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Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)

  • 1Email authorView ORCID ID profile,
  • 1,
  • 1,
  • 2,
  • 2,
  • 3,
  • 4,
  • 4,
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  • 5,
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Contributed equally
Hereditary Cancer in Clinical Practice201917:3

https://doi.org/10.1186/s13053-019-0104-x

  • Received: 13 August 2018
  • Accepted: 9 January 2019
  • Published:
Open Peer Review reports

Abstract

Background

Approximately 5 to 10% of all cancers are caused by inherited germline mutations, many of which are associated with different Hereditary Cancer Syndromes (HCS). In the context of the Program of Hereditary Cancer of the Valencia Community, individuals belonging to specific HCS and their families receive genetic counselling and genetic testing according to internationally established guidelines. The current diagnostic approach is based on sequencing a few high-risk genes related to each HCS; however, this method is time-consuming, expensive and does not achieve a confirmatory genetic diagnosis in many cases. This study aims to test the level of improvement offered by a Next Generation Sequencing (NGS) gene-panel compared to the standard approach in a diagnostic reference laboratory setting.

Methods

A multi-gene NGS panel was used to test a total of 91 probands, previously classified as non-informative by analysing the high-risk genes defined in our guidelines.

Results

Nineteen deleterious mutations were detected in 16% of patients, some mutations were found in already-tested high-risk genes (BRCA1, BRCA2, MSH2) and others in non-prevalent genes (RAD51D, PALB2, ATM, TP53, MUTYH, BRIP1).

Conclusions

Overall, our findings reclassify several index cases into different HCS, and change the mutational status of 14 cases from non-informative to gene mutation carriers. In conclusion, we highlight the necessity of incorporating validated multi-gene NGS panels into the HCSs diagnostic routine to increase the performance of genetic diagnosis.

Keywords

  • Hereditary Cancer syndrome
  • Genetic counselling
  • Next generation sequencing
  • Multi-gene panel
  • Diagnostic accuracy

Background

Approximately 5 to 10% of all cancers are caused by inherited germline mutations and are termed Hereditary Cancer (HC) [13]. HC is generally driven by a single mutated gene which confers increased risk of developing certain tumours to the affected individual (mostly at an early age). Causative genes usually control functions in cell cycle or DNA repair damage machinery, and can be related to the same spectrum of tumours inducing similar phenotypes and defining different Hereditary Cancer Syndromes (HCSs) [4]. Hence, the identification of gene mutation carriers constitutes a challenge for the Public Health System in terms of prevention and early diagnosis of tumours associated with each HCS.

To date, more than 200 HCSs have been described and the majority of the associated genes have been identified [1, 4, 5]. The identification of gene mutation carriers in relatives of HCS families has important implications in the field of cancer prevention, early diagnosis and in reproductive decision-making. In order to manage these high-risk individuals, clinical practice guidelines and specific genetic counselling programmes have been incorporated in the context of health care institutions. Furthermore, our better understanding of tumour genetics together the availability of cutting-edge sequencing technologies requires a continuous evaluation of clinical guidelines and analytical procedures to improve the performance of genetic counselling programmes.

The Oncology Plan of the Valencia Community was an initiative of the Public Health Ministry from the Valencia Government to follow World Health Organization (WHO) recommendations from the National Cancer Control Programme (NCCP). This Plan included the institution of a Hereditary Cancer Programme (HCP) in 2005 to identify gene mutation carriers associated with a HCS, aiming to improve cancer prevention and early diagnosis and reduce cancer specific mortality. The HCP involves professionals from different specialities (Oncologists, Epidemiologists, Pathologists, Geneticists, Nurses, and Psychologists) and four reference laboratories for performing the genetic analysis. This multidisciplinary team shares a common database and an HC Clinical Practice Guideline that regulates the multi-centre diagnostic process of individuals with an increased risk of developing cancer. This guideline also defines the prevention and surveillance recommendations for mutation carriers and their relatives.

We aim to incorporate the study of a large NGS multi-gene panel related to HCSs in the clinical routine of one of the reference laboratories in the context of the HCP of the Valencia Community.

