Table 1.
Eligibility criteria | Index cases (number / percent)d |
---|---|
An index case in a family that fulfils clinical criteria for a hereditary cancer syndrome | 28 (14.4) |
An index case with two primary cancers (either synchronous or metachronous) diagnosed at 60 years or younger | 83 (42.6) |
An index case with three primary cancers diagnosed at 70 years or younger | 52 (26.7) |
Index case with colorectal polyposis defined as per InSiGHTa or eviQb testing guidelines for MUTYH and/or APC | 29 (14.9) |
A cancer-affected individual fulfilling two or more of the following criteria: • Early age at onset (under 40 years for adult cancer or < 10 years younger than the mean age of cancer diagnosis for that tumour type and sexc) • One or more first-degree relatives with the same kind of cancer • Two or more first- or second-degree relatives with different cancers, where at least one cancer is very rare |
42 (21.5) |
aThe International Society for Gastrointestinal Hereditary Tumours (InSiGHT), as per https://www.insight-group.org/
beviQ, as per https://www.eviq.org.au/
cAustralian Institute of Health and Welfare 2017. Cancer in Australia 2017. Cancer series no. 101. Cat. no. CAN 100. Canberra: AIHW
dPercent does not add to 100% as index cases may have met more than one eligibility criteria