Literature DB >> 30607672

TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.

J J Bakhuizen1, F B Hogervorst2, M E Velthuizen3, M W Ruijs2, K van Engelen4, T A van Os4, J J Gille4, M Collée5, A M van den Ouweland5, C J van Asperen6, C M Kets7, A R Mensenkamp7, E M Leter8, M J Blok8, M M de Jong9, M G Ausems3.   

Abstract

Early-onset breast cancer may be due to Li-Fraumeni Syndrome (LFS). Current national and international guidelines recommend that TP53 genetic testing should be considered for women with breast cancer diagnosed before the age of 31 years. However, large studies investigating TP53 mutation prevalence in this population are scarce. We collected nationwide laboratory records for all young breast cancer patients tested for TP53 mutations in the Netherlands. Between 2005 and 2016, 370 women diagnosed with breast cancer younger than 30 years of age were tested for TP53 germline mutations, and eight (2.2%) were found to carry a (likely) pathogenic TP53 sequence variant. Among BRCA1/BRCA2 mutation negative women without a family history suggestive of LFS or a personal history of multiple LFS-related tumours, the TP53 mutation frequency was < 1% (2/233). Taking into consideration that TP53 mutation prevalence was comparable or even higher in some studies selecting patients with breast cancer onset at older ages or HER2-positive breast cancers, raises the question of whether a very early age of onset is an appropriate single TP53 genetic testing criterion.

Entities:  

Keywords:  Breast cancer; Genetic testing; Hereditary; Li–Fraumeni syndrome; TP53

Mesh:

Substances:

Year:  2019        PMID: 30607672     DOI: 10.1007/s10689-018-00118-0

Source DB:  PubMed          Journal:  Fam Cancer        ISSN: 1389-9600            Impact factor:   2.375


  46 in total

1.  Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.

Authors:  Chantal R M Lammens; Neil K Aaronson; Anja Wagner; Rolf H Sijmons; Margreet G E M Ausems; Annette H J T Vriends; Mariëlle W G Ruijs; Theo A M van Os; Liesbeth Spruijt; Encarna B Gómez García; Irma Kluijt; Tanja Nagtegaal; Senno Verhoef; Eveline M A Bleiker
Journal:  J Clin Oncol       Date:  2010-05-17       Impact factor: 44.544

2.  Genetic testing in a cohort of young patients with HER2-amplified breast cancer.

Authors:  D M Eccles; N Li; R Handwerker; T Maishman; E R Copson; L T Durcan; S M Gerty; L Jones; D G Evans; L Haywood; I Campbell
Journal:  Ann Oncol       Date:  2015-12-17       Impact factor: 32.976

3.  A molecular approach for identifying individuals with Li-Fraumeni syndrome who have a limited family history.

Authors:  P Ang; I H K Lim; R Y Y Yong; A S G Lee
Journal:  Clin Genet       Date:  2009-03       Impact factor: 4.438

4.  2009 version of the Chompret criteria for Li Fraumeni syndrome.

Authors:  Julie Tinat; Gaelle Bougeard; Stéphanie Baert-Desurmont; Stéphanie Vasseur; Cosette Martin; Emilie Bouvignies; Olivier Caron; Brigitte Bressac-de Paillerets; Pascaline Berthet; Catherine Dugast; Catherine Bonaïti-Pellié; Dominique Stoppa-Lyonnet; Thierry Frébourg
Journal:  J Clin Oncol       Date:  2009-08-03       Impact factor: 44.544

5.  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

6.  Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing.

Authors:  Huma Q Rana; Rebecca Gelman; Holly LaDuca; Rachel McFarland; Emily Dalton; Jennifer Thompson; Virginia Speare; Jill S Dolinsky; Elizabeth C Chao; Judy E Garber
Journal:  J Natl Cancer Inst       Date:  2018-08-01       Impact factor: 13.506

Review 7.  [CHEK2-mutation in Dutch breast cancer families: expanding genetic testing for breast cancer].

