Berrington de Gonzalez Amy, Berg Christine D, Visvanathan Kala, Robson Mark
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, 615 N Wolfe St, Baltimore, MD 21205, USA.
J Natl Cancer Inst. 2009 Feb 4;101(3):205-9. doi: 10.1093/jnci/djn440. Epub 2009 Jan 27.
BRCA mutation carriers are recommended to start mammographic screening for breast cancer as early as age 25-30 years. We used an excess relative risk model (based on a pooled analysis of three cohorts with 7600 subjects who received radiation exposure) to estimate the lifetime risk of radiation-induced breast cancer from five annual mammographic screenings in young (<40 years) BRCA mutation carriers. We then estimated the reduction in breast cancer mortality required to outweigh the radiation risk. Breast cancer rates for mutation carriers were based on a pooled analysis of 22 pedigree studies with 8139 subjects. For BRCA1 mutation carriers, the estimated lifetime risk of radiation-induced breast cancer mortality per 10,000 women resulting from annual mammography was 26 (95% confidence interval [CI] = 14 to 49) for screening at age 25-29 years, 20 (95% CI = 11 to 39) for screening at age 30-34 years, and 13 (95% CI = 7 to 23) for screening at age 35-39 years. To outweigh these risks, screening would have to reduce breast cancer mortality by 51% (95% CI = 27% to 96%) at age 25-29 years, by 12% (95% CI = 6% to 23%) at age 30-34 years, and by 4% (95% CI = 2% to 7%) at age 35-39 years; estimates were similar for BRCA2 mutation carriers. If we assume that the mortality reduction from mammography is 15%-25% or less for young women, these results suggest that there would be no net benefit from annual mammographic screening of BRCA mutation carriers at age 25-29 years; the net benefit would be zero or small at age 30-34 years, but there should be some net benefit at age 35 or older. These results depend on a number of assumptions due to the absence of empiric data. The impact of varying these assumptions was therefore examined.
BRCA突变携带者建议早在25至30岁时就开始进行乳腺癌的乳房X光筛查。我们使用了一种超额相对风险模型(基于对三个队列中7600名接受辐射暴露的受试者的汇总分析)来估计年轻(<40岁)BRCA突变携带者进行五次年度乳房X光筛查导致辐射诱发乳腺癌的终生风险。然后,我们估计了为超过辐射风险所需的乳腺癌死亡率降低幅度。突变携带者的乳腺癌发病率基于对22项有8139名受试者的家系研究的汇总分析。对于BRCA1突变携带者,每10000名女性中,因年度乳房X光检查在25至29岁时进行筛查导致的辐射诱发乳腺癌死亡的估计终生风险为26(95%置信区间[CI]=14至49),在30至34岁时进行筛查为20(95%CI=11至39),在35至39岁时进行筛查为13(95%CI=7至23)。为超过这些风险,筛查在25至29岁时必须将乳腺癌死亡率降低51%(95%CI=27%至96%),在30至34岁时降低12%(95%CI=6%至23%),在35至39岁时降低4%(95%CI=2%至7%);BRCA2突变携带者的估计结果相似。如果我们假设乳房X光检查对年轻女性的死亡率降低为15% - 25%或更低,这些结果表明,对25至29岁的BRCA突变携带者进行年度乳房X光筛查不会有净益处;在30至34岁时净益处为零或很小,但在35岁及以上应该会有一些净益处。由于缺乏实证数据,这些结果取决于许多假设。因此,研究了改变这些假设的影响。