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DC Field | Value | Language |
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dc.contributor.author | Wendt C. | en |
dc.contributor.author | Van Leeuwen F.E. | en |
dc.contributor.author | Van Ongeval C. | en |
dc.contributor.author | Van't Veer L.J. | en |
dc.contributor.author | Wang Q. | en |
dc.contributor.author | Westenend P.J. | en |
dc.contributor.author | Schmidt M.K. | en |
dc.contributor.author | Hooning M.J. | en |
dc.contributor.author | Giardiello D. | en |
dc.contributor.author | Steyerberg E.W. | en |
dc.contributor.author | Hauptmann M. | en |
dc.contributor.author | Adank M.A. | en |
dc.contributor.author | Akdeniz D. | en |
dc.contributor.author | Blomqvist C. | en |
dc.contributor.author | Bojesen S.E. | en |
dc.contributor.author | Bolla M.K. | en |
dc.contributor.author | Brinkhuis M. | en |
dc.contributor.author | Chang-Claude J. | en |
dc.contributor.author | Czene K. | en |
dc.contributor.author | Devilee P. | en |
dc.contributor.author | Dunning A.M. | en |
dc.contributor.author | Easton D.F. | en |
dc.contributor.author | Eccles D.M. | en |
dc.contributor.author | Fasching P.A. | en |
dc.contributor.author | Figueroa J. | en |
dc.contributor.author | Flyger H. | en |
dc.contributor.author | Garcia-Closas M. | en |
dc.contributor.author | Haeberle L. | en |
dc.contributor.author | Haiman C.A. | en |
dc.contributor.author | Hall P. | en |
dc.contributor.author | Hamann U. | en |
dc.contributor.author | Hopper J.L. | en |
dc.contributor.author | Jager A. | en |
dc.contributor.author | Jakubowska A. | en |
dc.contributor.author | Jung A. | en |
dc.contributor.author | Keeman R. | en |
dc.contributor.author | Kramer I. | en |
dc.contributor.author | Lambrechts D. | en |
dc.contributor.author | Le Marchand L. | en |
dc.contributor.author | Lindblom A. | en |
dc.contributor.author | Lubinski J. | en |
dc.contributor.author | Manoochehri M. | en |
dc.contributor.author | Mariani L. | en |
dc.contributor.author | Nevanlinna H. | en |
dc.contributor.author | Oldenburg H.S.A. | en |
dc.contributor.author | Pelders S. | en |
dc.contributor.author | Pharoah P.D.P. | en |
dc.contributor.author | Shah M. | en |
dc.contributor.author | Siesling S. | en |
dc.contributor.author | Smit V.T.H.B.M. | en |
dc.contributor.author | Southey M.C. | en |
dc.contributor.author | Tapper W.J. | en |
dc.contributor.author | Tollenaar R.A.E.M. | en |
dc.contributor.author | Van Den Broek A.J. | en |
dc.contributor.author | Van Deurzen C.H.M. | en |
dc.date.accessioned | 2021-05-14T11:58:19Z | en |
dc.date.available | 2021-05-14T11:58:19Z | en |
dc.date.copyright | 2019 | en |
dc.date.created | 20200106 | en |
dc.date.issued | 2020-01-06 | en |
dc.identifier.citation | Breast Cancer Research. 21 (1) (no pagination), 2019. Article Number: 144. Date of Publication: 17 Dec 2019. | en |
dc.identifier.issn | 1465-5411 | en |
dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/35432 | en |
dc.description.abstract | Background: Breast cancer survivors are at risk for contralateral breast cancer (CBC), with the consequent burden of further treatment and potentially less favorable prognosis. We aimed to develop and validate a CBC risk prediction model and evaluate its applicability for clinical decision-making. Method(s): We included data of 132,756 invasive non-metastatic breast cancer patients from 20 studies with 4682 CBC events and a median follow-up of 8.8 years. We developed a multivariable Fine and Gray prediction model (PredictCBC-1A) including patient, primary tumor, and treatment characteristics and BRCA1/2 germline mutation status, accounting for the competing risks of death and distant metastasis. We also developed a model without BRCA1/2 mutation status (PredictCBC-1B) since this information was available for only 6% of patients and is routinely unavailable in the general breast cancer population. Prediction performance was evaluated using calibration and discrimination, calculated by a time-dependent area under the curve (AUC) at 5 and 10 years after diagnosis of primary breast cancer, and an internal-external cross-validation procedure. Decision curve analysis was performed to evaluate the net benefit of the model to quantify clinical utility. Result(s): In the multivariable model, BRCA1/2 