Authors:  Muriel A Adank; Frederik J Hes; Wendy A G van Zelst-Stams; M Petrousjka van den Tol; Caroline Seynaeve; Jan C Oosterwijk
Journal:  Ned Tijdschr Geneeskd       Date:  2015

8.  A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations.

Authors:  J R F Wilson; A C Bateman; H Hanson; Q An; G Evans; N Rahman; J L Jones; D M Eccles
Journal:  J Med Genet       Date:  2010-08-30       Impact factor: 6.318

9.  Radio-induced malignancies after breast cancer postoperative radiotherapy in patients with Li-Fraumeni syndrome.

Authors:  Steve Heymann; Suzette Delaloge; Arslane Rahal; Olivier Caron; Thierry Frebourg; Lise Barreau; Corinne Pachet; Marie-Christine Mathieu; Hugo Marsiglia; Céline Bourgier
Journal:  Radiat Oncol       Date:  2010-11-08       Impact factor: 3.481

10.  Attitude towards pre-implantation genetic diagnosis for hereditary cancer.

Authors:  Chantal Lammens; Eveline Bleiker; Neil Aaronson; Annette Vriends; Margreet Ausems; Maaike Jansweijer; Anja Wagner; Rolf Sijmons; Ans van den Ouweland; Rob van der Luijt; Liesbeth Spruijt; Encarna Gómez García; Mariëlle Ruijs; Senno Verhoef
Journal:  Fam Cancer       Date:  2009-07-30       Impact factor: 2.375

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  7 in total

1.  New surveillance guidelines for Li-Fraumeni and hereditary TP53 related cancer syndrome: implications for germline TP53 testing in breast cancer.

Authors:  D Gareth Evans; Emma R Woodward
Journal:  Fam Cancer       Date:  2021-01       Impact factor: 2.375

2.  Gail Model Underestimates Breast Cancer Risk in Thai Population.

Authors:  Doonyapat Sa-Nguanraksa; Thanyawat Sasanakietkul; Chayanuch O-Charoenrat; Anchalee Kulprom; Pornchai O-Charoenrat
Journal:  Asian Pac J Cancer Prev       Date:  2019-08-01

3.  Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population.

Authors:  Emilia Rogoża-Janiszewska; Karolina Malińska; Bohdan Górski; Rodney J Scott; Cezary Cybulski; Wojciech Kluźniak; Marcin Lener; Anna Jakubowska; Jacek Gronwald; Tomasz Huzarski; Jan Lubiński; Tadeusz Dębniak
Journal:  Breast Cancer       Date:  2020-09-04       Impact factor: 4.239

4.  Feedback of extended panel sequencing in 1530 patients referred for suspicion of hereditary predisposition to adult cancers.

Authors:  Mathias Cavaillé; Nancy Uhrhammer; Maud Privat; Flora Ponelle-Chachuat; Mathilde Gay-Bellile; Mathis Lepage; Sandrine Viala; Yannick Bidet; Yves-Jean Bignon
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5.  TP53 germline mutations in the context of families with hereditary breast and ovarian cancer: a clinical challenge.

Authors:  Sabine Grill; Juliane Ramser; Heide Hellebrand; Nicole Pfarr; Melanie Boxberg; Christine Brambs; Nina Ditsch; Alfons Meindl; Eva Groß; Thomas Meitinger; Marion Kiechle; Anne S Quante
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6.  Somatic Mutational Profile of High-Grade Serous Ovarian Carcinoma and Triple-Negative Breast Carcinoma in Young and Elderly Patients: Similarities and Divergences.

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Journal:  Cells       Date:  2021-12-20       Impact factor: 6.600

7.  Breast cancer characteristics and surgery among women with Li-Fraumeni syndrome in Germany-A retrospective cohort study.

Authors:  Nathalie Rippinger; Christine Fischer; Hans-Peter Sinn; Nicola Dikow; Christian Sutter; Kerstin Rhiem; Sabine Grill; Friedrich W Cremer; Huu P Nguyen; Nina Ditsch; Karin Kast; Simone Hettmer; Christian P Kratz; Sarah Schott
Journal:  Cancer Med       Date:  2021-09-26       Impact factor: 4.452

  7 in total

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