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对HER2低表达乳腺癌这一新兴实体的见解。

Insights Into the Emerging Entity of HER2-Low Breast Cancer.

作者信息

El Haddad Georges, Diab Ernest, Hajjar Michel, Aoun Maroun, Mallat Farid, Zalaquett Ziad, Kourie Hampig-Raphael

机构信息

Hematology-Oncology Department Hôtel-Dieu de France University Hospital Saint Joseph University of Beirut, Beirut, Lebanon.

出版信息

Int J Breast Cancer. 2024 Jun 13;2024:2853007. doi: 10.1155/2024/2853007. eCollection 2024.


DOI:10.1155/2024/2853007
PMID:38962672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11221987/
Abstract

Human epidermal growth factor receptor 2 (HER2)-low breast cancer (BC) is a subtype of BC that has been recently recognized as a separate clinical entity with distinct clinical and molecular characteristics. It is defined by a low level of HER2 protein expression, which distinguishes it from other more aggressive BC subtypes. Early studies suggest that it may have a more favorable prognosis than HER2-positive BC, as it is less likely to spread to other parts of the body and may be more responsive to standard BC treatments such as chemotherapy, radiation therapy, and hormone therapy. Given the relative new emergence of HER2-low BC, there is still much to be learned about this subtype; ongoing research is focused on identifying the underlying genetic mutations that contribute to HER2-low BC as well as developing targeted therapies that can improve outcomes for patients with this disease. This review is aimed at summarizing the current clinical knowledge on HER2-low BC, with the aim of creating a better understanding of this entity and paving the way for potential interventions and a new standard of care.

摘要

人表皮生长因子受体2(HER2)低表达乳腺癌(BC)是乳腺癌的一种亚型,最近被确认为具有独特临床和分子特征的独立临床实体。它由HER2蛋白低水平表达所定义,这使其有别于其他侵袭性更强的乳腺癌亚型。早期研究表明,与HER2阳性乳腺癌相比,它可能具有更有利的预后,因为它扩散到身体其他部位的可能性较小,并且可能对化疗、放疗和激素治疗等标准乳腺癌治疗更敏感。鉴于HER2低表达乳腺癌相对较新出现,关于这一亚型仍有许多有待了解之处;正在进行的研究集中于确定导致HER2低表达乳腺癌的潜在基因突变,以及开发能够改善该疾病患者治疗结果的靶向疗法。本综述旨在总结目前关于HER2低表达乳腺癌的临床知识,以便更好地了解这一实体,并为潜在干预措施和新的护理标准铺平道路。

相似文献

[1]
Insights Into the Emerging Entity of HER2-Low Breast Cancer.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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引用本文的文献

[1]
Intratumoral and peritumoral ultrasound radiomics analysis for predicting HER2-low expression in HER2-negative breast cancer patients: a retrospective analysis of dual-central study.

Discov Oncol. 2025-6-5

[2]
Molecular Subtypes and Mechanisms of Breast Cancer: Precision Medicine Approaches for Targeted Therapies.

Cancers (Basel). 2025-3-25

[3]
Prognostic Impact of HER2 Low Status in Male Breast Cancer: Prospective Cohort Analysis.

Cancers (Basel). 2024-10-5

本文引用的文献

[1]
Cost-effectiveness and Value-based Pricing of Trastuzumab Deruxtecan in Metastatic Breast Cancer With Low HER2 Expression.

Clin Breast Cancer. 2023-7

[2]
Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment.

EBioMedicine. 2023-5

[3]
Clinicopathological characteristics and prognosis of early-stage HER2 low-expression breast cancer: A single-center retrospective study.

Front Oncol. 2023-3-29

[4]
Evolution and clinical significance of HER2-low status after neoadjuvant therapy for breast cancer.

Front Oncol. 2023-2-22

[5]
Discordance of HER2-Low between Primary Tumors and Matched Distant Metastases in Breast Cancer.

Cancers (Basel). 2023-2-23

[6]
Comparison of clinicopathological characteristics and response to neoadjuvant systemic therapy in patients with HER2-low-positive and HER2-zero breast cancer.

J Investig Med. 2023-4

[7]
The impact of HER2-low status on response to neoadjuvant chemotherapy in clinically HER2-negative breast cancer.

Clin Transl Oncol. 2023-6

[8]
Comparison of clinicopathological characteristics and response to neoadjuvant chemotherapy between HER2-low and HER2-zero breast cancer.

Breast. 2023-2

[9]
Economic Evaluation of Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer in the United States.

Breast Cancer (Dove Med Press). 2022-12-9

[10]
Trastuzumab deruxtecan chemotherapy for patients with HER2-low advanced breast cancer: A US-based cost-effectiveness analysis.

Front Pharmacol. 2022-10-28

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