Literature DB >> 32485079

Suggested application of HER2+ breast tumor phenotype for germline TP53 variant classification within ACMG/AMP guidelines.

Cristina Fortuno1, Jessica Mester2, Tina Pesaran3, Jeffrey N Weitzel4, Jill Dolinsky3, Amal Yussuf3, Kelly McGoldrick3, Judy E Garber5, Sharon A Savage6, Payal P Khincha6, D Gareth Evans7, Maria Isabel Achatz8, Kim E Nichols9, Kara N Maxwell10, Joshua D Schiffman11, Renata Sandoval8, Paul A James12, Amanda B Spurdle1.   

Abstract

Early onset breast cancer is the most common malignancy in women with Li-Fraumeni syndrome, caused by germline TP53 pathogenic variants. It has repeatedly been suggested that breast tumors from TP53 carriers are more likely to be HER2+ than those of noncarriers, but this information has not been incorporated into variant interpretation models for TP53. Breast tumor pathology is already being used quantitatively for assessing pathogenicity of germline variants in other genes, and it has been suggested that this type of evidence can be incorporated into current American College of Medical Genetics and Genomics/Association for Molecular Pathology (ACMG/AMP) guidelines for germline variant classification. Here, by reviewing published data and using internal datasets separated by different age groups, we investigated if breast tumor HER2+ status has utility as a predictor of TP53 germline variant pathogenicity, considering age at diagnosis. Overall, our results showed that the identification of HER2+ breast tumors diagnosed before the age of 40 can be conservatively incorporated into the current TP53-specific ACMG/AMP PP4 criterion, following a point system detailed in this manuscript. Further larger studies will be needed to reassess the value of HER2+ breast tumors diagnosed at a later age.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  ACMG; HER2; TP53; variant classification

Mesh:

Substances:

Year:  2020        PMID: 32485079      PMCID: PMC7484289          DOI: 10.1002/humu.24060

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.700


  28 in total

1.  Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis.

Authors:  Mandy L Ballinger; Ana Best; Phuong L Mai; Payal P Khincha; Jennifer T Loud; June A Peters; Maria Isabel Achatz; Rubens Chojniak; Alexandre Balieiro da Costa; Karina Miranda Santiago; Judy Garber; Allison F O'Neill; Rosalind A Eeles; D Gareth Evans; Eveline Bleiker; Gabe S Sonke; Marielle Ruijs; Claudette Loo; Joshua Schiffman; Anne Naumer; Wendy Kohlmann; Louise C Strong; Jasmina Bojadzieva; David Malkin; Surya P Rednam; Elena M Stoffel; Erika Koeppe; Jeffrey N Weitzel; Thomas P Slavin; Bita Nehoray; Mark Robson; Michael Walsh; Lorenzo Manelli; Anita Villani; David M Thomas; Sharon A Savage
Journal:  JAMA Oncol       Date:  2017-12-01       Impact factor: 31.777

2.  A quantitative model to predict pathogenicity of missense variants in the TP53 gene.

Authors:  Cristina Fortuno; Arcadi Cipponi; Mandy L Ballinger; Sean V Tavtigian; Magali Olivier; Vatsal Ruparel; Ygal Haupt; Sue Haupt; International Sarcoma Kindred Study; Kathy Tucker; Amanda B Spurdle; David M Thomas; Paul A James
Journal:  Hum Mutat       Date:  2019-03-18       Impact factor: 4.878

3.  Detection of somatic variants in peripheral blood lymphocytes using a next generation sequencing multigene pan cancer panel.

Authors:  Bradford Coffee; Hannah C Cox; John Kidd; Scott Sizemore; Krystal Brown; Susan Manley; Debora Mancini-DiNardo
Journal:  Cancer Genet       Date:  2017-01-16

4.  Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.

Authors:  Ella R Thompson; Simone M Rowley; Na Li; Simone McInerny; Lisa Devereux; Michelle W Wong-Brown; Alison H Trainer; Gillian Mitchell; Rodney J Scott; Paul A James; Ian G Campbell
Journal:  J Clin Oncol       Date:  2016-01-19       Impact factor: 44.544

5.  Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.

Authors:  Gaëlle Bougeard; Mariette Renaux-Petel; Jean-Michel Flaman; Camille Charbonnier; Pierre Fermey; Muriel Belotti; Marion Gauthier-Villars; Dominique Stoppa-Lyonnet; Emilie Consolino; Laurence Brugières; Olivier Caron; Patrick R Benusiglio; Brigitte Bressac-de Paillerets; Valérie Bonadona; Catherine Bonaïti-Pellié; Julie Tinat; Stéphanie Baert-Desurmont; Thierry Frebourg
Journal:  J Clin Oncol       Date:  2015-05-26       Impact factor: 44.544

6.  Prevalence of germline TP53 mutations in HER2+ breast cancer patients.

Authors:  Michelle G Rath; Serena Masciari; Rebecca Gelman; Alexander Miron; Penelope Miron; Kathleen Foley; Andrea L Richardson; Ian E Krop; Sigitas J Verselis; Deborah A Dillon; Judy E Garber
Journal:  Breast Cancer Res Treat       Date:  2013-04-12       Impact factor: 4.872

