General Session 1 (available abstracts)
Publication Number: GS1-01:
Peter Schmid, Javier Cortes, Rebecca Dent, et al.
The authors conclude that the EFS sensitivity analyzes revealed a robust and generally consistent treatment benefit of neoadjuvant pembro + chemotherapy followed by adjuvant pembro across a wide range of patient subgroups in previously untreated, non-metastatic triple-negative breast cancer.
Publication Number: GS1-02
Javier Cortes, David W. Cescon, Hope S. Rugo, et al.
The authors conclude that the study shows that CPS ≥ 10 is a reasonable cut-off to define the patient population with metastatic triple negative breast cancer who could benefit from Pembro + chemotherapy.
Publication Number: GS1-05
Ian Krop, Dejan Juric, Toshio Shimizu, et al.
The authors conclude that Dato-DXd has shown promise in antitumor activity in patients with previously treated advanced / metastatic triple negative breast cancer. The security profile is manageable.
Publication Number: GS1-06
Binghe Xu, Qingyuan Zhang, Xichun Hu, et al.
The authors conclude that compared with exemestane monotherapy, entinostat plus exemestane significantly improved progression-free survival in HR-positive, HER2-negative breast cancer that had progressed after previous endocrine therapy. The combination was generally tolerated and may offer important clinical benefit in these patients.
Publication Number: GS1-07
Michael Gnant, Amylou C Dueck, Sophie Frantal, et al.
The authors conclude that this analysis of the PALLAS study shows that adding 2 years of palbociclib to ongoing adjuvant endocrine therapy did not improve survival endpoints for patients with HR + / HER2-eBC stage II-III.
Publication Number: GS1-09
Inhibition of GPX4 induces preferential death of p53-mutant triple-negative breast cancer cells
William M Tahaney, Jing Qian, Reid Powell, et al.
With their studies, the authors provide the scientific basis for the further development of ferroptosis inducers for the targeted treatment of p53-mutated breast cancer. For more information see the abstract.