Evidence map›Paper›PMID 25910169›Full record

ArticleBMC cancer2015

A model-based assessment of the cost-utility of strategies to identify Lynch syndrome in early-onset colorectal cancer patients.

Tristan Snowsill, Nicola Huxley, Martin Hoyle, Tracey Jones-Hughes, Helen Coelho, Chris Cooper, Ian Frayling, Chris Hyde

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
4.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Validity of a two-antibody testing algorithm for mismatch repair deficiency testing in cancer; a systematic literature review and meta-analysis.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Pooled it
  2. A systematic review of the methodological quality of economic evaluations in genetic screening and testing for monogenic disorders.Genetics in medicine : official journal of the American College of Medical Genetics · 2022
    Pooled it
  3. Which Lynch syndrome screening programs could be implemented in the "real world"? A systematic review of economic evaluations.Genetics in medicine : official journal of the American College of Medical Genetics · 2018
    Pooled it
  4. Article
  5. Article
  6. Young-onset colorectal cancer.Nature reviews. Disease primers · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Cost-effectiveness of precision medicine: a scoping review.International journal of public health · 2019
    Article
  11. Article
  12. Article
  13. Mutational Analysis Identifies Therapeutic Biomarkers in Inflammatory Bowel Disease-Associated Colorectal Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Deficient mismatch repair: Read all about it (Review).International journal of oncology · 2015
    Review
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Tristan SnowsillInstitute of Health Research, University of Exeter Medical School, University of Exeter, Exeter, UK. t.m.snowsill@exeter.ac.uk.
Nicola HuxleyInstitute of Health Research, University of Exeter Medical School, University of Exeter, Exeter, UK. n.j.huxley@exeter.ac.uk.
Martin HoyleInstitute of Health Research, University of Exeter Medical School, University of Exeter, Exeter, UK. m.w.hoyle@exeter.ac.uk.
Tracey Jones-HughesInstitute of Health Research, University of Exeter Medical School, University of Exeter, Exeter, UK. t.jones-hughes@exeter.ac.uk.
Helen CoelhoInstitute of Health Research, University of Exeter Medical School, University of Exeter, Exeter, UK. h.coelho@exeter.ac.uk.
Chris CooperInstitute of Health Research, University of Exeter Medical School, University of Exeter, Exeter, UK. christopher.cooper@exeter.ac.uk.
Ian FraylingInstitute of Cancer & Genetics, Cardiff University, Cardiff, UK. fraylingim@cardiff.ac.uk.
Chris HydeInstitute of Health Research, University of Exeter Medical School, University of Exeter, Exeter, UK. c.j.hyde@exeter.ac.uk.
University of Exeter · GBCardiff University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLynch syndrome is an autosomal dominant cancer predisposition syndrome caused by mutations in the DNA mismatch repair genes MLH1, MSH2, MSH6 and PMS2. Individuals with Lynch syndrome have an increased risk of colorectal cancer, endometrial cancer, ovarian and other cancers. Lynch syndrome remains underdiagnosed in the UK. Reflex testing for Lynch syndrome in early-onset colorectal cancer patients is proposed as a method to identify more families affected by Lynch syndrome and offer surveillance to reduce cancer risks, although cost-effectiveness is viewed as a barrier to implementation. The objective of this project was to estimate the cost-utility of strategies to identify Lynch syndrome in individuals with early-onset colorectal cancer in the NHS.

methodsA decision analytic model was developed which simulated diagnostic and long-term outcomes over a lifetime horizon for colorectal cancer patients with and without Lynch syndrome and for relatives of those patients. Nine diagnostic strategies were modelled which included microsatellite instability (MSI) testing, immunohistochemistry (IHC), BRAF mutation testing (methylation testing in a scenario analysis), diagnostic mutation testing and Amsterdam II criteria. Biennial colonoscopic surveillance was included for individuals diagnosed with Lynch syndrome and accepting surveillance. Prophylactic hysterectomy with bilateral salpingo-oophorectomy (H-BSO) was similarly included for women diagnosed with Lynch syndrome. Costs from NHS and Personal Social Services perspective and quality-adjusted life years (QALYs) were estimated and discounted at 3.5% per annum.

resultsAll strategies included for the identification of Lynch syndrome were cost-effective versus no testing. The strategy with the greatest net health benefit was MSI followed by BRAF followed by diagnostic genetic testing, costing £5,491 per QALY gained over no testing. The effect of prophylactic H-BSO on health-related quality of life (HRQoL) is uncertain and could outweigh the health benefits of testing, resulting in overall QALY loss.

conclusionsReflex testing for Lynch syndrome in early-onset colorectal cancer patients is predicted to be a cost-effective use of limited financial resources in England and Wales. Research is recommended into the cost-effectiveness of reflex testing for Lynch syndrome in other associated cancers and into the impact of prophylactic H-BSO on HRQoL.

Indexed as

AgedAge of OnsetColorectal Neoplasms, Hereditary NonpolyposisCost-Benefit AnalysisDecision Making, Computer-AssistedDNA Mutational AnalysisFemaleHumansMaleMiddle AgedModels, EconomicMolecular Diagnostic TechniquesQuality-Adjusted Life YearsRiskSensitivity and Specificity

Identifiers

PMID25910169
PMCPMC4428233
OpenAlexW2082072262

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.