Phenotypic characteristics of hereditary non-polyposis colorectal cancer by the Amsterdam criteria: an Asian perspective

ANZ J Surg. 2008 Jul;78(7):556-60. doi: 10.1111/j.1445-2197.2008.04570.x.

Abstract

Background: Hereditary non-polyposis colorectal cancer (HNPCC) is an autosomal disease with a 68-82% lifetime risk of colorectal cancer (CRC). This study examined the phenotypic characteristics of CRC in Amsterdam criteria-positive Asian patients from the Singapore Polyposis Registry.

Methods: Hereditary non-polyposis CRC patients, defined by the Amsterdam I and II criteria, prospectively monitored in the Singapore Polyposis Registry over a 16-year period were reviewed. Clinical data were obtained from a computerized database and parameters, such as age of diagnosis, type and location of CRC, other associated cancers in the pedigree, cancer recurrence and survival were analysed.

Results: Fifty-two patients (31 men and 21 women) from 42 unrelated families, with a median age of 44.5 years (range 27-73 years), fulfilled either Amsterdam I or II criteria and were included in our analysis. The racial distribution was 91% (n = 47) Chinese and 9% (n = 5) Malays, with a median follow up of 44.9 months (range 2-183 months). Significantly, 69% of tumours in this Amsterdam-defined cohort were left sided, with most being sigmoid cancers. Sixty per cent of all the tumours presented at a late stage (Dukes' C or D). Left-sided tumours presented with more advanced Dukes' stage (P = 0.096) and a higher rate of metastatic disease (P = 0.08) compared with right-sided lesions. There were, however, no significant differences in either disease-free or overall survival between right-sided and left-sided tumours.

Conclusion: This study emphasized the significant left-sided predominance of CRC in Amsterdam I and II-defined patients from our predominantly Chinese population, in contrast to those classically described in Lynch syndrome. Amsterdam criteria thus may not be suitable for diagnosing HNPCC in Asian populations and a greater emphasis should be made towards routine molecular diagnosis of mismatch repair gene defects in suspected HNPCC patients of Asian decent.

MeSH terms

  • Adult
  • Aged
  • Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis
  • Colorectal Neoplasms, Hereditary Nonpolyposis / ethnology*
  • Colorectal Neoplasms, Hereditary Nonpolyposis / pathology*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Singapore / epidemiology
  • Survival Analysis