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Record W4400024448 · doi:10.17615/c9rj-vf19

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

2024· article· en· W4400024448 on OpenAlexfundno aff
Stella Koutros, Wolfgang Janni, B Rack, D.F. Easton, Per Hall, Clare L. Scott, Volker Arndt, Sebastian Nielsen, Arif B. Ekici, Mikael Eriksson, José Á. García-Sáenz, Nick Orr, Sara Margolin, Ting Cheng, Agnes Jager, Christine L. Clarke, Bette J. Caan, Argyrios Ziogas, Mitul Shah, Harald Surowy, A.F. Olshan, Valerie Rhenius, T. Brüning, R. Kaaks, Kyriaki Michailidou, Georgia Chenevix‐Trench, Kamila Czene, Paul L. Auer, Rebecca Roylance, Ian Tomlinson, Hiltrud Brauch, Angela Cox, Henrik Flyger, Nadège Presneau, ABCTB Investigators, Peter Kraft, A. Wolk, Esther M. John, Wei He, D. Gareth Evans, Matthias Ruebner, Joe Dennis, Pascal Guénel, Annelie Augustinsson, Thomas U. Ahearn, Dijana Plaseska-Karanfilska, Graham G. Giles, Reiner Hoppe, kConFab Investigators, Q. Wang, RM Tamimi, Tjoung‐Won Park‐Simon, Bernard Peissel, Audrey Jung, NBCS Collaborators, Sabine Behrens, Marı́a Elena Martı́nez, Jose E. Castelao, Heli Nevanlinna, A. Lindblom, A Swerdlow, Snezhana Smichkoska, William Tapper, Anthony Howell, Machteld Keupers, SS Buys, Martha S. Linet, Simon S. Cross, A.V. Patel, A. Heather Eliassen, Manuela Gago-Domínguez, A. Schneeweiss, R.A.E.M. Tollenaar, Jan Lubiński, Steven N. Hart, Masood Manoochehri, Diether Lambrechts, K. Prajzendanc, Michael Lush, Anna Marie Mulligan, Emmanouil Saloustros, Thilo Dörk, Heiko Becher, M.W. Beckmann, Niclas Håkansson, David J. Hunter, Alain Hartmann, P. Peterlongo, Atocha Romero, Allison W. Kurian, M. Bolla, Laure Dossus, Peter A. Fasching, Melissa C. Southey, Robert Winqvist, Thérèse Truong, J. Lacey, Montserrat García‐Closas, William G. Newman, L. Le Marchand, Hermann Brenner, Celine M. Vachon, Melanie Gündert, U. Hamann, Diana Eccles, Håkan Olsson, Arto Mannermaa, Emma Sawyer, Jennifer Stone, Børge G. Nordestgaard, Stig E. Bojesen, Ross L. Prentice, G. Rennert, Daniele Campa, Sander Canisius, Maria Escala-Garcia, A.M. Dunning, Lin Fritschi, Lauren R. Teras, C.A. Haiman, Hedy S. Rennert, Anna Jakubowska, R Schmutzler, Renske Keeman, Mary Beth Terry, Robert Luben, M Schmidt, Anna Morra, M.B. Daly, Laura E. Beane Freeman, Roger L. Milne, M.A. Troester, Sarah V. Colonna, Jenny Chang‐Claude, J.W.M. Martens, Cari M. Kitahara, Jaana M. Hartikainen, Maartje J. Hooning, T.A. Muranen, Amber N. Hurson, Vessela N. Kristensen, Paul D.P. Pharoah, J. Beesley, Federico Canzian, I.L. Andrulis, Miriam Dwek, H. Anton-Culver, Mervi Grip, D. Mavroudis, F.J. Couch, JL Hopper, S.J. Chanock

