ArticleNPJ precision oncology2026
A Phase II study of SHR-A1921, a TROP2-targeted antibody-drug conjugate, in patients with recurrent or metastatic salivary gland carcinoma.
Article in NPJ precision oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05924256 (A Phase II Study of Advanced Salivary Gland Carcinoma Based on Molecular Typing), which is not on this map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
A Phase II Study of Advanced Salivary Gland Carcinoma Based on Molecular Typing
Who cites it
2 citing papers in PubMed.
- Comprehensive analysis of antibody-drug conjugate (ADC) targets in adenoid cystic carcinoma: examining antigen expression in relation to clinicopathological features, prognosis, and initial therapeutic outcomes.Translational oncology · 2026Article
- Durable Intracranial Response to Sacituzumab Tirumotecan in HER2-Negative Salivary Duct Carcinoma With High TROP2 Expression: A Case Report.Cancer reports (Hoboken, N.J.) · 2026Article
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Authors and funding
14 authors.
Funding
Abstract
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.
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