Targeted next-generation sequencing of plasma DNA from cancer patients: factors influencing consistency with tumour DNA and prospective investigation of its utility for diagnosis

Use of circulating tumour DNA (ctDNA) as a liquid biopsy has been proposed for potential identification and monitoring of solid tumours. We investigate a next-generation sequencing approach for mutation detection in ctDNA in two related studies using a targeted panel. The first study was retrospecti...

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Main Authors: Kaisaki, P, Cutts, A, Popitsch, N, Camps, C, Pentony, M, Wilson, G, Page, S, Kaur, K, Vavoulis, D, Henderson, S, Gupta, A, Middleton, M, Karydis, I, Talbot, D, Schuh, A, Taylor, J
Format: Journal article
Language:English
Published: Public Library of Science 2016
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author Kaisaki, P
Cutts, A
Popitsch, N
Camps, C
Pentony, M
Wilson, G
Page, S
Kaur, K
Vavoulis, D
Henderson, S
Gupta, A
Middleton, M
Karydis, I
Talbot, D
Schuh, A
Taylor, J
author_facet Kaisaki, P
Cutts, A
Popitsch, N
Camps, C
Pentony, M
Wilson, G
Page, S
Kaur, K
Vavoulis, D
Henderson, S
Gupta, A
Middleton, M
Karydis, I
Talbot, D
Schuh, A
Taylor, J
author_sort Kaisaki, P
collection OXFORD
description Use of circulating tumour DNA (ctDNA) as a liquid biopsy has been proposed for potential identification and monitoring of solid tumours. We investigate a next-generation sequencing approach for mutation detection in ctDNA in two related studies using a targeted panel. The first study was retrospective, using blood samples taken from melanoma patients at diverse timepoints before or after treatment, aiming to evaluate correlation between mutations identified in biopsy and ctDNA, and to acquire a first impression of influencing factors. We found good concordance between ctDNA and tumour mutations of melanoma patients when blood samples were collected within one year of biopsy or before treatment. In contrast, when ctDNA was sequenced after targeted treatment in melanoma, mutations were no longer found in 9 out of 10 patients, suggesting the method might be useful for detecting treatment response. Building on these findings, we focused the second study on ctDNA obtained before biopsy in lung patients, i.e. when a tentative diagnosis of lung cancer had been made, but no treatment had started. The main objective of this prospective study was to evaluate use of ctDNA in diagnosis, investigating the concordance of biopsy and ctDNA-derived mutation detection. Here we also found positive correlation between diagnostic lung biopsy results and pre-biopsy ctDNA sequencing, providing support for using ctDNA as a cost-effective, non-invasive solution when the tumour is inaccessible or when biopsy poses significant risk to the patient.
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spelling oxford-uuid:58d818fd-2de7-42e0-a198-b09a771e2cdb2022-03-26T17:06:30ZTargeted next-generation sequencing of plasma DNA from cancer patients: factors influencing consistency with tumour DNA and prospective investigation of its utility for diagnosisJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:58d818fd-2de7-42e0-a198-b09a771e2cdbEnglishSymplectic Elements at OxfordPublic Library of Science2016Kaisaki, PCutts, APopitsch, NCamps, CPentony, MWilson, GPage, SKaur, KVavoulis, DHenderson, SGupta, AMiddleton, MKarydis, ITalbot, DSchuh, ATaylor, JUse of circulating tumour DNA (ctDNA) as a liquid biopsy has been proposed for potential identification and monitoring of solid tumours. We investigate a next-generation sequencing approach for mutation detection in ctDNA in two related studies using a targeted panel. The first study was retrospective, using blood samples taken from melanoma patients at diverse timepoints before or after treatment, aiming to evaluate correlation between mutations identified in biopsy and ctDNA, and to acquire a first impression of influencing factors. We found good concordance between ctDNA and tumour mutations of melanoma patients when blood samples were collected within one year of biopsy or before treatment. In contrast, when ctDNA was sequenced after targeted treatment in melanoma, mutations were no longer found in 9 out of 10 patients, suggesting the method might be useful for detecting treatment response. Building on these findings, we focused the second study on ctDNA obtained before biopsy in lung patients, i.e. when a tentative diagnosis of lung cancer had been made, but no treatment had started. The main objective of this prospective study was to evaluate use of ctDNA in diagnosis, investigating the concordance of biopsy and ctDNA-derived mutation detection. Here we also found positive correlation between diagnostic lung biopsy results and pre-biopsy ctDNA sequencing, providing support for using ctDNA as a cost-effective, non-invasive solution when the tumour is inaccessible or when biopsy poses significant risk to the patient.
spellingShingle Kaisaki, P
Cutts, A
Popitsch, N
Camps, C
Pentony, M
Wilson, G
Page, S
Kaur, K
Vavoulis, D
Henderson, S
Gupta, A
Middleton, M
Karydis, I
Talbot, D
Schuh, A
Taylor, J
Targeted next-generation sequencing of plasma DNA from cancer patients: factors influencing consistency with tumour DNA and prospective investigation of its utility for diagnosis
title Targeted next-generation sequencing of plasma DNA from cancer patients: factors influencing consistency with tumour DNA and prospective investigation of its utility for diagnosis
title_full Targeted next-generation sequencing of plasma DNA from cancer patients: factors influencing consistency with tumour DNA and prospective investigation of its utility for diagnosis
title_fullStr Targeted next-generation sequencing of plasma DNA from cancer patients: factors influencing consistency with tumour DNA and prospective investigation of its utility for diagnosis
title_full_unstemmed Targeted next-generation sequencing of plasma DNA from cancer patients: factors influencing consistency with tumour DNA and prospective investigation of its utility for diagnosis
title_short Targeted next-generation sequencing of plasma DNA from cancer patients: factors influencing consistency with tumour DNA and prospective investigation of its utility for diagnosis
title_sort targeted next generation sequencing of plasma dna from cancer patients factors influencing consistency with tumour dna and prospective investigation of its utility for diagnosis
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