Membrane-specific HER2 expression by artificial intelligence-based quantitative scoring for prediction of efficacy of trastuzumab deruxtecan in biliary tract cancer (HERB trial): Exploratory analysis of a multicenter, single arm, phase II trial.

M Mitsuho Imai (Translational Research Supporting Office, National Cancer Center Hospital East, Kashiwa, Japan) C Chigusa Morizane W Woochan Hwang (7Lunit Inc., Seoul, Korea) A Akihiro Ohba (Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Sunto-Gun, Japan) Y Yasuyuki Kawamoto Y Yoshito Komatsu M Makoto Ueno S Satoshi Kobayashi M Masafumi Ikeda M Mitsuhito Sasaki (Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan) N Nobuyoshi Hiraoka H Hiroshi Yoshida A Aya Kuchiba R Ryo Sadachi (Clinical Research Support Office, National Cancer Center Hospital, Tokyo, Japan) K Kenichi Nakamura (National Cancer Center Hospital, Tokyo, Japan) N Naoko Matsui (Department of Stem Cell Transplantation, National Cancer Center, Tokyo, Japan) C Chang Ho Ahn (Lunit Inc., Seoul, South Korea) C Chan-Young Ock Y Yoshiaki Nakamura T Takayuki Yoshino (National Cancer Center Hospital East, Kashiwa, Japan)

Abstract

4097 Background: Trastuzumab deruxtecan (T-DXd) showed promising results in patients with HER2-positive biliary tract cancer (BTC). With T-DXd's expanding indication into HER2-low cancers, quantitative Artificial Intelligence (AI)-based scoring of HER2 expression at the cellular level becomes increasingly important. This study investigated whether the intensity and subcellular pattern of HER2 staining would correlate with response to T-DXd. Methods: HER2 immunohistochemistry (IHC) whole slide images from the phase II HERB trial were analyzed. These participants had unresectable or recurrent BTC refractory or intolerant to gemcitabine-containing regimen and received T-DXd based on confirmed HER2-positive or low status. Lunit SCOPE universal IHC, a deep learning based IHC analyzer, was used to provide cell level classes (AI-H0, H1+, H2+, H3+) and continuous scoring of HER2 staining intensities of subcellular compartments (membrane, cytoplasm and nucleus) for each tumor cell. Membrane specificity was calculated for each cell as the ratio of membrane intensity to the sum of all three subcellular compartments. Results: The 29 patients analyzed showed continuous improvement in response rates with an increasing proportion of AI-H3+ cells. The ORR was 37.5%, 42.9% and 50.0% for patients with more than 10%, 25%, and 50% of tumor cells classified as AI-H3+, respectively. The HER2 intense cohort (n=4), defined by tumors with over 50% of tumor cells classified as AI-H3+, had a significantly better PFS (HR 0.15, p<0.05) and OS (HR 0.10, p<0.05) compared to the rest of the treatment group. The high membrane specificity group defined by ≥80% of tumor cells with membrane specificity ≥0.4 (N=6) had a confirmed ORR of 50%. These patients also demonstrated significantly longer PFS (HR 0.30, p<0.05) and OS (HR 0.27, p<0.05). The six cases identified by membrane specificity included all four cases of the HER2 intense cohort and two more cases, showing improved sensitivity in identifying likely responders. Conclusions: AI based quantification of HER2 intensity and membrane specificity was predictive of therapeutic response to T-DXd in HER2 expressing BTC. Membrane specificity analysis was more sensitive in identifying exceptional responders compared to intensity alone. Confirmed response and survival based on AI defined biomarkers. By AI-H3+ proportion By AI-MB specific cell proportion < 50% ≥ 50% < 80% ≥ 80% Sample size 25 4 23 6 ORR, % 28.0 50.0 26.1 50.0 mPFS 4.21 (2.83-4.40) 11.04 (5.68-12.91) 4.21 (2.83-4.40) 11.04 (1.45-12.91) HR (95% CI, p-value) REF 0.15 (0.03-0.67, <0.05) REF 0.30 (0.10-0.92, <0.05) mOS 7.00 (4.37-8.94) NR (5.68-NR) 7.00 (4.27-8.94) NR (9.63-NR) HR (95% CI, p-value) REF 0.10 (0.01-0.79, <0.05) REF 0.27 (0.08-0.93, <0.05)

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 4097-4097
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

M

Mitsuho Imai

Translational Research Supporting Office, National Cancer Center Hospital East, Kashiwa, Japan

C

Chigusa Morizane

W

Woochan Hwang

7Lunit Inc., Seoul, Korea

A

Akihiro Ohba

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Sunto-Gun, Japan

Y

Yasuyuki Kawamoto

Y

Yoshito Komatsu

M

Makoto Ueno

S

Satoshi Kobayashi

M

Masafumi Ikeda

M

Mitsuhito Sasaki

Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Kashiwa, Japan

N

Nobuyoshi Hiraoka

H

Hiroshi Yoshida

A

Aya Kuchiba

R

Ryo Sadachi

Clinical Research Support Office, National Cancer Center Hospital, Tokyo, Japan

K

Kenichi Nakamura

National Cancer Center Hospital, Tokyo, Japan

N

Naoko Matsui

Department of Stem Cell Transplantation, National Cancer Center, Tokyo, Japan

C

Chang Ho Ahn

Lunit Inc., Seoul, South Korea

C

Chan-Young Ock

Y

Yoshiaki Nakamura

T

Takayuki Yoshino

National Cancer Center Hospital East, Kashiwa, Japan