July 23, 2025

Recurrent FGFR2 and PIK3CA mutations in sialoblastoma

Key Points

FGFR2 p.C382R is identified as the main driver mutation in sialoblastoma, found in 80% of analyzed cases.
A cohort of five tumors exhibited growth patterns with varying mitotic activities and histologic features.
Targeted next-generation sequencing revealed concurrent mutations in PIK3CA and CTNNB1 in some cases.
These findings expand the molecular understanding of sialoblastoma, indicating possible therapeutic avenues targeting FGFR and PI3K pathways.

Abstract

Abstract Purpose Sialoblastoma is an extremely rare low-grade malignant salivary gland neoplasm that presents at birth or early infancy and has heterogeneous clinical behavior. Due to its rarity, the molecular landscape remains incompletely characterized. We aimed to expand the current understanding of the genetic alterations in sialoblastoma through comprehensive molecular analysis. Methods Five sialoblastoma cases were retrieved from four institutional archives. Clinical and pathologic review was performed, and targeted next-generation sequencing was conducted using clinically validated panels. Copy number analysis was performed on four cases. Results The cohort included five patients with tumors located in parotid gland (n = 2), minor salivary glands (n = 2), and submandibular gland (n = 1). Four patients were diagnosed before 6 months of age. Histologically, all tumors showed solid organoid nests with primitive basaloid cells, dense fibrous stroma, and mitotic activity ranging from 8–25 per 10 high-power fields. Recurrent FGFR2 p.C382R variants were identified in 80% (4/5) of cases. Additional alterations were seen in FGFR2 p.C382R mutated tumors, including PIK3CA hotspot mutations in two cases (p.R88Q, p.R38H) and a truncating FGFR2 variant (p.L776Rfs) in one. The single tumor that lacked FGFR2 mutations harbored a CTNNB1 p.I35T variant and showed more favorable histologic features. Copy number analysis revealed recurrent whole-chromosome gains of chromosomes 8, 10, and 11. Conclusion This study validates FGFR2 p.C382R hotspot mutation as the predominant driver mutation in sialoblastoma. Tumors with this mutation tend to have solid growth pattern, aggressive histologic features, and clinical behavior. The identification of concurrent genomic alterations and alternative drivers like CTNNB1 mutations expands the molecular landscape of this rare tumor. These findings support potential therapeutic targeting of FGFR and PI3K pathways in the management of sialoblastoma.

Ask AI

Helpful

Bookmark

View Full Paper