Skip to main content
Erschienen in: Breast Cancer Research and Treatment 1/2017

12.07.2017 | Brief Report

Hereditary diffuse gastric cancer and lynch syndromes in a BRCA1/2 negative breast cancer patient

verfasst von: Scolastica W. Njoroge, Kelly R. Burgess, Melody A. Cobleigh, Hussein H. Alnajar, Paolo Gattuso, Lydia Usha

Erschienen in: Breast Cancer Research and Treatment | Ausgabe 1/2017

Einloggen, um Zugang zu erhalten

Abstract

Introduction

Genetic counseling and testing is recommended for women with a personal and/or family history of breast and other cancers (ovarian, pancreatic, male breast and others). Mutations in the BRCA1 and BRCA2 genes (BRCA1/2) are the most common causes of hereditary breast and ovarian cancer. Additional genetic counseling and testing with a multi-gene panel may be considered in breast cancer patients who tested negative for mutations in these two genes. In about 11% of BRCA1/2-negative patients, further genetic testing reveals pathogenic mutations in other high or moderate cancer risk genes. In 0.2% of cases, an individual may carry pathogenic mutations in more than one high penetrance gene (a double heterozygote). Finding one or more pathogenic mutations is important for cancer prevention in patients and/or their families.

Case presentation

Here we present a case of a breast cancer patient who did not have a pathogenic mutation in BRCA1/2 and had a family history of breast and stomach cancers. On an additional multi-gene panel testing, she was found to carry pathogenic mutations in the CDH1 and PMS2 genes, which cause Hereditary Diffuse Gastric Cancer and Lynch syndromes, respectively. To our knowledge, this is the first description of such a double heterozygote.

Discussion

Clinical manifestations, genetics, and management of both syndromes are reviewed, including prophylactic surgery and screening for unaffected family members. Management challenges for a mutation carrier with advanced breast cancer are discussed. Our case supports the clinical utility of additional multi-gene panel testing for breast cancer patients who do not have a pathogenic mutation in BRCA1/2 genes.
Fußnoten
1
The NCCN Guidelines are a work in progress that may be refined as often as new significant data becomes available. The NCCN Guidelines are a statement of consensus of its authors regarding their views of currently accepted approaches to treatment. Any clinician seeking to apply or consult any NCCN Guidelines is expected to use independent medical judgment in the context of individual clinical circumstances to determine any patient’s care or treatment. The National Comprehensive Cancer Network makes no warranties of any kind whatsoever regarding their content, use or application and disclaims any responsibility for their application or use in any way.
 
