This clinical trial examines the integration of cancer genetic testing in various ethnic populations. Studying individuals and families at risk of cancer may help identify cancer genes and other persons at risk. The information from this study may provide an opportunity for cancer risk stratification and individualized screening in these ethnic populations.
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Prevalence of pathogenic germline mutations in enrolled patients within each cancer site
Timeframe: Study completion (2 years)
Prevalence of positive pathogenic germline mutations
Timeframe: Study completion (2 years)
Rate of mutation detection via genetic testing to clinical practice guidelines of traditional family history criteria
Timeframe: Study completion (2 years)
Impact of germline genetic testing on both therapeutic management and targeted cancer prevention
Timeframe: Study completion (2 years)