Epidermal Growth Factor Receptor Inhibition in Lung Cancer Status 2012

被引:95
作者
Hirsch, Fred R. [1 ,2 ]
Jaenne, Pasi A. [3 ]
Eberhardt, Wilfried E. [4 ]
Cappuzzo, Federico [5 ]
Thatcher, Nick [6 ]
Pirker, Robert [7 ]
Choy, Hak [8 ]
Kim, Edward S. [9 ]
Paz-Ares, Luis [10 ]
Gandara, David R. [11 ,12 ]
Wu, Yi-Long [13 ,14 ]
Ahn, Myung-Ju [15 ]
Mitsudomi, Tetsuya [16 ]
Shepherd, Frances A. [17 ,18 ]
Mok, Tony S. [19 ]
机构
[1] Univ Colorado, Dept Med, Div Med Oncol, Ctr Canc, Aurora, CO 80045 USA
[2] Univ Colorado, Dept Pathol, Ctr Canc, Aurora, CO 80045 USA
[3] Dana Farber Canc Inst, Lowe Ctr Thorac Oncol, Boston, MA 02115 USA
[4] West German Canc Ctr, Dept Med Canc Res, Essen, Germany
[5] Osped Civile, Dept Oncol, Inst Toscano Tumori, Venice, Livorno, Italy
[6] Christie Hosp NHS Trust, Dept Med Oncol, Manchester M20 4BX, Lancs, England
[7] Med Univ Vienna, Dept Med 1, Vienna, Austria
[8] Univ Texas SW Med Ctr Dallas, Dept Therapeut Radiat Oncol, Dallas, TX 75390 USA
[9] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[10] Univ Hosp Virgen del Rocio, Dept Med, Inst Biomed Sevilla, Seville, Spain
[11] UC Davis Canc Ctr, Dept Internal Med, Div Hematol Oncol, Sacramento, CA USA
[12] UC Davis Canc Ctr, Dept Radiat Oncol, Sacramento, CA USA
[13] Guangdong Gen Hosp, Dept Med, Guangdong Lung Canc Inst, Guangzhou, Guangdong, Peoples R China
[14] Guangdong Acad Med Sci, Guangzhou, Guangdong, Peoples R China
[15] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Med,Div Hematol Oncol, Seoul, South Korea
[16] Kinki Univ, Dept Surg, Div Thorac Surg, Sch Med, Higashiosaka, Osaka 577, Japan
[17] Princess Margaret Hosp, Dept Med, Div Med Oncol & Hematol, Univ Hlth Network, Toronto, ON M4X 1K9, Canada
[18] Univ Toronto, Toronto, ON, Canada
[19] Chinese Univ Hong Kong, Dept Clin Oncol, Prince Wales Hosp, Hong Kong, Hong Kong, Peoples R China
关键词
EGFR antibodies; Carcinoma; non-small-cell lung; Molecular targeted therapy; Epidermal growth factor receptor; Tyrosine kinase inhibitors; PHASE-III TRIAL; TYROSINE KINASE INHIBITORS; PREVIOUSLY TREATED PATIENTS; ACQUIRED-RESISTANCE; MET AMPLIFICATION; 1ST-LINE CHEMOTHERAPY; MOLECULAR PREDICTORS; EGFR MUTATION; OPEN-LABEL; GEFITINIB RESISTANCE;
D O I
10.1097/JTO.0b013e31827ed0ff
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is the most common cause of cancer deaths. Most patients present with advanced-stage disease, and the prognosis is generally poor. However, with the understanding of lung cancer biology, and development of molecular targeted agents, there have been improvements in treatment outcomes for selected subsets of patients with non-small-cell lung cancer (NSCLC). Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) have demonstrated significantly improved tumor responses and progression-free survival in subsets of patients with advanced NSCLC, particularly those with tumors harboring activating EGFR mutations. Testing for EGFR mutations is a standard procedure for identification of patients who will benefit from first-line EGFR TKIs. For patients with advanced NSCLC and no activating EGFR mutations (EGFR wild-type) or no other driving oncogenes such as ALK-gene rearrangement, chemotherapy is still the standard of care. A new generation of EGFR TKIs, targeting multiple receptors and with irreversible bindings to the receptors, are in clinical trials and have shown encouraging effects. Research on primary and acquired resistant mechanisms to EGFR TKIs are ongoing. Monoclonal antibodies (e.g. cetuximab), in combination with chemotherapy, have demonstrated improved outcomes, particularly for subsets of NSCLC patients, but further validations are needed. Novel monoclonal antibodies are combined with chemotherapy, and randomized comparative studies are ongoing. This review summarizes the current status of EGFR inhibitors in NSCLC in 2012 and some of the major challenges we are facing.
引用
收藏
页码:373 / 384
页数:12
相关论文
共 113 条
[1]  
[Anonymous], J CLIN ONCOL S
[2]  
[Anonymous], J CLIN ONCOL S
[3]  
[Anonymous], 2012, ANN ONCOL
[4]  
[Anonymous], J CLIN ONCOL S
[5]   Prevalence, Clinicopathologic Associations, and Molecular Spectrum of ERBB2 (HER2) Tyrosine Kinase Mutations in Lung Adenocarcinomas [J].
Arcila, Maria E. ;
Chaft, Jamie E. ;
Nafa, Khedoudja ;
Roy-Chowdhuri, Sinchita ;
Lau, Christopher ;
Zaidinski, Michael ;
Paik, Paul K. ;
Zakowski, Maureen F. ;
Kris, Mark G. ;
Ladanyi, Marc .
CLINICAL CANCER RESEARCH, 2012, 18 (18) :4910-4918
[6]   MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib [J].
Bean, James ;
Brennan, Cameron ;
Shih, Jin-Yuan ;
Riely, Gregory ;
Viale, Agnes ;
Wang, Lu ;
Chitale, Dhananjay ;
Motoi, Noriko ;
Szoke, Janos ;
Broderick, Stephen ;
Balak, Marissa ;
Chang, Wen-Cheng ;
Yu, Chong-Jen ;
Gazdar, Adi ;
Pass, Harvey ;
Rusch, Valerie ;
Gerald, William ;
Huang, Shiu-Feng ;
Yang, Pan-Chyr ;
Miller, Vincent ;
Ladany, Marc ;
Yang, Chih-Hsin ;
Pao, William .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (52) :20932-20937
[7]  
BELANI CP, 2010, ASCO M S, V28, P7506
[8]   Phase II Study of Cetuximab in Combination With Chemoradiation in Patients With Stage IIIA/B Non-Small-Cell Lung Cancer: RTOG 0324 [J].
Blumenschein, George R., Jr. ;
Paulus, Rebecca ;
Curran, Walter J. ;
Robert, Francisco ;
Fossella, Frank ;
Werner-Wasik, Maria ;
Herbst, Roy S. ;
Doescher, Philip O. ;
Choy, Hak ;
Komaki, Ritsuko .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (17) :2312-2318
[9]   Radiotherapy plus cetuximab for squamous-cell carcinoma of the head and neck [J].
Bonner, JA ;
Harari, PM ;
Giralt, J ;
Azarnia, N ;
Shin, DM ;
Cohen, RB ;
Jones, CU ;
Sur, R ;
Raben, D ;
Jassem, J ;
Ove, R ;
Kies, MS ;
Baselga, J ;
Youssoufian, H ;
Amellal, N ;
Rowinsky, EK ;
Ang, KK .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) :567-578
[10]  
Bradley J, 2011, 53 ANN M AM SOC RAD