Triple-Negative Breast Cancer and the Need for New Therapeutic Targets

被引:140
作者
Engebraaten, Olav [1 ,2 ,3 ]
Vollan, Hans Kristian Moen [1 ,2 ,4 ]
Borresen-Dale, Anne-Lise [2 ,4 ]
机构
[1] Oslo Univ Hosp, Dept Oncol, Div Canc Med Surg & Transplantat, N-0407 Oslo, Norway
[2] Univ Oslo, Inst Clin Med, Fac Med, KG Jebsen Ctr Breast Canc Res, Oslo, Norway
[3] Norwegian Radium Hosp, Inst Canc Res, Oslo Univ Hosp, Dept Tumor Biol, Oslo, Norway
[4] Norwegian Radium Hosp, Inst Canc Res, Oslo Univ Hosp, Dept Genet, Oslo, Norway
关键词
PLATINUM-BASED CHEMOTHERAPY; PHASE-II TRIAL; NEOADJUVANT CHEMOTHERAPY; MOLECULAR PORTRAITS; MESENCHYMAL TRANSITION; MUTATIONAL PROCESSES; INTRINSIC SUBTYPES; SYNTHETIC LETHAL; MICROARRAY DATA; TUMOR SUBTYPES;
D O I
10.1016/j.ajpath.2013.05.033
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Triple-negative breast cancers (TNBCs) are a diverse and heterogeneous group of tumors that by definition lack estrogen and progesterone receptors and amplification of the HER2 gene. The majority of the tumors classified as TNBCs are highly malignant, and only a subgroup responds to conventional chemotherapy with a favorable prognosis. Results from decades of research have identified important molecular characteristics that can subdivide this group of breast cancers further. High-throughput molecular analyses including sequencing, pathway analyses, and integrated analyses of alterations at the genomic and transcriptomic Levels have improved our understanding of the molecular alterations involved in tumor development and progression. How this knowledge should be used for rational selection of therapy is a challenging task and the subject of numerous ongoing research programs. This review summarizes the current knowledge on the clinical characteristics and molecular alterations of TNBCs. Currently used conventional therapeutic strategies and targeted therapy studies are discussed, with references to recently published results on the molecular characterization of TNBCs.
引用
收藏
页码:1064 / 1074
页数:11
相关论文
共 92 条
[1]   A randomized phase II trial of platinum salts in basal-like breast cancer patients in the neoadjuvant setting. Results from the GEICAM/2006-03, multicenter study [J].
Alba, E. ;
Chacon, J. I. ;
Lluch, A. ;
Anton, A. ;
Estevez, L. ;
Cirauqui, B. ;
Carrasco, E. ;
Calvo, L. ;
Segui, M. A. ;
Ribelles, N. ;
Alvarez, R. ;
Sanchez-Munoz, A. ;
Sanchez, R. ;
Lopez Garcia-Asenjo, J. A. ;
Rodriguez-Martin, C. ;
Escudero, M. J. ;
Albanell, J. .
BREAST CANCER RESEARCH AND TREATMENT, 2012, 136 (02) :487-493
[2]   Comparisons between different polychemotherapy regimens for early breast cancer: meta-analyses of long-term outcome among 100 000 women in 123 randomised trials [J].
Albain, K. ;
Anderson, S. ;
Arriagada, R. ;
Barlow, W. ;
Bergh, J. ;
Bliss, J. ;
Buyse, M. ;
Cameron, D. ;
Carrasco, E. ;
Clarke, M. ;
Correa, C. ;
Coates, A. ;
Collins, R. ;
Costantino, J. ;
Cutter, D. ;
Cuzick, J. ;
Darby, S. ;
Davidson, N. ;
Davies, C. ;
Davies, K. ;
Delmestri, A. ;
Di Leo, A. ;
Dowsett, M. ;
Elphinstone, P. ;
Evans, V. ;
Ewertz, M. ;
Gelber, R. ;
Gettins, L. ;
Geyer, C. ;
Goldhirsch, A. ;
Godwin, J. ;
Gray, R. ;
Gregory, C. ;
Hayes, D. ;
Hill, C. ;
Ingle, J. ;
Jakesz, R. ;
James, S. ;
Kaufmann, M. ;
Kerr, A. ;
MacKinnon, E. ;
McGale, P. ;
McHugh, T. ;
Norton, L. ;
Ohashi, Y. ;
Paik, S. ;
Pan, H. C. ;
Perez, E. ;
Peto, R. ;
Piccart, M. .
LANCET, 2012, 379 (9814) :432-444
[3]   Descriptive analysis of estrogen receptor (ER)negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype - A population-based study from the California Cancer Registry [J].
Bauer, Katrina R. ;
Brown, Monica ;
Cress, Rosemary D. ;
Parise, Carol A. ;
Caggiano, Vincent .
CANCER, 2007, 109 (09) :1721-1728
[4]   Bevacizumab Added to Neoadjuvant Chemotherapy for Breast Cancer [J].
Bear, Harry D. ;
Tang, Gong ;
Rastogi, Priya ;
Geyer, Charles E., Jr. ;
Robidoux, Andre ;
Atkins, James N. ;
Baez-Diaz, Luis ;
Brufsky, Adam M. ;
Mehta, Rita S. ;
Fehrenbacher, Louis ;
Young, James A. ;
Senecal, Francis M. ;
Gaur, Rakesh ;
Margolese, Richard G. ;
Adams, Paul T. ;
Gross, Howard M. ;
Costantino, Joseph P. ;
Swain, Sandra M. ;
Mamounas, Eleftherios P. ;
Wolmark, Norman .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (04) :310-320
[5]   Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer [J].
