drug_type
RELEVANT_DRUG
intervention_type
Drug
drug_description
An anti-HER2 antibody–drug conjugate (ADC) consisting of trastuzumab linked to a cleavable topoisomerase I inhibitor payload (DXd). It binds ERBB2/HER2 on tumor cells, is internalized, and releases the cytotoxic payload in lysosomes to induce tumor cell death.
nci_thesaurus_concept_id
C128799
nci_thesaurus_preferred_term
Trastuzumab Deruxtecan
nci_thesaurus_definition
An antibody-drug conjugate (ADC) composed of trastuzumab, a monoclonal antibody targeting human epidermal growth factor receptor 2 (ERBB2; EGFR2; HER2) conjugated to deruxtecan, a derivative of the camptothecin analog exatecan (DXd; DX-8951 derivative), a DNA topoisomerase 1 (topoisomerase I; Top1) inhibitor, with antineoplastic activity. Upon administration of trastuzumab deruxtecan, trastuzumab targets and binds to HER2 on tumor cells. Upon antibody/antigen binding and internalization, deruxtecan binds to and inhibits Top1-DNA complexes, which results in an inhibition of DNA replication, cell cycle arrest and tumor cell apoptosis. HER2, a tyrosine kinase receptor, is overexpressed by many cancer cell types. In addition, trastuzumab deruxtecan induces antibody-dependent cell-mediated cytotoxicity (ADCC) and causes a bystander killing effect.
drug_mesh_term
Trastuzumab Deruxtecan
drug_category
ANTIBODY DRUG CONJUGATE
drug_class
Conjugate
drug_delivery_route
Intravenous
drug_mechanism_of_action
Trastuzumab deruxtecan is a HER2-targeted monoclonal antibody linked via a cleavable linker to a topoisomerase I inhibitor payload (deruxtecan, DXd). After binding ERBB2/HER2 on tumor cells, the complex is internalized and the payload is released in lysosomes, inhibiting Top1 to cause DNA damage, replication arrest, and apoptosis. It also mediates ADCC and produces a bystander killing effect due to a membrane-permeable payload.
drug_name
Trastuzumab deruxtecan
nct_id_drug_ref
NCT06492447