Literature DB >> 25475920

Testing for Hereditary Breast Cancer: Panel or Targeted Testing? Experience from a Clinical Cancer Genetics Practice.

Jennifer Doherty1, Danielle C Bonadies, Ellen T Matloff.   

Abstract

Approaches to hereditary breast cancer testing are shifting as multi-gene panels become more widely available. This paper describes our center's experience and outcomes of a 6-gene panel test as a first-tier approach in patients who were candidates for BRCA testing. Between July and December 2013, a 6-gene panel test was ordered for patients meeting criteria for BRCA testing. A retrospective review detailed the mutation and variant of uncertain significance (VUS) rates for the genes analyzed. The mutation rate was 5.2 % (n = 7) and the VUS rate was 6.7 % (n = 9). A subsequent review determined the number of BRCA-negative patients who would have been offered additional single gene testing had BRCA, only, been their first-tier test. Applying consensus criteria revealed 7.1 % (n = 9) cases that met criteria for additional testing. Pedigree analysis by a certified genetic counselor revealed 26.8 % (n = 34) cases that would have been offered additional testing based on personal and/or family history. Our results suggest that this panel may be warranted as a first-tier test for a small subset of patients, but likely represents over testing for the majority of patients who are candidates for BRCA testing. The genes selected for panels, the extra costs per patient and the chance of VUS must be considered before we uniformly switch from BRCA to full panel testing on all patients.

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Year:  2014        PMID: 25475920     DOI: 10.1007/s10897-014-9796-2

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  16 in total

Review 1.  The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?

Authors:  F S M Hilbers; M P G Vreeswijk; C J van Asperen; P Devilee
Journal:  Clin Genet       Date:  2013-09-12       Impact factor: 4.438

Review 2.  American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.

Authors:  Mark E Robson; Courtney D Storm; Jeffrey Weitzel; Dana S Wollins; Kenneth Offit
Journal:  J Clin Oncol       Date:  2010-01-11       Impact factor: 44.544

3.  Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.

Authors:  Nicholas Hearle; Valérie Schumacher; Fred H Menko; Sylviane Olschwang; Lisa A Boardman; Johan J P Gille; Josbert J Keller; Anne Marie Westerman; Rodney J Scott; Wendy Lim; Jill D Trimbath; Francis M Giardiello; Stephen B Gruber; G Johan A Offerhaus; Felix W M de Rooij; J H Paul Wilson; Anika Hansmann; Gabriela Möslein; Brigitte Royer-Pokora; Tilman Vogel; Robin K S Phillips; Allan D Spigelman; Richard S Houlston
Journal:  Clin Cancer Res       Date:  2006-05-15       Impact factor: 12.531

4.  Rapid development of post-radiotherapy sarcoma and breast cancer in a patient with a novel germline 'de-novo' TP53 mutation.

Authors:  A Salmon; D Amikam; N Sodha; S Davidson; L Basel-Vanagaite; R A Eeles; D Abeliovich; T Peretz
Journal:  Clin Oncol (R Coll Radiol)       Date:  2007-06-14       Impact factor: 4.126

5.  F18-fluorodeoxyglucose-positron emission tomography/computed tomography screening in Li-Fraumeni syndrome.

Authors:  Serena Masciari; Annick D Van den Abbeele; Lisa R Diller; Iryna Rastarhuyeva; Jeffrey Yap; Katherine Schneider; Lisa Digianni; Frederick P Li; Joseph F Fraumeni; Sapna Syngal; Judy E Garber
Journal:  JAMA       Date:  2008-03-19       Impact factor: 56.272

Review 6.  Systematic review: comparative effectiveness of medications to reduce risk for primary breast cancer.

Authors:  Heidi D Nelson; Rongwei Fu; Jessica C Griffin; Peggy Nygren; M E Beth Smith; Linda Humphrey
Journal:  Ann Intern Med       Date:  2009-11-17       Impact factor: 25.391

7.  Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations.

Authors:  Kelly D Gonzalez; Katie A Noltner; Carolyn H Buzin; Dongqing Gu; Cindy Y Wen-Fong; Vu Q Nguyen; Jennifer H Han; Katrina Lowstuter; Jeffrey Longmate; Steve S Sommer; Jeffrey N Weitzel
Journal:  J Clin Oncol       Date:  2009-02-09       Impact factor: 44.544

8.  The integration of next-generation sequencing panels in the clinical cancer genetics practice: an institutional experience.

Authors:  Caitlin B Mauer; Sara M Pirzadeh-Miller; Linda D Robinson; David M Euhus
Journal:  Genet Med       Date:  2013-10-10       Impact factor: 8.822

9.  Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research.

Authors:  Rebecca C Fitzgerald; Richard Hardwick; David Huntsman; Fatima Carneiro; Parry Guilford; Vanessa Blair; Daniel C Chung; Jeff Norton; Krishnadath Ragunath; J Han Van Krieken; Sarah Dwerryhouse; Carlos Caldas
Journal:  J Med Genet       Date:  2010-07       Impact factor: 6.318

Review 10.  Hereditary diffuse gastric cancer: association with lobular breast cancer.