7.  Gene panel testing of 5589 BRCA1/2-negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer.

Authors:  Jan Hauke; Judit Horvath; Eva Groß; Andrea Gehrig; Ellen Honisch; Karl Hackmann; Gunnar Schmidt; Norbert Arnold; Ulrike Faust; Christian Sutter; Julia Hentschel; Shan Wang-Gohrke; Mateja Smogavec; Bernhard H F Weber; Nana Weber-Lassalle; Konstantin Weber-Lassalle; Julika Borde; Corinna Ernst; Janine Altmüller; Alexander E Volk; Holger Thiele; Verena Hübbel; Peter Nürnberg; Katharina Keupp; Beatrix Versmold; Esther Pohl; Christian Kubisch; Sabine Grill; Victoria Paul; Natalie Herold; Nadine Lichey; Kerstin Rhiem; Nina Ditsch; Christian Ruckert; Barbara Wappenschmidt; Bernd Auber; Andreas Rump; Dieter Niederacher; Thomas Haaf; Juliane Ramser; Bernd Dworniczak; Christoph Engel; Alfons Meindl; Rita K Schmutzler; Eric Hahnen
Journal:  Cancer Med       Date:  2018-03-09       Impact factor: 4.452

8.  Somatic TP53 variants frequently confound germ-line testing results.

Authors:  Jeffrey N Weitzel; Elizabeth C Chao; Bita Nehoray; Lily R Van Tongeren; Holly LaDuca; Kathleen R Blazer; Thomas Slavin; D A B M D Facmg; Tina Pesaran; Christina Rybak; Ilana Solomon; Mariana Niell-Swiller; Jill S Dolinsky; Danielle Castillo; Aaron Elliott; Chia-Ling Gau; Virginia Speare; Kory Jasperson
Journal:  Genet Med       Date:  2017-11-30       Impact factor: 8.822

9.  Mutant p53 gain of function induces HER2 over-expression in cancer cells.

Authors:  A A Román-Rosales; E García-Villa; L A Herrera; P Gariglio; J Díaz-Chávez
Journal:  BMC Cancer       Date:  2018-07-03       Impact factor: 4.430

10.  Breast cancer receptor status and stage at diagnosis in over 1,200 consecutive public hospital patients in Soweto, South Africa: a case series.

Authors:  Valerie A McCormack; Maureen Joffe; Eunice van den Berg; Nadine Broeze; Isabel dos Santos Silva; Isabelle Romieu; Judith S Jacobson; Alfred I Neugut; Joachim Schüz; Herbert Cubasch
Journal:  Breast Cancer Res       Date:  2013       Impact factor: 6.466

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  6 in total

1.  Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants.

Authors:  Cristina Fortuno; Kristy Lee; Magali Olivier; Tina Pesaran; Phuong L Mai; Kelvin C de Andrade; Laura D Attardi; Stephanie Crowley; D Gareth Evans; Bing-Jian Feng; Ann K M Foreman; Megan N Frone; Robert Huether; Paul A James; Kelly McGoldrick; Jessica Mester; Bryce A Seifert; Thomas P Slavin; Leora Witkowski; Liying Zhang; Sharon E Plon; Amanda B Spurdle; Sharon A Savage
Journal:  Hum Mutat       Date:  2020-12-25       Impact factor: 4.700

2.  Breast Cancer Phenotype Associated With Li-Fraumeni Syndrome: A Brazilian Cohort Enriched by TP53 p.R337H Carriers.

Authors:  Renata Lazari Sandoval; Natalia Polidorio; Ana Carolina Rathsam Leite; Mariana Cartaxo; Janina Pontes Pisani; Carla Vanessa Quirino; Loureno Cezana; Natálya Gonçalves Pereira; Allan Andresson Lima Pereira; Benedito Mauro Rossi; Maria Isabel Achatz
Journal:  Front Oncol       Date:  2022-03-16       Impact factor: 6.244

3.  Expanding ACMG variant classification guidelines into a general framework.

Authors:  Emmanuelle Masson; Wen-Bin Zou; Emmanuelle Génin; David N Cooper; Gerald Le Gac; Yann Fichou; Na Pu; Vinciane Rebours; Claude Férec; Zhuan Liao; Jian-Min Chen
Journal:  Hum Genomics       Date:  2022-08-16       Impact factor: 6.481

4.  An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes.

Authors:  Alison Schwartz; Danielle K Manning; Diane R Koeller; Anu Chittenden; Raymond A Isidro; Connor P Hayes; Feruza Abraamyan; Monica Devi Manam; Meaghan Dwan; Justine A Barletta; Lynette M Sholl; Matthew B Yurgelun; Huma Q Rana; Judy E Garber; Arezou A Ghazani
Journal:  Front Oncol       Date:  2022-08-25       Impact factor: 5.738

5.  The role of TP53 pathogenic variants in early-onset HER2-positive breast cancer.

Authors:  Carla Escudeiro; Carla Pinto; Joana Vieira; Ana Peixoto; Pedro Pinto; Manuela Pinheiro; Catarina Santos; Joana Guerra; Susana Lisboa; Rui Santos; João Silva; Conceição Leal; Nuno Coimbra; Paula Lopes; Marco Ferreira; Ana B Sousa; Manuel R Teixeira
Journal:  Fam Cancer       Date:  2020-10-14       Impact factor: 2.375

6.  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

  6 in total

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