ASTEFANIA: adjuvant ado-trastuzumab emtansine and atezolizumab for high-risk, HER2-positive breast cancer.
Sara Alsterlind HurvitzThomas BachelotGiampaolo BianchiniNadia HarbeckSherene LoiYeon Hee ParkAleix PratLeslie GilhamThomas BouletNino GochitashviliEstefania MonturusChiara LambertiniBeatrice NyawiraAdam KnottEleonora RestucciaPeter SchmidPublished in: Future oncology (London, England) (2022)
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).
Keyphrases
- positive breast cancer
- early stage
- end stage renal disease
- metastatic breast cancer
- clinical trial
- newly diagnosed
- ejection fraction
- chronic kidney disease
- peritoneal dialysis
- epidermal growth factor receptor
- open label
- minimally invasive
- randomized controlled trial
- coronary artery disease
- patient reported outcomes
- phase iii
- rectal cancer
- acute coronary syndrome
- adipose tissue
- study protocol
- young adults
- atrial fibrillation
- metabolic syndrome
- bone marrow
- weight loss
- percutaneous coronary intervention
- insulin resistance