UCCL-IKF-AIO-STO-0124 NeoART—an international phase Ib/II platform trial investigating trastuzumab deruxtecan (T-DXd) combined with neoadjuvant chemotherapy for HER2-positive, resectable esophagogastric adenocarcinoma (EGA)

Background: Despite advances in the multimodal treatment of resectable esophagogastric adenocarcinoma (EGA), relapse rates remain high, resulting in a cure rate of <50%. Recently, perioperative durvalumab in combination with chemotherapy (ctx) has shown improved event-free survival in biomarker-unselected patients with resectable EGA. However, human epidermal growth factor receptor 2 (HER2)-targeted therapy has not yet been established as a treatment for this disease in the perioperative setting. While the combination of HER2-targeting antibodies and neoadjuvant ctx leads to an increased histopathological response rate, a survival benefit has not yet been demonstrated. Trastuzumab deruxtecan (T-DXd), a HER2-targeting antibody-drug conjugate, has demonstrated superior efficacy in second- and third-line treatment of metastatic HER2-positive EGA compared with chemotherapies, as well as high response rates when combined with ctx in the first-line setting. Aim: This study aims to evaluate the feasibility, safety, and activity of various neoadjuvant T-DXd-based combination regimens in patients with HER2-positive, locally advanced, resectable EGA. The primary endpoint is the feasibility rate across the different cohorts. Trial design: UCCL-IKF-NeoART is an international, open-label, non-randomized phase Ib/II platform trial evaluating T-DXd in sequential cohorts, each combining the drug with a different ctx regimen. Every cohort includes an initial safety run-in phase.

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Publication Details

Journal
ESMO Gastrointestinal Oncology
Published
2026-04-21
DOI
https://doi.org/10.1016/j.esmogo.2025.100256
Primary Topic
Esophageal Cancer Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

UCCL-IKF-AIO-STO-0124 NeoART—an international phase Ib/II platform trial investigating trastuzumab deruxtecan (T-DXd) combined with neoadjuvant chemotherapy for HER2-positive, resectable esophagogastric adenocarcinoma (EGA)

U.T. Hacker, A. Ilhan-Mutlu, C. Pauligk, T.O. Goetze et al.
ESMO Gastrointestinal Oncology
Esophageal Cancer Research and Treatment
article

UCCL-IKF-AIO-STO-0124 NeoART—an international phase Ib/II platform trial investigating trastuzumab deruxtecan (T-DXd) combined with neoadjuvant chemotherapy for HER2-positive, resectable esophagogastric adenocarcinoma (EGA)

U.T. Hacker, A. Ilhan-Mutlu, C. Pauligk, T.O. Goetze, G. Stocker, F. Lordick, S.-E. Al-Batran, S. Junge, R. Lordick Obermannová
article en

Abstract

Background: Despite advances in the multimodal treatment of resectable esophagogastric adenocarcinoma (EGA), relapse rates remain high, resulting in a cure rate of <50%. Recently, perioperative durvalumab in combination with chemotherapy (ctx) has shown improved event-free survival in biomarker-unselected patients with resectable EGA. However, human epidermal growth factor receptor 2 (HER2)-targeted therapy has not yet been established as a treatment for this disease in the perioperative setting. While the combination of HER2-targeting antibodies and neoadjuvant ctx leads to an increased histopathological response rate, a survival benefit has not yet been demonstrated. Trastuzumab deruxtecan (T-DXd), a HER2-targeting antibody-drug conjugate, has demonstrated superior efficacy in second- and third-line treatment of metastatic HER2-positive EGA compared with chemotherapies, as well as high response rates when combined with ctx in the first-line setting. Aim: This study aims to evaluate the feasibility, safety, and activity of various neoadjuvant T-DXd-based combination regimens in patients with HER2-positive, locally advanced, resectable EGA. The primary endpoint is the feasibility rate across the different cohorts. Trial design: UCCL-IKF-NeoART is an international, open-label, non-randomized phase Ib/II platform trial evaluating T-DXd in sequential cohorts, each combining the drug with a different ctx regimen. Every cohort includes an initial safety run-in phase.

ESMO Gastrointestinal OncologyVol. 12
Goethe University Frankfurt (DE), Masaryk University (CZ), Masaryk Memorial Cancer Institute (CZ), Institute of Clinical Cancer Research (DE), University Hospital Leipzig (DE), University Hospital Frankfurt (DE), Frankfurt Cancer Institute (DE), Medical University of Vienna (AT), Leipzig University (DE)
Falk Foundation, Amgen, Eli Lilly and Company, AstraZeneca, Sanofi, Gilead Sciences, Celgene, BeiGene, Incyte, Deutsche Forschungsgemeinschaft, Daiichi-Sankyo, Astellas Pharma, Deutsche Krebshilfe, Vifor Pharma, Servier, Ipsen, Daiichi Sankyo Europe
Partnerships for the goals
Openalex Percentile: Top 13%
Esophageal Cancer Research and Treatment
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