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.
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页数:17
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