Methods

Samples

Germline DNA samples extracted by conventional methods were requested to the IBSP-CV Biobank, which currently holds a collection of more than 4000 DNA samples from individuals enrolled in the HCP of the Valencia Community. Selected samples correspond to 91 non-informative probands of high-risk families classified into different HCSs (Additional file 1 Table S1).

This study (Fam-Can) was approved by the Ethical Committee of the Public Health Ministry on March 30th, 2015 and all probands gave informed consent for using their DNA for research purposes.

NGS analysis

The TruSight™ Cancer Sequencing Panel (Illumina©) was used for library preparation. DNA sequencing was performed with the MiSeq Reagent Kit v2 300 cycles (Illumina©) on a MiSeq platform (Illumina©). This pan-hereditary-cancer panel comprises oligo probes targeting 94 genes and 284 SNPs associated with an increased cancer predisposition. All procedures were performed according to the manufacturer’s instructions.

Four independent experiments were performed. Sequences were mapped to the human reference genome GRCh37/hg19. Data output files (gVCF) were imported into the open source Illumina VariantStudio™ Data Analysis Software v2.2 (Illumina©) for analysis. Custom filters were created to improve variant annotation and interpretation according to the assay. These included: alternative variant frequency higher than 30% (for detecting germline variants), and a minimum read depth of 50x per variant. Personalized reports for each sample were generated.

The five-tier terminology system of the American College of Medical Genetics and Genomics (ACMG) was used for variant classification [6] including: Pathogenic (P), Likely Pathogenic (LP), Variant of Unknown Significance (VUS), Likely Benign (LB) and Benign (B). Additional categories according to ClinVar interpretation including NA (Not Available) or Other, Risk Factor, Drug Response, Protective and Conflicting Interpretation, were merged with VUS.

Variants automatically annotated by software were manually checked on the main human genomic databases: ClinVar (www.ncbi.nlm.nih.gov/clinvar), dbSNP (www.ncbi.nlm.nih.gov/projects/SNP) and Ensembl (http://www.ensembl.org), and were categorized according to the available clinical interpretation.

Validation of pathogenic and likely pathogenic variants

Only those variants classified as P/LP were validated: 16 by Sanger Sequencing using specific primers (Additional file 2 Table S2); and 3 by an alternative NGS multi-gene panel [Hereditary Cancer Solution v1.1 panel (SOPHiA GENETICS®)]. Variant validation analyses were performed with SeqScape® Software v2.6 (Applied Biosystems) and Sequencing Analysis Software v5.2 (Applied Biosystems) for Sanger Sequencing, and Sophia DDM® Platform v4.4.2.1 (SOPHiA GENETICS®) for NGS.

Results

NGS analysis

The 91 samples included in the study were sequenced in four consecutive experiments. The output data yielded similar results in all experiments (Additional file 3 Table S3).

Coverage uniformity was higher than 90% in all tested samples. The average value of total aligned reads was 1,040,207 (89%), and average percentage of target coverage at 50x was 88.6%, the median region coverage depth being 206x (range: 29–549).

A total of 27,941 variants were identified in the 91 samples, 23,427 (83.8%) of which passed the established custom filters. The median number of filtered variants per sample was 274 (range: 17–326). Overall, filtered variants were annotated as follows: 45 P, 57 LP, 15,028 VUS, 636 LB and 7661 B. Detailed classification of variants per sample is indicated in Additional file 4 Table S4: 102 P/LP (0.4%), 15,028 VUS (64.1%), and 8297 B/LB (35.4%). Focusing on P/LP variants, 30 of 91 samples (33%) presented the same P variant in EHBP1 (NM_015252.3:c.1290 + 30064G > A, rs721048), and 54 of 91 samples (59%) carried the same LP variant in CCDC170 (NC_000006.12:g.151627231G > A, rs2046210). Both were eliminated from the analysis due to their high frequency, in fact these variants are classified as B in Varsome, because they meet the BA1 rule (Allele frequency is > 5% in Exome Sequencing Project, 1000 Genomes Project, or Exome Aggregation Consortium).

