Literature DB >> 28766224

Clinical Decision-Making in Patients with Variant of Uncertain Significance in BRCA1 or BRCA2 Genes.

Jessemae L Welsh1, Tanya L Hoskin2, Courtney N Day2, Abigail S Thomas2, Jodie A Cogswell2, Fergus J Couch3, Judy C Boughey4.   

Abstract

BACKGROUND: How diagnosis with a variant of uncertain significance (VUS) in a BRCA gene impacts clinical decision-making is not well known.
METHODS: We queried for all patients attending Mayo Clinic Rochester from 2004 to 2016 who tested positive for BRCA1 or BRCA2 VUS and reviewed patient management choices. Groups were compared by using Wilcoxon rank-sum and Chi-square tests.
RESULTS: We identified 97 patients (95 females, 2 males) with BRCA VUS. For patients without cancer history (n = 20), 80% had a mother or sister with breast cancer, and median Tyrer-Cuzick (IBIS) lifetime breast cancer risk score was 27% (range 16-62%). Management included bilateral prophylactic mastectomy (BPM) in 39%, where choice for BPM was significantly associated with IBIS score (median 32 vs. 24%, p = 0.02) and first-degree family history of breast cancer (100 vs. 64%, p = 0.03) but not Gail score or total number of family members with cancer. For patients with breast cancer who had known VUS status prior to surgery (n = 9), the rate of contralateral prophylactic mastectomy (CPM) was 22% compared with 25% without known VUS and 83% with known BRCA pathogenic mutation. In 21 of 97 (22%) patients, the BRCA VUS has been reclassified (95% benign, 5% deleterious).
CONCLUSIONS: BRCA VUS carriers with cancer elected surgical choices similar to average-risk breast cancer patients. However, VUS carriers without cancer had high rates of BPM, associated with first-degree family history and IBIS score. Over time, a significant proportion of BRCA VUS were reclassified, illustrating the importance of appropriate counseling regarding VUS.

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Year:  2017        PMID: 28766224      PMCID: PMC6171336          DOI: 10.1245/s10434-017-5959-3

Source DB:  PubMed          Journal:  Ann Surg Oncol        ISSN: 1068-9265            Impact factor:   5.344


  8 in total

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Authors:  J M Eggington; K R Bowles; K Moyes; S Manley; L Esterling; S Sizemore; E Rosenthal; A Theisen; J Saam; C Arnell; D Pruss; J Bennett; L A Burbidge; B Roa; R J Wenstrup
Journal:  Clin Genet       Date:  2013-12-20       Impact factor: 4.438

2.  State Variation in the Receipt of a Contralateral Prophylactic Mastectomy Among Women Who Received a Diagnosis of Invasive Unilateral Early-Stage Breast Cancer in the United States, 2004-2012.

Authors:  Rebecca Nash; Michael Goodman; Chun Chieh Lin; Rachel A Freedman; Laura S Dominici; Kevin Ward; Ahmedin Jemal
Journal:  JAMA Surg       Date:  2017-07-01       Impact factor: 14.766

3.  Variants of uncertain significance in BRCA testing: evaluation of surgical decisions, risk perception, and cancer distress.

Authors:  J O Culver; C D Brinkerhoff; J Clague; K Yang; K E Singh; S R Sand; J N Weitzel
Journal:  Clin Genet       Date:  2013-02-20       Impact factor: 4.438

4.  Impact that Timing of Genetic Mutation Diagnosis has on Surgical Decision Making and Outcome for BRCA1/BRCA2 Mutation Carriers with Breast Cancer.

Authors:  Akiko Chiba; Tanya L Hoskin; Emily J Hallberg; Jodie A Cogswell; Courtney N Heins; Fergus J Couch; Judy C Boughey
Journal:  Ann Surg Oncol       Date:  2016-06-23       Impact factor: 5.344

5.  Use of immediate breast reconstruction and choice for contralateral prophylactic mastectomy.

Authors:  Tanya L Hoskin; Tina J Hieken; Amy C Degnim; James W Jakub; Steven R Jacobson; Judy C Boughey
Journal:  Surgery       Date:  2015-12-17       Impact factor: 3.982

6.  Variants of unknown significance in BRCA testing: impact on risk perception, worry, prevention and counseling.

Authors:  S Richter; I Haroun; T C Graham; A Eisen; A Kiss; E Warner
Journal:  Ann Oncol       Date:  2013-11       Impact factor: 32.976

7.  Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.

