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<p>Advanced salivary gland carcinoma (SGC) lacking both human epidermal growth factor receptor 2 (HER2) and androgen receptor (AR) expression has limited treatment options. In this single-center, phase II trial, patients with recurrent/metastatic HER2-negative/AR-negative SGC received SHR-A1921, a TROP-2-directed antibody-drug conjugate, every 3 weeks until disease progression or unacceptable toxicity. The primary endpoint was objective response rate (ORR) per RECIST v1.1; secondary endpoints included progression-free survival (PFS), safety, and exploratory analyses of baseline TROP-2 expression by immunohistochemistry. As of August 1, 2025, 17 patients were treated and 15 were evaluable for efficacy, including 10 with non-adenoid cystic carcinoma (non-ACC) and 5 with adenoid cystic carcinoma (ACC). In non-ACC SGC, confirmed ORR was 20.0%, disease control rate was 80.0%, and clinical benefit rate was 60.0%. All patients with ACC achieved stable disease, with median PFS of 15.4 months. Treatment-related adverse events were manageable; oral mucositis was most common. No grade 4–5 treatment-related adverse events or treatment-related serious adverse events occurred; one patient discontinued treatment due to toxicity. Baseline TROP-2 expression was heterogeneous, with numerically higher H-scores in responders but no significant association with PFS. SHR-A1921 showed preliminary activity in non-ACC SGC and disease stabilization in ACC, supporting further evaluation in stratified cohorts. Trial registration: ClinicalTrials.gov, NCT05924256. Registered on June 29, 2023.</p>

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A Phase II study of SHR-A1921, a TROP2-targeted antibody–drug conjugate, in patients with recurrent or metastatic salivary gland carcinoma

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年5月13日

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  • Guang-Liang Chen,
  • Yanjing Guo,
  • Ya’nan Yang,
  • Youzhou Sang,
  • Si Sun,
  • Xin Liu,
  • Xin Zhou,
  • Chun-ying Sheng,
  • Xiayun He,
  • Jianfei Wang,
  • Rongliang Shi,
  • Yu Wang,
  • Qinghai Ji,
  • Dongmei Ji

摘要

Advanced salivary gland carcinoma (SGC) lacking both human epidermal growth factor receptor 2 (HER2) and androgen receptor (AR) expression has limited treatment options. In this single-center, phase II trial, patients with recurrent/metastatic HER2-negative/AR-negative SGC received SHR-A1921, a TROP-2-directed antibody-drug conjugate, every 3 weeks until disease progression or unacceptable toxicity. The primary endpoint was objective response rate (ORR) per RECIST v1.1; secondary endpoints included progression-free survival (PFS), safety, and exploratory analyses of baseline TROP-2 expression by immunohistochemistry. As of August 1, 2025, 17 patients were treated and 15 were evaluable for efficacy, including 10 with non-adenoid cystic carcinoma (non-ACC) and 5 with adenoid cystic carcinoma (ACC). In non-ACC SGC, confirmed ORR was 20.0%, disease control rate was 80.0%, and clinical benefit rate was 60.0%. All patients with ACC achieved stable disease, with median PFS of 15.4 months. Treatment-related adverse events were manageable; oral mucositis was most common. No grade 4–5 treatment-related adverse events or treatment-related serious adverse events occurred; one patient discontinued treatment due to toxicity. Baseline TROP-2 expression was heterogeneous, with numerically higher H-scores in responders but no significant association with PFS. SHR-A1921 showed preliminary activity in non-ACC SGC and disease stabilization in ACC, supporting further evaluation in stratified cohorts. Trial registration: ClinicalTrials.gov, NCT05924256. Registered on June 29, 2023.