Bibliographic record

VenueUNC Libraries · 2024
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBRCA gene mutations in cancer
Canadian institutionsnot available
FundersMedical Research and Materiel CommandServicio Gallego de SaludUniversitätsklinikum Hamburg-EppendorfInstituto de Salud Carlos IIICancer Council TasmaniaCancer Council NSWNational Health and Medical Research CouncilWorld Cancer Research FundMedical Research CouncilCanadian Institutes of Health ResearchProgramme Grants for Applied ResearchManchester Biomedical Research CentreUniversity of California, San FranciscoImperial Experimental Cancer Medicine CentreNational Institutes of HealthHellenic Health FoundationFreistaat SachsenDeutschen Konsortium für Translationale KrebsforschungXunta de GaliciaMutuelle Générale de l'Education NationaleInstitut Gustave-RoussyCenters for Disease Control and PreventionLeids Universitair Medisch CentrumInstitut National Du CancerNorges ForskningsrådDeutsche KrebshilfeInstitut National de la Santé et de la Recherche MédicaleUniversity of CreteVetenskapsrådetStockholms Läns LandstingUniversity of Southern CaliforniaStavros Niarchos FoundationKuopion Yliopistollinen SairaalaHarvard T.H. Chan School of Public HealthKarolinska InstitutetGovernment of CanadaMinisterio de Sanidad, Servicios Sociales e IgualdadBundesministerium für Bildung und ForschungOvarian Cancer Research FundMinisterio de Economía y CompetitividadCancer AustraliaAgence Nationale de la RechercheDeutsche Gesetzliche UnfallversicherungGentofte HospitalDeutsche ForschungsgemeinschaftCancer Council South AustraliaFonds Wetenschappelijk OnderzoekCancerfondenNational Cancer InstituteCancer Institute NSWEuropean Regional Development FundKing's College LondonNational Institute for Health and Care ResearchCancer Research UKRobert Bosch StiftungEberhard Karls Universität TübingenRheinische Friedrich-Wilhelms-Universität BonnBreast Cancer Research TrustFondation du cancer du sein du QuébecDavid F. and Margaret T. Grohne Family FoundationU.S. ArmyUniversity of WestminsterLigue Contre le CancerDeutsches KrebsforschungszentrumBrigham and Women's HospitalAssociazione Italiana per la Ricerca sul CancroGenome CanadaItä-Suomen YliopistoFondation de FranceSundhed og Sygdom, Det Frie ForskningsrådCancer Council VictoriaCalifornia Department of Public HealthNational Breast Cancer FoundationCancer Council Western AustraliaEuropean CommissionBreast Cancer Research Foundation
KeywordsGermlinePathologicalBreast cancerOncologyBiologyCancerGenetic associationInternal medicineMedicineGeneticsGenotypeGeneSingle-nucleotide polymorphism

Abstract

fetched live from OpenAlex

Background: Given the high heterogeneity among breast tumors, associations between common germline genetic variants and survival that may exist within specific subgroups could go undetected in an unstratified set of breast cancer patients. Methods: We performed genome-wide association analyses within 15 subgroups of breast cancer patients based on prognostic factors, including hormone receptors, tumor grade, age, and type of systemic treatment. Analyses were based on 91,686 female patients of European ancestry from the Breast Cancer Association Consortium, including 7531 breast cancer-specific deaths over a median follow-up of 8.1 years. Cox regression was used to assess associations of common germline variants with 15-year and 5-year breast cancer-specific survival. We assessed the probability of these associations being true positives via the Bayesian false discovery probability (BFDP < 0.15). Results: Evidence of associations with breast cancer-specific survival was observed in three patient subgroups, with variant rs5934618 in patients with grade 3 tumors (15-year-hazard ratio (HR) [95% confidence interval (CI)] 1.32 [1.20, 1.45], P = 1.4E−08, BFDP = 0.01, per G allele); variant rs4679741 in patients with ER-positive tumors treated with endocrine therapy (15-year-HR [95% CI] 1.18 [1.11, 1.26], P = 1.6E−07, BFDP = 0.09, per G allele); variants rs1106333 (15-year-HR [95% CI] 1.68 [1.39,2.03], P = 5.6E−08, BFDP = 0.12, per A allele) and rs78754389 (5-year-HR [95% CI] 1.79 [1.46,2.20], P = 1.7E−08, BFDP = 0.07, per A allele), in patients with ER-negative tumors treated with chemotherapy. Conclusions: We found evidence of four loci associated with breast cancer-specific survival within three patient subgroups. There was limited evidence for the existence of associations in other patient subgroups. However, the power for many subgroups is limited due to the low number of events. Even so, our results suggest that the impact of common germline genetic variants on breast cancer-specific survival might be limited.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.220
Threshold uncertainty score0.425

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.012
GPT teacher head0.256
Teacher spread0.244 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2024
Admission routes1
Has abstractyes

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