Authors:  Mitzi L Murray; Felecia Cerrato; Robin L Bennett; Gail P Jarvik
Journal:  Genet Med       Date:  2011-12       Impact factor: 8.822

8.  Understanding of BRCA VUS genetic results by breast cancer specialists.

Authors:  B K Eccles; E Copson; T Maishman; J E Abraham; D M Eccles
Journal:  BMC Cancer       Date:  2015-11-25       Impact factor: 4.430

  8 in total
  16 in total

1.  A Multiplex Homology-Directed DNA Repair Assay Reveals the Impact of More Than 1,000 BRCA1 Missense Substitution Variants on Protein Function.

Authors:  Lea M Starita; Muhtadi M Islam; Tapahsama Banerjee; Aleksandra I Adamovich; Justin Gullingsrud; Stanley Fields; Jay Shendure; Jeffrey D Parvin
Journal:  Am J Hum Genet       Date:  2018-09-12       Impact factor: 11.025

2.  Physician interpretation of variants of uncertain significance.

Authors:  Sarah K Macklin; Jessica L Jackson; Paldeep S Atwal; Stephanie L Hines
Journal:  Fam Cancer       Date:  2019-01       Impact factor: 2.375

3.  Contralateral Risk-Reducing Mastectomy in Breast Cancer Patients Who Undergo Multigene Panel Testing.

Authors:  Brittany L Murphy; Min Yi; Banu K Arun; Angelica M Gutierrez Barrera; Isabelle Bedrosian
Journal:  Ann Surg Oncol       Date:  2020-07-27       Impact factor: 5.344

4.  Timely cancer genetic counseling and testing for young women with breast cancer: impact on surgical decision-making for contralateral risk-reducing mastectomy.

Authors:  Shenin A Dettwyler; Darcy L Thull; Priscilla F McAuliffe; Jennifer G Steiman; Ronald R Johnson; Emilia J Diego; Phuong L Mai
Journal:  Breast Cancer Res Treat       Date:  2022-05-21       Impact factor: 4.872

5.  Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?

Authors:  Paul S Appelbaum; Wylie Burke; Erik Parens; David A Zeevi; Laura Arbour; Nanibaa' A Garrison; Vence L Bonham; Wendy K Chung
Journal:  Am J Hum Genet       Date:  2022-06-02       Impact factor: 11.043

6.  Risk-reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system.

Authors:  Sarah Knerr; Boya Guo; Kathleen F Mittendorf; Heather Spencer Feigelson; Marian J Gilmore; Gail P Jarvik; Tia L Kauffman; Erin Keast; Frances L Lynch; Kristin R Muessig; Sonia Okuyama; David L Veenstra; Jamilyn M Zepp; Katrina A B Goddard; Beth Devine
Journal:  Cancer       Date:  2022-06-09       Impact factor: 6.921

7.  Association Between Genetic Testing for Hereditary Breast Cancer and Contralateral Prophylactic Mastectomy Among Multiethnic Women Diagnosed With Early-Stage Breast Cancer.

Authors:  Vicky Ro; Julia E McGuinness; Boya Guo; Meghna S Trivedi; Tarsha Jones; Wendy K Chung; Roshni Rao; Elana Levinson; Carrie Koval; Donna Russo; Ilana Chilton; Rita Kukafka; Katherine D Crew
Journal:  JCO Oncol Pract       Date:  2021-10-27

8.  Clinical management among individuals with variant of uncertain significance in hereditary cancer: A systematic review and meta-analysis.

Authors:  Sukh Makhnoon; Erica M Bednar; Kate J Krause; Susan K Peterson; Maria A Lopez-Olivo
Journal:  Clin Genet       Date:  2021-04-21       Impact factor: 4.438

9.  Postgraduate training in Cancer Genetics-a cross-specialty survey exploring experience of clinicians in Ireland.

Authors:  Jana K McHugh; Gozie Offiah; Sean Daly; Nazmy El Beltagi; Michael Kevin Barry; Seamus O'Reilly; Terri P McVeigh
Journal:  Ir J Med Sci       Date:  2021-06-30       Impact factor: 2.089

10.  Men seeking counselling in a Breast Cancer Risk Evaluation Clinic.

Authors:  Ana Catarina Freitas; Ana Opinião; Sofia Fragoso; Hugo Nunes; Madalena Santos; Ana Clara; Sandra Bento; Ana Luis; Jorge Silva; Cecília Moura; Bruno Filipe; Patrícia Machado; Sidónia Santos; Saudade André; Paula Rodrigues; Joana Parreira; Fátima Vaz
Journal:  Ecancermedicalscience       Date:  2018-01-30
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