Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients.

Personalized healthcare relies on accurate companion diagnostic assays that enable the most appropriate treatment decision for cancer patients. Extensive assay validation prior to use in a clinical setting is essential for providing a reliable test result. This poses a challenge for low prevalence m...

Full description

Bibliographic Details
Main Authors: Elza C de Bruin, Jessica L Whiteley, Claire Corcoran, Pauline M Kirk, Jayne C Fox, Javier Armisen, Justin P O Lindemann, Gaia Schiavon, Helen J Ambrose, Alexander Kohlmann
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5417426?pdf=render
id doaj-3e485ea657ce4bf09a2d0717817f9dbd
record_format Article
spelling doaj-3e485ea657ce4bf09a2d0717817f9dbd2020-11-25T01:30:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01125e017577910.1371/journal.pone.0175779Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients.Elza C de BruinJessica L WhiteleyClaire CorcoranPauline M KirkJayne C FoxJavier ArmisenJustin P O LindemannGaia SchiavonHelen J AmbroseAlexander KohlmannPersonalized healthcare relies on accurate companion diagnostic assays that enable the most appropriate treatment decision for cancer patients. Extensive assay validation prior to use in a clinical setting is essential for providing a reliable test result. This poses a challenge for low prevalence mutations with limited availability of appropriate clinical samples harboring the mutation. To enable prospective screening for the low prevalence AKT1 E17K mutation, we have developed and validated a competitive allele-specific TaqMan® PCR (castPCR™) assay for mutation detection in formalin-fixed paraffin-embedded (FFPE) tumor tissue. Analysis parameters of the castPCR™ assay were established using an FFPE DNA reference standard and its analytical performance was assessed using 338 breast cancer and gynecological cancer FFPE samples. With recent technical advances for minimally invasive mutation detection in circulating tumor DNA (ctDNA), we subsequently also evaluated the OncoBEAM™ assay to enable plasma specimens as additional diagnostic opportunity for AKT1 E17K mutation testing. The analysis performance of the OncoBEAM™ test was evaluated using a novel AKT1 E17K ctDNA reference standard consisting of sheared genomic DNA spiked into human plasma. Both assays are employed at centralized testing laboratories operating according to quality standards for prospective identification of the AKT1 E17K mutation in ER+ breast cancer patients in the context of a clinical trial evaluating the AKT inhibitor AZD5363 in combination with endocrine (fulvestrant) therapy.http://europepmc.org/articles/PMC5417426?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Elza C de Bruin
Jessica L Whiteley
Claire Corcoran
Pauline M Kirk
Jayne C Fox
Javier Armisen
Justin P O Lindemann
Gaia Schiavon
Helen J Ambrose
Alexander Kohlmann
spellingShingle Elza C de Bruin
Jessica L Whiteley
Claire Corcoran
Pauline M Kirk
Jayne C Fox
Javier Armisen
Justin P O Lindemann
Gaia Schiavon
Helen J Ambrose
Alexander Kohlmann
Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients.
PLoS ONE
author_facet Elza C de Bruin
Jessica L Whiteley
Claire Corcoran
Pauline M Kirk
Jayne C Fox
Javier Armisen
Justin P O Lindemann
Gaia Schiavon
Helen J Ambrose
Alexander Kohlmann
author_sort Elza C de Bruin
title Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients.
title_short Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients.
title_full Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients.
title_fullStr Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients.
title_full_unstemmed Accurate detection of low prevalence AKT1 E17K mutation in tissue or plasma from advanced cancer patients.
title_sort accurate detection of low prevalence akt1 e17k mutation in tissue or plasma from advanced cancer patients.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Personalized healthcare relies on accurate companion diagnostic assays that enable the most appropriate treatment decision for cancer patients. Extensive assay validation prior to use in a clinical setting is essential for providing a reliable test result. This poses a challenge for low prevalence mutations with limited availability of appropriate clinical samples harboring the mutation. To enable prospective screening for the low prevalence AKT1 E17K mutation, we have developed and validated a competitive allele-specific TaqMan® PCR (castPCR™) assay for mutation detection in formalin-fixed paraffin-embedded (FFPE) tumor tissue. Analysis parameters of the castPCR™ assay were established using an FFPE DNA reference standard and its analytical performance was assessed using 338 breast cancer and gynecological cancer FFPE samples. With recent technical advances for minimally invasive mutation detection in circulating tumor DNA (ctDNA), we subsequently also evaluated the OncoBEAM™ assay to enable plasma specimens as additional diagnostic opportunity for AKT1 E17K mutation testing. The analysis performance of the OncoBEAM™ test was evaluated using a novel AKT1 E17K ctDNA reference standard consisting of sheared genomic DNA spiked into human plasma. Both assays are employed at centralized testing laboratories operating according to quality standards for prospective identification of the AKT1 E17K mutation in ER+ breast cancer patients in the context of a clinical trial evaluating the AKT inhibitor AZD5363 in combination with endocrine (fulvestrant) therapy.
url http://europepmc.org/articles/PMC5417426?pdf=render
work_keys_str_mv AT elzacdebruin accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT jessicalwhiteley accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT clairecorcoran accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT paulinemkirk accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT jaynecfox accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT javierarmisen accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT justinpolindemann accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT gaiaschiavon accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT helenjambrose accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
AT alexanderkohlmann accuratedetectionoflowprevalenceakt1e17kmutationintissueorplasmafromadvancedcancerpatients
_version_ 1725089838958379008