Carcinoma of the breast: incidence, epidemiology, RFs Flashcards
1
Q
- how common is breast cancer?
- how common in terms of mortality?
- prevailing form of the cancer?
- genetic subtypes most common?
A
- most common non-skin malignancy in women
- second only to lung cancer in death count
- most are adenocarcinoma
- HER-/ER+, HER-/ER-, HER+/ER(+/-): most are HER-/ER+
2
Q
- Significance of benign epithelial changes:
- nonproliferative changes
- proliferative changes without atypia
- proliferative changes with atypia
A
- associated with invasive carcinoma
- nonprolif changes do not increase risk of cancer
- prolif changes without atypia increase risk 1.5-2x
- prolif changes with atypia increase risk 4-5x
3
Q
age associations
A
rare before 25, rapidly increases after 30
4
Q
RFs:
- hereditary
- ethnicity
- peak-age
- menarche association
- conception association
- benign breast disease associations
A
- First degree relatives with breast cancer increase the risk by 15-20%
- Non-hispanic white women have the highest incidence in the US
- Ashkenazi Jews have high BRCA1/BRCA2 rate
- menarche before age 11 increases risk of breast cancer by 20%
- peak of breast cancer between 70-80
- conception before age 20 lowers a woman’s risk of BC by 50%
- prolif changes and atypical hyperplasia increase risk of invasive carcinoma
5
Q
RFS
- estrogen exposure
- oophrectomy
- breast density
- radiation
- carcinoma of contralateral breast or ovaries
- obesity
A
- menopausal estrogen hormone therapy increases risk
- oral contraceptives do not increase risk
- most “excess cancers” are small ER+ carcinomas
- oophrectomy: reduces risk of developing breast cancer by 75% because it reduces estrogen exposure
- breast density: very dense breasts increase risk 4-6 times
- radiation increases
- 1% increased risk of developing a 2nd carcinoma per year
- obesity lowers risk because of anovulation–> reduces estrogen exposure
6
Q
major known susceptibility genes
A
BRCA1, BRCA2, TP53, CHEK2
7
Q
20-40% increase in ovarian cancers associated with what gene
A
BRCA1
8
Q
- 10-20% increased risk for developing ovarian cancer associated with what gene?
- which gene is most commonly associated with male breast cancer?
- chrom 17
- chrom 13
- germline mutations
A
- BRCA2: male breast cancer more commonly associated
- BRCA2: less commonly associated with ovarian carcinoma as BRCA1
- BRCA1
- BRCA2
- TP53 in li fraumeni syndrome, CHEK2,
9
Q
BRCA2 chromosome, associations
A
chrom 13, ashkenazi jews 1/40, more often ER+ than BRCA1, poorly differentiated carcinoma
10
Q
BRCA1 chromosome, associations
A
Chromosome 17, ashkenazi jew 1/40, more commonly poorly differentiated with “medullary features”