共 50 条
Endocrine therapy plus HER2-targeted therapy, another favorable option for HR+/HER2+advanced breast cancer patients
被引:1
|作者:
Liang, Yuehua
[1
]
Liu, Xiaoran
[1
]
Yun, Zehui
[1
]
Li, Kun
[1
]
Li, Huiping
[1
]
机构:
[1] Peking Univ Canc Hosp & Inst, Dept Breast Oncol, Key Lab Carcinogenesis & Translat Res, Minist Educ Beijing, Beijing, Peoples R China
关键词:
antibody-drug conjugates;
chemotherapy;
combination therapy;
endocrine therapy;
HER2+breast cancer;
hormone receptor-positive breast cancer;
hormone therapy;
targeted therapy;
ESTROGEN-RECEPTOR-ALPHA;
EPIDERMAL-GROWTH-FACTOR;
DOUBLE-BLIND;
1ST-LINE TREATMENT;
TRASTUZUMAB DERUXTECAN;
TAMOXIFEN RESISTANCE;
AROMATASE INHIBITORS;
CROSS-TALK;
FOLLOW-UP;
PLACEBO;
D O I:
10.1177/17588359231220501
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Advanced breast cancer (ABC) that is positive for hormone receptors (HRs) and human epidermal growth factor receptor 2 (HER2) is a cancer subtype with distinctive characteristics. The primary treatment guidelines suggest that a combination therapy comprising anti-HER2 therapy and chemotherapy should be administered as the initial treatment for HR-positive/ HER2-positive (HR+/HER2+) ABC. However, crosstalk between the HR and HER2 pathways can partially account for the resistance of HR+/HER2+ disease to HER2-targeted therapy. This, in turn, provides a rationale for the concomitant administration of HER2-targeted therapy and endocrine therapy (ET). Many clinical studies have confirmed that the combination of HER2-targeted therapy and ET as a first-line treatment is not inferior to the combination of HER2-targeted therapy and chemotherapy, and support its use as a first-line treatment choice for HR+/HER2+ ABC. Other drugs, such as antibody-drug conjugates, cyclin-dependent kinase 4/6 inhibitors, phosphatidylinositol 3-kinase-protein kinase B (AKT)-mammalian target of rapamycin inhibitors, and programmed cell death protein 1 or programmed cell death ligand 1 inhibitors, may also improve the prognosis of patients with breast cancer by blocking signaling pathways associated with tumor proliferation and break new ground for the treatment of HR+/HER2+ ABC.
引用
收藏
页数:17
相关论文