Biomarker-Stratified Phase II Trial of Trastuzumab Rezetecan in Advanced Salivary Gland Carcinoma Across Cohorts With High and Low Human Epidermal Growth Factor Receptor 2 Expression

G Guang-Liang Chen (Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China) Y Yanjing Guo X Xin Liu Y Ya'nan Yang (School of Materials Science and Engineering Harbin Institute of Technology (Weihai) Weihai 264209 China) Y Youzhou Sang (Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China) X Xueguan Lu (Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China) S Si Sun X Xiao Shi Y Yan Zhang T Tong-Zhen Chen (Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China) N Ning Qu (Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China) D Duo Wen X Xiao-Shuang Niu (Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China) S Shu Dong (Department of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai, China) Y Yu Wang Y Yulong Wang (State Key Laboratory of High Pressure and Superhard Materials, College of Physics) J Jiachen Wang L Lu Zhang C Chaosu Hu (Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China) Q Qinghai Ji (Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China) D Dongmei ji

Abstract

PURPOSE Systemic treatment options for advanced salivary gland carcinoma (SGC) are limited, and prospective data for human epidermal growth factor receptor 2 (HER2)–directed therapy remain sparse, particularly in HER2-low disease. We evaluated trastuzumab rezetecan (SHR-A1811), a HER2-directed antibody-drug conjugate, in prospectively defined HER2-high and HER2-low cohorts. PATIENTS AND METHODS In this phase II trial, patients with unresectable locally advanced or recurrent/metastatic SGC were enrolled in separate HER2-high (immunohistochemistry [IHC] 3+ or IHC 2+/in situ hybridization [ISH]+) and HER2-low (IHC 1+ or IHC 2+/ISH–) cohorts. Each cohort was independently evaluated using Simon's optimal two-stage design. SHR-A1811 was administered intravenously once every 3 weeks at a recommended starting dose of 4.8 mg/kg. The primary end point was confirmed objective response rate (ORR) per RECIST version 1.1. RESULTS Forty-six patients were enrolled and treated, including 24 in the HER2-high cohort and 22 in the HER2-low cohort. The median follow-up was 21.9 months (95% CI, 16.9 to 26.9) and 11.3 months (95% CI, 6.9 to 15.7), respectively. The confirmed ORR was 91.7% (95% CI, 73.0 to 99.0), including four complete responses, in the HER2-high cohort and 45.5% (95% CI, 24.4 to 67.8) in the HER2-low cohort. Median progression-free survival (PFS) and overall survival (OS) were not reached in the HER2-high cohort. In the HER2-low cohort, the median PFS was 12.7 months and the median OS was 21.3 months. Grade 3 or higher treatment-related adverse events occurred in 41.3% of patients, most commonly neutrophil count decreased (32.6%). Interstitial lung disease occurred in 6.5% of patients, all grade 1. No treatment-related deaths occurred. CONCLUSION SHR-A1811 showed high antitumor activity in HER2-high SGC and promising activity in HER2-low SGC, with a manageable safety profile.

Article Details

Volume / Issue Vol. 1, Issue 1
Published August 11, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (21)

G

Guang-Liang Chen

Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China

Y

Yanjing Guo

X

Xin Liu

Y

Ya'nan Yang

School of Materials Science and Engineering Harbin Institute of Technology (Weihai) Weihai 264209 China

Y

Youzhou Sang

Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China

X

Xueguan Lu

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China

S

Si Sun

X

Xiao Shi

Y

Yan Zhang

T

Tong-Zhen Chen

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China

N

Ning Qu

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China

D

Duo Wen

X

Xiao-Shuang Niu

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China

S

Shu Dong

Department of Integrative Oncology, Fudan University Shanghai Cancer Center, Shanghai, China

Y

Yu Wang

Y

Yulong Wang

State Key Laboratory of High Pressure and Superhard Materials, College of Physics

J

Jiachen Wang

L

Lu Zhang

C

Chaosu Hu

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China

Q

Qinghai Ji

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China

D

Dongmei ji