Trastuzumab Emtansine: Mechanisms of Action and Resistance, Clinical Progress, and Beyond

Trends Cancer. 2020 Feb;6(2):130-146. doi: 10.1016/j.trecan.2019.12.010. Epub 2020 Jan 21.

Abstract

The approval of ado-trastuzumab emtansine (T-DM1) for clinical use represented a turning point both in HER2-positive breast cancer treatment and antibody-drug conjugate (ADC) technology. T-DM1 has proved its value and effectiveness in advanced metastatic disease as well as in the adjuvant setting. However, its therapeutic potential extends beyond the treatment of breast cancer. Around 100 clinical trials have evaluated or are studying different aspects of T-DM1, such as its role in other HER2 malignancies, rational combinations with immunotherapy, or its function in brain metastasis. Conceptually, many lessons can be learned from this ADC. Understanding its mechanisms of action and the molecular basis underlying resistance to T-DM1 may be relevant to comprehend resistances raised to other ADCs and identify pitfalls that may be overcome.

Keywords: T-DM1; antibody–drug conjugates; drug resistance.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Ado-Trastuzumab Emtansine / pharmacology*
  • Ado-Trastuzumab Emtansine / therapeutic use
  • Antineoplastic Agents, Immunological / pharmacology*
  • Antineoplastic Agents, Immunological / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Breast / pathology
  • Breast / surgery
  • Breast Neoplasms / immunology
  • Breast Neoplasms / mortality
  • Breast Neoplasms / pathology
  • Breast Neoplasms / therapy*
  • Chemotherapy, Adjuvant / methods
  • Clinical Trials as Topic
  • Drug Resistance, Neoplasm / drug effects
  • Female
  • Humans
  • Immune Checkpoint Inhibitors / pharmacology
  • Immune Checkpoint Inhibitors / therapeutic use
  • Immunotoxins / pharmacology*
  • Immunotoxins / therapeutic use
  • Mastectomy
  • Neoadjuvant Therapy / methods
  • Progression-Free Survival
  • Receptor, ErbB-2 / antagonists & inhibitors
  • Receptor, ErbB-2 / metabolism

Substances

  • Antineoplastic Agents, Immunological
  • Immune Checkpoint Inhibitors
  • Immunotoxins
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • Ado-Trastuzumab Emtansine