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
[71]   Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor-Resistant Disease [J].
Ohashi, Kadoaki ;
Maruvka, Yosef E. ;
Michor, Franziska ;
Pao, William .
JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (08) :1070-1080
[72]   Lung cancers with acquired resistance to EGFR inhibitors occasionally harbor BRAF gene mutations but lack mutations in KRAS, NRAS, or MEK1 [J].
Ohashi, Kadoaki ;
Sequist, Lecia V. ;
Arcila, Maria E. ;
Moran, Teresa ;
Chmielecki, Juliann ;
Lin, Ya-Lun ;
Pan, Yumei ;
Wang, Lu ;
de Stanchina, Elisa ;
Shien, Kazuhiko ;
Aoe, Keisuke ;
Toyooka, Shinichi ;
Kiura, Katsuyuki ;
Fernandez-Cuesta, Lynnette ;
Fidias, Panos ;
Yang, James Chih-Hsin ;
Miller, Vincent A. ;
Riely, Gregory J. ;
Kris, Mark G. ;
Engelman, Jeffrey A. ;
Vnencak-Jones, Cindy L. ;
Dias-Santagata, Dora ;
Ladanyi, Marc ;
Pao, William .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (31) :E2127-E2133
[73]   Familial Lung Adenocarcinoma Caused by the EGFR V843I Germ-Line Mutation [J].
Ohtsuka, Kouki ;
Ohnishi, Hiroaki ;
Kurai, Daisuke ;
Matsushima, Satsuki ;
Morishita, Yukio ;
Shinonaga, Mayumi ;
Goto, Hajime ;
Watanabe, Takashi .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (08) :E191-E192
[74]   Natural History and Molecular Characteristics of Lung Cancers Harboring EGFR Exon 20 Insertions [J].
Oxnard, Geoffrey R. ;
Lo, Peter C. ;
Nishino, Mizuki ;
Dahlberg, Suzanne E. ;
Lindeman, Neal I. ;
Butaney, Mohit ;
Jackman, David M. ;
Johnson, Bruce E. ;
Jaenne, Pasi A. .
JOURNAL OF THORACIC ONCOLOGY, 2013, 8 (02) :179-184
[75]   Maintained Sensitivity to EGFR Tyrosine Kinase Inhibitors in EGFR-Mutant Lung Cancer Recurring after Adjuvant Erlotinib or Gefitinib [J].
Oxnard, Geoffrey R. ;
Janjigian, Yelena Y. ;
Arcila, Maria E. ;
Sima, Camelia S. ;
Kass, Samantha L. ;
Riely, Gregory J. ;
Pao, William ;
Kris, Mark G. ;
Ladanyi, Marc ;
Azzoli, Christopher G. ;
Miller, Vincent A. .
CLINICAL CANCER RESEARCH, 2011, 17 (19) :6322-6328
[76]   New Strategies in Overcoming Acquired Resistance to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Lung Cancer [J].
Oxnard, Geoffrey R. ;
Arcila, Maria E. ;
Chmielecki, Juliann ;
Ladanyi, Marc ;
Miller, Vincent A. ;
Pao, William .
CLINICAL CANCER RESEARCH, 2011, 17 (17) :5530-5537
[77]   EGFR mutations in lung cancer:: Correlation with clinical response to gefitinib therapy [J].
Paez, JG ;
Jänne, PA ;
Lee, JC ;
Tracy, S ;
Greulich, H ;
Gabriel, S ;
Herman, P ;
Kaye, FJ ;
Lindeman, N ;
Boggon, TJ ;
Naoki, K ;
Sasaki, H ;
Fujii, Y ;
Eck, MJ ;
Sellers, WR ;
Johnson, BE ;
Meyerson, M .
SCIENCE, 2004, 304 (5676) :1497-1500
[78]   KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib [J].
Pao, W ;
Wang, TY ;
Riely, GJ ;
Miller, VA ;
Pan, QL ;
Ladanyi, M ;
Zakowski, MF ;
Heelan, RT ;
Kris, MG ;
Varmus, HE .
PLOS MEDICINE, 2005, 2 (01) :57-61
[79]   Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain [J].
Pao, W ;
Miller, VA ;
Politi, KA ;
Riely, GJ ;
Somwar, R ;
Zakowski, MF ;
Kris, MG ;
Varmus, H .
PLOS MEDICINE, 2005, 2 (03) :225-235
[80]   EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib [J].
Pao, W ;
Miller, V ;
Zakowski, M ;
Doherty, J ;
Politi, K ;
Sarkaria, I ;
Singh, B ;
Heelan, R ;
Rusch, V ;
Fulton, L ;
Mardis, E ;
Kupfer, D ;
Wilson, R ;
Kris, M ;
Varmus, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (36) :13306-13311