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205P VERITAC update: Phase II study of ARV-471, a PROteolysis TArgeting Chimera (PROTAC) estrogen receptor (ER) degrader in ER+/human epidermal growth factor receptor 2 (HER2)- advanced breast cancer

Sara A. Hurvitz, Anne F. Schott, X. Cynthia, Rita Nanda, G. Zahrah, N. Hunter, Adrienne Tan, Melinda L. Telli, Jesús Anampa, R. Jeselsohn, Pamela N. Münster, Eric Zhi, R. Gedrich, C. Mather, Hyo S. Han, E.P. Hamilton

2023ESMO Open10 citationsDOIOpen Access PDF

Abstract

The oral PROTAC protein degrader ARV-471 binds and degrades wild-type (WT) and mutant ER. The phase II expansion (VERITAC) of a phase I/II study (NCT04072952) tested 2 ARV-471 doses (200 mg once daily [QD] and 500 mg QD) in heavily pretreated patients (pts) with ER+/HER2- advanced breast cancer. ARV-471 200 mg QD was selected as the phase III monotherapy dose based on comparable efficacy and favorable tolerability vs 500 mg QD and robust ER degradation (data cutoff: Jun 6, 2022). We present updated data for ARV-471 200 mg QD after 5 additional months of follow-up.

Topics & Concepts

Chimera (genetics)Estrogen receptorCancer researchBreast cancerProteolysisEpidermal growth factor receptorMedicineReceptorHuman Epidermal Growth Factor Receptor 2CancerInternal medicineOncologyBiologyGeneBiochemistryEnzymeProtein Degradation and InhibitorsAdvanced Breast Cancer TherapiesHER2/EGFR in Cancer Research
205P VERITAC update: Phase II study of ARV-471, a PROteolysis TArgeting Chimera (PROTAC) estrogen receptor (ER) degrader in ER+/human epidermal growth factor receptor 2 (HER2)- advanced breast cancer | Litcius