Study design for DESTINY-Breast Respond HER2-low Europe: T-DXd in patients with HER2-low advanced breast cancer.
Valentina GuarneriJosé Luís Passos CoelhoFrancois P DuhouxDaniel EgleJosé Angel García-SaenzFrédérique Penault-LlorcaKatri SelanderHans WildiersKhalil ZamanPetra LaeisMarkus LucernaJean-Yves PiergaPublished in: Future oncology (London, England) (2024)
Trastuzumab deruxtecan (T-DXd) is approved for the treatment of human epidermal growth factor receptor 2 (HER2)-low metastatic breast cancer (mBC). Results on T-DXd treatment in HER2-low mBC have so far been limited to clinical trials. DESTINY-Breast Respond HER2-low Europe (NCT05945732) is a multi-center, multi-country, observational, prospective, non-interventional study planning to enroll 1350 patients from 216 sites receiving T-DXd or conventional chemotherapy as their routine clinical care for advanced stage breast cancer in 12 European countries. This non-interventional study will provide real-world insight into T-DXd treatment for HER2-low mBC with data on effectiveness, safety and tolerability, patient-reported outcomes, treatment patterns, geriatric health status and HER2 testing. This will be beneficial for improving guidance to maximize patient treatment benefit.
Keyphrases
- epidermal growth factor receptor
- patient reported outcomes
- randomized controlled trial
- healthcare
- systematic review
- squamous cell carcinoma
- metastatic breast cancer
- machine learning
- advanced non small cell lung cancer
- combination therapy
- tyrosine kinase
- case report
- rectal cancer
- quality improvement
- smoking cessation
- radiation therapy
- study protocol
- induced pluripotent stem cells