Abstract

Colorectal cancer (CRC) has a strong familial component which extends to discordant cancers (ie non-CRC tumors). This is best seen in cancer syndromes such as hereditary non-polyposis colorectal cancer (HNPCC) which predisposes to several tumor types. Population-based family studies have also found discordant associations for CRC but they have included cancers which manifest in HNPCC, and there is no convincing evidence of discordant associations beyond the known syndromes. We address familial associations of non-CRC tumors with CRC using the resources of the Swedish Family-Cancer Database and applying a powerful approach of assessing familial relative risks in families of increasing numbers of patients with discordant cancers. Among 1.8 million cancer patients and over 200,000 CRC cases consistent familial associations of CRC was observed for several HNPCC related cancers. However, for small intestinal, pancreatic and nervous system cancers RRs remained essentially unchanged when potential HNPCC families were excluded, suggesting involvement of genes not related to HNPCC. Two independent associations of CRC were found for melanoma, thyroid and eye cancers and these appeared not to be related to known syndromes. A number of other cancers associated with CRC in single analyses and independent studies are required to assess the relevance of such findings.

Highlights

  • About 13% of patients with colorectal cancer (CRC) have a parent or a sibling diagnosed with Colorectal cancer (CRC) and the familial relative risks (RRs) are 1.80 and 2.00, respectively[1, 2]

  • A total of 207,512 individuals were diagnosed with CRC, and of these 35,360 were in the 0–80 year old offspring generation used as index individuals to calculate RRs

  • As reference we show RRs for concordant CRC which increased from 1.76 (1 proband diagnosed with CRC) to 5.13

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Summary

Introduction

About 13% of patients with colorectal cancer (CRC) have a parent or a sibling diagnosed with CRC and the familial relative risks (RRs) are 1.80 and 2.00, respectively[1, 2]. Hereditary non-polyposis colorectal cancer (HNPCC) is the most common CRC syndrome, accounting for some 10% of familial CRC3, 4 (for distinction between HNPCC and Lynch syndrome see Methods). Numerous (at least 50) low-risk susceptibility loci have been identified[6] As their RRs are low they combined contribute to the familial risk no more than the high-risk genes[7]. HNPCC, familial adenomatous polyposis (FAP) and other rare CRC-related cancer syndromes manifest cancers other than CRC; in HNPCC the risk of at least 8 cancers is increased[4, 8, 9]. Risk in offspring Stomach Colorectum Small intestine Colorectum Colorectum Pancreas Colorectum Lung Colorectum Breast Colorectum Endometrium Colorectum Ovary Colorectum Prostate Colorectum Melanoma Colorectum Eye Colorectum Nervous system Colorectum Thyroid gland Colorectum Myeloma Colorectum CUP7 Colorectum cancer case in the family

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