Evidence map›Paper›PMID 32614418›Full record

ArticleJAMA oncology2020

Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).

Valentina Silvestri, Goska Leslie, Daniel R Barnes, CIMBA Group, Bjarni A Agnarsson, Kristiina Aittomäki, Elisa Alducci, Irene L Andrulis, Rosa B Barkardottir, Alicia Barroso and 114 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in JAMA oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
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  8. Article
  9. Exploring the One Health Paradigm in Male Breast Cancer.Journal of mammary gland biology and neoplasia · 2024
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  10. Review
  11. Haematologica · 2024
    Article
  12. Frontiers in oncology · 2024
    Article
  13. Article
  14. Article
  15. Molecular characteristics of Asian male BRCA-related cancers.Breast cancer research and treatment · 2023
    Article
  16. Cancer risk in relatives ofCancer biology & medicine · 2023
    Article
  17. Hereditary cancer syndromes.World journal of clinical oncology · 2023
    Review
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

124 authors at 20 institutions in 29 countries.

Valentina SilvestriDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Goska LeslieCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
Daniel R BarnesCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
CIMBA Group
Bjarni A AgnarssonDepartment of Pathology, Landspitali University Hospital, Reykjavik, Iceland.
Kristiina AittomäkiDepartment of Clinical Genetics, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
Elisa AlducciImmunology and Molecular Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Irene L AndrulisLunenfeld-Tanenbaum Research Institute, Fred A. Litwin Center for Cancer Genetics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Rosa B BarkardottirDepartment of Pathology, Landspitali University Hospital, Reykjavik, Iceland.
Alicia BarrosoHuman Genetics Group, Human Cancer Genetics Programme, Spanish National Cancer Research Centre, Madrid, Spain.
Daniel BarrowdaleCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
Javier BenitezHuman Genetics Group and Genotyping Unit, CEGEN, Human Cancer Genetics Programme, Spanish National Cancer Research Centre, Madrid, Spain.
Bernardo BonanniDivision of Cancer Prevention and Genetics-IEO, European Institute of Oncology IRCCS, Milan, Italy.
Ake BorgDepartment of Oncology, Lund University, Skåne University Hospital, Lund, Sweden.
Saundra S BuysHuntsman Cancer Institute, Department of Internal Medicine, University of Utah Health, Salt Lake City.
Trinidad CaldésInstituto de Investigación Sanitaria San Carlos (IdISSC), Centro Investigación Biomédica en Red de Cáncer (CIBERONC), Medical Oncology Department, Hospital Clínico San Carlos, Madrid, Spain.
Maria A CaligoSection of Molecular Genetics, Department of Laboratory Medicine, University Hospital of Pisa, Pisa, Italy.
Carlo CapalboDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Ian CampbellSir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Victoria, Australia.
Wendy K ChungDepartments of Pediatrics and Medicine, Columbia University, New York, New York.
Kathleen B M ClaesCentre for Medical Genetics, Ghent University, Gent, Belgium.
Sarah V ColonnaHuntsman Cancer Institute, Department of Internal Medicine, University of Utah Health, Salt Lake City.
Laura CortesiDepartment of Oncology and Haematology, University of Modena and Reggio Emilia, Modena, Italy.
Fergus J CouchDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Miguel de la HoyaInstituto de Investigación Sanitaria San Carlos (IdISSC), Centro Investigación Biomédica en Red de Cáncer (CIBERONC), Medical Oncology Department, Hospital Clínico San Carlos, Madrid, Spain.
Orland DiezHereditary Cancer Genetics Group, Vall d'Hebron Institute of Oncology, Barcelona, Spain.
Yuan Chun DingDepartment of Population Sciences, Beckman Research Institute of City of Hope, Duarte, California.
Susan DomchekAbramson Cancer Center, Perelman School of Medicine, Department of Medicine, University of Pennsylvania, Philadelphia.
Douglas F EastonCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
Bent EjlertsenDepartment of Oncology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Christoph EngelInstitute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.
D Gareth EvansGenomic Medicine, Manchester Academic Health Sciences Centre, Division of Evolution and Genomic Science, Manchester University, Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom.
Lidia FeliubadalòMolecular Diagnostic Unit, Hereditary Cancer Program, IDIBELL (Bellvitge Biomedical Research Institute), Catalan Institute of Oncology, CIBERONC, Barcelona, Spain.
Lenka ForetovaDepartment of Cancer Epidemiology and Genetics, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Florentia FostiraMolecular Diagnostics Laboratory, INRASTES, National Centre for Scientific Research "Demokritos", Athens, Greece.
Lajos GécziMedical Oncology Center, National Institute of Oncology, Budapest, Hungary.
