ASCENT
Regimen
- Experimental
- Sacituzumab govitecan-hziy 10 mg/kg IV D1, D8 Q3W until progression or toxicity.
- Control
- Single-agent treatment of physician's choice: eribulin, vinorelbine, capecitabine, or gemcitabine.
Population
Metastatic triple-negative breast cancer (excluding brain metastases in primary analysis) previously treated with >=2 prior lines of chemotherapy including a taxane.
Key finding
ASCENT established sacituzumab govitecan as standard of care in pretreated metastatic TNBC (NCCN category 1 preferred >=2L; FDA approved April 2021). First TROP2 ADC with OS benefit in any tumor.
Source: PMID 33882206
Timeline
- Publication: 2021 Apr 22
Guideline citations
- NCCN BREAST