Loman Niklas, Bladström Anna, Johannsson Oskar, Borg Ake, Olsson Håkan
Department of Oncology, Lund University Hospital, Lund, Sweden.
Breast Cancer Res. 2003;5(6):R175-86. doi: 10.1186/bcr632. Epub 2003 Aug 7.
Relatives of breast cancer cases have an increased risk of the disease. The risk increases with increasing numbers and decreasing age of onset of affected relatives. In families with a BRCA1 or a BRCA2 mutation, individual carrier status predicts the risk of breast cancer. In relatives of cases where both BRCA1 and BRCA2 mutations are excluded, the risk remains undetermined.
Standardized incidence ratios (SIRs) and cumulative cancer incidences were calculated for relatives of a population-based set of early-onset breast cancer index cases (younger than age 41 years) with a defined BRCA mutation status (n = 203).
In first-degree relatives (FDRs) of mutation-negative cases, breast cancer incidences (SIR = 2.3), prostate cancer incidences (SIR = 1.7), cervix cancer incidences (SIR = 3.3) and nonmelanoma skin cancer incidences (SIR = 2.8) were increased. The risks of breast cancer, prostate cancer and nonmelanoma skin cancer were further increased in FDRs of breast cancer cases younger than 36 years of age. In high-risk individuals with at least one relative with breast cancer apart from the index case, but no BRCA mutation in the family, breast cancer incidence was increased (SIR = 5.3); again the prostate cancer incidence was elevated (SIR = 2.5). The cumulative incidence of breast cancer at ages 50 and 70 years for FDRs of index cases without a BRCA mutation was 3.6% and 12.8%, respectively. Similarly, the cumulative incidence of breast cancer for high-risk women was 6.3% and 21.1% at ages 50 and 70 years, and that for FDRs of BRCA mutation carriers was 17.2% and 27.7% at the same ages.
The incidence of breast cancer is increased for FDRs of women with early-onset breast cancer irrespective of the BRCA status in the family. Risk increases with decreasing age and with increasing number of affected relatives. The incidences of prostate cancer, cervix cancer and nonmelanoma skin cancer are elevated for FDRs of early-onset breast cancer cases without a BRCA mutation, indicating a possible association between these cancers and early-onset breast cancer.
乳腺癌患者的亲属患该病的风险增加。风险随着受影响亲属数量的增加和发病年龄的降低而增加。在携带BRCA1或BRCA2突变的家族中,个体携带者状态可预测患乳腺癌的风险。在排除BRCA1和BRCA2突变的病例的亲属中,风险仍未确定。
计算了一组基于人群的早发性乳腺癌索引病例(年龄小于41岁)且具有明确BRCA突变状态(n = 203)的亲属的标准化发病率(SIR)和累积癌症发病率。
在突变阴性病例的一级亲属(FDR)中,乳腺癌发病率(SIR = 2.3)、前列腺癌发病率(SIR = 1.7)、宫颈癌发病率(SIR = 3.3)和非黑色素瘤皮肤癌发病率(SIR = 2.8)均升高。在年龄小于36岁的乳腺癌病例的FDR中,乳腺癌、前列腺癌和非黑色素瘤皮肤癌的风险进一步增加。在除索引病例外至少有一名亲属患乳腺癌但家族中无BRCA突变的高危个体中,乳腺癌发病率升高(SIR = 5.3);前列腺癌发病率同样升高(SIR = 2.5)。无BRCA突变的索引病例的FDR在50岁和70岁时的乳腺癌累积发病率分别为3.6%和12.8%。同样,高危女性在50岁和70岁时的乳腺癌累积发病率分别为6.3%和21.1%,而BRCA突变携带者的FDR在相同年龄时的累积发病率分别为17.2%和27.7%。
早发性乳腺癌女性的FDR患乳腺癌的发病率增加,与家族中的BRCA状态无关。风险随着年龄的降低和受影响亲属数量的增加而增加。在无BRCA突变的早发性乳腺癌病例的FDR中,前列腺癌、宫颈癌和非黑色素瘤皮肤癌的发病率升高,表明这些癌症与早发性乳腺癌之间可能存在关联。