Literature DB >> 32923877

Pathogenic Variants in CHEK2 Are Associated With an Adverse Prognosis in Symptomatic Early-Onset Breast Cancer.

Stephanie L Greville-Heygate1,2,3, Tom Maishman1, William J Tapper1, Ramsey I Cutress1, Ellen Copson1, Alison M Dunning4, Linda Haywood5, Louise J Jones5, Diana M Eccles1,2.   

Abstract

PURPOSE: Checkpoint kinase 2 (CHEK2) is frequently included in multigene panels. We describe the associated outcomes among carriers of CHEK2 pathogenic variants in young patients with symptomatic breast cancer. PATIENTS AND METHODS: Participants (N = 2,344) in the Prospective Outcomes in Sporadic Versus Hereditary Breast Cancer study had a diagnosis of primary invasive breast cancer at age ≤ 40 years. Summary statistics were used to compare tumor characteristics among CHEK2+ carriers with those who were CHEK2-. Kaplan-Meier curves were used to demonstrate overall survival (OS) and distant disease-free survival.
RESULTS: Overall, 53 of the 2,344 participants (2.3%) had a pathogenic CHEK2 variant. CHEK2+-associated tumors were significantly more likely to be grade 2, estrogen receptor and progesterone receptor-positive compared with CHEK2- tumors (grade 2, n = 28 of 52 [53.8%] v n = 803 of 2,229 [36.0%]; P = .029). CHEK2-associated tumors were significantly more likely to have nodal involvement (N1, n = 37 of 53 [69.8%] v 1,169 of 2,253 [51.9%]; P = .0098) and demonstrated a trend toward multifocality. A higher proportion of participants with CHEK2+ variants with invasive breast cancer were obese than were those with CHEK2- variant (28.3% v 18.8%; P = .039). Univariate and multivariable analyses revealed that OS and distant disease-free survival were significantly worse in CHEK2+ versus CHEK2- carriers (OS hazard ratio, 1.58; 95% CI, 1.01 to 2.48; P = .043).
CONCLUSION: This work highlights the adverse prognosis associated with breast cancer in carriers of CHEK2 pathogenic variants. It also identifies a potential association among obesity, family history, and breast cancer risk in young CHEK2 gene carriers.
© 2020 by American Society of Clinical Oncology.

Entities:  

Year:  2020        PMID: 32923877      PMCID: PMC7446368          DOI: 10.1200/PO.19.00178

Source DB:  PubMed          Journal:  JCO Precis Oncol        ISSN: 2473-4284


  27 in total

1.  Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer.

Authors:  Cezary Cybulski; Dominika Wokołorczyk; Anna Jakubowska; Tomasz Huzarski; Tomasz Byrski; Jacek Gronwald; Bartłomiej Masojć; Tadeusz Deebniak; Bohdan Górski; Paweł Blecharz; Steven A Narod; Jan Lubiński
Journal:  J Clin Oncol       Date:  2011-08-29       Impact factor: 44.544

2.  Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2*1100delC germline mutation.

Authors:  Marjanka K Schmidt; Rob A E M Tollenaar; Sanne R de Kemp; Annegien Broeks; Cees J Cornelisse; Vincent T H B M Smit; Johannes L Peterse; Flora E van Leeuwen; Laura J Van't Veer
Journal:  J Clin Oncol       Date:  2006-11-28       Impact factor: 44.544

3.  Family history and outcome of young patients with breast cancer in the UK (POSH study).

Authors:  B K Eccles; E R Copson; R I Cutress; T Maishman; D G Altman; P Simmonds; S M Gerty; L Durcan; L Stanton; D M Eccles
Journal:  Br J Surg       Date:  2015-05-20       Impact factor: 6.939

4.  Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2*1100delC variant.

Authors:  G H de Bock; M Schutte; E M M Krol-Warmerdam; C Seynaeve; J Blom; C T M Brekelmans; H Meijers-Heijboer; C J van Asperen; C J Cornelisse; P Devilee; R A E M Tollenaar; J G M Klijn
Journal:  J Med Genet       Date:  2004-10       Impact factor: 6.318

Review 5.  CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls.

