did not express ERCC1 had partial response (PR) compared to 33% whose tumors expressed the protein (P = 0.022). Similarly, 54% patients whose tumor did not express RRM1 had PR compared to 36% whose tumors expression the protein (P = 0.042). Further, patients whose tumors lacked of ERCC1 but not RRM1 expression had a longer median survival time than those tumors expressed ERCC1 (13.4 months versus 9.1 months; P = 0.006), which is independent of other prognostic factors (P = 0.0066). In conclusion, tumor ERCC1 expression is associated with tumor response and patients’ survival in Chinese advanced NSCLC patients treated with platinum-based regimen and may serve as a biomarker in predicting tumor response and clinical outcome in the patient population.
引用
收藏
页码:484 / 490
页数:6
相关论文
共 50 条
  • [21] DNA repair by ERCC1 in non-small-cell lung cancer
    Cecere, Fabiana
    Bria, Emilio
    Rosell, Rafael
    NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (24): : 2590 - 2591
  • [22] Randomized Prospective Biomarker Trial of ERCC1 for Comparing Platinum and Nonplatinum Therapy in Advanced Non-Small-Cell Lung Cancer: ERCC1 Trial (ET)
    Lee, Siow Ming
    Falzon, Mary
    Blackhall, Fiona
    Spicer, James
    Nicolson, Marianne
    Chaudhuri, Abhro
    Middleton, Gary
    Ahmed, Samreen
    Hicks, Jonathan
    Crosse, Barbara
    Napier, Mark
    Singer, Julian M.
    Ferry, David
    Lewanski, Conrad
    Forster, Martin
    Rolls, Sally-Ann
    Capitanio, Arrigo
    Rudd, Robin
    Iles, Natasha
    Ngai, Yenting
    Gandy, Michael
    Lillywhite, Rachel
    Hackshaw, Allan
    JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (04) : 402 - +
  • [23] ERCC1 protein expression is not associated with survival after platinum-based chemotherapy in patients with metastatic non-small cell lung cancer (NSCLC)
    Pennell, Nathan A.
    Chirieac, Lucian R.
    El Karak, Fadi
    Lynch, Thomas J.
    Heist, Rebecca S.
    Christiani, David C.
    JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (06) : S238 - S239
  • [24] Expression of ERCC1 protein in biopsy specimen predicts survival in advanced ovarian cancer patients treated with platinum-based chemotherapy
    Milovic-Kovacevic, M.
    Srdic-Rajic, T.
    Radulovic, S.
    Bjelogrlic, S.
    Gavrilovic, D.
    JOURNAL OF BUON, 2011, 16 (04): : 708 - 714
  • [25] Role of ERCC5 promoter polymorphisms in response to platinum-based chemotherapy in patients with advanced non-small-cell lung cancer
    He, Caiyun
    Duan, Zhipeng
    Li, Ping
    Xu, Qian
    Yuan, Yuan
    ANTI-CANCER DRUGS, 2013, 24 (03) : 300 - 305
  • [26] Pharmacogenetics of platinum-based chemotherapy in non-small cell lung cancer: predictive validity of polymorphisms of ERCC1
    Hamilton, Gerhard
    Rath, Barbara
    EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2018, 14 (01) : 17 - 24
  • [27] Association between ERCC1 polymorphisms and nephrotoxicity in non-small cell lung cancer patients undergoing platinum-based chemotherapy
    de Jong, Corine
    Deneer, Vera Henriette
    Kelder, Johannes
    Hunting, Cornelis Bernardus
    Herder, Gerarda
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
  • [28] Prognostic Value of EGFR Mutation and ERCC1 in Patients with Non-Small Cell Lung Cancer Undergoing Platinum-Based Chemotherapy
    Yamashita, Fumie
    Azuma, Koichi
    Yoshida, Tsukasa
    Yamada, Kazuhiko
    Kawahara, Akihiko
    Hattori, Satoshi
    Takeoka, Hiroaki
    Zaizen, Yoshiaki
    Kawayama, Tomotaka
    Kage, Masayoshi
    Hoshino, Tomoaki
    PLOS ONE, 2013, 8 (08):
  • [29] ERCC1 SNPs as Potential Predictive Biomarkers in Non-Small Cell Lung Cancer Patients Treated With Platinum-Based Chemotherapy
    Kalikaki, Aristea
    Voutsina, Alexandra
    Koutsopoulos, Anastasios
    Papadaki, Chara
    Sfakianaki, Maria
    Yachnakis, Emmanouel
    Xyrafas, Alexandros
    Kotsakis, Athanasios
    Agelaki, Sofia
    Souglakos, John
    Mavroudis, Dimitrios
    Georgoulias, Vassilis
    CANCER INVESTIGATION, 2015, 33 (04) : 107 - 113
  • [30] Association Between Polymorphisms of ERCC1 and XPD and Clinical Response to Platinum-Based Chemotherapy in Advanced Non-Small Cell Lung Cancer
    Li, Fan
    Sun, Xinchen
    Sun, Ning
    Qin, Shukui
    Cheng, Hongyan
    Feng, Jifeng
    Chen, Baoan
    Cheng, Lu
    Lu, Zuhong
    Ji, Jiazhong
    Zhou, Yingfeng
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2010, 33 (05): : 489 - 494