Bergamaschi, Anna ;
Kim, Young H. ;
Wang, Pei ;
Sorlie, Therese ;
Hernandez-Boussard, Tina ;
Lonning, Per E. ;
Tibshirani, Robert ;
Borresen-Dale, Anne-Lise ;
Pollack, Jonathan R. .
GENES CHROMOSOMES & CANCER, 2006, 45 (11) :1033-1040
[6]   Why don't we get more cancer? A proposed role of the microenvironment in restraining cancer progression [J].
Bissell, Mina J. ;
Hines, William C. .
NATURE MEDICINE, 2011, 17 (03) :320-329
[7]   Subtyping of Breast Cancer by Immunohistochemistry to Investigate a Relationship between Subtype and Short and Long Term Survival: A Collaborative Analysis of Data for 10,159 Cases from 12 Studies [J].
Blows, Fiona M. ;
Driver, Kristy E. ;
Schmidt, Marjanka K. ;
Broeks, Annegien ;
van Leeuwen, Flora E. ;
Wesseling, Jelle ;
Cheang, Maggie C. ;
Gelmon, Karen ;
Nielsen, Torsten O. ;
Blomqvist, Carl ;
Heikkila, Paivi ;
Heikkinen, Tuomas ;
Nevanlinna, Heli ;
Akslen, Lars A. ;
Begin, Louis R. ;
Foulkes, William D. ;
Couch, Fergus J. ;
Wang, Xianshu ;
Cafourek, Vicky ;
Olson, Janet E. ;
Baglietto, Laura ;
Giles, Graham G. ;
Severi, Gianluca ;
McLean, Catriona A. ;
Southey, Melissa C. ;
Rakha, Emad ;
Green, Andrew R. ;
Ellis, Ian O. ;
Sherman, Mark E. ;
Lissowska, Jolanta ;
Anderson, William F. ;
Cox, Angela ;
Cross, Simon S. ;
Reed, Malcolm W. R. ;
Provenzano, Elena ;
Dawson, Sarah-Jane ;
Dunning, Alison M. ;
Humphreys, Manjeet ;
Easton, Douglas F. ;
Garcia-Closas, Montserrat ;
Caldas, Carlos ;
Pharoah, Paul D. ;
Huntsman, David .
PLOS MEDICINE, 2010, 7 (05)
[8]   Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium [J].
Broeks, Annegien ;
Schmidt, Marjanka K. ;
Sherman, Mark E. ;
Couch, Fergus J. ;
Hopper, John L. ;
Dite, Gillian S. ;
Apicella, Carmel ;
Smith, Letitia D. ;
Hammet, Fleur ;
Southey, Melissa C. ;
Van 't Veer, Laura J. ;
de Groot, Renate ;
Smit, Vincent T. H. B. M. ;
Fasching, Peter A. ;
Beckmann, Matthias W. ;
Jud, Sebastian ;
Ekici, Arif B. ;
Hartmann, Arndt ;
Hein, Alexander ;
Schulz-Wendtland, Ruediger ;
Burwinkel, Barbara ;
Marme, Frederik ;
Schneeweiss, Andreas ;
Sinn, Hans-Peter ;
Sohn, Christof ;
Tchatchou, Sandrine ;
Bojesen, Stig E. ;
Nordestgaard, Borge G. ;
Flyger, Henrik ;
Orsted, David D. ;
Kaur-Knudsen, Diljit ;
Milne, Roger L. ;
Perez, Jose I. Arias ;
Zamora, Pilar ;
Menendez Rodriguez, Primitiva ;
Benitez, Javier ;
Brauch, Hiltrud ;
Justenhoven, Christina ;
Ko, Yon-Dschun ;
Hamann, Ute ;
Fischer, Hans-Peter ;
Bruening, Thomas ;
Pesch, Beate ;
Chang-Claude, Jenny ;
Wang-Gohrke, Shan ;
Bremer, Michael ;
Karstens, Johann H. ;
Hillemanns, Peter ;
Doerk, Thilo ;
Nevanlinna, Heli A. .
HUMAN MOLECULAR GENETICS, 2011, 20 (16) :3289-3303
[9]   Pathologic Complete Response Rates in Young Women With BRCA1-Positive Breast Cancers After Neoadjuvant Chemotherapy [J].
Byrski, Tomasz ;
Gronwald, Jacek ;
Huzarski, Tomasz ;
Grzybowska, Ewa ;
Budryk, Magdalena ;
Stawicka, Malgorzata ;
Mierzwa, Tomasz ;
Szwiec, Marek ;
Wisniowski, Rafal ;
Siolek, Monika ;
Dent, Rebecca ;
Lubinski, Jan ;
Narod, Steven .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (03) :375-379
[10]   Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study [J].
Carey, Lisa A. ;
Perou, Charles M. ;
Livasy, Chad A. ;
Dressler, Lynn G. ;
Cowan, David ;
Conway, Kathleen ;
Karaca, Gamze ;
Troester, Melissa A. ;
Tse, Chiu Kit ;
Edmiston, Sharon ;
Deming, Sandra L. ;
Geradts, Joseph ;
Cheang, Maggie C. U. ;
Nielsen, Torsten O. ;
Moorman, Patricia G. ;
Earp, H. Shelton ;
Millikan, Robert C. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (21) :2492-2502