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Interval breast cancer risk associations with breast density, family history and breast tissue aging.
Nguyen, Tuong L; Li, Shuai; Dite, Gillian S; Aung, Ye K; Evans, Christopher F; Trinh, Ho N; Baglietto, Laura; Stone, Jennifer; Song, Yun-Mi; Sung, Joohon; English, Dallas R; Jenkins, Mark A; Dugué, Pierre-Antoine; Milne, Roger L; Southey, Melissa C; Giles, Graham G; Pike, Malcolm C; Hopper, John L.
Afiliação
  • Nguyen TL; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Li S; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Dite GS; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Aung YK; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Evans CF; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Trinh HN; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Baglietto L; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
  • Stone J; Centre for Genetic Origins of Health and Disease, University of Western Australia, Perth, WA, Australia.
  • Song YM; Department of Family Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • Sung J; Department of Epidemiology School of Public Health, Seoul National University, Seoul, South Korea.
  • English DR; Institute of Health and Environment, Seoul National University, Seoul, South Korea.
  • Jenkins MA; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Dugué PA; Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, VIC, Australia.
  • Milne RL; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Southey MC; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
  • Giles GG; Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, VIC, Australia.
  • Pike MC; Precision Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia.
  • Hopper JL; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia.
Int J Cancer ; 147(2): 375-382, 2020 07 15.
Article em En | MEDLINE | ID: mdl-31609476
ABSTRACT
Interval breast cancers (those diagnosed between recommended mammography screens) generally have poorer outcomes and are more common among women with dense breasts. We aimed to develop a risk model for interval breast cancer. We conducted a nested case-control study within the Melbourne Collaborative Cohort Study involving 168 interval breast cancer patients and 498 matched control subjects. We measured breast density using the CUMULUS software. We recorded first-degree family history by questionnaire, measured body mass index (BMI) and calculated age-adjusted breast tissue aging, a novel measure of exposure to estrogen and progesterone based on the Pike model. We fitted conditional logistic regression to estimate odds ratio (OR) or odds ratio per adjusted standard deviation (OPERA) and calculated the area under the receiver operating characteristic curve (AUC). The stronger risk associations were for unadjusted percent breast density (OPERA = 1.99; AUC = 0.66), more so after adjusting for age and BMI (OPERA = 2.26; AUC = 0.70), and for family history (OR = 2.70; AUC = 0.56). When the latter two factors and their multiplicative interactions with age-adjusted breast tissue aging (p = 0.01 and 0.02, respectively) were fitted, the AUC was 0.73 (95% CI 0.69-0.77), equivalent to a ninefold interquartile risk ratio. In summary, compared with using dense breasts alone, risk discrimination for interval breast cancers could be doubled by instead using breast density, BMI, family history and hormonal exposure. This would also give women with dense breasts, and their physicians, more information about the major consequence of having dense breasts-an increased risk of developing an interval breast cancer.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progesterona / Neoplasias da Mama / Mamografia / Estrogênios / Anamnese Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged País como assunto: Oceania Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progesterona / Neoplasias da Mama / Mamografia / Estrogênios / Anamnese Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged País como assunto: Oceania Idioma: En Ano de publicação: 2020 Tipo de documento: Article