Real world impact of epidermal growth factor receptor mutation status on treatment patterns in patients with non-small cell lung cancer

被引:10
|
作者
Sun, Jong-Mu [1 ]
Rampal, Sanjay [2 ,3 ]
Lee, Genehee [4 ,5 ]
Lee, Jeeyun [1 ]
Choi, Yoon-La [6 ,7 ]
Parasuraman, Bhash [8 ]
Guallar, Eliseo [2 ]
Cho, Juhee [2 ,7 ]
Shim, Young Mog [5 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Hematol Oncol,Dept Med, Seoul 135710, South Korea
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol & Med, Welch Ctr Prevens Epidemiol & Clin Res, Baltimore, MD USA
[3] Univ Malaya, Fac Med, Julius Ctr, Dept Social & Prevent Med, Kuala Lumpur, Malaysia
[4] Sungkyunkwan Univ, Sch Med, Dept Nursing, Samsung Med Ctr, Seoul 135710, South Korea
[5] Sungkyunkwan Univ, Sch Med, Dept Thorac Surg, Samsung Med Ctr, Seoul 135710, South Korea
[6] Sungkyunkwan Univ, Sch Med, Dept Pathol, Samsung Med Ctr, Seoul 135710, South Korea
[7] Sungkyunkwan Univ, Dept Hlth Sci & Technol, Samsung Adv Inst Hlth Sci & Technol, Seoul 135710, South Korea
[8] AstraZeneca, Wilmington, DE USA
关键词
Epidermal growth factor receptor; Non-small cell lung cancer; Mutation; Real-world practice; Tyrosine kinase inhibitor; PHASE-III; 1ST-LINE TREATMENT; NEVER-SMOKERS; OPEN-LABEL; GEFITINIB; CHEMOTHERAPY; ADENOCARCINOMA; DOCETAXEL; ERLOTINIB; TRIAL;
D O I
10.1016/j.lungcan.2013.01.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Epidermal growth factor receptor (EGFR) mutation status is an important predictor of the efficacy of EGFR tyrosine kinase inhibitor (TKI) therapy in patients with non-small cell lung cancer (NSCLC). We evaluated the real impact of EGFR mutation status on chemotherapy patterns of NSCLC patients. Patients and methods: This is a retrospective cohort study of consecutive advanced NSCLC patients attended at the Samsung Medical Centre in Seoul, Korea, from January 2007 through July 2010. EGFR mutation was analyzed by direct sequencing testing. Results: Among 1164 patients treated during the study period, 166 (14.3%) were EGFR mutation positive, 275 (23.6%) were mutation negative, and 723 (62.1%) had mutation status unknown. Overall, 605 (52%) received TKI therapy as a first-, second-, or third-line therapy. The proportions of patients receiving TKI therapy among those with positive, negative and unknown EGFR mutation status were 88.0, 46.5, and 45.8%, respectively. After adjustment for other factors, patients with a positive EGFR mutation status (odds ratio [OR] 7.88, 95% CI 4.58, 13.57), and those who were female (OR 2.83, 95% CI 2.04, 3.92) or had poor performance status (OR 1.58, 95% CI 1.13, 2.22) were significantly more likely to receive TKI treatment. Furthermore, the temporal relationship between EGFR mutation reporting and initiation of TKI therapy significantly differed by EGFR mutation status. Conclusion: EGFR mutation status significantly affected the chemotherapy patterns in advanced NSCLC. More widespread EGFR testing and the use of faster and more sensitive mutation tests will result in more timely and appropriate use of TKI therapy in advanced NSCLC. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:191 / 196
页数:6
相关论文
共 50 条
  • [31] Rad51 in regulating the radiosensitivity of non-small cell lung cancer with different epidermal growth factor receptor mutation status
    Zhong, Xing
    Luo, Guomin
    Zhou, Xiaojuan
    Luo, Wen
    Wu, Xia
    Zhong, Renming
    Wang, Yanping
    Xu, Feng
    Wang, Jin
    THORACIC CANCER, 2016, 7 (01) : 50 - 60
  • [32] Epidermal growth factor receptor mutation subtypes and geographical distribution among Indian non-small cell lung cancer patients
    Choughule, A.
    Noronha, V
    Joshi, A.
    Desai, S.
    Jannbhekar, N.
    Utture, S.
    Thavamanni, A.
    Prabhash, K.
    Dutt, A.
    INDIAN JOURNAL OF CANCER, 2013, 50 (02) : 107 - 111
  • [33] Comparison of plasma and tissue samples in epidermal growth factor receptor mutation by ARMS in advanced non-small cell lung cancer
    Ma, MeiLi
    Shi, ChunLei
    Qian, JiaLin
    Teng, JiaJun
    Zhong, Hua
    Han, BaoHui
    GENE, 2016, 591 (01) : 58 - 64
  • [34] An observational study of the epidermal growth factor receptor-tyrosine kinase inhibitor resistance mechanism in epidermal growth factor receptor gene mutation-positive non-small cell lung cancer
    Yoshimura, Akihiro
    Uchino, Junji
    Tanimura, Keiko
    Chihara, Yusuke
    Tamiya, Nobuyo
    Kaneko, Yoshiko
    Takeda, Takayuki
    Hiranuma, Osamu
    Hasegawa, Isao
    Kubota, Yutaka
    Shiotsu, Shinsuke
    Takumi, Chieko
    Hiraoka, Noriya
    Yamada, Tadaaki
    Takayama, Koichi
    MEDICINE, 2018, 97 (40)
  • [35] Osimertinib for the treatment of epidermal growth factor receptor-mutated non-small cell lung cancer patients with leptomeningeal metastases and different T790M status
    Xu, Haiyan
    Chen, Hengqi
    Kong, Jianxin
    Zhang, Ye
    Liu, Shan
    Yang, Guangjian
    Yang, Lu
    Wang, Yan
    ANNALS OF TRANSLATIONAL MEDICINE, 2021, 9 (11)
  • [36] Resistance to epidermal growth factor receptor inhibition in non-small cell lung cancer
    Van Der Steen, Nele
    Giovannetti, Elisa
    Carbone, Daniela
    Leonetti, Alessandro
    Rolfo, Christian D.
    Peters, Godefridus J.
    CANCER DRUG RESISTANCE, 2018, 1 (04) : 230 - 249
  • [37] Optimal Management of Patients with Non-Small Cell Lung Cancer and Epidermal Growth Factor Receptor Mutations
    Chia-Chi Lin
    James Chih-Hsin Yang
    Drugs, 2011, 71 : 79 - 88
  • [38] The evolving first-line treatment of advanced non-small cell lung cancer harbouring epidermal growth factor receptor mutations
    Decoster, Lore
    Giron, Philippe
    Mignon, Sacha
    De Greve, Jacques
    TRANSLATIONAL LUNG CANCER RESEARCH, 2018, 7 : S134 - S137
  • [39] Epidermal growth factor receptor tyrosine kinase inhibitors in elderly or poor performance status patients with advanced non-small cell lung cancer
    Chia-Chi Lin
    Chih-Hsin Yang
    Targeted Oncology, 2009, 4 : 37 - 44
  • [40] Osimertinib a new weapon in epidermal growth factor receptor-mutated non-small cell lung cancer patients
    Rossi, Antonio
    TRANSLATIONAL CANCER RESEARCH, 2017, 6 : S610 - S613