drug_type
RELEVANT_DRUG
intervention_type
Drug
drug_description
Antibody–drug conjugate targeting HER2 that delivers DXd, a membrane-permeable topoisomerase I inhibitor via a cathepsin-cleavable linker; enables receptor-mediated internalization and bystander effect.
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
HER2-targeted monoclonal antibody (trastuzumab) linked via a cathepsin-cleavable linker to deruxtecan (DXd), a membrane-permeable topoisomerase I inhibitor. Binding to HER2 triggers receptor-mediated internalization; linker cleavage releases DXd, which stabilizes Top1–DNA complexes, inhibiting DNA replication and inducing apoptosis. Also mediates bystander killing and antibody-dependent cell-mediated cytotoxicity (ADCC).
drug_name
Trastuzumab Deruxtecan
nct_id_drug_ref
NCT06328387