Anne-Marie GerdesDepartment of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.
Gord GlendonLunenfeld-Tanenbaum Research Institute, Fred A. Litwin Center for Cancer Genetics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Andrew K GodwinDepartment of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City.
David E GoldgarHuntsman Cancer Institute, Department of Dermatology, University of Utah School of Medicine, Salt Lake City.
Eric HahnenCenter for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
Frans B L HogervorstFamily Cancer Clinic, Netherlands Cancer Institute, Amsterdam, the Netherlands.
John L HopperCentre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Victoria, Australia.
Peter J HulickCenter for Medical Genetics, NorthShore University HealthSystem, Evanston, Illinois.
Claudine IsaacsLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC.
Angel IzquierdoGenetic Counseling Unit, Hereditary Cancer Program, IDIBGI (Institut d'Investigació Biomèdica de Girona), Catalan Institute of Oncology, CIBERONC, Girona, Spain.
Paul A JamesSir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Victoria, Australia.
Ramunas JanaviciusHematology, Oncology and Transfusion Medicine Center, Department of Molecular and Regenerative Medicine, Vilnius University Hospital Santariskiu Clinics, Vilnius, Lithuania.
Uffe Birk JensenDepartment of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
Esther M JohnDepartment of Epidemiology and Population Health, Division of Oncology, Department of Medicine, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California.
Vijai JosephClinical Genetics Research Lab, Department of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Irene KonstantopoulouMolecular Diagnostics Laboratory, INRASTES, National Centre for Scientific Research "Demokritos", Athens, Greece.
Allison W KurianDepartment of Epidemiology and Population Health, Division of Oncology, Department of Medicine, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California.
Ava KwongHong Kong Hereditary Breast Cancer Family Registry, Cancer Genetics Centre, Happy Valley, Hong Kong.
Elisabetta LanducciUO Oncologia Medica, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
Fabienne LesueurGenetic Epidemiology of Cancer Team, Inserm, U900, Paris, France.
Jennifer T LoudClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
Eva MachackovaDepartment of Cancer Epidemiology and Genetics, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Phuong L MaiMagee-Womens Hospital, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Keivan Majidzadeh-ABreast Cancer Research Center, Genetics Department, Motamed Cancer Institute, ACECR, Tehran, Iran.
Siranoush ManoukianUnit of Medical Genetics, Department of Medical Oncology and Hematology, Fondazione IRCCS Istituto Nazionale dei Tumori (INT), Milan, Italy.
Marco MontagnaImmunology and Molecular Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Lidia MoserleImmunology and Molecular Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Anna Marie MulliganDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Katherine L NathansonAbramson Cancer Center, Perelman School of Medicine, Department of Medicine, University of Pennsylvania, Philadelphia.
Heli NevanlinnaDepartment of Obstetrics and Gynecology, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
Joanne NgeowCancer Genetics Service, National Cancer Centre Singapore, Singapore.
Liene Nikitina-ZakeLatvian Biomedical Research and Study Centre, Riga, Latvia.
Kenneth OffitClinical Genetics Research Lab, Department of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Edith OlahDepartment of Molecular Genetics, National Institute of Oncology, Budapest, Hungary.
Olufunmilayo I OlopadeCenter for Clinical Cancer Genetics, The University of Chicago, Chicago, Illinois.
Ana OsorioHuman Genetics Group, Human Cancer Genetics Programme, Spanish National Cancer Research Centre, Madrid, Spain.
Laura PapiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy.
Sue K ParkDepartment of Preventive Medicine, Seoul National University College of Medicine, Seoul, Korea.
Inge Sokilde PedersenMolecular Diagnostics, Department of Clinical Medicine, Aalborg University Hospital, Aalborg University, Aalborg, Denmark.
Pedro Perez-SeguraInstituto de Investigación Sanitaria San Carlos (IdISSC), Centro Investigación Biomédica en Red de Cáncer (CIBERONC), Medical Oncology Department, Hospital Clínico San Carlos, Madrid, Spain.
Annabeth H PetersenDepartment of Clinical Genetics, Vejle Hospital, Vejle, Denmark.
Pedro PintoDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Berardino PorfirioDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy.
Miquel Angel PujanaProCURE, Catalan Institute of Oncology, IDIBELL (Bellvitge Biomedical Research Institute), Barcelona, Spain.
Paolo RadiceUnit of Molecular Bases of Genetic Risk and Genetic Testing, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori (INT), Milan, Italy.
Johanna RantalaClinical Genetics, Karolinska Institutet, Stockholm, Sweden.
