Targeting FGFR pathway in breast cancer

被引:92
作者
Perez-Garcia, J. [1 ,2 ]
Munoz-Couselo, E. [3 ,5 ]
Soberino, J. [1 ]
Racca, F. [1 ]
Cortes, J. [2 ,4 ,5 ,6 ,7 ]
机构
[1] Quiron Univ Hosp, Baselga Inst Oncol, Barcelona, Spain
[2] Med Sci Innovat Res MedSIR, Barcelona, Spain
[3] Vall dHebron Univ Hosp, Dept Med Oncol, Breast Canc Unit, Barcelona, Spain
[4] Ramon y Cajal Univ Hosp, Madrid 28034, Spain
[5] Vall dHebron Inst Oncol VHIO, Barcelona, Spain
[6] Baselga Inst Oncol, Madrid, Spain
[7] Baselga Inst Oncol, Barcelona, Spain
关键词
Fibroblast growth factor receptor (FGFR); Breast cancer; Tyrosine kinase receptor; Tyrosine kinase inhibitors; FGFR amplification; Multitargeted TKIs; Selective FGFR inhibitors; GROWTH-FACTOR RECEPTORS; MOLECULAR PORTRAITS; GENETIC ALTERATIONS; THERAPEUTIC TARGET; DOSE-ESCALATION; PHASE-II; EXPRESSION; AMPLIFICATION; INHIBITOR; PLUS;
D O I
10.1016/j.breast.2017.10.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Developments in breast cancer biology over the last years have permitted deconstructing the molecular profile of the most relevant breast cancer subtypes. This has led to an increase in therapeutic options, including more effective personalized therapy for breast cancer and substantial improvements in patient outcomes. Although currently there are only a few targeted therapies approved for metastatic breast cancer, the discovery of druggable kinase gene alterations has radically changed cancer treatment by providing novel and successfully actionable drug targets. Fibroblast growth factors and their receptors (FGFRs) participate in different physiologic processes and also play an essential role in cancer cell proliferation, survival, differentiation, migration, and apoptosis. This article summarizes the main molecular alterations of FGFRs, as well as the available preclinical and clinical data with FGFR inhibitors in breast cancer, and discusses new opportunities for the clinical development of these agents in patients with breast cancer. (c) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:126 / 133
页数:8
相关论文
共 50 条
[1]  
Andre F, 2013, P AACR 104 ANN M 201
[2]   Rationale for targeting fibroblast growth factor receptor signaling in breast cancer [J].
Andre, Fabrice ;
Cortes, Javier .
BREAST CANCER RESEARCH AND TREATMENT, 2015, 150 (01) :1-8
[3]   Targeting FGFR with Dovitinib (TKI258): Preclinical and Clinical Data in Breast Cancer [J].
Andre, Fabrice ;
Bachelot, Thomas ;
Campone, Mario ;
Dalenc, Florence ;
Perez-Garcia, Jose M. ;
Hurvitz, Sara A. ;
Turner, Nicholas ;
Rugo, Hope ;
Smith, John W. ;
Deudon, Stephanie ;
Shi, Michael ;
Zhang, Yong ;
Kay, Andrea ;
Porta, Diana Graus ;
Yovine, Alejandro ;
Baselga, Jose .
CLINICAL CANCER RESEARCH, 2013, 19 (13) :3693-3702
[4]  
[Anonymous], 2015, J CLIN ONCOL S
[5]   Advances and challenges in targeting FGFR signalling in cancer [J].
Babina, Irina S. ;
Turner, Nicholas C. .
NATURE REVIEWS CANCER, 2017, 17 (05) :318-332
[6]   Everolimus in Postmenopausal Hormone-Receptor-Positive Advanced Breast Cancer [J].
Baselga, Jose ;
Campone, Mario ;
Piccart, Martine ;
Burris, Howard A., III ;
Rugo, Hope S. ;
Sahmoud, Tarek ;
Noguchi, Shinzaburo ;
Gnant, Michael ;
Pritchard, Kathleen I. ;
Lebrun, Fabienne ;
Beck, J. Thaddeus ;
Ito, Yoshinori ;
Yardley, Denise ;
Deleu, Ines ;
Perez, Alejandra ;
Bachelot, Thomas ;
Vittori, Luc ;
Xu, Zhiying ;
Mukhopadhyay, Pabak ;
Lebwohl, David ;
Hortobagyi, Gabriel N. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (06) :520-529
[7]   Pertuzumab plus Trastuzumab plus Docetaxel for Metastatic Breast Cancer [J].
Baselga, Jose ;
Cortes, Javier ;
Kim, Sung-Bae ;
Im, Seock-Ah ;
Hegg, Roberto ;
Im, Young-Hyuck ;
Roman, Laslo ;
Pedrini, Jose Luiz ;
Pienkowski, Tadeusz ;
Knott, Adam ;
Clark, Emma ;
Benyunes, Mark C. ;
Ross, Graham ;
Swain, Sandra M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (02) :109-119
[8]   E-3810 Is a Potent Dual Inhibitor of VEGFR and FGFR that Exerts Antitumor Activity in Multiple Preclinical Models [J].
Bello, Ezia ;
Colella, Gennaro ;
Scarlato, Valentina ;
Oliva, Paolo ;
Berndt, Alexander ;
Valbusa, Giovanni ;
Serra, Sonia Colombo ;
D'Incalci, Maurizio ;
Cavalletti, Ennio ;
Giavazzi, Raffaella ;
Damia, Giovanna ;
Camboni, Gabriella .
CANCER RESEARCH, 2011, 71 (04) :1396-1405
[9]   Large-Scale Profiling of Kinase Dependencies in Cancer Cell Lines [J].
Campbell, James ;
Ryan, Colm J. ;
Brough, Rachel ;
Bajrami, Ilirjana ;
Pemberton, Helen N. ;
Chong, Irene Y. ;
Costa-Cabral, Sara ;
Frankum, Jessica ;
Gulati, Aditi ;
Holme, Harriet ;
Miller, Rowan ;
Postel-Vinay, Sophie ;
Rafiq, Rumana ;
Wei, Wenbin ;
Williamson, Chris T. ;
Quigley, David A. ;
Tym, Joe ;
Al-Lazikani, Bissan ;
Fenton, Timothy ;
Natrajan, Rachael ;
Strauss, Sandra J. ;
Ashworth, Alan ;
Lord, Christopher J. .
CELL REPORTS, 2016, 14 (10) :2490-2501
[10]   Neratinib after trastuzumab-based adjuvant therapy in patients with HER2-positive breast cancer (ExteNET): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial [J].
Chan, Arlene ;
Delaloge, Suzette ;
Holmes, Frankie A. ;
Moy, Beverly ;
Iwata, Hiroji ;
Harvey, Vernon J. ;
Robert, Nicholas J. ;
Silovski, Tajana ;
Gokmen, Erhan ;
von Minckwitz, Gunter ;
Ejlertsen, Bent ;
Chia, Stephen K. L. ;
Mansi, Janine ;
Barrios, Carlos H. ;
Gnant, Michael ;
Buyse, Marc ;
Gore, Ira ;
Smith, John, II ;
Harker, Graydon ;
Masuda, Norikazu ;
Petrakova, Katarina ;
Guerrero Zotano, Angel ;
Iannotti, Nicholas ;
Rodriguez, Gladys ;
Tassone, Pierfrancesco ;
Wong, Alvin ;
Bryce, Richard ;
Ye, Yining ;
Yao, Bin ;
Martin, Miguel .
LANCET ONCOLOGY, 2016, 17 (03) :367-377