Your browser doesn't support javascript.
loading
Association of mammographic density measures and breast cancer "intrinsic" molecular subtypes.
Kleinstern, Geffen; Scott, Christopher G; Tamimi, Rulla M; Jensen, Matthew R; Pankratz, V Shane; Bertrand, Kimberly A; Norman, Aaron D; Visscher, Daniel W; Couch, Fergus J; Brandt, Kathleen; Shepherd, John; Wu, Fang-Fang; Chen, Yunn-Yi; Cummings, Steven R; Winham, Stacey; Kerlikowske, Karla; Vachon, Celine M.
Afiliação
  • Kleinstern G; School of Public Health, University of Haifa, Haifa, Israel.
  • Scott CG; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Tamimi RM; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Jensen MR; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
  • Pankratz VS; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • Bertrand KA; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Norman AD; University of New Mexico, Albuquerque, NM, USA.
  • Visscher DW; Slone Epidemiology Center, Boston University School of Medicine, Boston, MA, USA.
  • Couch FJ; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Brandt K; Department of Anatomic Pathology, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Shepherd J; Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Wu FF; Department of Radiology, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Chen YY; University of Hawaii, Honolulu, HI, USA.
  • Cummings SR; Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic College of Medicine, 200 First St. SW, Rochester, MN, 55905, USA.
  • Winham S; Department of Pathology and Laboratory Services, University of California, San Francisco, CA, USA.
  • Kerlikowske K; San Francisco Coordinating Center, California Pacific Medical Center Research Institute, San Francisco, CA, USA.
  • Vachon CM; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, MN, USA.
Breast Cancer Res Treat ; 187(1): 215-224, 2021 May.
Article em En | MEDLINE | ID: mdl-33392844
PURPOSE: We evaluated the association of percent mammographic density (PMD), absolute dense area (DA), and non-dense area (NDA) with risk of "intrinsic" molecular breast cancer (BC) subtypes. METHODS: We pooled 3492 invasive BC and 10,148 controls across six studies with density measures from prediagnostic, digitized film-screen mammograms. We classified BC tumors into subtypes [63% Luminal A, 21% Luminal B, 5% HER2 expressing, and 11% as triple negative (TN)] using information on estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2), and tumor grade. We used polytomous logistic regression to calculate odds ratio (OR) and 95% confidence intervals (CI) for density measures (per SD) across the subtypes compared to controls, adjusting for age, body mass index and study, and examined differences by age group. RESULTS: All density measures were similarly associated with BC risk across subtypes. Significant interaction of PMD by age (P = 0.001) was observed for Luminal A tumors, with stronger effect sizes seen for younger women < 45 years (OR = 1.69 per SD PMD) relative to women of older ages (OR = 1.53, ages 65-74, OR = 1.44 ages 75 +). Similar but opposite trends were seen for NDA by age for risk of Luminal A: risk for women: < 45 years (OR = 0.71 per SD NDA) was lower than older women (OR = 0.83 and OR = 0.84 for ages 65-74 and 75 + , respectively) (P < 0.001). Although not significant, similar patterns of associations were seen by age for TN cancers. CONCLUSIONS: Mammographic density measures were associated with risk of all "intrinsic" molecular subtypes. However, findings of significant interactions between age and density measures may have implications for subtype-specific risk models.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Densidade da Mama Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Israel

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Densidade da Mama Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Israel