Erschienen in:
01.08.2013 | Translational Research and Biomarkers
Molecular Staging of Surgical Margins in Oral Squamous Cell Carcinoma Using Promoter Methylation of p16INK4A, Cytoglobin, E-cadherin, and TMEFF2
verfasst von:
Richard J. Shaw, MD, Andrew J. Hobkirk, MBChB, BDS, George Nikolaidis, PhD, Julia A. Woolgar, PhD, Asterios Triantafyllou, PhD, James S. Brown, MD, Triantafillos Liloglou, PhD, Janet M. Risk, PhD
Erschienen in:
Annals of Surgical Oncology
|
Ausgabe 8/2013
Einloggen, um Zugang zu erhalten
Abstract
Background
Local recurrence in oral squamous cell carcinoma (OSCC) despite clear surgical margins may indicate the presence of residual, sub-microscopic disease. Molecular assessment of surgical margins may provide a greater prognostic sensitivity compared to histopathology. We aimed to determine whether promoter methylation in deep and mucosal resection margins can predict recurrence in OSCC.
Methods
Forty-eight consecutive OSCC cases were recruited and a 5 mm3 tumor sample plus 5 deep and 5 mucosal margin samples were snap frozen. Clinical, pathological, adjuvant therapy, and outcome data were recorded. Tumors were informative if >5 % promoter methylation was found for ≥1 of 4 genes using qMSP. Margins were declared molecularly positive if >1 % promoter methylation was found in any margin.
Results
Thirty (63 %) of 48 cases were methylation informative. Mucosal margin samples were largely positive for methylation (26 of 30, 87 %), indicating the presence of field cancerization. Methylation at ≥1 gene promoters in ≥1 deep margin correlated with the presence of close/involved mucosal margins (P = 0.027) and increased pT status (P = 0.027) but not the status of deep margins, recurrence, or survival.
Conclusions
The current gene panel did not add prognostic information to histopathological reporting of resection margins. Future efforts should concentrate on improving gene selection, informativity, and assay performance in the patient group with intermediate indications for adjuvant therapy.