Tumor immune microenvironment components and the other markers can predict the efficacy of neoadjuvant chemotherapy for breast cancer

被引:7
|
作者
Zhang, Weiqian [1 ,2 ]
Xu, Ke [1 ,2 ]
Li, Zhengfa [1 ,2 ]
Wang, Linwei [3 ]
Chen, Honglei [1 ,2 ]
机构
[1] Wuhan Univ, Dept Pathol, Zhongnan Hosp, Wuhan 430071, Peoples R China
[2] Wuhan Univ, Sch Basic Med Sci, Dept Pathol, Wuhan 430071, Peoples R China
[3] Wuhan Univ, Dept Oncol, Zhongnan Hosp, Wuhan 430071, Peoples R China
关键词
Breast cancer; Neoadjuvant chemotherapy; Predictors; Tumor microenvironment; Immune checkpoints; PATHOLOGICAL COMPLETE RESPONSE; INFILTRATING LYMPHOCYTES; CLINICAL-SIGNIFICANCE; PROGNOSTIC VALUE; EXPRESSION; THERAPY; COMBINATION; CYCLOPHOSPHAMIDE; DOXORUBICIN; DOCETAXEL;
D O I
10.1007/s12094-023-03075-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer is an epithelial malignant tumor that occurs in the terminal ducts of the breast. Neoadjuvant chemotherapy (NACT) is an important part of breast cancer treatment. Its purpose is to use systemic treatment for some locally advanced breast cancer patients, to decrease the tumor size and clinical stage so that non-operable breast cancer patients can have a chance to access surgical treatment, or patients who are not suitable for breast-conserving surgery can get the opportunity of breast-conserving. However, some patients who do not respond to NACT will lead deterioration in their condition. Therefore, prediction of NACT efficacy in breast cancer is vital for precision therapy. The tumor microenvironment (TME) has a crucial role in the carcinogenesis and therapeutic response of breast cancer. In this review, we summarized the immune cells, immune checkpoints, and other biomarkers in the TME that can evaluate the efficacy of NACT in treating breast cancer. We believe that the detection and evaluation of the TME components in breast cancer are helpful to predict the efficacy of NACT, and the prediction methods are in the prospect. In addition, we also summarized other predictive factors of NACT, such as imaging examination, biochemical markers, and multigene/multiprotein profiling.
引用
收藏
页码:1579 / 1593
页数:15
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