Finally, a total of 19 P/LP variants were identified in 15 probands (16%) affecting 11 different genes (Table 1). These alterations represented 10 Single Nucleotide Variants (SNVs), 6 deletions and 1 duplication, all in heterozygosis, and resulted in: 7 missense variants (2 affecting the splice site region), 6 frameshift variants (1 not yet reported in consulted databases), 3 nonsense variants (resulting in premature termination codon), and 1 in-frame deletion variant.
Table 1

P/LP variants. cDNA and Protein changes are named according to HGVS nomenclature

ID

HCS

Gene

cDNA change

Protein change

Variant Type

Consequence

Variant Classific.

S14

HBOC

RAD51D

c.958C > T

p.(Arg320Ter)

SNV

Nonsense

LP

S22

CRC

APC

c.2805C > A

(p.Tyr935Ter)

SNV

Nonsense

P

MUTYH

c.1187G > A

(p.Gly396Asp)

SNV

Missense

P

TP53

c.845G > A

(p.Arg282Gln)

SNV

Missense

P

S36

HBOC

XPC

c.1001C > A

p.(Pro334His)

SNV

Missense

P

S38

LS

MSH2

c.792G > C

p.(Gln264His)

SNV

Missense a

LP

S39

LS

MUTYH

c.536A > G

p.(Tyr179Cys)

SNV

Missense

P

S51

FAP

MUTYH

c.1187G > A

p.(Gly396Asp)

SNV

Missense a

P

MUTYH

c.1437_1439delGGA

p.(Glu480del)

del

Missense

P

S58

HBOC

MUTYH

c.1101dupC

p.(Arg368GlnfsTer164)

dup

Frameshift

P

S63

HBOC

ATM

c.8249_8252delTAAC

p.(Thr2751SerfsTer54)

del

Frameshift a

LP

MUTYH

c.1101dupC

p.(Arg368GlnfsTer164)

dup

Frameshift

P

S69

HBOC

PALB2

c.2964delA

p.(Val989Ter)

del

Frameshift

P

S70

HBOC

BRCA1

c.115 T > C

p.(Cys39Arg)

SNV

Missense

P

S77

HBOC

BRCA1

c.3770_3771delAG

p.(Glu1257GlyfsTer9)

del

Frameshift

P

S84

LS

BRIP1

c.2990_2993delCAAA

p.(Thr997ArgfsTer61)

del

Frameshift

LP

S87

LS

TP53

c.638G > A

p.(Arg213Gln)

SNV

Missense

P

S89

LS

BRCA2

c.5980C > T

p.(Gln1994Ter)

SNV

Nonsense

P

S91

HBOC

BRCA2

c.9025_9029delTATCA

p.(Tyr3009SerfsTer7)

del

Frameshift

P

Reference sequence: RAD51D: NM_001142571.1; TP53: NM_000546.5; APC: NM_000038.5; MUTYH: NM_001128425.1; XPC: NM_004628.4; MSH2: NM_000251.2; ATM: NM_000051.3; PALB2: NM_024675.3; BRCA1: NM_007300.3; BRIP1: NM_032043.2; BRCA2: NM_032043.3

aRemarked missense variants which affect splice site regions and novel frameshift variant

The most frequently mutated gene was MUTYH with 6 variants (32%), 4 were monoallelic and 2 biallelic (Table 1). The second most frequently mutated genes were TP53, BRCA1 and BRCA2 (11% each). One mutation was reported in the following genes: RAD51D, APC, MSH2, ATM, PALB2, BRIP1 and XPC (5% each).

The mutation rate in each HCS was: 9 P/LP variants in 49 Hereditary Breast and Ovarian Cancer (HBOC) cases (18%), 5 in 21 Lynch Syndrome (LS) samples (24%), 3 in one unique sample within the 16 Colorectal Cancer (CRC) group (19%), and 2 MUTYH mutations in one of the 4 Familiar Adenomatous Polyposis (FAP) samples (25%) (Table 1). Over half of the P/LP variants corresponded to probands diagnosed with HBOC (9/19, 53%), almost one third of them with LS (5/19, 33%), followed by CRC and FAP (1/9, 7% each) (Fig. 1).
Fig. 1
Fig. 1

Distribution of P/LP variants by gene (a) and HCS (b)

Validation of pathogenic variants

All P/LP variants listed in Table 1 were successfully confirmed by Sanger Sequencing or by an alternative NGS multi-gene panel. A concordance of 100% was achieved.

