Abstract LB010: First-line (1L) trastuzumab deruxtecan (T-DXd) regimens in advanced HER2-positive (HER2+) gastric cancer (GC), gastroesophageal junction adenocarcinoma (GEJA), or esophageal adenocarcinoma (EA): Exploratory analysis of baseline HER2-r

Abstract Background: DG-03 Part 2 showed promising antitumor activity for 1L T-DXd regimens in advanced HER2+ GCs. We report concordance rates between local and central HER2 IHC results, and ORRs according to baseline HER2-related biomarkers, in DG-03 Part 2. Methods: DG-03 (NCT04379596) is a Phase 1b/2, open-label, multipart trial. In Part 2, patients (pts) with previously untreated advanced HER2+ (IHC 3+ or IHC 2+/ISH+; local test) GC/GEJA/EA were enrolled across six arms and received either trastuzumab + chemotherapy (CT; fluoropyrimidine [FP; 5-fluorouracil or capecitabine] + cisplatin/oxaliplatin), T-DXd 6.4 mg/kg, T-DXd 6.4 mg/kg + FP, T-DXd 6.4 mg/kg + FP + pembrolizumab (pembro), T-DXd 6.4 mg/kg + pembro, or T-DXd 5.4 mg/kg + FP + pembro. Confirmed investigator-assessed ORRs were reported by local and central HER2 IHC/ISH status (HercepTest for central IHC) and by plasma (GuardantOMNI) and tumoral (FoundationOne CDx) HER2 (ERBB2) amplification (amp). Results: As of Feb 28, 2025, 230 pts were enrolled; 229 received treatment. Overall (n/N), 80% (160/199) of HER2+ (IHC 3+ or IHC 2+/ISH+) GCs by local test were centrally scored as HER2+; 86% (143/166) and 52% (17/33) of IHC 3+ and IHC 2+/ISH+ GCs by local test were centrally scored as HER2+, respectively (missing/unknown data for n=2 local IHC, n=1 local ISH, n=3 central ISH, and n=24 central IHC results). Baseline HER2-related biomarker analyses are in the Table. Conclusions: Concordance results were broadly consistent with prior studies in GC. Elevated baseline HER2 IHC expression and HER2 amp were generally associated with higher ORRs for pts with HER2+ GCs treated with 1L T-DXd regimens, versus those with lower HER2 expression and/or without amplified HER2. Data provide further evidence of antitumor activity for 1L T-DXd combinations in HER2+ GCs. Citation Format: Yelena Y. Janjigian, Hanneke van Laarhoven, Sun Young Rha, Vadim Kozlov, Keun-Wook Lee, Do-Youn Oh, Adriano Gravina, Min-Hee Ryu, Liane Rapatoni, Luís Antunes, Filippo Pietrantonio, Hirokazu Shoji, Ralf-Dieter Hofheinz, Maxime Chénard-Poirier, Li-Tzong Chen, Aleksandr Vasiliev, Svetlana Kutukova, Arthur W. Lambert, Kun Yu, Megan Scott, Roy Rabbie, Jeeyun Lee. First-line (1L) trastuzumab deruxtecan (T-DXd) regimens in advanced HER2-positive (HER2+) gastric cancer (GC), gastroesophageal junction adenocarcinoma (GEJA), or esophageal adenocarcinoma (EA): Exploratory analysis of baseline HER2-related biomarkers in DESTINY-Gastric03 (DG-03) Part 2 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(8_Suppl):Abstract nr LB010.

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Journal
Cancer Research
Published
2026-04-17
DOI
https://doi.org/10.1158/1538-7445.am2026-lb010
Primary Topic
HER2/EGFR in Cancer Research
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article

Abstract LB010: First-line (1L) trastuzumab deruxtecan (T-DXd) regimens in advanced HER2-positive (HER2+) gastric cancer (GC), gastroesophageal junction adenocarcinoma (GEJA), or esophageal adenocarcinoma (EA): Exploratory analysis of baseline HER2-r

Adriano Gravina, С. И. Кутукова, Liane Rapatoni, Yelena Y. Janjigian et al.
Cancer Research
HER2/EGFR in Cancer Research
article

Abstract LB010: First-line (1L) trastuzumab deruxtecan (T-DXd) regimens in advanced HER2-positive (HER2+) gastric cancer (GC), gastroesophageal junction adenocarcinoma (GEJA), or esophageal adenocarcinoma (EA): Exploratory analysis of baseline HER2-r

Adriano Gravina, С. И. Кутукова, Liane Rapatoni, Yelena Y. Janjigian, Luís Antunes, Vadim Kozlov, Roy Rabbie, Arthur W. Lambert, Maxime Chénard-Poirier, ALEKSANDR VASILIEV, Hanneke van Laarhoven, Jeeyun Lee, Keun-Wook Lee, Do-Youn Oh, Filippo Pietrantonio, Ralf-Dieter Hofheinz, Megan Scott, Sun Young Rha, Kun Yu, Li-Tzong Chen, Min-Hee Ryu, Hirokazu Shoji
article en

