Answers are grounded in this paper and cite their sources.
Treatment options for advanced recurrent or metastatic (R/M) adenoid cystic carcinoma (ACC) remain limited, with few effective molecular-based therapies.Advances in targeted protein panels provide an approach for identifying potentially targetable protein expression patterns and supporting individualized treatment considerations; however, their feasibility and decision-support potential in R/M ACC remain poorly defined.The present proof-of-concept study evaluated the feasibility and decision-support potential of a predefined immunohistochemistry-based 11-protein panel in heavily pretreated patients with R/M ACC.Among 10 patients with advanced R/M ACC, seven underwent tumor profiling using the panel.Potentially actionable targets, including epidermal growth factor receptor (EGFR), MET proto-oncogene, receptor tyrosine kinase, KIT proto-oncogene, receptor tyrosine kinase, and platelet-derived growth factor receptor, were identified in 86% of profiled cases.Based on these findings, panel-based therapy recommendations were issued for the majority of patients.In one illustrative case, EGFR-directed therapy with gefitinib was associated with ~3 years of disease stability.In conclusion, these findings support the feasibility of a pragmatic immunohistochemistry-based approach to inform treatment discussions in advanced R/M ACC.However, the clinical relevance of these findings requires further validation in larger prospective cohorts.
No takes yet. Share an insight, caveat, or question.
Thölken et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: