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Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings

Bonache, Sandra ; Esteban, Irene ; Moles-Fernández, Alejandro ; Tenés, Anna ; Duran-Lozano, Laura LU ; Montalban, Gemma ; Bach, Vanessa ; Carrasco, Estela ; Gadea, Neus and López-Fernández, Adrià , et al. (2018) In Journal of Cancer Research and Clinical Oncology 144(12). p.2495-2513
Abstract

PURPOSE: Few and small studies have been reported about multigene testing usage by massively parallel sequencing in European cancer families. There is an open debate about what genes should be tested, and the actionability of some included genes is under research.

METHODS: We investigated a panel of 34 known high/moderate-risk cancer genes, including 16 related to breast or ovarian cancer (BC/OC) genes, and 63 candidate genes to BC/OC in 192 clinically suspicious of hereditary breast/ovarian cancer (HBOC) Spanish families without pathogenic variants in BRCA1 or BRCA2 (BRCA1/2).

RESULTS: We identified 16 patients who carried a high- or moderate-risk pathogenic variant in eight genes: 4 PALB2, 3 ATM, 2 RAD51D, 2 TP53, 2 APC, 1... (More)

PURPOSE: Few and small studies have been reported about multigene testing usage by massively parallel sequencing in European cancer families. There is an open debate about what genes should be tested, and the actionability of some included genes is under research.

METHODS: We investigated a panel of 34 known high/moderate-risk cancer genes, including 16 related to breast or ovarian cancer (BC/OC) genes, and 63 candidate genes to BC/OC in 192 clinically suspicious of hereditary breast/ovarian cancer (HBOC) Spanish families without pathogenic variants in BRCA1 or BRCA2 (BRCA1/2).

RESULTS: We identified 16 patients who carried a high- or moderate-risk pathogenic variant in eight genes: 4 PALB2, 3 ATM, 2 RAD51D, 2 TP53, 2 APC, 1 BRIP1, 1 PTEN and 1 PMS2. These findings led to increased surveillance or prevention options in 12 patients and predictive testing in their family members. We detected 383 unique variants of uncertain significance in known cancer genes, of which 35 were prioritized in silico. Eighteen loss-of-function variants were detected in candidate BC/OC genes in 17 patients (1 BARD1, 1 ERCC3, 1 ERCC5, 2 FANCE, 1 FANCI, 2 FANCL, 1 FANCM, 1 MCPH1, 1 PPM1D, 2 RBBP8, 3 RECQL4 and 1 with SLX4 and XRCC2), three of which also carry pathogenic variants in known cancer genes.

CONCLUSIONS: Eight percent of the BRCA1/2 negative patients carry pathogenic variants in other actionable genes. The multigene panel usage improves the diagnostic yield in HBOC testing and it is an effective tool to identify potentially new candidate genes.

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Please use this url to cite or link to this publication:
@article{c068b60e-1306-4c9d-80a1-5cfc0059c188,
  abstract     = {{<p>PURPOSE: Few and small studies have been reported about multigene testing usage by massively parallel sequencing in European cancer families. There is an open debate about what genes should be tested, and the actionability of some included genes is under research.</p><p>METHODS: We investigated a panel of 34 known high/moderate-risk cancer genes, including 16 related to breast or ovarian cancer (BC/OC) genes, and 63 candidate genes to BC/OC in 192 clinically suspicious of hereditary breast/ovarian cancer (HBOC) Spanish families without pathogenic variants in BRCA1 or BRCA2 (BRCA1/2).</p><p>RESULTS: We identified 16 patients who carried a high- or moderate-risk pathogenic variant in eight genes: 4 PALB2, 3 ATM, 2 RAD51D, 2 TP53, 2 APC, 1 BRIP1, 1 PTEN and 1 PMS2. These findings led to increased surveillance or prevention options in 12 patients and predictive testing in their family members. We detected 383 unique variants of uncertain significance in known cancer genes, of which 35 were prioritized in silico. Eighteen loss-of-function variants were detected in candidate BC/OC genes in 17 patients (1 BARD1, 1 ERCC3, 1 ERCC5, 2 FANCE, 1 FANCI, 2 FANCL, 1 FANCM, 1 MCPH1, 1 PPM1D, 2 RBBP8, 3 RECQL4 and 1 with SLX4 and XRCC2), three of which also carry pathogenic variants in known cancer genes.</p><p>CONCLUSIONS: Eight percent of the BRCA1/2 negative patients carry pathogenic variants in other actionable genes. The multigene panel usage improves the diagnostic yield in HBOC testing and it is an effective tool to identify potentially new candidate genes.</p>}},
  author       = {{Bonache, Sandra and Esteban, Irene and Moles-Fernández, Alejandro and Tenés, Anna and Duran-Lozano, Laura and Montalban, Gemma and Bach, Vanessa and Carrasco, Estela and Gadea, Neus and López-Fernández, Adrià and Torres-Esquius, Sara and Mancuso, Francesco and Caratú, Ginevra and Vivancos, Ana and Tuset, Noemí and Balmaña, Judith and Gutiérrez-Enríquez, Sara and Diez, Orland}},
  issn         = {{1432-1335}},
  keywords     = {{Adult; Alleles; Biomarkers, Tumor; Computational Biology/methods; Female; Genes, BRCA1; Genes, BRCA2; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Hereditary Breast and Ovarian Cancer Syndrome/diagnosis; High-Throughput Nucleotide Sequencing; Humans; Middle Aged; Neoplasm Staging; Sequence Analysis, DNA; Spain; Young Adult}},
  language     = {{eng}},
  number       = {{12}},
  pages        = {{2495--2513}},
  publisher    = {{Springer}},
  series       = {{Journal of Cancer Research and Clinical Oncology}},
  title        = {{Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings}},
  url          = {{http://dx.doi.org/10.1007/s00432-018-2763-9}},
  doi          = {{10.1007/s00432-018-2763-9}},
  volume       = {{144}},
  year         = {{2018}},
}