germline mutation status, family history, and systemic adjuvant treatment showed the strongest associations with CBC risk. The AUC of PredictCBC-1A was 0.63 (95% prediction interval (PI) at 5 years, 0.52-0.74; at 10 years, 0.53-0.72). Calibration-in-the-large was-0.13 (95% PI:-1.62-1.37), and the calibration slope was 0.90 (95% PI: 0.73-1.08). The AUC of Predict-1B at 10 years was 0.59 (95% PI: 0.52-0.66); calibration was slightly lower. Decision curve analysis for preventive contralateral mastectomy showed potential clinical utility of PredictCBC-1A between thresholds of 4-10% 10-year CBC risk for BRCA1/2 mutation carriers and non-carriers. Conclusion(s): We developed a reasonably calibrated model to predict the risk of CBC in women of European-descent; however, prediction accuracy was moderate. Our model shows potential for improved risk counseling, but decision-making regarding contralateral preventive mastectomy, especially in the general breast cancer population where limited information of the mutation status in BRCA1/2 is available, remains challenging.Copyright © 2019 The Author(s). | en |
dc.language | English | en |
dc.language | en | en |
dc.publisher | BioMed Central Ltd. (E-mail: info@biomedcentral.com) | en |
dc.relation.ispartof | Breast Cancer Research | en |
dc.subject.mesh | mastectomy | - |
dc.subject.mesh | risk | - |
dc.subject.mesh | cancer risk | - |
dc.subject.mesh | germline mutation | - |
dc.subject.mesh | heterozygote | - |
dc.subject.mesh | validation study | - |
dc.subject.mesh | contralateral breast cancer | - |
dc.subject.mesh | distant metastasis/co | - |
dc.subject.mesh | family history | - |
dc.subject.mesh | breast cancer | - |
dc.subject.mesh | cancer adjuvant therapy | - |
dc.subject.mesh | cancer patient | - |
dc.subject.mesh | clinical decision making | - |
dc.subject.mesh | mutational analysis | - |
dc.subject.mesh | research | - |
dc.subject.mesh | tumor suppressor gene | - |
dc.title | Prediction and clinical utility of a contralateral breast cancer risk model. | en |
dc.type | Article | en |
dc.identifier.affiliation | Monash University - School of Clinical Sciences at Monash Health | - |
dc.identifier.doi | http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1186/s13058-019-1221-1 | - |
dc.publisher.place | United Kingdom | en |
dc.identifier.pubmedid | 31847907 [http://www.ncbi.nlm.nih.gov/pubmed/?term=31847907] | en |
dc.identifier.source | 630285125 | en |
dc.identifier.institution | (Giardiello, Keeman, Kramer, Van Den Broek, Van't Veer, Schmidt) Division of Molecular Pathology, Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital, Amsterdam, Netherlands (Giardiello, Steyerberg) Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, Netherlands (Steyerberg) Department of Public Health, Erasmus MC Cancer Institute, Rotterdam, Netherlands (Hauptmann) Institute of Biometry and Registry Research, Brandenburg Medical School, Neuruppin, Germany (Hauptmann) Department of Epidemiology and Biostatistics, Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital, Amsterdam, Netherlands (Adank) Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital, Family Cancer Clinic, Amsterdam, Netherlands (Akdeniz, Pelders, Hooning) Department of Medical Oncology, Family Cancer Clinic, Erasmus MC Cancer Institute, Rotterdam, Netherlands (Blomqvist) Department of Oncology, Helsinki University Hospital, University of Helsinki, Helsinki, Finland (Blomqvist) Department of Oncology, Orebro University Hospital, Orebro, Sweden (Bojesen) Copenhagen General Population Study, Herlev and Gentofte Hospital, Copenhagen University Hospital, Herlev, Denmark (Bojesen) Department of Clinical Biochemistry, Herlev and Gentofte Hospital, Copenhagen University Hospital, Herlev, Denmark (Bojesen) Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark (Bolla, Easton, Pharoah, Wang) Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom (Brinkhuis) East-Netherlands, Laboratory for Pathology, Hengelo, Netherlands (Chang-Claude, Jung) Division of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany (Chang-Claude) Cancer Epidemiology Group, University Cancer Center Hamburg (UCCH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany (Czene, Hall) Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden (Devilee, Smit) Department of