Rakha Emad, Reis-Filho Jorge S
Department of Histopathology, Nottingham City Hospital NHS Trust, Nottingham University, Nottingham, UK.
Arch Pathol Lab Med. 2009 Jun;133(6):860-8. doi: 10.5858/133.6.860.
Advances in the understanding of the molecular and genetic mechanisms of breast cancer have led to realization of the heterogeneity of the disease and the promise of a new era of individualized management for patients with breast cancer. The advent and use of high-throughput molecular methods for the study of breast cancer have brought to the forefront the existence of the so-called basal-like breast cancers, which have been shown to have distinct biologic and clinical characteristics.
To critically assess the clinicopathologic features of basal-like breast cancer, discuss the morphologic and immunophenotypic features of basal-like cancer, and explore the criteria that can be used to identify these tumors in routine practice.
A Medline/PubMed search was conducted using the terms "basal-like," "(basal OR basaloid OR basal-like) AND breast cancer." All articles in English language were retrieved and critically reviewed.
Basal-like breast cancers constitute a distinct, yet heterogeneous, class of neoplasms associated with specific histologic features and poor prognosis despite high response rates to neoadjuvant chemotherapy. Basal-like breast cancers have features that recapitulate those of tumors arising in BRCA1 mutation carriers, and the majority of patients with BRCA1 germline mutations develop basal-like breast cancers. At the molecular level, basal-like cancers harbor a transcriptome that is distinct from that of hormone-receptor-positive or HER2-amplified tumors, being characterized by the expression of genes usually found in basal/myoepithelial cells of the breast. However, translating the new concepts about basal-like cancer into clinical practice has proven a Herculean task, given the lack of an internationally accepted definition for these tumors and for the method of identification in routine practice.
对乳腺癌分子和遗传机制认识的进展,已使人们认识到该疾病的异质性以及乳腺癌患者个体化治疗新时代的前景。用于研究乳腺癌的高通量分子方法的出现和应用,使所谓的基底样乳腺癌的存在成为焦点,已表明其具有独特的生物学和临床特征。
严格评估基底样乳腺癌的临床病理特征,讨论基底样癌的形态学和免疫表型特征,并探索在常规实践中可用于识别这些肿瘤的标准。
使用术语“基底样”、“(基底或基底样或基底样)与乳腺癌”进行了Medline/PubMed检索。检索了所有英文文章并进行严格审查。
基底样乳腺癌构成一类独特但异质性的肿瘤,与特定的组织学特征相关,尽管对新辅助化疗反应率高,但预后较差。基底样乳腺癌具有与BRCA1突变携带者中发生的肿瘤相似的特征,并且大多数BRCA1种系突变患者会发生基底样乳腺癌。在分子水平上,基底样癌具有与激素受体阳性或HER2扩增肿瘤不同的转录组,其特征是通常在乳腺基底/肌上皮细胞中发现的基因表达。然而,鉴于缺乏这些肿瘤及其在常规实践中的识别方法的国际公认定义,将关于基底样癌的新概念转化为临床实践已被证明是一项艰巨的任务。