Integrating genotype–phenotype correlations into the diagnostic workflow of odontogenic tumors and cysts: insights from a 69 lesion cohort

Odontogenic tumors (OTs) represent a heterogeneous group of lesions ranging from hamartomatous or non-neoplastic proliferations to benign and malignant neoplasms with metastatic potential. Their classification remains challenging due to morphological and molecular variability. In this study, we performed comprehensive molecular profiling of odontogenic lesions—excluding previously analyzed ameloblastomas—to identify genomic alterations that define molecular subtypes and evaluate their diagnostic significance and potential therapeutic implications. A total of 88 odontogenic lesions were analyzed, including 25 cysts and 63 benign or malignant tumors, classified according to the 2022 5th edition of the World Health Organization (WHO) classification. Targeted next-generation sequencing (NGS) was performed to detect somatic mutations. Mutational patterns were correlated with histological subtypes and clinical parameters such as age, gender, lesion location, and recurrence. Somatic mutations were identified in 46 of 69 lesions successfully sequenced (66.7%). Among malignant tumors, genomic alterations—including gene fusions and mutations—were detected in 75% of cases. The highest mutation frequency was observed in OTs of epithelial origin. Notably, 11 of the 46 mutated cases harbored concurrent alterations in two genes. Molecular profiling serves as a valuable diagnostic adjunct in evaluating odontogenic tumors and cysts. Incorporating mutational analysis into routine workflows may enhance diagnostic precision, particularly in small or ambiguous biopsies, and may provide preliminary insights for future development of targeted therapeutic approaches. This study highlights the diagnostic value of integrating somatic mutation analysis into the standard evaluation of odontogenic lesions and highlights its potential adjunctive role in diagnostically challenging cases and as a basis for future therapeutic investigations.

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Publication Details

Journal
Clinical Oral Investigations
Published
2025-12-09
DOI
https://doi.org/10.1007/s00784-025-06642-5
Primary Topic
Oral and Maxillofacial Pathology
Type
article
Field-Weighted Citation Impact
0.00

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article

Integrating genotype–phenotype correlations into the diagnostic workflow of odontogenic tumors and cysts: insights from a 69 lesion cohort

Reinhard Büttner, Burcu Şengüven, Sibel Elif Gültekin, Carina Heydt
Clinical Oral Investigations
Oral and Maxillofacial Pathology
article

Integrating genotype–phenotype correlations into the diagnostic workflow of odontogenic tumors and cysts: insights from a 69 lesion cohort

Reinhard Büttner, Burcu Şengüven, Sibel Elif Gültekin, Carina Heydt
article en

Abstract

Odontogenic tumors (OTs) represent a heterogeneous group of lesions ranging from hamartomatous or non-neoplastic proliferations to benign and malignant neoplasms with metastatic potential. Their classification remains challenging due to morphological and molecular variability. In this study, we performed comprehensive molecular profiling of odontogenic lesions—excluding previously analyzed ameloblastomas—to identify genomic alterations that define molecular subtypes and evaluate their diagnostic significance and potential therapeutic implications. A total of 88 odontogenic lesions were analyzed, including 25 cysts and 63 benign or malignant tumors, classified according to the 2022 5th edition of the World Health Organization (WHO) classification. Targeted next-generation sequencing (NGS) was performed to detect somatic mutations. Mutational patterns were correlated with histological subtypes and clinical parameters such as age, gender, lesion location, and recurrence. Somatic mutations were identified in 46 of 69 lesions successfully sequenced (66.7%). Among malignant tumors, genomic alterations—including gene fusions and mutations—were detected in 75% of cases. The highest mutation frequency was observed in OTs of epithelial origin. Notably, 11 of the 46 mutated cases harbored concurrent alterations in two genes. Molecular profiling serves as a valuable diagnostic adjunct in evaluating odontogenic tumors and cysts. Incorporating mutational analysis into routine workflows may enhance diagnostic precision, particularly in small or ambiguous biopsies, and may provide preliminary insights for future development of targeted therapeutic approaches. This study highlights the diagnostic value of integrating somatic mutation analysis into the standard evaluation of odontogenic lesions and highlights its potential adjunctive role in diagnostically challenging cases and as a basis for future therapeutic investigations.

Clinical Oral InvestigationsVol. 30(1)
University of Cologne (DE), Gazi University (TR)
Deutsche Krebshilfe
Openalex Percentile: Top 46%
Oral and Maxillofacial Pathology
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