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Is mammographic density differentially associated with breast cancer according to receptor status? A meta-analysis
被引:0
|作者:
Sebastien Antoni
Annie J. Sasco
Isabel dos Santos Silva
Valerie McCormack
机构:
[1] International Agency for Research on Cancer,Department of Non
[2] Centre INSERM U897-Epidemiologie-Biostatistique,Communicable Disease Epidemiology
[3] INSERM,undefined
[4] ISPED,undefined
[5] Centre INSERM U897-Epidemiologie-Biostatistique,undefined
[6] ISPED,undefined
[7] Université de Bordeaux,undefined
[8] London School of Hygiene and Tropical Medicine,undefined
来源:
Breast Cancer Research and Treatment
|
2013年
/
137卷
关键词:
Breast cancer;
Breast density;
Receptor subtypes;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Mammographic density (MD) is a strong marker of breast cancer risk, but it is debated whether the association holds, and is of a similar magnitude, for different subtypes of breast cancer defined by receptor status or gene expression profiles. A literature search conducted in June 2012 was used to identify all studies that had investigated the association of MD with subtype-specific breast cancer, independent of age. 7 cohort/case–control and 12 case-only studies were included, comprising a total of >24,000 breast cancer cases. Random effects meta-analysis models were used to combine relative risks (RR) of MD with subtype-specific breast cancer for case–control studies, and in case-only studies to combine relative risk ratios (RRR) of receptor positive versus negative breast tumors. In case–control/cohort studies, relative to women in the lowest density category, women in the highest density category had 3.1-fold (95 % confidence interval [CI] 2.2, 4.2) and 3.2-fold (1.7, 5.9) increased risk of estrogen receptor positive (ER+) and ER− breast cancer, respectively. In case-only analyses, RRRs of breast tumors being ER+ versus ER− were 1.13 (95 % CI 0.89, 1.42) for medium versus minimal MD. MD remained associated with screen-detected ER+ tumors, despite the expectation of this association to be attenuated due to masking bias and overdiagnoses of ER+ tumors. In eight contributing studies, the association of MD did not differ by HER2 status. This combined evidence strengthens the importance of MD as a strong marker of overall and of subtype-specific risk, and confirms its value in overall breast cancer risk assessment and monitoring for both research and clinical purposes.
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页码:337 / 347
页数:10
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