期刊
BREAST
卷 66, 期 -, 页码 169-177出版社
CHURCHILL LIVINGSTONE
DOI: 10.1016/j.breast.2022.10.007
关键词
Antibody drug conjugate (ADC); Trophoblast cell surface antigen-2 (TROP-2); Sacituzumab govitecan; Datopotamab deruxtecan; Metastatic breast cancer
Antibody drug conjugates (ADCs) combine the cytotoxicity of chemotherapy and the targeted therapy of antibodies into a single molecule. TROP-2, a transmembrane glycoprotein, is expressed in multiple tumor types, especially in HER2-negative breast tumors, and is associated with worse survival. Sacituzumab govitecan (SG) is a first-in-class TROP-2-directed ADC that has shown significant improvement in progression-free survival and overall survival in pretreated metastatic triple-negative breast cancer. Datopotamab deruxtecan (Dato-DXd) is another TROP-2 ADC that has demonstrated preliminary efficacy in unselected metastatic TNBC. Both SG and Dato-DXd have the potential to deliver enhanced efficacy with reduced toxicity in breast cancer.
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 demon-strated 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 effi-cacy 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).
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