Antibody-drug conjugates in breast cancer: Marching from HER2-overexpression into HER2-low

被引:7
|
作者
Fan, Pinchao [1 ]
Xu, Kun [2 ,3 ,4 ]
机构
[1] Nanjing Med Univ, Clin Med Coll 1, Nanjing 211166, Peoples R China
[2] Nanjing Med Univ, Jiangsu Canc Hosp, Dept Oncol, 42 Baiziting, Nanjing 210009, Peoples R China
[3] Nanjing Med Univ, Jiangsu Inst Canc Res, 42 Baiziting, Nanjing 210009, Peoples R China
[4] Nanjing Med Univ, Affiliated Canc Hosp, 42 Baiziting, Nanjing 210009, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2023年 / 1878卷 / 01期
关键词
Antibody-drug conjugate; Breast cancer; HER2-overexpression; HER2-low; TRASTUZUMAB EMTANSINE T-DM1; SACITUZUMAB GOVITECAN; SINGLE-ARM; CHEMOTHERAPY; EXPRESSION; METASTASES; THERAPY; DISEASE; COHORT; TUMORS;
D O I
10.1016/j.bbcan.2022.188849
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The recent decade has witnessed a vigorous prosper of antibody-drug conjugates (ADCs) in solid tumors including breast cancer. Integrating the specificity of monoclonal antibodies and potency of cytotoxic drugs, ADCs are capable of delivering cytotoxic agents directly to tumor cells and surrounding accomplices with het-erogeneous antigen expression by exerting the distinctive bystander effect. Up till now, three ADCs (T-DM1, T-DXd and SG) have attained the official approval and stepped into clinical practices in breast cancer, with numerous promising products in the pipeline. As an unprecedented breast cancer subgroup identified following solidified drug benefit, the cognitive and therapeutic paradigm of HER2-low population which was previously thought lacking definite targets and efficacious regimens has been thoroughly rewritten by ADCs, and several encouraging achievements are expected in ongoing trials. Herein, we discuss the contrived knowledge, latest advancements and future perspectives of ADCs in HER2-overexpressing and HER2-low breast cancer.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] HER2-Low Breast Cancer: a New Subtype?
    Chiara Corti
    Federica Giugliano
    Eleonora Nicolò
    Paolo Tarantino
    Carmen Criscitiello
    Giuseppe Curigliano
    Current Treatment Options in Oncology, 2023, 24 : 468 - 478
  • [32] HER2-low breast cancer: where are we?
    Molinelli, Chiara
    Jacobs, Flavia
    Marchio, Caterina
    Pitto, Francesca
    Cosso, Maurizio
    Spinaci, Stefano
    de Azambuja, Evandro
    Schettini, Francesco
    Agostinetto, Elisa
    Lambertini, Matteo
    BREAST CARE, 2022, 17 (06) : 533 - 544
  • [33] Current Biological, Pathological and Clinical Landscape of HER2-Low Breast Cancer
    Zhang, Huina
    Peng, Yan
    CANCERS, 2023, 15 (01)
  • [34] Novel development strategies and challenges for anti-Her2 antibody-drug conjugates
    Zhang, Xinling
    Huang, Andrew C.
    Chen, Fahai
    Chen, Hu
    Li, Lele
    Kong, Nana
    Luo, Wenting
    Fang, Jianmin
    ANTIBODY THERAPEUTICS, 2022, 5 (01) : 18 - 29
  • [35] Recent advances in the development of anti-HER2 antibodies and antibody-drug conjugates
    Wong, Deborah J. L.
    Hurvitz, Sara A.
    ANNALS OF TRANSLATIONAL MEDICINE, 2014, 2 (12)
  • [36] Antibody-drug conjugates in breast cancer
    Zhu, Yinxing
    Song, Yaqi
    Zhou, Xilei
    Zhang, Wenwen
    Luo, Honglei
    CARCINOGENESIS, 2025, 46 (01)
  • [37] Lung toxicity induced by anti-HER2 antibody - drug conjugates for breast cancer
    Chai, Mengting
    Li, Li
    Wu, Huachao
    Liu, Yue
    Yi, Zongbi
    Yu, Haijun
    CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2024, 195
  • [38] Antibody drug conjugates targeting HER2: Clinical development in metastatic breast cancer
    Rassy, Elie
    Rached, Layal
    Pistilli, Barbara
    BREAST, 2022, 66 : 217 - 226
  • [39] Current Updates in Management of HER2-Positive and HER2-Low Breast Cancer
    Arushi Thaper
    Jennifer Tran
    Azka Ali
    Current Breast Cancer Reports, 2023, 15 : 135 - 141
  • [40] HER2-Low Breast Cancers New Opportunities and Challenges
    Zhang, Huina
    Katerji, Hani
    Turner, Bradley M.
    Hicks, David G.
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2022, 157 (03) : 328 - 336