Exploratory analysis of HER2 status based on central and local testing results from the DESTINY-Gastric04 study.

K Kohei Shitara E Eric Van Cutsem (University Hospitals Gasthuisberg, Leuven, Belgium) L Lin Shen F Filippo Pietrantonio S Sara Lonardi M Mike R. Zou (Daiichi Sankyo, Inc., Basking Ridge, NJ) J Jennifer Lin (AbbVie, North Chicago, Illinois, United States) J John Allard (Daiichi Sankyo, Inc., Basking Ridge, NJ) H Holly Hilton (Daiichi Sankyo, Inc., Basking Ridge, NJ) S Sutan Wu (Daiichi Sankyo, Inc., Basking Ridge, NJ) X Xiaoyang Ma F Fabricio Souza (Daiichi Sankyo, Basking Ridge, NJ) Y Yoshihiko Yamasaki (Daiichi Sankyo, Inc., Basking Ridge, NJ) V Victor Gazdoiu (Daiichi Sankyo, Inc., Basking Ridge, NJ) A Aziz Zaanan (Department of Gastroenterology and Digestive Oncology, Paris-Cité University, Paris) M Mahmut Gümüş (Istanbul Medeniyet University, Istanbul, Turkey)

Abstract

434 Background: In the phase 3 DESTINY-Gastric04 study (NCT04704934), T-DXd significantly improved overall survival versus ramucirumab + paclitaxel as second-line treatment in patients (pts) with HER2-positive (HER2+) metastatic gastric cancer. Accurate determination of HER2+ status is crucial to reliably identify pts likely to benefit from T-DXd. Methods: In DESTINY-Gastric04, biopsies were obtained from pts after progression following prior trastuzumab-based therapy. HER2 status was determined by central testing using immunohistochemistry (IHC; Agilent HercepTest) and in situ hybridization (ISH; Agilent IQ-FISH) from first tissue screening in 2021 until a protocol amendment in 2023, and by central or local testing thereafter. We analyzed HER2 status based on central testing and evaluated concordance between local and central HER2 testing. HER2+ was defined as IHC 3+ or IHC 2+/ISH+. Results: Of 1088 pts who underwent tissue screening, 638 pts underwent main screening, and 494 pts were randomly assigned to the treatment arms. Of 833 pre-randomized subjects with central HER2 testing results, 68% were HER2+ with consistent rates in primary and metastatic tissue specimens (Table) and across laboratory locations. Retrospective central HER2 testing was done for 122 of 133 pts who were randomized in DESTINY-Gastric04 based on HER2+ status by local test. In these pts, positive percentage agreement (PPA) was ~80% regardless of biopsy site (Table). PPA was higher for specimens that were IHC 3+ vs IHC 2+/ISH+ by local test (91% [95% CI, 84%-96%] vs 43% [95% CI, 25%-63%]). Concordance between local and central HER2 status varied across assay types. Conclusions: Results support the use of existing HER2 assays to select pts with gastric cancer for second-line treatment when needed and suggest that both primary and metastatic tissue specimens may be suitable for HER2 testing. Clinical trial information: NCT04704934 . All cases Primary tissue Metastatic tissue Cases with central testing results n = 833 n = 550 n = 283 HER2+, n (%) 564 (68) 366 (67) 198 (70) IHC 3+ 488 (59) 323 (59) 165 (58) IHC 2+/ISH+ 76 (9) 43 (8) 33 (12) Cases with local and central testing results (retrospective) n = 122 n = 82 n = 40 PPA (95% CI), % 80 (71-86) 79 (69-87) 80 (64-91)

Article Details

Volume / Issue Vol. 44, Issue 2_suppl
Published January 10, 2026
Pages 434-434
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (16)

K

Kohei Shitara

E

Eric Van Cutsem

University Hospitals Gasthuisberg, Leuven, Belgium

L

Lin Shen

F

Filippo Pietrantonio

S

Sara Lonardi

M

Mike R. Zou

Daiichi Sankyo, Inc., Basking Ridge, NJ

J

Jennifer Lin

AbbVie, North Chicago, Illinois, United States

J

John Allard

Daiichi Sankyo, Inc., Basking Ridge, NJ

H

Holly Hilton

Daiichi Sankyo, Inc., Basking Ridge, NJ

S

Sutan Wu

Daiichi Sankyo, Inc., Basking Ridge, NJ

X

Xiaoyang Ma

F

Fabricio Souza

Daiichi Sankyo, Basking Ridge, NJ

Y

Yoshihiko Yamasaki

Daiichi Sankyo, Inc., Basking Ridge, NJ

V

Victor Gazdoiu

Daiichi Sankyo, Inc., Basking Ridge, NJ

A

Aziz Zaanan

Department of Gastroenterology and Digestive Oncology, Paris-Cité University, Paris

M

Mahmut Gümüş

Istanbul Medeniyet University, Istanbul, Turkey