Known and putative mechanisms of resistance to EGFR targeted therapies in NSCLC patients with EGFR mutations-a review

被引:295
作者
Stewart, Erin L. [1 ,2 ]
Tan, Samuel Zhixing [1 ,3 ]
Liu, Geoffrey [1 ,2 ,4 ]
Tsao, Ming-Sound [1 ,2 ,3 ]
机构
[1] Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[3] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[4] Univ Toronto, Dept Med, Toronto, ON, Canada
关键词
Epidermal growth factor receptor (EGFR); molecular targeted therapy; drug resistance; antineoplastic;
D O I
10.3978/j.issn.2218-6751.2014.11.06
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is the leading cause of cancer related deaths in Canada with non-small cell lung cancer (NSCLC) being the predominant form of the disease. Tumor characterization can identify cancerdriving mutations as treatment targets. One of the most successful examples of cancer targeted therapy is inhibition of mutated epidermal growth factor receptor (EGFR), which occurs in similar to 10-30% of NSCLC patients. While this treatment has benefited many patients with activating EGFR mutations, almost all who initially benefited will eventually acquire resistance. Approximately 50% of cases of acquired resistance (AR) are due to a secondary T790M mutation in exon 20 of the EGFR gene; however, many of the remaining mechanisms of resistance are still unknown. Much work has been done to elucidate the remaining mechanisms of resistance. This review aims to highlight both the mechanisms of resistance that have already been identified in patients and potential novel mechanisms identified in preclinical models which have yet to be validated in the patient settings.
引用
收藏
页码:67 / 81
页数:15
相关论文
共 141 条
[41]   JAK2-related pathway induces acquired erlotinib resistance in lung cancer cells harboring an epidermal growth factor receptor-activating mutation [J].
Harada, Daijiro ;
Takigawa, Nagio ;
Ochi, Nobuaki ;
Ninomiya, Takashi ;
Yasugi, Masayuki ;
Kubo, Toshio ;
Takeda, Hiromasa ;
Ichihara, Eiki ;
Ohashi, Kadoaki ;
Takata, Saburo ;
Tanimoto, Mitsune ;
Kiura, Katsuyuki .
CANCER SCIENCE, 2012, 103 (10) :1795-1802
[42]   Rebiopsy of Non-Small Cell Lung Cancer Patients With Acquired Resistance to Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor [J].
Hata, Akito ;
Katakami, Nobuyuki ;
Yoshioka, Hiroshige ;
Takeshita, Jumpei ;
Tanaka, Kosuke ;
Nanjo, Shigeki ;
Fujita, Shiro ;
Kaji, Reiko ;
Imai, Yukihiro ;
Monden, Kazuya ;
Matsumoto, Takeshi ;
Nagata, Kazuma ;
Otsuka, Kyoko ;
Tachikawa, Ryo ;
Tomii, Keisuke ;
Kunimasa, Kei ;
Iwasaku, Masahiro ;
Nishiyama, Akihiro ;
Ishida, Tadashi ;
Nishimura, Yoshihiro .
CANCER, 2013, 119 (24) :4325-4332
[43]   Novel germline mutation:: EGFR V843I in patient with multiple lung adenocarcinomas and family members with lung cancer [J].
Ikeda, Koei ;
Nomori, Hiroaki ;
Mori, Takeshi ;
Sasaki, Jiichiro ;
Kobayashi, Toshiaki .
ANNALS OF THORACIC SURGERY, 2008, 85 (04) :1430-1432
[44]   Presence of epidermal growth factor receptor gene T790M mutation as a minor clone in non-small cell lung cancer [J].
Inukai, Michio ;
Toyooka, Shinichi ;
Ito, Sachio ;
Asano, Hiroaki ;
Ichihara, Shuji ;
Soh, Junichi ;
Suehisa, Hiroshi ;
Ouchida, Mamoru ;
Aoe, Keisuke ;
Aoe, Motoi ;
Kiura, Katsuyuki ;
Shimizu, Nobuyoshi ;
Date, Hiroshi .
CANCER RESEARCH, 2006, 66 (16) :7854-7858
[45]   Long Term Therapeutic Plan for Patients with Non-Small Cell Lung Cancer Harboring EGFR Mutation [J].
Jang, Seung Hun .
TUBERCULOSIS AND RESPIRATORY DISEASES, 2014, 76 (01) :8-14
[46]   Dual Inhibition of EGFR with Afatinib and Cetuximab in Kinase Inhibitor-Resistant EGFR-Mutant Lung Cancer with and without T790M Mutations [J].
Janjigian, Yelena Y. ;
Smit, Egbert F. ;
Groen, Harry J. M. ;
Horn, Leora ;
Gettinger, Scott ;
Camidge, D. Ross ;
Riely, Gregory J. ;
Wang, Bushi ;
Fu, Yali ;
Chand, Vikram K. ;
Miller, Vincent A. ;
Pao, William .
CANCER DISCOVERY, 2014, 4 (09) :1036-1045
[47]   A rapid and sensitive enzymatic method for epidermal growth factor receptor mutation screening [J].
Jänne, PA ;
Borras, AM ;
Kuang, YN ;
Rogers, AM ;
Joshi, VA ;
Liyanage, H ;
Lindeman, N ;
Lee, JC ;
Halmos, B ;
Maher, EA ;
Distel, RJ ;
Meyerson, M ;
Johnson, BE .
CLINICAL CANCER RESEARCH, 2006, 12 (03) :751-758
[48]  
Janne PA, 2014, J CLIN ONCOL, V32
[49]  
Janne PA, 2009, J CLIN ONCOL, P15
[50]   MALDI-TOF mass spectrometry - A versatile tool for high-performance DNA analysis [J].
Jurinke, C ;
Oeth, P ;
van den Boom, D .
MOLECULAR BIOTECHNOLOGY, 2004, 26 (02) :147-163