Abstract

Abstract Background: DG-03 Part 2 showed promising antitumor activity for 1L T-DXd regimens in advanced HER2+ GCs. We report concordance rates between local and central HER2 IHC results, and ORRs according to baseline HER2-related biomarkers, in DG-03 Part 2. Methods: DG-03 (NCT04379596) is a Phase 1b/2, open-label, multipart trial. In Part 2, patients (pts) with previously untreated advanced HER2+ (IHC 3+ or IHC 2+/ISH+; local test) GC/GEJA/EA were enrolled across six arms and received either trastuzumab + chemotherapy (CT; fluoropyrimidine [FP; 5-fluorouracil or capecitabine] + cisplatin/oxaliplatin), T-DXd 6.4 mg/kg, T-DXd 6.4 mg/kg + FP, T-DXd 6.4 mg/kg + FP + pembrolizumab (pembro), T-DXd 6.4 mg/kg + pembro, or T-DXd 5.4 mg/kg + FP + pembro. Confirmed investigator-assessed ORRs were reported by local and central HER2 IHC/ISH status (HercepTest for central IHC) and by plasma (GuardantOMNI) and tumoral (FoundationOne CDx) HER2 (ERBB2) amplification (amp). Results: As of Feb 28, 2025, 230 pts were enrolled; 229 received treatment. Overall (n/N), 80% (160/199) of HER2+ (IHC 3+ or IHC 2+/ISH+) GCs by local test were centrally scored as HER2+; 86% (143/166) and 52% (17/33) of IHC 3+ and IHC 2+/ISH+ GCs by local test were centrally scored as HER2+, respectively (missing/unknown data for n=2 local IHC, n=1 local ISH, n=3 central ISH, and n=24 central IHC results). Baseline HER2-related biomarker analyses are in the Table. Conclusions: Concordance results were broadly consistent with prior studies in GC. Elevated baseline HER2 IHC expression and HER2 amp were generally associated with higher ORRs for pts with HER2+ GCs treated with 1L T-DXd regimens, versus those with lower HER2 expression and/or without amplified HER2. Data provide further evidence of antitumor activity for 1L T-DXd combinations in HER2+ GCs. Citation Format: Yelena Y. Janjigian, Hanneke van Laarhoven, Sun Young Rha, Vadim Kozlov, Keun-Wook Lee, Do-Youn Oh, Adriano Gravina, Min-Hee Ryu, Liane Rapatoni, Luís Antunes, Filippo Pietrantonio, Hirokazu Shoji, Ralf-Dieter Hofheinz, Maxime Chénard-Poirier, Li-Tzong Chen, Aleksandr Vasiliev, Svetlana Kutukova, Arthur W. Lambert, Kun Yu, Megan Scott, Roy Rabbie, Jeeyun Lee. First-line (1L) trastuzumab deruxtecan (T-DXd) regimens in advanced HER2-positive (HER2+) gastric cancer (GC), gastroesophageal junction adenocarcinoma (GEJA), or esophageal adenocarcinoma (EA): Exploratory analysis of baseline HER2-related biomarkers in DESTINY-Gastric03 (DG-03) Part 2 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(8_Suppl):Abstract nr LB010.

Cancer ResearchVol. 86(8_Supplement)
Memorial Sloan Kettering Cancer Center (US), Kaohsiung Medical University (TW), Cancer Research Institute (US), German Cancer Research Center (DE), Yonsei University (KR), Heidelberg University (DE), First Pavlov State Medical University of St. Petersburg (RU), Asan Medical Center (KR), Samsung Medical Center (KR), Seoul National University Hospital (KR), Seoul National University Bundang Hospital (KR), Universidade Federal de Santa Maria (BR), National Cancer Center (US), Hospital Universitário de Santa Maria (BR), AstraZeneca (South Korea) (KR), Centre hospitalier universitaire de Québec (CA), Novosibirsk Tuberculosis Research Institute (RU), AstraZeneca (Singapore) (SG), AstraZeneca (Brazil) (BR), City Clinical Oncology Center (RU), AstraZeneca (Poland) (PL), City Clinical Hospital No 31 (RU), Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" (IT), National Cancer Center Hospital East (JP), AstraZeneca (Spain) (ES), AstraZeneca (United States) (US), Amsterdam University Medical Centers (NL), Clinics Hospital of Ribeirão Preto (BR), Fondazione IRCCS Istituto Nazionale dei Tumori (IT), Sungkyunkwan University (KR), University of Amsterdam (NL)
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Openalex Percentile: Top 20%
HER2/EGFR in Cancer Research
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