Acute skin radiation toxicity seen with concurrent T-DM1: A single institutional report of 35 patients

Breast. 2023 Feb:67:26-29. doi: 10.1016/j.breast.2022.12.002. Epub 2022 Dec 17.

Abstract

Trastuzumab emtansine (T-DM1) is a novel therapeutic for HER2+ breast cancer patients with residual disease after neoadjuvant chemotherapy. Concurrent radiotherapy (RT) is offered to a subset of patients based on results from the KATHERINE trial which showed a favorable safety profile. With emerging therapies that necessitate concurrent RT, we must closely follow rates of skin toxicity. Our first 35 patients who underwent concurrent T-DM1 treatment with breast/chest wall (CW) ± nodal irradiation are reported. Most patients (22/35) had grade 2+ toxicity and 3 patients had grade 3 toxicities. We add our experience with radiation dermatitis and concurrent T-DM1 to contribute to existing reports.

Keywords: Adjuvant radiation; Chemo-immunotherapy; Concurrent chemo radiation; Skin toxicity.

MeSH terms

  • Ado-Trastuzumab Emtansine / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Breast Neoplasms* / chemically induced
  • Breast Neoplasms* / radiotherapy
  • Female
  • Humans
  • Maytansine* / adverse effects
  • Receptor, ErbB-2
  • Trastuzumab / adverse effects

Substances

  • Trastuzumab
  • Receptor, ErbB-2
  • Maytansine
  • Ado-Trastuzumab Emtansine