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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes.

Authors :
Whitworth J
Smith PS
Martin JE
West H
Luchetti A
Rodger F
Clark G
Carss K
Stephens J
Stirrups K
Penkett C
Mapeta R
Ashford S
Megy K
Shakeel H
Ahmed M
Adlard J
Barwell J
Brewer C
Casey RT
Armstrong R
Cole T
Evans DG
Fostira F
Greenhalgh L
Hanson H
Henderson A
Hoffman J
Izatt L
Kumar A
Kwong A
Lalloo F
Ong KR
Paterson J
Park SM
Chen-Shtoyerman R
Searle C
Side L
Skytte AB
Snape K
Woodward ER
Tischkowitz MD
Maher ER
Source :
American journal of human genetics [Am J Hum Genet] 2018 Jul 05; Vol. 103 (1), pp. 3-18. Date of Electronic Publication: 2018 Jun 14.
Publication Year :
2018

Abstract

Multiple primary tumors (MPTs) affect a substantial proportion of cancer survivors and can result from various causes, including inherited predisposition. Currently, germline genetic testing of MPT-affected individuals for variants in cancer-predisposition genes (CPGs) is mostly targeted by tumor type. We ascertained pre-assessed MPT individuals (with at least two primary tumors by age 60 years or at least three by 70 years) from genetics centers and performed whole-genome sequencing (WGS) on 460 individuals from 440 families. Despite previous negative genetic assessment and molecular investigations, pathogenic variants in moderate- and high-risk CPGs were detected in 67/440 (15.2%) probands. WGS detected variants that would not be (or were not) detected by targeted resequencing strategies, including low-frequency structural variants (6/440 [1.4%] probands). In most individuals with a germline variant assessed as pathogenic or likely pathogenic (P/LP), at least one of their tumor types was characteristic of variants in the relevant CPG. However, in 29 probands (42.2% of those with a P/LP variant), the tumor phenotype appeared discordant. The frequency of individuals with truncating or splice-site CPG variants and at least one discordant tumor type was significantly higher than in a control population (χ <superscript>2</superscript> = 43.642; p ≤ 0.0001). 2/67 (3%) probands with P/LP variants had evidence of multiple inherited neoplasia allele syndrome (MINAS) with deleterious variants in two CPGs. Together with variant detection rates from a previous series of similarly ascertained MPT-affected individuals, the present results suggest that first-line comprehensive CPG analysis in an MPT cohort referred to clinical genetics services would detect a deleterious variant in about a third of individuals.<br /> (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1537-6605
Volume :
103
Issue :
1
Database :
MEDLINE
Journal :
American journal of human genetics
Publication Type :
Academic Journal
Accession number :
29909963
Full Text :
https://doi.org/10.1016/j.ajhg.2018.04.013