Rios-Hoyo Alejandro, Shan Naing-Lin, Karn Philipp L, Pusztai Lajos
Yale Cancer Center, Yale School of Medicine, New Haven, CT, USA.
University of Ulm, Ulm, Germany.
Adv Exp Med Biol. 2025;1464:435-448. doi: 10.1007/978-3-031-70875-6_21.
Estrogen receptor-positive (ER+) and estrogen receptor-negative (ER-) breast cancers have different genomic architecture and show large-scale gene expression differences consistent with different cellular origins, which is reflected in the luminal (i.e., ER+) versus basal-like (i.e., ER-) molecular class nomenclature. These two major molecular subtypes have distinct epidemiological risk factors and different clinical behaviors. Luminal cancers can be subdivided further based on proliferative activity and ER signaling. Those with a high expression of proliferation-related genes and a low expression of ER-associated genes, called luminal B, have a high risk of early recurrence (i.e., within 5 years), derive significant benefit from adjuvant chemotherapy, and may benefit from adding immunotherapy to chemotherapy. This subset of luminal cancers is identified as the genomic high-risk ER+ cancers by the MammaPrint, Oncotype DX Recurrence Score, EndoPredict, Prosigna, and several other molecular prognostic assays. Luminal A cancers are characterized by low proliferation and high ER-related gene expression. They tend to have excellent prognosis with adjuvant endocrine therapy. Adjuvant chemotherapy may not improve their outcome further. These cancers correspond to the genomic low-risk categories. However, these cancers remain at risk for distant recurrence for extended periods of time, and over 50% of distant recurrences occur after 5 years. Basal-like cancers are uniformly highly proliferative and tend to recur within 3-5 years of diagnosis. In the absence of therapy, basal-like breast cancers have the worst survival, but these also include many highly chemotherapy-sensitive cancers. Basal-like cancers are often treated with preoperative chemotherapy combined with an immune checkpoint inhibitor which results in 60-65% pathologic complete response rates that herald excellent long-term survival. Patients with residual cancer after neoadjuvant therapy can receive additional postoperative chemotherapy that improves their survival. Currently, there is no clinically actionable molecular subclassification for basal-like cancers, although cancers with high androgen receptor (AR)-related gene expression and those with high levels of immune infiltration have better prognosis, but currently their treatment is not different from basal-like cancers in general. A clinically important, minor subset of breast cancers are characterized by frequent HER2 gene amplification and high expression of a few dozen genes, many residing on the HER2 amplicon. This is an important subset because of the highly effective HER2 targeted therapies which are synergistic with endocrine therapy and chemotherapy. The clinical behavior of HER2-enriched cancers is dominated by the underlying ER subtype. ER+/HER2-enriched cancers tend to have more indolent course and lesser chemotherapy sensitivity than their ER counterparts.
雌激素受体阳性(ER+)和雌激素受体阴性(ER-)乳腺癌具有不同的基因组结构,并表现出与不同细胞起源一致的大规模基因表达差异,这反映在管腔型(即ER+)与基底样型(即ER-)分子分类命名中。这两种主要分子亚型具有不同的流行病学危险因素和不同的临床行为。管腔型癌症可根据增殖活性和ER信号进一步细分。那些增殖相关基因高表达且ER相关基因低表达的癌症,称为管腔B型,具有早期复发(即5年内)的高风险,从辅助化疗中获益显著,并且可能从化疗联合免疫治疗中获益。管腔型癌症的这一亚组通过MammaPrint、Oncotype DX复发评分、EndoPredict、Prosigna以及其他几种分子预后检测方法被确定为基因组高风险ER+癌症。管腔A型癌症的特征是低增殖和高ER相关基因表达。它们通过辅助内分泌治疗往往预后良好。辅助化疗可能不会进一步改善其预后。这些癌症对应于基因组低风险类别。然而,这些癌症在很长一段时间内仍有远处复发的风险,超过50%的远处复发发生在5年后。基底样型癌症普遍具有高增殖性,倾向于在诊断后3至5年内复发。在未接受治疗的情况下,基底样型乳腺癌的生存率最差,但其中也包括许多对化疗高度敏感的癌症。基底样型癌症通常采用术前化疗联合免疫检查点抑制剂治疗,其病理完全缓解率可达60%至65%,预示着良好的长期生存率。新辅助治疗后有残留癌的患者可接受额外的术后化疗,这可提高他们的生存率。目前,对于基底样型癌症尚无临床上可操作的分子亚分类,尽管雄激素受体(AR)相关基因高表达的癌症和免疫浸润水平高的癌症预后较好,但目前它们的治疗与一般基底样型癌症并无不同。一小部分临床上重要的乳腺癌以频繁的HER2基因扩增和几十种基因的高表达为特征,其中许多基因位于HER2扩增子上。这是一个重要的亚组,因为高效的HER2靶向治疗与内分泌治疗和化疗具有协同作用。HER2富集型癌症的临床行为主要由潜在的ER亚型决定。ER+/HER2富集型癌症往往病程较惰性,化疗敏感性低于其ER亚型对应癌症。