ER-/PR+ breast cancer: from diagnostic discordance to precision therapy.

IF 3.4 3区 医学 Q2 ONCOLOGY
Frontiers in Oncology Pub Date : 2026-10-05 eCollection Date: 2026-01-01 DOI:10.3389/fonc.2026.1961666
Yuanhao Shao, Meng Zhou, Zhenwei Hu, Bin Wu, Jing Zhou
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引用次数: 0

Abstract

Estrogen receptor-negative/progesterone receptor-positive/human epidermal growth factor receptor 2-negative (ER-/PR+/HER2-)breast cancer is a rare, controversial type that makes up about 0. 3% of all breast cancer cases and does not follow the traditional ER→PR regulatory hierarchy. This review synthesizes the available evidence on the diagnostic evaluation, clinicopathological characteristics, molecular mechanisms, prognosis, and treatment of ER-/PR+/HER2-(ER-/PR+) breast cancer. Although there are false-negative ER staining results and pre-analytical/analytical factors, a number of clinical and transcriptomic data support the existence of a reproducible ER-/PR+subgroup with molecular heterogeneity. These tumors often have a high histological grade, elevated Ki-67 expression, TP53 alterations, and basal-like features, and are closer to triple-negative breast cancer than luminal disease. Potential drivers include ER-independent non-canonical PR activation, epigenetic dysregulation, kinase-mediated receptor phosphorylation, membrane-associated progesterone signaling and receptor network reprogramming. Direct subtype-specific evidence remains limited, and the effectiveness of conventional endocrine therapy is unknown. Current guidelines classify these tumors as hormone receptor-positive/HER2-negative, obscuring clinically relevant heterogeneity. Standardized repeat testing and multi-omic characterization are thus required. Future studies should prioritize prospective multicenter cohorts with paired pre-treatment and post-treatment receptor testing, spatial or single-cell characterization, biomarker-guided stratification and adaptive clinical trials. A PR-oriented precision-medicine framework may improve diagnostic classification and help identify therapeutic vulnerabilities in biologically distinct patient subsets. In addition, this rare phenotype may serve as a useful model for investigating lineage plasticity and endocrine resistance.

ER-/PR+乳腺癌:从诊断不一致到精准治疗。
雌激素受体阴性/孕激素受体阳性/人表皮生长因子受体2阴性(ER-/PR+/HER2-)乳腺癌是一种罕见的、有争议的类型,约占乳腺癌发病率的1%。占所有乳腺癌病例的3%并且不遵循传统的ER→PR调节等级。本文就ER-/PR+/HER2-(ER-/PR+)乳腺癌的诊断评价、临床病理特征、分子机制、预后及治疗等方面的研究进展进行综述。尽管存在假阴性ER染色结果和分析前/分析因素,但许多临床和转录组学数据支持存在可重复的ER-/PR+亚群,且具有分子异质性。这些肿瘤通常具有高组织学分级、Ki-67表达升高、TP53改变和基底样特征,比腔内疾病更接近三阴性乳腺癌。潜在的驱动因素包括内质网非典型PR激活、表观遗传失调、激酶介导的受体磷酸化、膜相关孕激素信号传导和受体网络重编程。直接的亚型特异性证据仍然有限,传统内分泌治疗的有效性尚不清楚。目前的指南将这些肿瘤分类为激素受体阳性/ her2阴性,模糊了临床相关的异质性。因此,需要标准化的重复测试和多组学表征。未来的研究应优先考虑前瞻性多中心队列,配对治疗前和治疗后受体检测,空间或单细胞表征,生物标志物引导分层和适应性临床试验。以pr为导向的精准医学框架可以改善诊断分类,并有助于识别生物学上不同患者亚群的治疗脆弱性。此外,这种罕见的表型可以作为研究谱系可塑性和内分泌抗性的有用模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Oncology
Frontiers in Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
6.20
自引率
10.60%
发文量
6641
审稿时长
14 weeks
期刊介绍: Cancer Imaging and Diagnosis is dedicated to the publication of results from clinical and research studies applied to cancer diagnosis and treatment. The section aims to publish studies from the entire field of cancer imaging: results from routine use of clinical imaging in both radiology and nuclear medicine, results from clinical trials, experimental molecular imaging in humans and small animals, research on new contrast agents in CT, MRI, ultrasound, publication of new technical applications and processing algorithms to improve the standardization of quantitative imaging and image guided interventions for the diagnosis and treatment of cancer.
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