Correlation of BRAF mutational status with clinical characteristics and survival outcomes of patients with ameloblastoma: The experience of 11 Italian centres

Riccardo Bonacina, Alice Indini, Gabriella Massazza, Eliana Rulli, Andrea Gianatti, Mario Mandalà

Research output: Contribution to journalArticlepeer-review

Abstract

Aims: Ameloblastoma is a rare odontogenic tumour with an aggressive local behaviour. Mutations in the mitogen-activated protein kinase pathway, namely BRAF V600E mutations, are a common finding. To date, there is no clear correlation between BRAF V600 mutation and clinical outcome. Methods: We retrospectively reviewed the medical records of patients who underwent surgery for ameloblastoma between May 1998 and June 2018, at 11 participating Italian centres. BRAF mutational status was evaluated by quantitative PCR/pyrosequencing. The primary end points were to determine BRAF mutational status in primitive and recurrent ameloblastoma, and to assess the relapse-free interval (RFI); the secondary end point was to investigate the correlation of BRAF mutational status with the clinical features of the tumour and survival outcomes. Results: Overall, 74 patients were included: 33 (44.5%) were BRAF wild type and 41 (55.4%) BRAF V600 mutated. BRAF V600 mutated ameloblastomas occurred more frequently in younger patients (p=0.0031), were located at the mandible (p=0.0009) and presented with unicystic variant. After a median follow-up of 60 months, 21 (28.3%) patients relapsed (30.3% and 26.8% in the BRAF wild type and BRAF mutated group, respectively). At univariable Cox models, none of the investigated variables, including microscopic margin involvement, was associated with RFI. Conclusions: Local recurrence occurs in 30% of patients with ameloblastoma. BRAFV600 mutation is associated with younger age, mandibular localisation and with unicystic ameloblastoma. Neither BRAF mutation nor microscopically positive surgical margins were associated with RFI. Further studies are needed to elucidate outcomes of this rare disease according to clinical, histopathological and comprehensive molecular features.

Original languageEnglish
Article numberjclinpath-2021-207527
JournalJournal of Clinical Pathology
DOIs
Publication statusAccepted/In press - 2021

Keywords

  • bone neoplasms
  • neoplasms
  • oncogenes

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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