Dey Nandini, Aske Jennifer, De Pradip
Translational Oncology Laboratory, Avera Cancer Institute, Sioux Falls, SD 57105, USA.
Cancers (Basel). 2021 Jan 26;13(3):458. doi: 10.3390/cancers13030458.
A strong association of pCR (pathological complete response) with disease-free survival or overall survival is clinically desirable. The association of pCR with disease-free survival or overall survival in ER+/HER2-breast cancers following neoadjuvant systemic therapy (NAT) or neoadjuvant endocrine therapy (NET) is relatively low as compared to the other two subtypes of breast cancers, namely triple-negative and HER2+ amplified. On the bright side, a neoadjuvant model offers a potential opportunity to explore the efficacy of novel therapies and the associated genomic alterations, thus providing a rare personalized insight into the tumor's biology and the tumor cells' response to the drug. Several decades of research have taught us that the disease's biology is a critical factor determining the tumor cells' response to any therapy and hence the final outcome of the disease. Here we propose two scenarios wherein apoptosis can be induced in ER+/HER2- breast cancers expressing wild type TP53 and RB genes following combinations of BCL2 inhibitor, MDM2 inhibitor, and cell-cycle inhibitor. The suggested combinations are contextual and based on the current understanding of the cell signaling in the ER+/HER2- breast cancers. The two combinations of drugs are (1) BCL2 inhibitor plus a cell-cycle inhibitor, which can prime the tumor cells for apoptosis, and (2) BCL2 inhibitor plus an MDM2 inhibitor.
pCR(病理完全缓解)与无病生存期或总生存期之间存在强关联在临床上是理想的。与乳腺癌的其他两种亚型(即三阴性和HER2+扩增型)相比,新辅助全身治疗(NAT)或新辅助内分泌治疗(NET)后ER+/HER2-乳腺癌中pCR与无病生存期或总生存期的关联相对较低。好的一面是,新辅助模型提供了一个潜在机会来探索新疗法的疗效以及相关的基因组改变,从而为肿瘤生物学和肿瘤细胞对药物的反应提供罕见的个性化见解。几十年的研究告诉我们,疾病生物学是决定肿瘤细胞对任何治疗的反应以及疾病最终结局的关键因素。在此,我们提出两种情况,即在联合使用BCL2抑制剂、MDM2抑制剂和细胞周期抑制剂后,可在表达野生型TP53和RB基因的ER+/HER2-乳腺癌中诱导细胞凋亡。所建议的联合用药是基于对ER+/HER2-乳腺癌细胞信号传导的当前理解而确定的。这两种药物联合方案为:(1)BCL2抑制剂加细胞周期抑制剂,可使肿瘤细胞易于凋亡;(2)BCL2抑制剂加MDM2抑制剂。