Literature DB >> 21913181

Earlier age of onset of BRCA mutation-related cancers in subsequent generations.

Jennifer K Litton1, Kaylene Ready, Huiqin Chen, Angelica Gutierrez-Barrera, Carol J Etzel, Funda Meric-Bernstam, Ana M Gonzalez-Angulo, Huong Le-Petross, Karen Lu, Gabriel N Hortobagyi, Banu K Arun.   

Abstract

BACKGROUND: Women who are diagnosed with a deleterious mutation in either breast cancer (BRCA) gene have a high risk of developing breast and ovarian cancers at young ages. In this study, the authors assessed age at diagnosis in 2 generations of families with known mutations to investigate for earlier onset in subsequent generations.
METHODS: Of the 132 BRCA-positive women with breast cancer who participated in a high-risk protocol at The University of Texas MD Anderson Cancer Center (Gen 2), 106 women could be paired with a family member in the previous generation (Gen 1) who was diagnosed with a BRCA-related cancer (either breast cancer or ovarian cancer). Age at diagnosis, location of the mutation, and year of birth were recorded. A previously published parametric anticipation model was applied in these genetically predisposed families.
RESULTS: The median age of cancer diagnosis was 42 years (range, 28-55 years) in Gen 2 and 48 years (range, 30-72 years) in Gen 1 (P < .001). [corrected]. In the parametric model, the estimated change in the expected age at onset for the entire cohort was 7.9 years (P < .0001). Statistically significant earlier ages at diagnosis also were observed within subgroups of BRCA1 and BRCA2 mutations, maternal inheritance, paternal inheritance, breast cancer only, and breast cancer-identified and ovarian cancer-identified families.
CONCLUSIONS: Breast and ovarian cancers in BRCA mutation carriers appeared to be diagnosed at an earlier age in later generations. The authors concluded that patients who are younger at the onset of BRCA-related cancers should continue to be tracked to offer appropriate screening modalities at appropriate ages.
Copyright © 2011 American Cancer Society.

Entities:  

Mesh:

Year:  2011        PMID: 21913181      PMCID: PMC4369377          DOI: 10.1002/cncr.26284

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  15 in total

1.  Evidence for genetic anticipation in non-Mendelian diseases.

Authors:  A D Paterson; J L Kennedy; A Petronis
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

2.  The interval between cancer diagnosis among mothers and offspring in a population-based cohort.

Authors:  Ora Paltiel; Yehiel Friedlander; Lisa Deutsch; Rebecca Yanetz; Ronit Calderon-Margalit; Efrat Tiram; Hagit Hochner; Micha Barchana; Susan Harlap; Orly Manor
Journal:  Fam Cancer       Date:  2007       Impact factor: 2.375

3.  Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

Authors:  R Wooster; S L Neuhausen; J Mangion; Y Quirk; D Ford; N Collins; K Nguyen; S Seal; T Tran; D Averill
Journal:  Science       Date:  1994-09-30       Impact factor: 47.728

4.  Role for genetic anticipation in Lynch syndrome.

Authors:  Mef Nilbert; Susanne Timshel; Inge Bernstein; Klaus Larsen
Journal:  J Clin Oncol       Date:  2008-12-15       Impact factor: 44.544

5.  A parametric model for analyzing anticipation in genetically predisposed families.

Authors:  Klaus Larsen; Janne Petersen; Inge Bernstein; Mef Nilbert
Journal:  Stat Appl Genet Mol Biol       Date:  2009-06-02

6.  Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.

Authors:  D F Easton; D T Bishop; D Ford; G P Crockford
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

7.  Further segregation analysis of the fragile X syndrome with special reference to transmitting males.

Authors:  S L Sherman; P A Jacobs; N E Morton; U Froster-Iskenius; P N Howard-Peebles; K B Nielsen; M W Partington; G R Sutherland; G Turner; M Watson
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease.

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Journal:  Am J Hum Genet       Date:  1995-09       Impact factor: 11.025

9.  Meta-analysis of BRCA1 and BRCA2 penetrance.

Authors:  Sining Chen; Giovanni Parmigiani
Journal:  J Clin Oncol       Date:  2007-04-10       Impact factor: 44.544

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  26 in total

Review 1.  Impact of germline and somatic BRCA1/2 mutations: tumor spectrum and detection platforms.

Authors:  H Wu; X Wu; Z Liang
Journal:  Gene Ther       Date:  2017-08-03       Impact factor: 5.250

2.  Earlier age of onset in BRCA carriers-anticipation or cohort effect?: A Countercurrents Series.

Authors:  S A Narod
Journal:  Curr Oncol       Date:  2011-12       Impact factor: 3.677

3.  Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing.

Authors:  C L Scherr; N M Lindor; T L Malo; F J Couch; S T Vadaparampil
Journal:  Clin Genet       Date:  2015-02-26       Impact factor: 4.438

4.  Promoting guideline-based cancer genetic risk assessment for hereditary breast and ovarian cancer in ethnically and geographically diverse cancer survivors: Rationale and design of a 3-arm randomized controlled trial.

Authors:  Anita Y Kinney; Rachel Howell; Rachel Ruckman; Jean A McDougall; Tawny W Boyce; Belinda Vicuña; Ji-Hyun Lee; Dolores D Guest; Randi Rycroft; Patricia A Valverde; Kristina M Gallegos; Angela Meisner; Charles L Wiggins; Antoinette Stroup; Lisa E Paddock; Scott T Walters
Journal:  Contemp Clin Trials       Date:  2018-09-18       Impact factor: 2.226

5.  Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.

Authors:  Deborah Cragun; Anne Weidner; Courtney Lewis; Devon Bonner; Jongphil Kim; Susan T Vadaparampil; Tuya Pal
Journal:  Cancer       Date:  2017-02-09       Impact factor: 6.860

6.  BRCA sequencing and large rearrangement testing in young Black women with breast cancer.

Authors:  Tuya Pal; Devon Bonner; Deborah Cragun; Sharland Johnson; Mohammad Akbari; Lily Servais; Steven Narod; Susan Vadaparampil
Journal:  J Community Genet       Date:  2013-08-29

7.  Breast care.

Authors: 
Journal:  Breast Care (Basel)       Date:  2012-12       Impact factor: 2.860

Review 8.  Genetic counseling for hereditary breast and ovarian cancer among Puerto Rican women living in the United States.

Authors:  Courtney L Scherr; Elsa Vasquez; Gwendolyn P Quinn; Susan T Vadaparampil
Journal:  Rev Recent Clin Trials       Date:  2014

Review 9.  Genetic risk assessments in individuals at high risk for inherited breast cancer in the breast oncology care setting.

Authors:  Tuya Pal; Susan T Vadaparampil
Journal:  Cancer Control       Date:  2012-10       Impact factor: 3.302

10.  Living With Genetic Vulnerability: a Life Course Perspective.

Authors:  Rebekah J Hamilton; Nancy A Innella; Dawn T Bounds
Journal:  J Genet Couns       Date:  2015-09-02       Impact factor: 2.537

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