Literatur
1.
Zurück zum Zitat NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) (2016) Genetic/Familial High Risk Assessment: Breast and Ovarian. Version 2.2017—December 7, 2016. © 2016 National Comprehensive Cancer Network, Inc. NCCN.org. Accessed 15 Oct 2016 NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) (2016) Genetic/Familial High Risk Assessment: Breast and Ovarian. Version 2.2017—December 7, 2016. © 2016 National Comprehensive Cancer Network, Inc. NCCN.org. Accessed 15 Oct 2016
2.
Zurück zum Zitat Desmond A, Kurian AW, Gabree M et al (2015) Clinical actionability of multigene panel testing for hereditary breast and ovarian cancer risk assessment. JAMA Oncol 1:943–951CrossRefPubMed Desmond A, Kurian AW, Gabree M et al (2015) Clinical actionability of multigene panel testing for hereditary breast and ovarian cancer risk assessment. JAMA Oncol 1:943–951CrossRefPubMed
3.
4.
Zurück zum Zitat Ford D, Easton D, Stratton M et al (1998) Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet 62:676–689CrossRefPubMedPubMedCentral Ford D, Easton D, Stratton M et al (1998) Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet 62:676–689CrossRefPubMedPubMedCentral
5.
Zurück zum Zitat Kurian AW, Hare EE, Mills MA et al (2014) Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment. J Clin Oncol 32:2001–2009CrossRefPubMedPubMedCentral Kurian AW, Hare EE, Mills MA et al (2014) Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment. J Clin Oncol 32:2001–2009CrossRefPubMedPubMedCentral
6.
Zurück zum Zitat Weitzel J, Blazer K, et al (2015) Assessment of the clinical presentation of patients with at least two pathogenic mutations on multigene panel testing. ASCO Annual meeting Abstract No: 1514 Weitzel J, Blazer K, et al (2015) Assessment of the clinical presentation of patients with at least two pathogenic mutations on multigene panel testing. ASCO Annual meeting Abstract No: 1514
7.
Zurück zum Zitat Plon SE, Pirics ML, Nuchtern J et al (2008) Multiple tumors in a child with germ-line mutations in TP53 and PTEN. N Engl J Med 359:537–539CrossRefPubMed Plon SE, Pirics ML, Nuchtern J et al (2008) Multiple tumors in a child with germ-line mutations in TP53 and PTEN. N Engl J Med 359:537–539CrossRefPubMed
8.
Zurück zum Zitat Augustyn AM, Agostino NM, Namey TL et al (2011) Two patients with germline mutations in both BRCA1 and BRCA2 discovered unintentionally: a case series and discussion of BRCA testing modalities. Breast Cancer Res Treat 129:629–634CrossRefPubMed Augustyn AM, Agostino NM, Namey TL et al (2011) Two patients with germline mutations in both BRCA1 and BRCA2 discovered unintentionally: a case series and discussion of BRCA testing modalities. Breast Cancer Res Treat 129:629–634CrossRefPubMed
10.
Zurück zum Zitat Rubenstein JH, Enns R, Heidelbaugh J et al (2015) American Gastroenterological Association Institute Guideline on the Diagnosis and Management of Lynch Syndrome. Gastroenterology 149:777–782CrossRefPubMed Rubenstein JH, Enns R, Heidelbaugh J et al (2015) American Gastroenterological Association Institute Guideline on the Diagnosis and Management of Lynch Syndrome. Gastroenterology 149:777–782CrossRefPubMed
11.
Zurück zum Zitat Berx G, Cleton-Jansen AM, Nollet F et al (1995) E-cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancers. EMBO J 14:6107–6115PubMedPubMedCentral Berx G, Cleton-Jansen AM, Nollet F et al (1995) E-cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancers. EMBO J 14:6107–6115PubMedPubMedCentral
12.
Zurück zum Zitat Takeichi M, Hirano S, Matsuyoshi N et al (1992) Cytoplasmic control of cadherin-mediated cell-cell adhesion. Cold Spring Harb Symp Quant Biol 57:327–334CrossRefPubMed Takeichi M, Hirano S, Matsuyoshi N et al (1992) Cytoplasmic control of cadherin-mediated cell-cell adhesion. Cold Spring Harb Symp Quant Biol 57:327–334CrossRefPubMed
13.
Zurück zum Zitat Buys SS, Sandbach JF, Gammon A et al (2017) A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes. Cancer 123(10):1721–1730CrossRefPubMed Buys SS, Sandbach JF, Gammon A et al (2017) A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes. Cancer 123(10):1721–1730CrossRefPubMed
14.
Zurück zum Zitat Kaurah P, MacMillan A, Boyd N et al (2007) Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer. JAMA 297:2360–2372CrossRefPubMed Kaurah P, MacMillan A, Boyd N et al (2007) Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer. JAMA 297:2360–2372CrossRefPubMed
15.
Zurück zum Zitat Pharoah PD, Guilford P, Caldas C et al (2001) Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families. Gastroenterology 121:1348–1353CrossRefPubMed Pharoah PD, Guilford P, Caldas C et al (2001) Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families. Gastroenterology 121:1348–1353CrossRefPubMed
16.
Zurück zum Zitat Schrader KA, Masciari S, Boyd N et al (2008) Hereditary diffuse gastric cancer: association with lobular breast cancer. Fam Cancer 7:73–82CrossRefPubMed Schrader KA, Masciari S, Boyd N et al (2008) Hereditary diffuse gastric cancer: association with lobular breast cancer. Fam Cancer 7:73–82CrossRefPubMed
18.
19.
Zurück zum Zitat Win AK, Lindor NM, Young JP et al (2012) Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome. J Natl Cancer Inst 104:1363–1372CrossRefPubMedPubMedCentral Win AK, Lindor NM, Young JP et al (2012) Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome. J Natl Cancer Inst 104:1363–1372CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Buerki N, Gautier L, Kovac M et al (2012) Evidence for breast cancer as an integral part of lynch syndrome. Genes Chromosom Cancer 51:83–91CrossRefPubMed Buerki N, Gautier L, Kovac M et al (2012) Evidence for breast cancer as an integral part of lynch syndrome. Genes Chromosom Cancer 51:83–91CrossRefPubMed
21.
Zurück zum Zitat LaDuca H, Horton C, Peseran T, et al (2014) Features of hereditary breast and ovarian cancer in a Lynch syndrome cohort ascertained through multi-gene panel testing. In: Abstract presented at the National Society of Genetic Counselors Annual Meeting LaDuca H, Horton C, Peseran T, et al (2014) Features of hereditary breast and ovarian cancer in a Lynch syndrome cohort ascertained through multi-gene panel testing. In: Abstract presented at the National Society of Genetic Counselors Annual Meeting
22.
Zurück zum Zitat Crispens MA (2012) Endometrial and ovarian cancer in lynch syndrome. Clin Colon Rectal Surg 25:097–102CrossRef Crispens MA (2012) Endometrial and ovarian cancer in lynch syndrome. Clin Colon Rectal Surg 25:097–102CrossRef
Metadaten
Titel
Hereditary diffuse gastric cancer and lynch syndromes in a BRCA1/2 negative breast cancer patient
verfasst von
Scolastica W. Njoroge
Kelly R. Burgess
Melody A. Cobleigh
Hussein H. Alnajar
Paolo Gattuso
Lydia Usha
Publikationsdatum
12.07.2017
Verlag
Springer US
Erschienen in
Breast Cancer Research and Treatment / Ausgabe 1/2017
Print ISSN: 0167-6806
Elektronische ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-017-4393-3

Weitere Artikel der Ausgabe 1/2017

Breast Cancer Research and Treatment 1/2017 Zur Ausgabe

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.