Abstract
Trastuzumab deruxtecan (T-DXd, DS-8201), an anti-HER2 antibody-drug conjugate, has shown significant clinical benefits in HER2+ metastatic breast cancer patients. In the phase 2 DESTINY-Breast01 trial, T-DXd demonstrated an objective response of 60.9% and median progression-free survival of 16.4 months, laying the foundation for accelerated approval in HER2+ metastatic breast cancer patients who have received two or more prior anti-HER2-based regimens in the metastatic setting. Moreover, T-DXd exhibited promising antitumor efficacy against HER2-low-expressing metastatic breast cancer. Its distinctive side effect was pneumonitis, with a 13.6% incidence. It is approved in the US with boxed warnings for interstitial lung disease and embryo-fetal toxicity. This review focuses on preclinical, pharmacokinetic and pharmacodynamic data on T-DXd and clinical evidence of its antitumor activity (both as monotherapy and in combination) and tolerability in metastatic breast cancer.
| Original language | English |
|---|---|
| Pages (from-to) | 7-19 |
| Number of pages | 13 |
| Journal | Future Oncology |
| Volume | 18 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2022 |
| Externally published | Yes |
Keywords
- breast cancer
- DESTINY-Breast01
- DS-8201
- HER2
- T-DXd
- trastuzumab deruxtecan