Pathology, Leiden University Medical Center, Leiden, Netherlands (Devilee) Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands (Dunning, Easton, Pharoah, Shah) Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, United Kingdom (Eccles) Cancer Sciences Academic Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom (Fasching) Department of Medicine Division of Hematology and Oncology, University of California at Los Angeles, David Geffen School of Medicine, Los Angeles, CA, United States (Fasching, Haeberle) Department of Gynecology and Obstetrics, Compreh. Cancer Ctr. ER-EMN, Univ. Hosp. Erlangen, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany (Figueroa) Usher Institute of Population Health Sciences and Informatics, University of Edinburgh Medical School, Edinburgh, United Kingdom (Figueroa) Cancer Research UK Edinburgh Centre, Edinburgh, United Kingdom (Figueroa, Garcia-Closas) Department of Health and Human Services, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States (Flyger) Department of Breast Surgery, Herlev and Gentofte Hospital, Copenhagen University Hospital, Herlev, Denmark (Garcia-Closas) Division of Genetics and Epidemiology, Institute of Cancer Research, London, United Kingdom (Haiman) Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States (Hall) Department of Oncology, Sodersjukhuset, Stockholm, Sweden (Hamann, Manoochehri) Molecular Genetics of Breast Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany (Hopper) Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, VIC, Australia (Jager) Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, Netherlands (Jakubowska, Lubinski) Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland (Jakubowska) Independent Laboratory of Molecular Biology and Genetic Diagnostics, Pomeranian Medical University, Szczecin, Poland (Lambrechts) VIB Center for Cancer Biology, VIB, Leuven, Belgium (Lambrechts) Laboratory for Translational Genetics, Department of Human Genetics, University of Leuven, Leuven, Belgium (Le Marchand) University of Hawaii Cancer Center, Epidemiology Program, Honolulu, HI, United States (Lindblom) Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden (Lindblom) Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden (Mariani) Unit of Clinical Epidemiology and Trial Organization, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy (Nevanlinna) Department of Obstetrics and Gynecology, Helsinki University Hospital, University of Helsinki, Helsinki, Finland (Oldenburg) Department of Surgical Oncology, Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital, Amsterdam, Netherlands (Siesling) Department of Research, Netherlands Comprehensive Cancer Organisation, Utrecht, Netherlands (Southey) Precision Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia (Southey) Department of Clinical Pathology, University of Melbourne, Melbourne, VIC, Australia (Tapper) Faculty of Medicine, University of Southampton, Southampton, United Kingdom (Tollenaar) Department of Surgery, Leiden University Medical Center, Leiden, Netherlands (Van Deurzen) Department of Pathology, Erasmus MC Cancer Institute, Rotterdam, Netherlands (Van Leeuwen, Schmidt) Division of Psychosocial Research and Epidemiology, Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital, Plesmanlaan 121, Amsterdam, CX 1066, Netherlands (Van Ongeval) Leuven Multidisciplinary Breast Center, Department of Oncology, Leuven Cancer Institute, University Hospitals Leuven, Leuven, Belgium (Wendt) Department of Clinical Science and Education, Sodersjukhuset, Karolinska Institutet, Stockholm, Sweden (Westenend) BOOG, Laboratory for Pathology Dordrecht, Dordrecht, Netherlands | en |
dc.description.address | M.K. Schmidt, Division of Molecular Pathology, Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital, Amsterdam, Netherlands. E-mail: mk.schmidt@nki.nl | en |
dc.description.publicationstatus | Embase | en |
dc.rights.statement | Copyright 2020 Elsevier B.V., All rights reserved. | en |
dc.subect.keywords | BRCA mutation carriers Clinical decision-making Contralateral breast cancer Risk prediction model | en |
dc.identifier.authoremail | Schmidt M.K.; mk.schmidt@nki.nl | en |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.openairetype | Article | - |
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