Phase Ib/II trial evaluates safety and activity of T-DXd with chemotherapy in HER2-positive EGA, indicating potential advancements in treatment.
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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Stocker et al. (2026) studied this question.
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