TY - JOUR
T1 - SOLTI-1805 TOT-HER3 Study Concept
T2 - A Window-of-Opportunity Trial of Patritumab Deruxtecan, a HER3 Directed Antibody Drug Conjugate, in Patients With Early Breast Cancer
AU - Pascual, Tomás
AU - Oliveira, Mafalda
AU - Ciruelos, Eva
AU - Bellet Ezquerra, Meritxell
AU - Saura, Cristina
AU - Gavilá, Joaquin
AU - Pernas, Sonia
AU - Muñoz, Montserrat
AU - Vidal, Maria J
AU - Margelí Vila, Mireia
AU - Cejalvo, Juan M
AU - González-Farré, Blanca
AU - Espinosa-Bravo, Martin
AU - Cruz, Josefina
AU - Salvador-Bofill, Francisco Javier
AU - Guerra, Juan Antonio
AU - Luna Barrera, Ana María
AU - Arumi de Dios, Miriam
AU - Esker, Stephen
AU - Fan, Pang-Dian
AU - Martínez-Sáez, Olga
AU - Villacampa, Guillermo
AU - Paré, Laia
AU - Ferrero-Cafiero, Juan M
AU - Villagrasa, Patricia
AU - Prat, Aleix
N1 - Copyright © 2021 Pascual, Oliveira, Ciruelos, Bellet Ezquerra, Saura, Gavilá, Pernas, Muñoz, Vidal, Margelí Vila, Cejalvo, González-Farré, Espinosa-Bravo, Cruz, Salvador-Bofill, Guerra, Luna Barrera, Arumi de Dios, Esker, Fan, Martínez-Sáez, Villacampa, Paré, Ferrero-Cafiero, Villagrasa and Prat.
PY - 2021
Y1 - 2021
N2 - Background: Preclinical data support a key role for the human epidermal growth factor receptor 3 (HER3) pathway in hormone receptor (HR)-positive breast cancer. Recently, new HER3 directed antibody drug conjugates have shown activity in breast cancer. Given the need to better understand the molecular biology, tumor microenvironment, and mechanisms of drug resistance in breast cancer, we designed this window-of-opportunity study with the HER3 directed antibody drug conjugate patritumab deruxtecan (HER3-DXd; U3-1402). Trial Design: Based on these data, a prospective, multicenter, single-arm, window-of-opportunity study was designed to evaluate the biological effect of patritumab deruxtecan in the treatment of naïve patients with HR-positive/HER2-negative early breast cancer whose primary tumors are ≥1 cm by ultrasound evaluation. Patients will be enrolled in four cohorts according to the mRNA-based ERBB3 expression by central assessment. The primary endpoint is a CelTIL score after one single dose. A translational research plan is also included to provide biological information and to evaluate secondary and exploratory objectives of the study. Trial Registration Number: EudraCT 2019-004964-23; NCT number: NCT04610528.
AB - Background: Preclinical data support a key role for the human epidermal growth factor receptor 3 (HER3) pathway in hormone receptor (HR)-positive breast cancer. Recently, new HER3 directed antibody drug conjugates have shown activity in breast cancer. Given the need to better understand the molecular biology, tumor microenvironment, and mechanisms of drug resistance in breast cancer, we designed this window-of-opportunity study with the HER3 directed antibody drug conjugate patritumab deruxtecan (HER3-DXd; U3-1402). Trial Design: Based on these data, a prospective, multicenter, single-arm, window-of-opportunity study was designed to evaluate the biological effect of patritumab deruxtecan in the treatment of naïve patients with HR-positive/HER2-negative early breast cancer whose primary tumors are ≥1 cm by ultrasound evaluation. Patients will be enrolled in four cohorts according to the mRNA-based ERBB3 expression by central assessment. The primary endpoint is a CelTIL score after one single dose. A translational research plan is also included to provide biological information and to evaluate secondary and exploratory objectives of the study. Trial Registration Number: EudraCT 2019-004964-23; NCT number: NCT04610528.
U2 - 10.3389/fonc.2021.638482
DO - 10.3389/fonc.2021.638482
M3 - Article
C2 - 33968735
SN - 2234-943X
VL - 11
SP - 638482
JO - Frontiers in Oncology
JF - Frontiers in Oncology
ER -