Toggle Main Menu Toggle Search

Open Access padlockePrints

The comprehensive English National Lynch Syndrome Registry: development and description of a new genomics data resource

Lookup NU author(s): Professor Sir John BurnORCiD

Downloads


Licence

This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

© 2024 The Author(s). Background: 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.


Publication metadata

Author(s): Huntley C, Loong L, Mallinson C, Bethell R, Rahman T, Alhaddad N, Tulloch O, Zhou X, Lee J, Eves P, Cook J, Armstrong R, Ahmed M, McVeigh T, DeSouza B, Kulkarni A, Bezuidenhout H, Martin R, Holliday D, Hart R, Lalloo F, Donaldson A, Cleaver R, Willis C, Kiesel V, O'Reilly M-A, Halliday D, Solomons J, Ong KR, McRonald F, Torr B, Burn J, Shaw A, Morris EJA, Monahan K, Hardy S, Turnbull C

Publication type: Article

Publication status: Published

Journal: eClinicalMedicine

Year: 2024

Volume: 69

Print publication date: 01/03/2024

Online publication date: 07/02/2024

Acceptance date: 17/01/2024

Date deposited: 20/02/2024

ISSN (electronic): 2589-5370

Publisher: Elsevier Ltd

URL: https://doi.org/10.1016/j.eclinm.2024.102465

DOI: 10.1016/j.eclinm.2024.102465


Altmetrics

Altmetrics provided by Altmetric


Funding

Funder referenceFunder name
203924/Z/16/Z
40tude Curing Colon Cancer
C8620/A8372
Cancer Research UK
Bowel Cancer UK
Wellcome Trust

Share