Table 1

Lynch syndrome cases of CRC and advanced adenomas tested for SEPTIN9 methylation in tissues

CRC group (%)Adenoma group (%)
All unique cases3614
Both CRC and adenoma44
Mean age at diagnosis, years (±SD)55.28 (±15.63)46.7 (±11.0)
Sex
 Males26 (72.2%)7 (50%)
 Females10 (27.8%)7 (50%)
Gene mutated
 MLH110 (27.8%)39 (64.3%)3
 MSH25 (13.9%)4 (28.6%)
 MSH610 (27.8%)11 (7.1%)1
 PMS211 (30.6%)0 (0.0%)
Neoplasia, n*3720
Location
 Left sided13 (35.1%)15 (75%)
 Right sided24 (64.9%)5 (25%)
StageNA
 I8 (21.6%)
 II17 (46.0%)
 III5 (13.5%)
 IV4 (10.8%)
 Unknown3 (8.1%)
Immunohistochemistry
 MLH13 IHC loss, 1 LOH, 6 NTNT
 MSH24 IHC loss, 1 NTNT
 MSH67 IHC loss, 3 IHC weak+somatic mutation†NT
 PMS211 IHC loss†NT
Matched NCM29 (28)‡13 (10)‡
  • Numbers in superscript indicate the number of cases who developed synchronous CRC and adenoma.

  • *Includes one CRC case developing two synchronous CRCs, and five adenoma cases developing two or more synchronous adenomas.

  • †Immunohistochemistry (IHC) or identification of a somatic second hit in tumour, as previously published.10

  • ‡Number of matched pairs of tumour-NCM with unique NCM samples (some cases developed more than one synchronous neoplasm).

  • CRC, colorectal cancer; LOH, loss of heterozygosity of normal allele; NA, not applicable; NCM, normal colorectal mucosa; NT, not tested.