<i>EGFR</i> <scp>T790M</scp> Mutations in Conventional and Langerhans Cell‐Rich Variants of <scp>CEOT</scp> : Unveiling Molecular Differences and Clinical Implications
The identification of EGFR c.2369C>T (p.T790M) mutations in both variants underscores its significant role in CEOT pathogenesis and suggests potential implications for targeted therapies. This comprehensive analysis enhances our understanding of the molecular landscape of CEOT variants and highlights the necessity for tailored diagnostic and treatment strategies.
Authors
- Jiang Xue (ORCID: https://orcid.org/0000-0002-1107-9207)
- Lisha Sun (ORCID: https://orcid.org/0000-0002-4571-3739)
- Wenyi Zhang (ORCID: https://orcid.org/0000-0002-2837-937X)
- Zhipeng Sun (ORCID: https://orcid.org/0000-0002-5491-4137)
Institutions
- King University (US)
- Peking University (CN)
- National Clinical Research Center for Digestive Diseases (CN)
- Peking University People's Hospital (CN)
Publication Details
- Journal
- Oral Diseases
- Published
- 2025-10-13
- DOI
- https://doi.org/10.1111/odi.70111
- Primary Topic
- Oral and Maxillofacial Pathology
- Type
- article
- Field-Weighted Citation Impact
- 0.00