Authors:  Maren Weischer; Stig Egil Bojesen; Christina Ellervik; Anne Tybjaerg-Hansen; Børge Grønne Nordestgaard
Journal:  J Clin Oncol       Date:  2008-01-02       Impact factor: 44.544

6.  Prospective observational study of breast cancer treatment outcomes for UK women aged 18-40 years at diagnosis: the POSH study.

Authors:  Ellen Copson; Bryony Eccles; Tom Maishman; Sue Gerty; Louise Stanton; Ramsey I Cutress; Douglas G Altman; Lorraine Durcan; Peter Simmonds; Gill Lawrence; Louise Jones; Judith Bliss; Diana Eccles
Journal:  J Natl Cancer Inst       Date:  2013-05-30       Impact factor: 13.506

7.  Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Authors:  Sue Richards; Nazneen Aziz; Sherri Bale; David Bick; Soma Das; Julie Gastier-Foster; Wayne W Grody; Madhuri Hegde; Elaine Lyon; Elaine Spector; Karl Voelkerding; Heidi L Rehm
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

8.  Body mass index had different effects on premenopausal and postmenopausal breast cancer risks: a dose-response meta-analysis with 3,318,796 subjects from 31 cohort studies.

Authors:  Yanzi Chen; Li Liu; Quan Zhou; Mustapha Umar Imam; Jialin Cai; Yaxuan Wang; Minjie Qi; Panpan Sun; Zhiguang Ping; Xiaoli Fu
Journal:  BMC Public Health       Date:  2017-12-08       Impact factor: 3.295

9.  Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol.

Authors:  Diana Eccles; Sue Gerty; Peter Simmonds; Victoria Hammond; Sarah Ennis; Douglas G Altman
Journal:  BMC Cancer       Date:  2007-08-15       Impact factor: 4.430

