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The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes Project

The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes Project
The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes Project

Background: the 100,000 Genomes Project established infrastructure for Whole Genome Sequencing (WGS) in the United Kingdom.

Methods: a retrospective study of cancer patients recruited to the 100,000 Genomes Project by the West Midlands Genomics Medicine Centre, evaluating clinical relevance of results.

Results: after excluding samples with no sequencing data (1678/4851; 34.6%), 3166 sample sets (germline and somatic) from 3067 participants were sequenced. Results of 1256 participants (41.0%) were interpreted (excluding participants who died (308/3067; 10.0%) or were clinically excluded (1503/3067; 49.0%)). Of these, 323 (25.7%) had no variants in genes which may alter management (Domain 1 genes). Of the remaining 933 participants, 552 (59.2%) had clinical recommendations made (718 recommendations in total). These included therapeutic recommendations (377/933; 40.4%), such as clinical trial, unlicensed or licensed therapies or high TMB recommendations, and germline variants warranting clinical genetics review (85/933; 9.1%). At the last follow up, 20.2% of all recommendations were followed (145/718). However, only a small proportion of therapeutic recommendations were followed (5.1%, 25/491).

Conclusions: the 100,000 Genomes Project has established infrastructure and regional experience to support personalised cancer care. The majority of those with successful sequencing had actionable variants. Ensuring GTAB recommendations are followed will maximise benefits for patients.

Humans, Neoplasms/genetics, Whole Genome Sequencing/methods, Retrospective Studies, Male, Female, United Kingdom, Middle Aged, Aged, Adult, Genomics/methods, Precision Medicine/methods, Aged, 80 and over
0007-0920
1805-1813
Leung, Elaine Y.L.
415aff1e-82ac-4261-9291-0fc64f0f3891
Robbins, Helen L.
47c59e1b-ab32-4473-8356-e4741bfcaa3f
Zaman, Shafquat
097d27c2-dece-43b6-b399-8ceea60d0f12
Lal, Neeraj
d6ac041d-d409-43ac-9f84-244dfd12d2ae
Morton, Dion
4c31306f-8af9-4f1b-aacc-7ee1619f56bc
Dew, Lisa
c170848d-3c2e-4657-a4c7-698d45642f98
Williams, Anthony P.
973ff46f-46f1-4d7c-b27d-0f53221e4c44
Wallis, Yvonne
06b18e73-df36-4601-9e55-52f71afd63d4
Bell, Jennie
8d250e06-2da2-4a5c-864d-1209950b859c
Raghavan, Manoj
f8141a72-8c17-4da2-b193-e42e978cbc4a
Middleton, Gary
31c645ca-3e55-491c-866e-370b6bbd91e5
Beggs, Andrew D.
fe399221-77bc-4be2-b45e-739e1d889581
Leung, Elaine Y.L.
415aff1e-82ac-4261-9291-0fc64f0f3891
Robbins, Helen L.
47c59e1b-ab32-4473-8356-e4741bfcaa3f
Zaman, Shafquat
097d27c2-dece-43b6-b399-8ceea60d0f12
Lal, Neeraj
d6ac041d-d409-43ac-9f84-244dfd12d2ae
Morton, Dion
4c31306f-8af9-4f1b-aacc-7ee1619f56bc
Dew, Lisa
c170848d-3c2e-4657-a4c7-698d45642f98
Williams, Anthony P.
973ff46f-46f1-4d7c-b27d-0f53221e4c44
Wallis, Yvonne
06b18e73-df36-4601-9e55-52f71afd63d4
Bell, Jennie
8d250e06-2da2-4a5c-864d-1209950b859c
Raghavan, Manoj
f8141a72-8c17-4da2-b193-e42e978cbc4a
Middleton, Gary
31c645ca-3e55-491c-866e-370b6bbd91e5
Beggs, Andrew D.
fe399221-77bc-4be2-b45e-739e1d889581

Leung, Elaine Y.L., Robbins, Helen L., Zaman, Shafquat, Lal, Neeraj, Morton, Dion, Dew, Lisa, Williams, Anthony P., Wallis, Yvonne, Bell, Jennie, Raghavan, Manoj, Middleton, Gary and Beggs, Andrew D. (2024) The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes Project. British Journal of Cancer, 131 (11), 1805-1813. (doi:10.1038/s41416-024-02890-6).

Record type: Article

Abstract

Background: the 100,000 Genomes Project established infrastructure for Whole Genome Sequencing (WGS) in the United Kingdom.

Methods: a retrospective study of cancer patients recruited to the 100,000 Genomes Project by the West Midlands Genomics Medicine Centre, evaluating clinical relevance of results.

Results: after excluding samples with no sequencing data (1678/4851; 34.6%), 3166 sample sets (germline and somatic) from 3067 participants were sequenced. Results of 1256 participants (41.0%) were interpreted (excluding participants who died (308/3067; 10.0%) or were clinically excluded (1503/3067; 49.0%)). Of these, 323 (25.7%) had no variants in genes which may alter management (Domain 1 genes). Of the remaining 933 participants, 552 (59.2%) had clinical recommendations made (718 recommendations in total). These included therapeutic recommendations (377/933; 40.4%), such as clinical trial, unlicensed or licensed therapies or high TMB recommendations, and germline variants warranting clinical genetics review (85/933; 9.1%). At the last follow up, 20.2% of all recommendations were followed (145/718). However, only a small proportion of therapeutic recommendations were followed (5.1%, 25/491).

Conclusions: the 100,000 Genomes Project has established infrastructure and regional experience to support personalised cancer care. The majority of those with successful sequencing had actionable variants. Ensuring GTAB recommendations are followed will maximise benefits for patients.

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More information

Accepted/In Press date: 21 October 2024
Published date: 30 October 2024
Keywords: Humans, Neoplasms/genetics, Whole Genome Sequencing/methods, Retrospective Studies, Male, Female, United Kingdom, Middle Aged, Aged, Adult, Genomics/methods, Precision Medicine/methods, Aged, 80 and over

Identifiers

Local EPrints ID: 497743
URI: http://eprints.soton.ac.uk/id/eprint/497743
ISSN: 0007-0920
PURE UUID: 2244b338-152d-45c4-a810-5fa059820081

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Date deposited: 30 Jan 2025 17:47
Last modified: 21 Aug 2025 03:18

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Contributors

Author: Elaine Y.L. Leung
Author: Helen L. Robbins
Author: Shafquat Zaman
Author: Neeraj Lal
Author: Dion Morton
Author: Lisa Dew
Author: Yvonne Wallis
Author: Jennie Bell
Author: Manoj Raghavan
Author: Gary Middleton
Author: Andrew D. Beggs

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