Ado-trastuzumab emtansine (T-DM1) is an antibody-drug conjugate (ADC) used in HER2-positive breast cancer.
Key points for oncology pharmacists:
- Composition:
- Combines the monoclonal antibody trastuzumab (targets HER2 receptor)
- Linked to the cytotoxic agent emtansine (DM1), a microtubule inhibitor
- Mechanism of Action:
- Trastuzumab binds HER2-expressing cancer cells → internalization of the conjugate → release of DM1 inside the cell → inhibits microtubule assembly → cancer cell death
- Also retains trastuzumab’s effects like HER2 signaling blockade and antibody-dependent cellular cytotoxicity (ADCC).
- Indications:
- HER2-positive metastatic breast cancer previously treated with trastuzumab and a taxane
- Early-stage HER2-positive breast cancer with residual invasive disease after neoadjuvant therapy
- Administration:
- Intravenous infusion, typically every 3 weeks
- Common Toxicities:
- Hepatotoxicity (monitor LFTs)
- Thrombocytopenia
- Peripheral neuropathy
- Cardiotoxicity (less frequent than trastuzumab alone)
- Infusion-related reactions
- Pharmacist considerations:
- Monitor liver function and platelets regularly
- Counsel on neuropathy symptoms
- Ensure cardiac monitoring per HER2 therapy protocols
- Educate patient on infusion reactions and supportive care
Synonyms
T-DM1, , Kadcyla

