The dawn of targeted therapies for triple negative breast cancer (TNBC): a snapshot of investigational drugs in phase I and II trials

被引:19
作者
Huynh, My-my [1 ]
Pambid, Mary Rose [1 ]
Jayanthan, Aarthi [1 ]
Dorr, Andrew [2 ]
Los, Gerrit [2 ]
Dunn, Sandra E. [1 ,2 ]
机构
[1] Phoenix Mol Designs, Preclin R&D, Vancouver, BC, Canada
[2] Phoenix Mol Designs, Clin Operat, San Diego, CA USA
关键词
Combination treatments; kinase inhibitors; metastatic disease; precision medicine; RSK2; targeted therapy; triple negative breast cancer; tnbc; breast cancer; clinical trials; EXPRESSION;
D O I
10.1080/13543784.2020.1818067
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction Triple negative breast cancer (TNBC) was once thought to be an insurmountable disease marked by a lack of targeted treatments. However, we are now witnessing the dawn of targeted therapies for TNBC in which progress has stemmed from an improved understanding of the components that make TNBC unique. The identification of biomarkers, such as BRCA1/2, PIK3CA and RSK2, have advanced the field remarkably and there is considerable interest in finding novel therapeutics for TNBC that offer durable clinical benefit with fewer adverse events. Areas covered We discuss phase I/II trials of new and emerging targeted therapies for TNBC, according to ClinicalTrials.gov up to June 2020. Although the emphasis is on ongoing and completed early phase trials, we also highlight pivotal studies that have led to the approval of new targeted classes of drugs for TNBC, with a focus on outcomes and common adverse events of each class of therapy. Expert opinion The way forward for TNBC treatment is through precision medicine. The use of novel agents matched with biomarkers to identify patients with the best chance of sustainable response offers new hope. We now have great potential for improving the outcomes for patients with TNBC.
引用
收藏
页码:1199 / 1208
页数:10
相关论文
共 65 条
[1]  
Adams S, 2019, ANN ONCOL, V30
[2]   The Management of Early-Stage and Metastatic Triple-Negative Breast Cancer: A Review [J].
Anders, Carey K. ;
Zagar, Timothy M. ;
Carey, Lisa A. .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2013, 27 (04) :737-+
[3]  
BARDIA A, 2019, N ENGL J MED, V380
[4]  
Brufsky A, 2019, JCO, V37
[5]   The triple negative paradox: Primary tumor chemosensitivity of breast cancer subtypes [J].
Carey, Lisa A. ;
Dees, E. Claire ;
Sawyer, Lynda ;
Gatti, Lisa ;
Moore, Dominic T. ;
Collichio, Frances ;
Ollila, David W. ;
Sartor, Carolyn I. ;
Graham, Mark L. ;
Perou, Charles M. .
CLINICAL CANCER RESEARCH, 2007, 13 (08) :2329-2334
[6]   Novel therapeutic avenues in triple-negative breast cancer: PI3K/AKT inhibition, androgen receptor blockade, and beyond [J].
Chan, Jack J. ;
Tan, Tira J. Y. ;
Dent, Rebecca A. .
THERAPEUTIC ADVANCES IN MEDICAL ONCOLOGY, 2019, 11
[7]  
CORTES J, 2019, ANN ONCOL, V30
[8]   Durvalumab compared to maintenance chemotherapy in patients with metastatic breast cancer: Results from phase II randomized trial SAFIR02-IMMUNO [J].
Dalenc, Florence ;
Garberis, Ingrid ;
Filleron, Thomas ;
Lusque, Amelie ;
Bachelot, Thomas ;
Arnedos, Monica ;
Campone, Mario ;
Sablin, Marie-Paule ;
Bonnefoi, Herve ;
Jimenez, Marta ;
Alexandra, Jacquet ;
Andre, Fabrice .
CANCER RESEARCH, 2020, 80 (04)
[9]   Androgen Receptor Expression and Association With Distant Disease-Free Survival in Triple Negative Breast Cancer: Analysis o 263 Patients Treated With Standard Therapy for Stage I-III Disease [J].
Dieci, Maria Vittoria ;
Tsvetkova, Vassilena ;
Griguolo, Gala ;
Miglietta, Federica ;
Mantiero, Mara ;
Tasca, Giulia ;
Cumerlato, Enrico ;
Giorgi, Carlo Alberto ;
Giarratano, Tommaso ;
Faggioni, Giovanni ;
Falci, Cristina ;
Vernaci, Grazia ;
Menichetti, Alice ;
Mioranza, Eleonora ;
Di Liso, Elisabetta ;
Frezzini, Simona ;
Saibene, Tania ;
Orvieto, Enrico ;
Guameri, Valentina .
FRONTIERS IN ONCOLOGY, 2019, 9
[10]   Triple-negative breast cancer in African-American women: disparities versus biology [J].
Dietze, Eric C. ;
Sistrunk, Christopher ;
Miranda-Carboni, Gustavo ;
O'Regan, Ruth ;
Seewaldt, Victoria L. .
NATURE REVIEWS CANCER, 2015, 15 (04) :248-254