Division of Medical Oncology, The Ohio State University Wexner Medical Center, James Cancer Hospital and Solove Research Institute, Columbus, OH, USA.
Expert Rev Anticancer Ther. 2021 Feb;21(2):135-148. doi: 10.1080/14737140.2021.1840984.
: Triple-negative breast cancer (TNBC) is an aggressive type of breast cancer associated with poor prognosis and limited treatment options. Validated prognostic and predictive biomarkers are needed to guide treatment decisions and prognostication.: In this review, we discuss established and developing prognostic and predictive biomarkers in TNBC and associated emerging and approved therapies. Biomarkers reviewed include epidermal growth factor receptor (EGFR), vascular endothelial growth factors (VEGF), fibroblast growth factor receptor (FGFR), human epidermal growth factor receptor 2 (HER2), androgen receptor, NOTCH signaling, oxidative stress/redox signaling, microRNAs, mutation, breast cancer susceptibility gene 1 or 2 () mutation/homologous recombination deficiency (HRD), NTRK gene fusion, PI3K/AKT/mTOR, immune biomarkers (programmed death-ligand 1 (PDL1), tumor-infiltrating lymphocytes (TILs), tumor mutational burden (TMB), neoantigens, defects in DNA mismatch repair proteins (dMMR)/microsatellite instability-high (MSI-H)), circulating tumor cells/cell-free DNA, novel targets of antibody-drug conjugates, and residual disease.: Biomarker-driven care in the management of TNBC is increasing and has helped expand options for patients diagnosed with this subtype of breast cancer. Research efforts are ongoing to identify additional biomarkers and targeted treatment options with the ultimate goal of improving clinical outcomes and survivorship.
三阴性乳腺癌(TNBC)是一种侵袭性乳腺癌,与预后不良和治疗选择有限有关。需要经过验证的预后和预测生物标志物来指导治疗决策和预后判断。在这篇综述中,我们讨论了 TNBC 中已确立和正在发展的预后和预测生物标志物,以及相关的新兴和已批准的治疗方法。综述的生物标志物包括表皮生长因子受体(EGFR)、血管内皮生长因子(VEGF)、成纤维细胞生长因子受体(FGFR)、人表皮生长因子受体 2(HER2)、雄激素受体、NOTCH 信号、氧化应激/还原信号、microRNAs、突变、乳腺癌易感基因 1 或 2(BRCA1/2)突变/同源重组缺陷(HRD)、NTRK 基因融合、PI3K/AKT/mTOR、免疫生物标志物(程序性死亡配体 1(PDL1)、肿瘤浸润淋巴细胞(TILs)、肿瘤突变负担(TMB)、新抗原、错配修复蛋白缺陷(dMMR)/微卫星不稳定高(MSI-H))、循环肿瘤细胞/游离 DNA、抗体药物偶联物的新靶点,以及残留疾病。在 TNBC 的管理中,基于生物标志物的治疗正在增加,并帮助扩大了诊断为这种乳腺癌亚型的患者的治疗选择。目前正在进行研究,以确定更多的生物标志物和靶向治疗方法,最终目标是改善临床结果和生存。