Sarah Cannon Research Institute, Nashville, TN, USA.
University of California San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA, USA.
Breast. 2022 Dec;66:169-177. doi: 10.1016/j.breast.2022.10.007. Epub 2022 Oct 18.
Antibody drug conjugates (ADCs) combine the potent cytotoxicity of chemotherapy with the antigen -specific targeted approach of antibodies into one single molecule. Trophoblast cell surface antigen 2 (TROP-2) is a transmembrane glycoprotein involved in calcium signal transduction and is expressed in multiple tumor types. TROP-2 expression is higher in HER2-negative breast tumors (HR+/HR-) and is associated with worse survival. Sacituzumab govitecan (SG) is a first-in-class TROP-2-directed ADC with an anti-TROP-2 antibody conjugated to SN-38, a topoisomerase inhibitor via a hydrolysable linker. This hydrolysable linker permits intracellular and extracellular release of the membrane permeable payload enabling the "bystander effect" contributing to the efficacy of this agent. There was significant improvement in progression free survival (PFS) and overall survival (OS) with SG versus chemotherapy in pretreated metastatic triple negative breast cancer (TNBC), resulting in regulatory approval. Common adverse events (AE) reported were neutropenia and diarrhea. SG also demonstrated clinical activity versus chemotherapy in a phase III trial of HR+/HER2-metastatic breast cancer (MBC) and is under evaluation in first-line metastatic and early stage TNBC as well. Datopotamab deruxtecan (Dato-DXd) is a TROP-2 ADC that differs from SG in that it has a cleavable tetrapeptide linker and a more potent topoisomerase inhibitor payload. This construct is highly stable in circulation with a longer half-life than SG, and undergoes cleavage in presence of intracellular lysosomal proteases. Dato-DXd demonstrated preliminary efficacy in unselected metastatic TNBC, with common AEs of low-grade nausea and stomatitis. Dato-DXd is being investigated in phase III studies in metastatic TNBC and HR+/HER2- MBC. These novel TROP-2 ADCs have the potential to deliver enhanced efficacy with reduced toxicity in MBC and possibly in early stage breast cancer (EBC).
抗体药物偶联物(ADC)将化疗的强大细胞毒性与抗体的抗原特异性靶向方法结合在一个单一分子中。滋养细胞表面抗原 2(TROP-2)是一种参与钙信号转导的跨膜糖蛋白,在多种肿瘤类型中表达。TROP-2 在 HER2 阴性乳腺癌(HR+/HR-)中表达更高,并且与更差的生存相关。Sacituzumab govitecan(SG)是一种首创的 TROP-2 定向 ADC,它将抗 TROP-2 抗体与 SN-38 连接,SN-38 是一种拓扑异构酶抑制剂,通过可水解的接头连接。这种可水解的接头允许膜渗透有效载荷在细胞内和细胞外释放,从而实现“旁观者效应”,有助于该药物的疗效。在预处理的转移性三阴性乳腺癌(TNBC)中,与化疗相比,SG 显著改善了无进展生存期(PFS)和总生存期(OS),从而获得了监管批准。报告的常见不良反应(AE)是中性粒细胞减少和腹泻。在 HR+/HER2-转移性乳腺癌(MBC)的 III 期试验中,SG 也显示出优于化疗的临床活性,并且正在评估一线转移性和早期 TNBC 中的疗效。Datopotamab deruxtecan(Dato-DXd)是一种 TROP-2 ADC,与 SG 不同的是,它具有可切割的四肽接头和更有效的拓扑异构酶抑制剂有效载荷。与 SG 相比,该构建体在循环中高度稳定,半衰期更长,并且在存在细胞内溶酶体蛋白酶时会发生切割。Dato-DXd 在未经选择的转移性 TNBC 中显示出初步疗效,常见的不良反应为低级别恶心和口腔炎。Dato-DXd 正在转移性 TNBC 和 HR+/HER2-MBC 的 III 期研究中进行研究。这些新型 TROP-2 ADC 有可能在 MBC 中提供更高的疗效,同时降低毒性,并且可能在早期乳腺癌(EBC)中也有效果。