Muhammad U RashidMolecular Genetics of Breast Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Barak RosenzweigMale High Risk Clinic, Uro-Oncology Service, Urology Department, Chaim Sheba Medical Center, Tel-Hashomer, Israel.
Maria RossingCenter for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Marta SantamariñaFundación Pública Galega Medicina Xenómica-SERGAS, Santiago de Compostela, Spain.
Rita K SchmutzlerCenter for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
Leigha SenterClinical Cancer Genetics Program, The Comprehensive Cancer Center, Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus.
Jacques SimardGenomics Center, Centre Hospitalier Universitaire de Québec-Université Laval, Research Centre, Québec City, Québec, Canada.
Christian F SingerComprehensive Cancer Center, Department of OB/GYN, Medical University of Vienna, Vienna, Austria.
Angela R SolanoINBIOMED, Faculty of Medicine/UBA-CONICET and Genotyping Laboratory, Department of Clinical Chemistry, Centro de Educacion Medica e Investigaciones Clinicas, CABA, Argentina.
Melissa C SoutheyPrecision Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia.
Linda SteeleDepartment of Population Sciences, Beckman Research Institute of City of Hope, Duarte, California.
Zoe SteinsnyderClinical Genetics Research Lab, Department of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, New York.
Dominique Stoppa-LyonnetService de Génétique, Institut Curie, Paris, France.
Yen Yen TanDepartment of OB/GYN, Medical University of Vienna, Vienna, Austria.
Manuel R TeixeiraDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Soo H TeoCancer Research Malaysia, Subang Jaya, Selangor, Malaysia.
Mary Beth TerryDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York.
Mads ThomassenDepartment of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Amanda E TolandDepartment of Cancer Biology and Genetics, The Ohio State University, Columbus.
Sara Torres-EsquiusHereditary Cancer Genetics Group, Vall d'Hebron Institute of Oncology, Barcelona, Spain.
Nadine TungDepartment of Medical Oncology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Christi J van AsperenDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
Ana VegaFundación Pública Galega Medicina Xenómica-SERGAS, Santiago de Compostela, Spain.
Alessandra VielDivision of Functional onco-genomics and genetics, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, Italy.
Jeroen VierstraeteCentre for Medical Genetics, Ghent University, Gent, Belgium.
Barbara WappenschmidtCenter for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
Jeffrey N WeitzelClinical Cancer Genetics, City of Hope, Duarte, California.
Greet WiemeCentre for Medical Genetics, Ghent University, Gent, Belgium.
Sook-Yee YoonCancer Research Malaysia, Subang Jaya, Selangor, Malaysia.
Kristin K ZornMagee-Womens Hospital, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Lesley McGuffogCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
Michael T ParsonsDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Ute HamannMolecular Genetics of Breast Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Mark H GreeneClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
Judy A KirkCentre for Cancer Research, University of Sydney at The Westmead Institute for Medical Research, and Familial Cancer Service, Westmead Hospital, New South Wales, Australia.
Susan L NeuhausenDepartment of Population Sciences, Beckman Research Institute of City of Hope, Duarte, California.
Timothy R RebbeckHarvard T.H. Chan School of Public Health, Boston, Massachusetts.
Marc TischkowitzProgram in Cancer Genetics, Departments of Human Genetics and Oncology, McGill University, Montréal, Quebec, Canada.
Georgia Chenevix-TrenchDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Antonis C AntoniouCentre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
Eitan FriedmanSackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, Israel.
Laura OttiniDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Memorial Sloan Kettering Cancer Center · USThe University of Melbourne · AUUniversity of Cambridge · GBUniversity of Cologne · DEGhent University · BEReykjavík University · ISTel Aviv University · ILUniversity of Pittsburgh · USGerman Cancer Research Center · DEHospital Clínico San Carlos · ESInserm · FRInstitut d'Investigació Biomédica de Bellvitge · ESMount Sinai Hospital · CANational Centre of Scientific Research "Demokritos" · GRQIMR Berghofer Medical Research Institute · AUUniversity of Helsinki · FIUniversity of Utah · USBeth Israel Deaconess Medical Center · USCity of Hope · USConsejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Using Integrated Omics to Identify Dysfunctional Genetic Mechanisms Influencing Schizophrenia and Sleep DisturbancesP20GM130423 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Kalyani Pyaram, Steven Allan Soper · 2019 to 2026
$21.5M
Cancer Research UK 20861Cancer Research UK 23382Cancer Research UK 26886NCI NIH HHS P30 CA008748NIGMS NIH HHS P20 GM130423Wellcome Trust 203477/Z/16/Z
6 · The paper itself