10.  PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

Authors:  Melissa C Southey; David E Goldgar; Robert Winqvist; Katri Pylkäs; Fergus Couch; Marc Tischkowitz; William D Foulkes; Joe Dennis; Kyriaki Michailidou; Elizabeth J van Rensburg; Tuomas Heikkinen; Heli Nevanlinna; John L Hopper; Thilo Dörk; Kathleen Bm Claes; Jorge Reis-Filho; Zhi Ling Teo; Paolo Radice; Irene Catucci; Paolo Peterlongo; Helen Tsimiklis; Fabrice A Odefrey; James G Dowty; Marjanka K Schmidt; Annegien Broeks; Frans B Hogervorst; Senno Verhoef; Jane Carpenter; Christine Clarke; Rodney J Scott; Peter A Fasching; Lothar Haeberle; Arif B Ekici; Matthias W Beckmann; Julian Peto; Isabel Dos-Santos-Silva; Olivia Fletcher; Nichola Johnson; Manjeet K Bolla; Elinor J Sawyer; Ian Tomlinson; Michael J Kerin; Nicola Miller; Federik Marme; Barbara Burwinkel; Rongxi Yang; Pascal Guénel; Thérèse Truong; Florence Menegaux; Marie Sanchez; Stig Bojesen; Sune F Nielsen; Henrik Flyger; Javier Benitez; M Pilar Zamora; Jose Ignacio Arias Perez; Primitiva Menéndez; Hoda Anton-Culver; Susan Neuhausen; Argyrios Ziogas; Christina A Clarke; Hermann Brenner; Volker Arndt; Christa Stegmaier; Hiltrud Brauch; Thomas Brüning; Yon-Dschun Ko; Taru A Muranen; Kristiina Aittomäki; Carl Blomqvist; Natalia V Bogdanova; Natalia N Antonenkova; Annika Lindblom; Sara Margolin; Arto Mannermaa; Vesa Kataja; Veli-Matti Kosma; Jaana M Hartikainen; Amanda B Spurdle; kConFab Investigators; Els Wauters; Dominiek Smeets; Benoit Beuselinck; Giuseppe Floris; Jenny Chang-Claude; Anja Rudolph; Petra Seibold; Dieter Flesch-Janys; Janet E Olson; Celine Vachon; Vernon S Pankratz; Catriona McLean; Christopher A Haiman; Brian E Henderson; Fredrick Schumacher; Loic Le Marchand; Vessela Kristensen; Grethe Grenaker Alnæs; Wei Zheng; David J Hunter; Sara Lindstrom; Susan E Hankinson; Peter Kraft; Irene Andrulis; Julia A Knight; Gord Glendon; Anna Marie Mulligan; Arja Jukkola-Vuorinen; Mervi Grip; Saila Kauppila; Peter Devilee; Robert A E M Tollenaar; Caroline Seynaeve; Antoinette Hollestelle; Montserrat Garcia-Closas; Jonine Figueroa; Stephen J Chanock; Jolanta Lissowska; Kamila Czene; Hatef Darabi; Mikael Eriksson; Diana M Eccles; Sajjad Rafiq; William J Tapper; Sue M Gerty; Maartje J Hooning; John W M Martens; J Margriet Collée; Madeleine Tilanus-Linthorst; Per Hall; Jingmei Li; Judith S Brand; Keith Humphreys; Angela Cox; Malcolm W R Reed; Craig Luccarini; Caroline Baynes; Alison M Dunning; Ute Hamann; Diana Torres; Hans Ulrich Ulmer; Thomas Rüdiger; Anna Jakubowska; Jan Lubinski; Katarzyna Jaworska; Katarzyna Durda; Susan Slager; Amanda E Toland; Christine B Ambrosone; Drakoulis Yannoukakos; Anthony Swerdlow; Alan Ashworth; Nick Orr; Michael Jones; Anna González-Neira; Guillermo Pita; M Rosario Alonso; Nuria Álvarez; Daniel Herrero; Daniel C Tessier; Daniel Vincent; Francois Bacot; Jacques Simard; Martine Dumont; Penny Soucy; Rosalind Eeles; Kenneth Muir; Fredrik Wiklund; Henrik Gronberg; Johanna Schleutker; Børge G Nordestgaard; Maren Weischer; Ruth C Travis; David Neal; Jenny L Donovan; Freddie C Hamdy; Kay-Tee Khaw; Janet L Stanford; William J Blot; Stephen Thibodeau; Daniel J Schaid; Joseph L Kelley; Christiane Maier; Adam S Kibel; Cezary Cybulski; Lisa Cannon-Albright; Katja Butterbach; Jong Park; Radka Kaneva; Jyotsna Batra; Manuel R Teixeira; Zsofia Kote-Jarai; Ali Amin Al Olama; Sara Benlloch; Stefan P Renner; Arndt Hartmann; Alexander Hein; Matthias Ruebner; Diether Lambrechts; Els Van Nieuwenhuysen; Ignace Vergote; Sandrina Lambretchs; Jennifer A Doherty; Mary Anne Rossing; Stefan Nickels; Ursula Eilber; Shan Wang-Gohrke; Kunle Odunsi; Lara E Sucheston-Campbell; Grace Friel; Galina Lurie; Jeffrey L Killeen; Lynne R Wilkens; Marc T Goodman; Ingo Runnebaum; Peter A Hillemanns; Liisa M Pelttari; Ralf Butzow; Francesmary Modugno; Robert P Edwards; Roberta B Ness; Kirsten B Moysich; Andreas du Bois; Florian Heitz; Philipp Harter; Stefan Kommoss; Beth Y Karlan; Christine Walsh; Jenny Lester; Allan Jensen; Susanne Krüger Kjaer; Estrid Høgdall; Bernard Peissel; Bernardo Bonanni; Loris Bernard; Ellen L Goode; Brooke L Fridley; Robert A Vierkant; Julie M Cunningham; Melissa C Larson; Zachary C Fogarty; Kimberly R Kalli; Dong Liang; Karen H Lu; Michelle A T Hildebrandt; Xifeng Wu; Douglas A Levine; Fanny Dao; Maria Bisogna; Andrew Berchuck; Edwin S Iversen; Jeffrey R Marks; Lucy Akushevich; Daniel W Cramer; Joellen Schildkraut; Kathryn L Terry; Elizabeth M Poole; Meir Stampfer; Shelley S Tworoger; Elisa V Bandera; Irene Orlow; Sara H Olson; Line Bjorge; Helga B Salvesen; Anne M van Altena; Katja K H Aben; Lambertus A Kiemeney; Leon F A G Massuger; Tanja Pejovic; Yukie Bean; Angela Brooks-Wilson; Linda E Kelemen; Linda S Cook; Nhu D Le; Bohdan Górski; Jacek Gronwald; Janusz Menkiszak; Claus K Høgdall; Lene Lundvall; Lotte Nedergaard; Svend Aage Engelholm; Ed Dicks; Jonathan Tyrer; Ian Campbell; Iain McNeish; James Paul; Nadeem Siddiqui; Rosalind Glasspool; Alice S Whittemore; Joseph H Rothstein; Valerie McGuire; Weiva Sieh; Hui Cai; Xiao-Ou Shu; Rachel T Teten; Rebecca Sutphen; John R McLaughlin; Steven A Narod; Catherine M Phelan; Alvaro N Monteiro; David Fenstermacher; Hui-Yi Lin; Jennifer B Permuth; Thomas A Sellers; Y Ann Chen; Ya-Yu Tsai; Zhihua Chen; Aleksandra Gentry-Maharaj; Simon A Gayther; Susan J Ramus; Usha Menon; Anna H Wu; Celeste L Pearce; David Van Den Berg; Malcolm C Pike; Agnieszka Dansonka-Mieszkowska; Joanna Plisiecka-Halasa; Joanna Moes-Sosnowska; Jolanta Kupryjanczyk; Paul Dp Pharoah; Honglin Song; Ingrid Winship; Georgia Chenevix-Trench; Graham G Giles; Sean V Tavtigian; Doug F Easton; Roger L Milne
Journal:  J Med Genet       Date:  2016-09-05       Impact factor: 6.318