Discussion

Genetic diagnosis of HCS is principally focussed on sequencing a few high-risk genes associated with each syndrome. To date the gold standard approach has been Sanger sequencing; nevertheless, it is expensive and time-consuming in comparison with NGS technologies [7]. Nowadays, thanks to the development and consolidation of NGS, many genes can be tested simultaneously, saving both time and resources. Moreover, the extensive use of NGS in research has allowed the identification of several new genes related to common HCSs [3]. NGS applications, such as multi-gene panels, are appropriate tools for improving the diagnostic performance within the HCS context, as they include analysis of the classic candidate genes as well as recently discovered ones. This broad approach has proved to be successful in several studies [811] responding to the increasing demand for genetic testing in oncology.

In our study, we used an NGS pan-hereditary-cancer gene panel to reanalyse DNA samples from probands that previously gave a non-informative single genetic testing result. It is important to highlight that this study was performed in the context of the HCP of the Valencia Community, supported and regulated by the Public Health Ministry, and constitutes the first attempt to introduce this technology in a multi-centre structure for the genetic diagnosis of HCS.

The variant rates obtained in our study are similar to those reported by others [10], in which the most frequent findings are VUS (64.1%), followed by non-informative variants (35.4%) and finally, deleterious mutations (0.5%). P/LP variants were detected in 16% of our samples, a higher rate than in studies performed with smaller NGS multi-gene panels [1113], but similar to others with the same pan-hereditary-cancer panel than us [8].

It is important to note that four of P/LP variants were detected in high-risk genes that had already been tested and were non-informative for any specific HCS: an MSH2 mutation in a LS (S38) and three mutations in BRCA1 (S70, S77) and BRCA2 (S91) in HBOC probands (4.4%). These findings emphasize the lack of sensitivity of some of the traditional screening methods used so far in our HCP, such as single strand conformation polymorphisms (SSCP) and High Resolution Melting (HRM) [14]. The remaining P/LP variants were detected in genes of high/moderate/low penetrance not previously analysed.

Using this approach, HCS diagnosis was improved, producing a corresponding clinical impact in terms of genetic counselling and surveillance indications. Specifically, this approach allowed the identification of new gene mutations associated with the affiliated HCS, as well as the reclassification of some cases as other HCSs. For instance: S89, initially classified as LS, carriers a deleterious mutation in BRCA2 being now associated with HBOC; and S51, clinically associated with FAP, presented a biallelic mutation in MUTYH matching criteria for MUTYH-Associated Polyposis (MAP). Detecting alterations in other genes associated with the same HCS may explain the different proband phenotypes, particularly in those cases with a difficult family history or when a non-confirmatory result was obtained by previous testing using a limited number of genes. For example, S14 and S69 were associated with HBOC (not informative by BRCA testing) and harboured deleterious mutations in RAD51D and PALB2, which are moderate-risk genes for Ovarian Cancer (OC) and Breast Cancer (BC) respectively [1520].

Interestingly, some cases displayed the simultaneous occurrence of pathogenic variants in different genes. S63, linked to an HBOC syndrome, carried mutations in ATM and MUTYH (monoallelic variant); and S22, associated with CRC syndrome, harboured deleterious mutations in three different genes: APC, TP53 and MUTYH (monoallelic variant). In both cases, and not considering monoallelic MUTYH variants, the altered genes are considered high-risk genes for their corresponding HCSs; however, such mutations would not have been detected with the limited stepwise approach. This reinforces the idea that NGS significantly increases diagnostic efficiency compared to conventional methodologies.

