SOLTI-1805 TOT-HER3 Study Concept: A Window-of-Opportunity Trial of Patritumab Deruxtecan, a HER3 Directed Antibody Drug Conjugate, in Patients With Early Breast Cancer.

dc.contributor.authorPascual, Tomás
dc.contributor.authorOliveira, Mafalda
dc.contributor.authorCiruelos, Eva
dc.contributor.authorBellet Ezquerra, Meritxell
dc.contributor.authorSaura, Cristina
dc.contributor.authorGavilá, Joaquin
dc.contributor.authorPernas, Sonia
dc.contributor.authorMuñoz, Montserrat
dc.contributor.authorVidal, Maria J
dc.contributor.authorMargelí Vila, Mireia
dc.contributor.authorCejalvo, Juan M
dc.contributor.authorGonzález-Farré, Blanca
dc.contributor.authorEspinosa-Bravo, Martin
dc.contributor.authorCruz, Josefina
dc.contributor.authorSalvador-Bofill, Francisco Javier
dc.contributor.authorGuerra, Juan Antonio
dc.contributor.authorLuna Barrera, Ana María
dc.contributor.authorArumi de Dios, Miriam
dc.contributor.authorEsker, Stephen
dc.contributor.authorFan, Pang-Dian
dc.contributor.authorMartínez-Sáez, Olga
dc.contributor.authorVillacampa, Guillermo
dc.contributor.authorParé, Laia
dc.contributor.authorFerrero-Cafiero, Juan M
dc.contributor.authorVillagrasa, Patricia
dc.contributor.authorPrat, Aleix
dc.date.accessioned2025-01-07T15:29:56Z
dc.date.available2025-01-07T15:29:56Z
dc.date.issued2021-04-23
dc.description.abstractBackground: 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.
dc.identifier.doi10.3389/fonc.2021.638482
dc.identifier.issn2234-943X
dc.identifier.pmcPMC8103897
dc.identifier.pmid33968735
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC8103897/pdf
dc.identifier.unpaywallURLhttps://www.frontiersin.org/articles/10.3389/fonc.2021.638482/pdf
dc.identifier.urihttps://hdl.handle.net/10668/27194
dc.journal.titleFrontiers in oncology
dc.journal.titleabbreviationFront Oncol
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen del Rocío
dc.page.number638482
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBreast Cancer
dc.subjectCelTIL Score
dc.subjectERBB3
dc.subjectHER3
dc.subjectHER3-DXd
dc.subjectU3-1402
dc.subjectpatritumab deruxtecan
dc.titleSOLTI-1805 TOT-HER3 Study Concept: A Window-of-Opportunity Trial of Patritumab Deruxtecan, a HER3 Directed Antibody Drug Conjugate, in Patients With Early Breast Cancer.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number11

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