TY - JOUR
T1 - Sacituzumab govitecan as second-line treatment for metastatic triple-negative breast cancer-phase 3 ASCENT study subanalysis
AU - Carey, Lisa A
AU - Loirat, Delphine
AU - Punie, Kevin
AU - Bardia, Aditya
AU - Diéras, Véronique
AU - Dalenc, Florence
AU - Diamond, Jennifer R
AU - Fontaine, Christel
AU - Wang, Grace
AU - Rugo, Hope S
AU - Hurvitz, Sara A
AU - Kalinsky, Kevin
AU - O'Shaughnessy, Joyce
AU - Loibl, Sibylle
AU - Gianni, Luca
AU - Piccart, Martine
AU - Zhu, Yanni
AU - Delaney, Rosemary
AU - Phan, See
AU - Cortés, Javier
N1 - © 2022. The Author(s).
PY - 2022/6/9
Y1 - 2022/6/9
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85131747486&partnerID=8YFLogxK
U2 - 10.1038/s41523-022-00439-5
DO - 10.1038/s41523-022-00439-5
M3 - Article
C2 - 35680967
VL - 8
SP - 1
EP - 72
JO - Breast Cancer
JF - Breast Cancer
SN - 1340-6868
IS - 1
M1 - 72
ER -