Lung toxicity induced by anti-HER2 antibody - drug conjugates for breast cancer

Crit Rev Oncol Hematol. 2024 Mar:195:104274. doi: 10.1016/j.critrevonc.2024.104274. Epub 2024 Jan 29.

Abstract

Human epidermal growth factor receptor 2 (HER2) serves as both a prognostic indicator and a therapeutic target for breast cancer. Therefore, anti-HER2 therapy plays a crucial role in the treatment of HER2-positive cancer. Antibody-drug conjugates (ADCs) are composed of a monoclonal antibody, a chemical linker and a payload, wherein their aim is to reduce the toxicity associated with chemotherapy drugs by utilizing specific antibodies. Among the anti-HER2 ADCs currently approved for clinical use, trastuzumab emtansine(T-DM1) and trastuzumab deruxtecan (T-Dxd) have demonstrated remarkable efficacy in treating HER2-positive breast cancer. However, it is essential to emphasize the occurrence of lung toxicity during the treatment process, which can be life-threatening. In this review, we provide an overview of the new epidemiological features associated with interstitial lung disease (ILD) related to anti-HER2 ADCs in breast cancer. We also summarize the potential pathogenesis and explore the diagnosis and treatment strategies within this field.

Keywords: Antibody-drug conjugate; HER2; Interstitial lung disease; T-DM1; T-Dxd.

Publication types

  • Review

MeSH terms

  • Ado-Trastuzumab Emtansine / adverse effects
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Antineoplastic Agents* / adverse effects
  • Breast Neoplasms* / complications
  • Breast Neoplasms* / drug therapy
  • Female
  • Humans
  • Immunoconjugates* / adverse effects
  • Lung Diseases, Interstitial* / chemically induced
  • Receptor, ErbB-2 / metabolism
  • Trastuzumab / adverse effects

Substances

  • Ado-Trastuzumab Emtansine
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Immunoconjugates
  • Receptor, ErbB-2
  • Trastuzumab