Elliot: Ethics of CRC Flashcards
What is diagnostic testing?
Establish diagnosis= genetic
What is diagnostic testing used for?
Tx choices
family risks
What is the purpose of predictive testing?
Risk and surveillance assessment
Clinical genomic programs help guide:
diagnoses
pharmacogenomic decisions
risk assessment
family based decision support
Who should have particular diagnostic testing?
Based on personal hx:
CRC at 50 yr or less
Synchronous (one then another)/metachronous (all at the same time) CRC or other HNPCC tumors
Polyps (10 or more adenomatous CRC polyps; 3-5 juvenile polyps in CR or multiple throughout GI)
CRC with first-degree relative with Lynch Syndrome-related tumor
Tissue based diagnostic testing is recommended for…
” to all people whose tumors are diagnosed as some form of CRC (regardless of family history or age)
genetic testing for Lynch Syndrome be offered
What percent of CRC are related at familial clusters?
20%
What percent of colon cancers are d/t a highly penetrant gene mutation that confers a high lifetime risk of dx?
5-10%
*importance of family hx
When should you consider predictive testing?
- Having information reduces morbidity and mortality of diagnosis
- Effective prevention, screening and treatment exist
- The predictive power of test (depends on penetrance of condition; family history)
When is predictive testing recommended?
1st degree relative w/ known GENE mutation!!
PATTERN of cancers in lineage suggesting syndrome (family history/genogram)
Relative with EARLY-onset diagnosis
REPRODUCTIVE decision concerns (pre-natal/pre- implantation)
What cancer details are used to make a family genagram?
Three or more closely realted family members w/ LS cancers (path confirmations)
Two successive generations w/ cancers
At least one person diagnosed <50 yrs
*Clustering of extra colonic cancers (endometerium, gastric, breast, thyroid)
What is the purpose of predictive genetic testing?
accurate risk assessment
What type of test is used for proband testing?
diagnostic test
If mutation found, gene test used to see if others have same mutation (true positives)
If no mutation in proband, test is uninformative for proband–and for others (false negatives)
What percent of CRC genetic testing is non-informative?
70%
What ethical issues are influenced by genetic testing?
Privacy / confidentiality Responsibility / Duty to warn Discrimination based on results of tests Genetic testing of minors Reproductive decision making
(beneficence- do good when we can, non-maleficence- do no harm, autonomy- individual decision making, justice)