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  5 in total

1.  Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast.

Authors:  Siddhartha Yadav; Chunling Hu; Katherine L Nathanson; Jeffrey N Weitzel; David E Goldgar; Peter Kraft; Rohan D Gnanaolivu; Jie Na; Hongyan Huang; Nicholas J Boddicker; Nicole Larson; Chi Gao; Song Yao; Clarice Weinberg; Celine M Vachon; Amy Trentham-Dietz; Jack A Taylor; Dale R Sandler; Alpa Patel; Julie R Palmer; Janet E Olson; Susan Neuhausen; Elena Martinez; Sara Lindstrom; James V Lacey; Allison W Kurian; Esther M John; Christopher Haiman; Leslie Bernstein; Paul W Auer; Hoda Anton-Culver; Christine B Ambrosone; Rachid Karam; Elizabeth Chao; Amal Yussuf; Tina Pesaran; Jill S Dolinsky; Steven N Hart; Holly LaDuca; Eric C Polley; Susan M Domchek; Fergus J Couch
Journal:  J Clin Oncol       Date:  2021-10-21       Impact factor: 44.544

2.  The impact of oophorectomy on survival from breast cancer in patients with CHEK2 mutations.

Authors:  Joanna Tomiczek-Szwiec; Marek Szwiec; Michal Falco; Cezary Cybulski; Dominika Wokolorczyk; Anna Jakubowska; Jacek Gronwald; Malgorzata Stawicka; Dariusz Godlewski; Ewa Kilar; Elzbieta Marczyk; Monika Siołek; Rafal Wiśniowski; Olga Haus; Robert Sibilski; Lubomir Bodnar; Ping Sun; Steven A Narod; Jan Lubinski; Tomasz Huzarski
Journal:  Br J Cancer       Date:  2022-03-07       Impact factor: 9.075

3.  Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome.

Authors:  Jaakko S Tyrmi; Riikka K Arffman; Natàlia Pujol-Gualdo; Venla Kurra; Laure Morin-Papunen; Eeva Sliz; Terhi T Piltonen; Triin Laisk; Johannes Kettunen; Hannele Laivuori
Journal:  Hum Reprod       Date:  2022-01-28       Impact factor: 6.918

4.  Management of Women With Breast Cancer and Pathogenic Variants in Genes Other Than BRCA1 or BRCA2.

Authors:  Mark Robson
Journal:  J Clin Oncol       Date:  2021-06-09       Impact factor: 50.717

5.  Cancer Predisposition Genes in Adolescents and Young Adults (AYAs): a Review Paper from the Italian AYA Working Group.

Authors:  Angela Toss; Paola Quarello; Fedro Alessandro Peccatori; Andrea Ferrari; Maurizio Mascarin; Giuseppe Luigi Banna; Marco Zecca; Saverio Cinieri
Journal:  Curr Oncol Rep       Date:  2022-03-23       Impact factor: 5.945

  5 in total

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