Triple-negative breast cancer: treatment challenges and solutions

被引:322
作者
Collignon, Joelle [1 ]
Lousberg, Laurence [1 ]
Schroeder, Helene [1 ]
Jerusalem, Guy [1 ,2 ]
机构
[1] Domaine Univ Sart Tilman, CHU Sart Tilman Liege, Med Oncol Dept, Liege, Belgium
[2] Univ Liege, Liege, Belgium
关键词
triple-negative breast cancer; molecular subtype; platinum-based chemotherapy; targeted therapy; androgen receptor; BRCA1/2; mutation;
D O I
10.2147/BCTT.S69488
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Triple-negative breast cancers (TNBCs) are defined by the absence of estrogen and progesterone receptors and the absence of HER2 overexpression. These cancers represent a heterogeneous breast cancer subtype with a poor prognosis. Few systemic treatment options exist besides the use of chemotherapy (CT). The heterogeneity of the disease has limited the successful development of targeted therapy in unselected patient populations. Currently, there are no approved targeted therapies for TNBC. However, intense research is ongoing to identify specific targets and develop additional and better systemic treatment options. Standard adjuvant and neoadjuvant regimens include anthracyclines, cyclophosphamide, and taxanes. Platinum-based CT has been proposed as another CT option of interest in TNBC. We review the role of this therapy in general, and particularly in patients carrying BRCA germ-line mutations. Available data concerning the role of platinum-based CT in TNBC were acquired primarily in the neoadjuvant setting. The routine use of platinum-based CT is not yet recommended by available guidelines. Many studies have reported the molecular characterization of TNBCs. Several actionable targets have been identified. Novel therapeutic strategies are currently being tested in clinical trials based on promising results observed in preclinical studies. These targets include androgen receptor, EGFR, PARP, FGFR, and the angiogenic pathway. We review the recent data on experimental drugs in this field. We also discuss the recent data concerning immunologic checkpoint inhibitors.
引用
收藏
页码:93 / 107
页数:15
相关论文
共 101 条
[1]
A Phase 2, randomized, open-label, multicenter, safety and efficacy study of oral lucitanib in patients with metastatic breast cancer with alterations in the FGF pathway [J].
Abu-Khalaf, Maysa ;
Mayer, Ingrid ;
Litten, Jason B. ;
Raponi, Mitch ;
Allen, Andrew R. ;
Pusztai, Lajos ;
Arteaga, Carlos L. .
CANCER RESEARCH, 2015, 75
[2]
Prognostic Value of Tumor-Infiltrating Lymphocytes in Triple-Negative Breast Cancers From Two Phase III Randomized Adjuvant Breast Cancer Trials: ECOG 2197 and ECOG 1199 [J].
Adams, Sylvia ;
Gray, Robert J. ;
Demaria, Sandra ;
Goldstein, Lori ;
Perez, Edith A. ;
Shulman, Lawrence N. ;
Martino, Silvana ;
Wang, Molin ;
Jones, Vicky E. ;
Saphner, Thomas J. ;
Wolff, Antonio C. ;
Wood, William C. ;
Davidson, Nancy E. ;
Sledge, George W. ;
Sparano, Joseph A. ;
Badve, Sunil S. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (27) :2959-+
[3]
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
[4]
Is androgen receptor targeting an emerging treatment strategy for triple negative breast cancer? [J].
Anestis, Aristomenis ;
Karamouzis, Michalis V. ;
Dalagiorgou, Georgia ;
Papavassiliou, Athanasios G. .
CANCER TREATMENT REVIEWS, 2015, 41 (06) :547-553
[5]
[Anonymous], 2014, CANC DISCOV, V4
[6]
Complete Response of Metastatic Androgen Receptor-Positive Breast Cancer to Bicalutamide: Case Report and Review of the Literature [J].
Arce-Salinas, Claudia ;
Riesco-Martinez, Maria Carmen ;
Hanna, Wedad ;
Bedard, Philippe ;
Warner, Ellen .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (04) :E21-E24
[7]
Androgen Receptor Biology in Triple Negative Breast Cancer: a Case for Classification as AR plus or Quadruple Negative Disease [J].
Barton, Valerie N. ;
D'Amato, Nicholas C. ;
Gordon, Michael A. ;
Christenson, Jessica L. ;
Elias, Anthony ;
Richer, Jennifer K. .
HORMONES & CANCER, 2015, 6 (5-6) :206-213
[8]
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
[9]
Comprehensive Genomic Analysis Identifies Novel Subtypes and Targets of Triple-Negative Breast Cancer [J].
Burstein, Matthew D. ;
Tsimelzon, Anna ;
Poage, Graham M. ;
Coyington, Kyle R. ;
Contreras, Alejandro ;
Fuqua, Suzanne A. W. ;
Sayage, Michelle I. ;
Osborne, C. Kent ;
Hilsenbeck, Susan G. ;
Chang, Jenny C. ;
Mills, Gordon B. ;
Lau, Ching C. ;
Brown, Powel H. .
CLINICAL CANCER RESEARCH, 2015, 21 (07) :1688-1698
[10]
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