Liquid biopsy in triple-negative breast cancer: unlocking the potential of precision oncology

被引:2
|
作者
Mazzeo, R. [1 ,2 ]
Sears, J. [3 ]
Palmero, L. [1 ,2 ]
Bolzonello, S. [1 ]
Davis, A. A. [4 ]
Gerratana, L. [1 ,2 ]
Puglisi, F. [1 ,2 ]
机构
[1] IRCCS, Natl Canc Inst, Dept Med Oncol, CRO Aviano, Via Franco Gallini 2, I-33081 Aviano, PN, Italy
[2] Univ Udine, Dept Med, Udine, Italy
[3] Washington Univ, Dept Med, St Louis, MO USA
[4] Washington Univ, Sch Med, Dept Med, Div Oncol, St Louis, MO USA
关键词
liquid biopsy; triple-negative breast cancer; precision oncology; novel biomarkers; circulating tumor DNA; circulating tumor cells; CIRCULATING TUMOR-CELLS; INFILTRATING LYMPHOCYTES; NEOADJUVANT CHEMOTHERAPY; PROGNOSTIC VALUE; DOUBLE-BLIND; DNA; EXPRESSION; MICRORNAS; HETEROGENEITY; PLASMAMATCH;
D O I
10.1016/j.esmoop.2024.103700
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the era of precision oncology, the management of triple-negative breast cancer (TNBC) is rapidly changing and becoming more complicated with a variety of chemotherapy, immunotherapy, and targeted treatment options. Currently, TNBC treatment is based on prognostic and predictive factors including immunohistochemical biomarkers [e.g. programmed death-ligand 1 (PD-L1)] and germline BRCA mutations. Given the current limitation of existing biomarkers, liquid biopsies may serve as clinically useful tools to determine treatment efficacy and response in both the (neo)adjuvant and metastatic settings, for detecting early relapse, and for monitoring clonal evolution during treatment. In this review, we comprehensively summarize current and future liquid biopsy applications. Specifically, we highlight the role of circulating tumor cell characterization, circulating tumor DNA, and other preclinical liquid biopsy technologies including circulating exosomes, RNA liquid biopsy, and circulating immune-based biomarkers. In the near future, these biomarkers may serve to identify early disease relapse, therapeutic targets, and disease clonality for patients with TNBC in the clinical setting.
引用
收藏
页数:12
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