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Antibody-drug conjugates targeting TROP-2: Clinical development in metastatic breast cancer
Mythili Shastry1, Saya Jacob2, Hope S Rugo2
1Sarah Cannon Research Institute, Nashville, TN, USA.
Abstract:
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).
Insights
Novel TROP-2 antibody-drug conjugates (ADCs) like sacituzumab govitecan and datopotamab deruxtecan show promise in treating metastatic breast cancer, offering improved survival and reduced toxicity.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Antibody drug conjugates (ADCs) merge targeted antibody therapy with potent chemotherapy for cancer treatment.
- Trophoblast cell surface antigen 2 (TROP-2) is a key target in various cancers, notably HER2-negative breast tumors, where its high expression correlates with poorer outcomes.
- Sacituzumab govitecan (SG) and datopotamab deruxtecan (Dato-DXd) are advanced TROP-2-targeting ADCs.
Purpose of the Study:
- To review the efficacy and safety of TROP-2 ADCs, specifically sacituzumab govitecan and datopotamab deruxtecan.
- To highlight their potential in treating metastatic breast cancer (MBC) and early-stage breast cancer (EBC).
Main Methods:
- Review of clinical trial data for sacituzumab govitecan (SG) and datopotamab deruxtecan (Dato-DXd).
- Comparison of ADC constructs, including linker technology and payload.
- Analysis of efficacy (progression-free survival, overall survival) and safety (adverse events).
Main Results:
- SG demonstrated significant improvements in PFS and OS compared to chemotherapy in pretreated metastatic triple-negative breast cancer (TNBC) and HR+/HER2- MBC.
- Dato-DXd showed preliminary efficacy in metastatic TNBC with a distinct safety profile (nausea, stomatitis).
- Both ADCs exhibit potential for enhanced efficacy and reduced toxicity.
Conclusions:
- TROP-2 ADCs represent a significant advancement in breast cancer therapy.
- Sacituzumab govitecan is approved for pretreated metastatic TNBC and shows activity in HR+/HER2- MBC.
- Datopotamab deruxtecan is under investigation and shows promise for MBC and potentially EBC.
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