From the results herein reported two challenging outcomes must be highlighted. First, we detected several monoallelic mutations in the MUTYH gene. Some of these variants occurred in the same individual, with other alterations in different genes (in S22 and S63 concomitant with APC and TP53, and ATM alterations respectively), but other MUTYH monoallelic mutations occurred as single variants in other cases such as S39 associated with LS and S58 pertaining to an HBOC family. In these cases, MUTYH monoallelic mutations were not causative for the patient phenotypes due to the consideration of MUTYH as a recessive gene [13, 21, 22]; however, alterations in this gene have recently been associated with low-risk for these HCSs [10]. Furthermore, some evidence has been reported about elevated cancer risk in monoallelic carriers and nowadays the associated cancer risks for MUTYH are controversial [13, 2123]. Second, we identified two deleterious alterations in TP53 (S87, S22), a very well-known tumour suppressor gene related to Li-Fraumeni syndrome (LFS), as well as to BC/OC (high-risk) and CRC (moderate-risk) [3, 24, 25]. So far, LFS is not included either for counselling or genetic testing within our HCP. However, the mutation rate of TP53 in our series together with the overlapping in different HCs prompts us to suggest considering alterations of this gene in the genetic diagnosis of HCs.

Overall, we found that most of the detected variants (79%) did not occur in the candidate genes established in our genetic counselling program for each HCS. In addition to those already mentioned, we identified BRIP1 (S84) and BRCA2 (S89) deleterious mutations in LS cases, and one XPC (S36) alteration in a HBOC individual. These genes are traditionally related to a different spectrum of tumours which were not diagnosed in our probands. However, some cases may be explained by the presence of other tumour types in proband relatives. As an example, BRIP1 is a moderate-risk gene related to BC, and although our proband (S84) was diagnosed with LS, cases of BC were present in the genetic pedigree (Fig. 2). Our findings support the inclusion of at least high and moderate genes in routine testing to better understand the cancer segregation in the affected families.
Fig. 2
Fig. 2

S84 family pedigree

Hence, NGS multi-gene panels have proven to be a feasible tool for inclusion in the routine laboratory workflow to improve HCS diagnosis. This approach is much more cost-effective than applying Sanger Sequencing to test the same number of genes in the same number of patients [2]. We obtained satisfactory sequencing parameters for 85 samples (93.4%) and all our informative results were successfully validated using alternative methods [9, 21], highlighting huge advantages in terms of time, sensitivity and cost effectiveness.

However, NGS has some limitations that still represent a challenge for clinical genetic labs and need to be considered when considering genetic tests in clinical decision making. Among these limitations we highlight the variable robustness of the methods employed, level of validation of the different NGS multi-gene panel (commercial vs. custom), technical and analytical capability of personnel, etc. Control of all these aspects should be mandatory and can be covered by implementing quality assurance management systems, some already internationally recognized such as the ISO15189 accreditation, and by participating in external quality controls, such as EMQN and UK NEQAS.

In addition to these technical aspects, NGS provides a huge amount of information that much of the time constitutes a bottle-neck for the proper interpretation of a genetic test. As with technical validation, data analysis and interpretation should also be validated and contrasted with the already existing databases. Information related to the quality of the sequencing run (raw data), such as covered and uncovered regions, noise, presence of pseudogenes, list of actionable variants, correlation with existing databases, etc., constitute some of the parameters that should be considered and validated to provide a proper genetic result guaranteeing the absence of both false positive or negative results. How different labs cover these analytical aspects varies (proprietary bioinformatics pipeline, free or commercial IT solutions, etc), but whichever approach used, they must be integrated as a key pillar within the comprehensive quality assurance systems of the genetic labs.

In conclusion, we advocate the implementation of NGS in routine clinical practice, combined with a robust quality assurance system to guarantee the utility of the genetic results.

Conclusions

Reanalysing negative samples of non-informative probands from high risk cancer families using a multi-gene NGS panel has resulted in the identification of 19 pathological mutations updating the mutation status of 14 families, which could take advantage from specific screening and cancer prevention programmes. Hence, we advocate the implementation of NGS in routine practice, combined with a robust quality assurance system to guarantee the clinical utility of the genetic results.

