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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

医学 曲妥珠单抗 队列 内科学 肿瘤科 临床终点 免疫组织化学 前瞻性队列研究 涎腺癌 临床研究阶段 不利影响 表皮生长因子受体 人表皮生长因子受体2 癌症 化疗 唾液腺 病理 胃肠病学 间质性肺病 存活率 回顾性队列研究 靶向治疗 表皮生长因子 临床试验 肺癌 实体瘤疗效评价标准 队列研究 总体生存率
作者
Guangliang Chen,Yanjing Guo,Xin Liu,Ya'nan Yang,Youzhou Sang,Xueguan Lu,Si Sun,Xiao Shi,Yan Zhang,Tongzhen Chen,Ning Qu,Duo Wen,Xiao-shuang Niu,Shu Dong,Yu Wang,Yulong Wang,Jiachen Wang,Lu Zhang,Chaosu Hu,Qinghai Ji
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:: JCO2600671-JCO2600671
标识
DOI:10.1200/jco-26-00671
摘要

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.
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