ASTEFANIA: adjuvant ado-trastuzumab emtansine and atezolizumab for high-risk, HER2-positive breast cancer

Future Oncol. 2022 Oct;18(32):3563-3572. doi: 10.2217/fon-2022-0485. Epub 2022 Nov 16.

Abstract

There is a strong rationale for combining HER2-targeted therapies with cancer immunotherapy to increase efficacy in breast cancer, particularly in the early-stage setting, where the immune system has not been weakened by heavy pretreatment. ASTEFANIA aims to evaluate the efficacy of adjuvant atezolizumab in combination with ado-trastuzumab emtansine in patients with high-risk, HER2-positive early breast cancer and residual disease following HER2-based neoadjuvant therapy. Eligible patients will be randomized to receive ado-trastuzumab emtansine in combination with either atezolizumab or placebo for 14 cycles within 12 weeks of primary surgery. The primary outcome is invasive disease-free survival and secondary outcomes include additional efficacy end points, safety and pharmacokinetics. The study plans to enroll 1700 patients across 32 counties. Clinical Trial Registration: NCT04873362 (ClinicalTrials.gov).

Keywords: HER2; ado-trastuzumab emtansine; atezolizumab; cancer immunotherapy; early breast cancer.

Publication types

  • Clinical Trial Protocol

MeSH terms

  • Adjuvants, Immunologic / therapeutic use
  • Ado-Trastuzumab Emtansine / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Breast Neoplasms*
  • Female
  • Humans
  • Randomized Controlled Trials as Topic
  • Receptor, ErbB-2
  • Trastuzumab / adverse effects

Substances

  • Ado-Trastuzumab Emtansine
  • atezolizumab
  • Trastuzumab
  • Receptor, ErbB-2
  • Adjuvants, Immunologic

Associated data

  • ClinicalTrials.gov/NCT04873362

Grants and funding