Authors:  Kasmintan A Schrader; Serena Masciari; Niki Boyd; Sara Wiyrick; Pardeep Kaurah; Janine Senz; Wylie Burke; Henry T Lynch; Judy E Garber; David G Huntsman
Journal:  Fam Cancer       Date:  2008       Impact factor: 2.375

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  11 in total

1.  Increased yield of actionable mutations using multi-gene panels to assess hereditary cancer susceptibility in an ethnically diverse clinical cohort.

Authors:  Charité Ricker; Julie O Culver; Katrina Lowstuter; Duveen Sturgeon; Julia D Sturgeon; Christopher R Chanock; William J Gauderman; Kevin J McDonnell; Gregory E Idos; Stephen B Gruber
Journal:  Cancer Genet       Date:  2016-01-12

2.  The Clinical Utility of Next Generation Sequencing Results in a Community-Based Hereditary Cancer Risk Program.

Authors:  A E Bunnell; C A Garby; E J Pearson; S A Walker; L E Panos; Joanne L Blum
Journal:  J Genet Couns       Date:  2016-06-09       Impact factor: 2.537

3.  Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort.

Authors:  Phuong L Mai; Ana F Best; June A Peters; Rosamma M DeCastro; Payal P Khincha; Jennifer T Loud; Renée C Bremer; Philip S Rosenberg; Sharon A Savage
Journal:  Cancer       Date:  2016-08-06       Impact factor: 6.860

4.  Genomic Disparities in Breast Cancer Among Latinas.

Authors:  Filipa Lynce; Kristi D Graves; Lina Jandorf; Charite Ricker; Eida Castro; Laura Moreno; Bianca Augusto; Laura Fejerman; Susan T Vadaparampil
Journal:  Cancer Control       Date:  2016-10       Impact factor: 3.302

5.  Mutation Rates in Cancer Susceptibility Genes in Patients With Breast Cancer With Multiple Primary Cancers.

Authors:  Kara N Maxwell; Brandon M Wenz; Abha Kulkarni; Bradley Wubbenhorst; Kurt D'Andrea; Benita Weathers; Noah Goodman; Joseph Vijai; Jenna Lilyquist; Steven N Hart; Thomas P Slavin; Kasmintan A Schrader; Vignesh Ravichandran; Tinu Thomas; Chunling Hu; Mark E Robson; Paolo Peterlongo; Bernardo Bonanni; James M Ford; Judy E Garber; Susan L Neuhausen; Payal D Shah; Angela R Bradbury; Angela M DeMichele; Kenneth Offit; Jeffrey N Weitzel; Fergus J Couch; Susan M Domchek; Katherine L Nathanson
Journal:  JCO Precis Oncol       Date:  2020-08-19

6.  Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries.

Authors:  Anne Brédart; Jean-Luc Kop; Antonis C Antoniou; Alex P Cunningham; Antoine De Pauw; Marc Tischkowitz; Hans Ehrencrona; Sylvie Dolbeault; Léonore Robieux; Kerstin Rhiem; Douglas F Easton; Peter Devilee; Dominique Stoppa-Lyonnet; Rita Schmutlzer
Journal:  Fam Cancer       Date:  2018-01       Impact factor: 2.375

7.  Patient-Centered Care in Breast Cancer Genetic Clinics.

Authors:  Anne Brédart; Amélie Anota; Julia Dick; Violetta Kuboth; Olivier Lareyre; Antoine De Pauw; Alejandra Cano; Dominique Stoppa-Lyonnet; Rita Schmutzler; Sylvie Dolbeault; Jean-Luc Kop
Journal:  Int J Environ Res Public Health       Date:  2018-02-12       Impact factor: 3.390

8.  Germline mutation landscape of Chinese patients with familial breast/ovarian cancer in a panel of 22 susceptibility genes.

Authors:  Jiayu Wang; Weiwei Li; Yujian Shi; Yan Huang; Tao Sun; Lili Tang; Qing Lu; Qiumo Lei; Ning Liao; Feng Jin; Hui Li; Tao Huang; Jun Qian; Danmei Pang; Shusen Wang; Peizhi Fan; Xinhong Wu; Ying Lin; Haiyan Qin; Binghe Xu
Journal:  Cancer Med       Date:  2019-04-13       Impact factor: 4.452

9.  Association between polymorphisms in estrogen metabolism genes and breast cancer development in Chinese women: A prospective case-control study.

Authors:  Juanjuan Qiu; Zhenggui Du; Jingping Liu; Yi Zhou; Faqing Liang; Qing Lü
Journal:  Medicine (Baltimore)       Date:  2018-11       Impact factor: 1.889

Review 10.  Multi gene panel testing for hereditary breast cancer - is it ready to be used?

Authors:  Andreea Catana; Adina Patricia Apostu; Razvan-Geo Antemie
Journal:  Med Pharm Rep       Date:  2019-07-31
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