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Review
. 2024 Jan 6:16:17588359231220501.
doi: 10.1177/17588359231220501. eCollection 2024.

Endocrine therapy plus HER2-targeted therapy, another favorable option for HR+/HER2+ advanced breast cancer patients

Affiliations
Review

Endocrine therapy plus HER2-targeted therapy, another favorable option for HR+/HER2+ advanced breast cancer patients

Yuehua Liang et al. Ther Adv Med Oncol. .

Abstract

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.

Keywords: HER2+ breast cancer; antibody–drug conjugates; chemotherapy; combination therapy; endocrine therapy; hormone receptor-positive breast cancer; hormone therapy; targeted therapy.

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Conflict of interest statement

The authors declare that there is no conflict of interest.

Figures

Figure 1.
Figure 1.
Crosstalk between HER2 signaling pathway and ER signaling pathway and drugs for HR+/HER2+ advanced breast cancer patients. HER, human epidermal growth factor receptor; HR, hormone receptor.

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References

    1. Sung H, Ferlay J, Siegel RL, et al.. Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021; 71: 209–249. - PubMed
    1. The National Health Commission of the People’s Republic of China. National guidelines for diagnosis and treatment of breast cancer 2022 in China (English version). Chin J Cancer Res 2022; 34: 151–175. - PMC - PubMed
    1. Vici P, Pizzuti L, Natoli C, et al.. Triple positive breast cancer: a distinct subtype? Cancer Treat Rev 2015; 41: 69–76. - PubMed
    1. Zhou P, Jiang YZ, Hu X, et al.. Clinicopathological characteristics of patients with HER2-positive breast cancer and the efficacy of trastuzumab in the People’s Republic of China. Onco Targets Ther 2016; 9: 2287–2295. - PMC - PubMed
    1. Colleoni M, Sun Z, Price KN, et al.. Annual hazard rates of recurrence for breast cancer during 24 years of follow-up: results from the International Breast Cancer Study Group trials I to V. J Clin Oncol 2016; 34: 927–935. - PMC - PubMed