Microsatellite analyses of recurrence or second primary tumor in head and neck cancer

Anticancer Res. 2005 Jul-Aug;25(4):2771-5.

Abstract

Background: In head and neck squamous cell carcinoma, distinguishing second primary tumours and recurrences may help to orient clinical decisions concerning therapy.

Patients and methods: A panel of eight microsatellite markers was used to analyse the loss of heterozygosity and genomic instability in a selected group of 32 patients experiencing a recurrence after having undergone surgery for oral or oropharyngeal carcinoma, in order to establish the clonality and origin of the recurrence.

Results: Twenty-three patients showed genetic changes in primary and/or relapsing tumour DNA: clonally-related patterns were detected in six cases, whereas the different patterns between paired tumours indicated the presence of a second primary tumour in 17 cases. None of the markers was informative in nine cases.

Conclusion: Our observations suggest that only a small proportion of patients have primary and secondary tumours developing from a single contiguous altered field (thus indicating a common clonal origin), whereas the metachronous tumour arises in unrelated fields in the majority of cases.

MeSH terms

  • Adult
  • Aged
  • Female
  • Genomic Instability
  • Humans
  • Loss of Heterozygosity
  • Male
  • Microsatellite Repeats / genetics*
  • Middle Aged
  • Mouth Neoplasms / genetics*
  • Neoplasm Recurrence, Local / genetics*
  • Neoplasms, Second Primary / genetics*
  • Oropharyngeal Neoplasms / genetics*