Notes

Abbreviations

ACMG: 

American College of Medical Genetics and Genomics

B: 

Benign variant

BC: 

Breast Cancer

CCDC170

COILED-COIL DOMAIN CONTAINING 170 GENE

CRC : 

Colorectal Cancer

CS : 

Cowden Syndrome

DNA : 

Deoxyribonucleic Acid

EMQN: 

European Molecular Genetics Quality Network

FAP: 

Familial Adenomatous Polyposis

GRCh37/hg19: 

Genome Reference Consortium human genome (build 37) or human genome19

gVCF: 

Genomic Variant Call Format

HBOC: 

Hereditary Breast and Ovarian Cancer

HC: 

Hereditary Cancer

HCP: 

Hereditary Cancer Programme

HCS: 

Hereditary Cancer Syndrome

HGVS: 

Human Genome Variation Society

HNPCC: 

Hereditary Non-Polyposis Colorectal Cancer

HRB: 

Hereditary Retinoblastoma

HRM: 

High Resolution Melting

IBSP-CV Biobank: 

Biobank for Biomedical Research and Public Health of the Valencian Community (Biobanco para la Investigación Biomédica y en Salud Pública de la Comunidad Valenciana)

LB: 

Likely Benign variant

LP: 

Likely Pathogenic variant

LS: 

Lynch Syndrome

MAP: 

MUTYH-Associated Polyposis

MEN: 

Multiple Endocrine Neoplasia

MEN1: 

Multiple Endocrine Neoplasia Type I

MEN2: 

Multiple Endocrine Neoplasia Type II

NA : 

Not Available

NCBI: 

National Center of Biological Information

NCCP: 

National Cancer Control Programme

NGS: 

Next Generation Sequencing

OC: 

Ovarian Cancer

OMIM: 

Online Mendelian Inheritance In Man

P: 

Pathogenic variant

PJS: 

Peutz-Jeghers Syndrome

SNP: 

Single Nucleotide Polimorfism

SNV: 

Single Nucleotide Variant

SSCP : 

Single strand conformation polymorphisms

UK NEQAS: 

United Kingdom National External Quality Assessment Service

VHL: 

von Hippel-Lindau disease

VUS: 

Variant of Unknown Significance

WHO: 

World Health Organization

Declarations

Acknowledgements

Authors want to thank Red Valenciana de Biobancos (RVB) and Biobanco Fundación Instituto Valenciano de Oncología for providing DNA samples to carry out this study.

Funding

There is no funding to be declared.

Availability of data and material

Data generated or analysed during this study are included in this published article (and its supplementary information files) or under request if necessary.

Authors’ contributions

M.R-C. and Z.G-C. contributed equally to the work. J.A.L-G. coordinated and supervised the study. All authors participate in the Hereditary Cancer Programme of the Valencia Community and provided clinical reviewing and information. M.R.C. and Z.G-C. carried out the experimental process and data analysis. M.R-C. and Z.G-C. wrote the manuscript with the contribution of all other authors. All authors read and approved the final manuscript

Ethics approval and consent to participate

This study (Fam-Can) was approved by the Ethical Committee of the Public Health General Management on March 30th, 2015 and all probands gave informed consent for using their DNA for research purposes.

Consent for publication

Not applicable.

Competing interests

No potential conflict of interest has been identified for any author of this paper according to the conventions and standards of the Hereditary Cancer in Clinical Practice.

Publisher’s Note

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Authors’ Affiliations

(1)
Laboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, C/Prof. Beltrán Báguena, 8-11, 46009 Valencia, Spain
(2)
Laboratory of Molecular Biology, Service of Clinical Analysis, Hospital Universitario y Politécnico La Fe, Valencia, Spain
(3)
Genetics Unit, Hospital Universitario y Politécnico La Fe, Valencia, Spain
(4)
Molecular Genetics Unit, Hospital General Universitario de Elche, Elche, Spain
(5)
Unit of Genetic Counselling in Cancer, Fundación Instituto Valenciano de Oncología, Valencia, Spain
(6)
Unit of Genetic Counselling in Cancer, Hospital Universitario y Politécnico La Fe, Valencia, Spain
(7)
Unit of Genetic Counselling in Cancer, Hospital Clínico, Valencia, Spain
(8)
Unit of Genetic Counselling in Cancer, Hospital General de Elche, Elche, Spain
(9)
Unit of Genetic Counselling in Cancer, Hospital General de Castellón, Castellón, Spain
(10)
Cancer and Public Health Area, FISABIO–Public Health, Valencia, Spain
(11)
General Directorate Public Health, Valencia, Spain
(12)
Epidemiology and Public Health Networking Biomedical Research Centre (CIBERESP), Madrid, Spain

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