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Record W2017761747 · doi:10.1186/1897-4287-8-s1-p5

Lynch syndrome-chasing a better ascertainment rate in British Columbia

2010· article· en· W2017761747 on OpenAlexaffabout
Carol Cremin, Morteza Bashash, Linlea Armstrong, Sharlene Gill, David Huntsman, Chris Bajdik

Bibliographic record

VenueHereditary Cancer in Clinical Practice · 2010
Typearticle
Languageen
FieldMedicine
TopicGenetic factors in colorectal cancer
Canadian institutionsBC Cancer Agency
Fundersnot available
KeywordsLynch syndromeMedicineMicrosatellite instabilityReferralPopulationGenetic testingColorectal cancerCancerFamily historyPediatricsFamily medicineInternal medicineDNA mismatch repairMicrosatelliteGenetics

Abstract

fetched live from OpenAlex

With a population of approximately 4.380 million people and an estimated Lynch syndrome mutation prevalence of 1/531, there are an expected 8000 individuals with Lynch syndrome in British Columbia. The Hereditary Cancer Program (HCP) of the BC Cancer Agency (BCCA) has provided clinical testing for Lynch syndrome since 2004 to patients across the province. Currently, there are approximately 100 patients with confirmed Lynch syndrome mutations in the BCCA database. Potential obstacles in ascertaining Lynch syndrome through a traditional clinic-based approach include physician awareness of referral criteria, patient's lack of knowledge of cancer family history, patient compliance, and availability of tumour tissue for testing. Given these obstacles, a population based approach to identifying Lynch syndrome through incident testing of newly diagnosed colorectal cancers under age 50 by microsatellite instability testing (MSI) was launched in BC in June of 2008. Chart review of a cohort of patients referred for genetic counselling at the RCP during 2004-2006 and a cohort of consecutive colorectal cancer cases referred directly for MSI testing to the BCCA Genetics Laboratory (June 2008-June 2009). Mutation prevalence and clinicopathologic characteristics will be compared between the two groups. Clinical and demographic characteristics of the groups will also be compared to non-referred cases diagnosed under 50 in the province. Our previous clinic-based results showed a 14.3% prevalence of Lynch syndrome mutations among the index cases tested for whom results were available. 76% of tumour results were microsatellite stable and intact for MLH1 and MSH2 proteins. The sensitivity of the program's referral criteria was about 83.3% with an approximate confidence interval of 68.2%-96.8% and the positive predictive value was about 38.3% with an approximate confidence interval of 17.7%-60.0%. The prevalence of Lynch syndrome mutations dropped to 3.2% among all patients referred for genetic counseling. From July 2008 to July 2009, a total of 37 incident colorectal cases diagnosed under age 50 were referred directly to the BC Cancer Agency's cancer genetics lab. 73% were microsatellite stable while additional testing is underway on the 10 MSI high cases. Further comparisons between the groups will be presented. Aside from becoming increasingly important for prognosis and predictive response to chemotherapy, population based MSI analysis on newly diagnosed colorectal cancer is expected to improve the rate of Lynch syndrome ascertainment in BC.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.003
metaresearch head score (Gemma)0.007
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow), Research integrity, Insufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.390
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0030.007
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.003
Insufficient payload (model declined to judge)0.0060.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.033
GPT teacher head0.384
Teacher spread0.351 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2010
Admission routes2
Has abstractyes

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