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Sacituzumab govitecan as second-line treatment for metastatic triple-negative breast cancer—phase 3 ASCENT study subanalysis
- Carey, Lisa A;
- Loirat, Delphine;
- Punie, Kevin;
- Bardia, Aditya;
- Diéras, Véronique;
- Dalenc, Florence;
- Diamond, Jennifer R;
- Fontaine, Christel;
- Wang, Grace;
- Rugo, Hope S;
- Hurvitz, Sara A;
- Kalinsky, Kevin;
- O’Shaughnessy, Joyce;
- Loibl, Sibylle;
- Gianni, Luca;
- Piccart, Martine;
- Zhu, Yanni;
- Delaney, Rosemary;
- Phan, See;
- Cortés, Javier
Published Web Location
https://doi.org/10.1038/s41523-022-00439-5Abstract
Patients with triple-negative breast cancer (TNBC) who relapse early after (neo)adjuvant chemotherapy have more aggressive disease. In the ASCENT trial, sacituzumab govitecan (SG), an antibody-drug conjugate composed of an anti-Trop–2 antibody coupled to SN-38 via a hydrolyzable linker, improved outcomes over single-agent chemotherapy of physician’s choice (TPC) in metastatic TNBC (mTNBC). Of 468 patients without known baseline brain metastases, 33/235 vs 32/233 patients (both 14%) in the SG vs TPC arms, respectively, received one line of therapy in the metastatic setting and experienced disease recurrence ≤12 months after (neo)adjuvant chemotherapy. SG prolonged progression-free survival (median 5.7 vs 1.5 months [HR, 0.41; 95% CI, 0.22–0.76]) and overall survival (median 10.9 vs 4.9 months [HR, 0.51; 95% CI, 0.28–0.91]) vs TPC, with a manageable safety profile in this subgroup consistent with the overall population. In this second-line setting, as with later-line therapy, SG improved survival over conventional chemotherapy for patients with mTNBC.
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