Abstract

Importance: The limited data on cancer phenotypes in men with germline BRCA1 and BRCA2 pathogenic variants (PVs) have hampered the development of evidence-based recommendations for early cancer detection and risk reduction in this population. Objective: To compare the cancer spectrum and frequencies between male BRCA1 and BRCA2 PV carriers. Design, Setting, and Participants: Retrospective cohort study of 6902 men, including 3651 BRCA1 and 3251 BRCA2 PV carriers, older than 18 years recruited from cancer genetics clinics from 1966 to 2017 by 53 study groups in 33 countries worldwide collaborating through the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA). Clinical data and pathologic characteristics were collected. Main Outcomes and Measures: BRCA1/2 status was the outcome in a logistic regression, and cancer diagnoses were the independent predictors. All odds ratios (ORs) were adjusted for age, country of origin, and calendar year of the first interview. Results: Among the 6902 men in the study (median [range] age, 51.6 [18-100] years), 1634 cancers were diagnosed in 1376 men (19.9%), the majority (922 of 1,376 [67%]) being BRCA2 PV carriers. Being affected by any cancer was associated with a higher probability of being a BRCA2, rather than a BRCA1, PV carrier (OR, 3.23; 95% CI, 2.81-3.70; P < .001), as well as developing 2 (OR, 7.97; 95% CI, 5.47-11.60; P < .001) and 3 (OR, 19.60; 95% CI, 4.64-82.89; P < .001) primary tumors. A higher frequency of breast (OR, 5.47; 95% CI, 4.06-7.37; P < .001) and prostate (OR, 1.39; 95% CI, 1.09-1.78; P = .008) cancers was associated with a higher probability of being a BRCA2 PV carrier. Among cancers other than breast and prostate, pancreatic cancer was associated with a higher probability (OR, 3.00; 95% CI, 1.55-5.81; P = .001) and colorectal cancer with a lower probability (OR, 0.47; 95% CI, 0.29-0.78; P = .003) of being a BRCA2 PV carrier. Conclusions and Relevance: Significant differences in the cancer spectrum were observed in male BRCA2, compared with BRCA1, PV carriers. These data may inform future recommendations for surveillance of BRCA1/2-associated cancers and guide future prospective studies for estimating cancer risks in men with BRCA1/2 PVs.

Indexed as

AdolescentAdultAgedAged, 80 and overBRCA1 ProteinBRCA2 ProteinGerm-Line MutationHumansMaleMiddle AgedNeoplasmsPhenotypeRetrospective StudiesYoung AdultBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, human

Identifiers

PMID32614418
PMCPMC7333177
OpenAlexW3038926436

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