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dc.contributor.authorHuntley, C
dc.contributor.authorLoong, L
dc.contributor.authorMallinson, C
dc.contributor.authorBethell, R
dc.contributor.authorRahman, T
dc.contributor.authorAlhaddad, N
dc.contributor.authorTulloch, O
dc.contributor.authorZhou, X
dc.contributor.authorLee, J
dc.contributor.authorEves, P
dc.contributor.authorGMSA Lynch Consortium,
dc.contributor.authorMcRonald, F
dc.contributor.authorTorr, B
dc.contributor.authorBurn, J
dc.contributor.authorShaw, A
dc.contributor.authorMorris, EJA
dc.contributor.authorMonahan, K
dc.contributor.authorHardy, S
dc.contributor.authorTurnbull, C
dc.date.accessioned2024-02-16T09:21:53Z
dc.date.available2024-02-16T09:21:53Z
dc.date.issued2024-03-01
dc.identifier102465
dc.identifier.citationEClinicalMedicine, 2024, 69 pp. 102465 - 102465
dc.identifier.issn2589-5370
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6155
dc.identifier.doi10.1016/j.eclinm.2024.102465
dc.identifier.doi10.1016/j.eclinm.2024.102465
dc.description.abstractBACKGROUND: Lynch Syndrome (LS) is a cancer predisposition syndrome caused by constitutional pathogenic variants in the mismatch repair (MMR) genes. To date, fragmentation of clinical and genomic data has restricted understanding of national LS ascertainment and outcomes, and precluded evaluation of NICE guidance on testing and management. To address this, via collaboration between researchers, the National Disease Registration Service (NDRS), NHS Genomic Medicine Service Alliances (GMSAs), and NHS Regional Clinical Genetics Services, a comprehensive registry of LS carriers in England has been established. METHODS: For comprehensive ascertainment of retrospectively identified MMR pathogenic variant (PV) carriers (diagnosed prior to January 1, 2023), information was retrieved from all clinical genetics services across England, then restructured, amalgamated, and validated via a team of trained experts in NDRS. An online submission portal was established for prospective ascertainment from January 1, 2023. The resulting data, stored in a secure database in NDRS, were used to investigate the demographic and genetic characteristics of the cohort, censored at July 25, 2023. Cancer outcomes were investigated via linkage to the National Cancer Registration Dataset (NCRD). FINDINGS: A total of 11,722 retrospective and 570 prospective data submissions were received, resulting in a comprehensive English National Lynch Syndrome Registry (ENLSR) comprising 9030 unique individuals. The most frequently identified pathogenic MMR genes were MSH2 and MLH1 at 37.2% (n = 3362) and 29.1% (n = 2624), respectively. 35.9% (n = 3239) of the ENLSR cohort received their LS diagnosis before their first cancer diagnosis (presumptive predictive germline test). Of these, 6.3% (n = 204) developed colorectal cancer, at a median age of initial diagnosis of 51 (IQR 40-62), compared to 73 years (IQR 64-80) in the general population (p < 0.0001). INTERPRETATION: The ENLSR represents the first comprehensive national registry of PV carriers in England and one of the largest cohorts of MMR PV carriers worldwide. The establishment of a secure, centralised infrastructure and mechanism for routine registration of newly identified carriers ensures sustainability of the data resource. FUNDING: This work was funded by the Wellcome Trust, Cancer Research UK and Bowel Cancer UK. The funder of this study had no role in study design, data collection, data analysis, data interpretation, or writing of the report.
dc.format.extent102465 - 102465
dc.languageen
dc.language.isoeng
dc.publisherELSEVIER
dc.relation.ispartofEClinicalMedicine
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleThe comprehensive English National Lynch Syndrome Registry: development and description of a new genomics data resource.
dc.typeJournal Article
dcterms.dateAccepted2024-05-01
dc.date.updated2024-02-12T10:27:17Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.eclinm.2024.102465
rioxxterms.licenseref.startdate2024-03-01
rioxxterms.typeJournal Article/Review
pubs.organisational-groupICR
pubs.organisational-groupICR/Students
pubs.organisational-groupICR/Students/PhD and MPhil
pubs.organisational-groupICR/Students/PhD and MPhil/20/21 Starting Cohort
pubs.publication-statusAccepted
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.eclinm.2024.102465
pubs.volume69
icr.researchteamTranslational Genetics
dc.contributor.icrauthorPronin, Lucy Wai Yee
dc.contributor.icrauthorTurnbull, Clare
icr.provenanceDeposited by Mr Arek Surman (impersonating Dr Lucy Pronin) on 2024-02-12. Deposit type is initial. No. of files: 1. Files: English National Lynch Syndrome Regsitry Profile.pdf


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