Ji Jianguang, Hemminki Kari
Department of Bioscience at Novum, Karolinska Institute, 141 57 Huddinge, Sweden.
Eur J Cancer. 2006 Sep;42(14):2343-9. doi: 10.1016/j.ejca.2005.11.043. Epub 2006 Jul 21.
We used the nation-wide Swedish Family-Cancer Database to examine the familial risks of histology-specific bone cancers in offspring by parental or sibling probands. Adjusted standardised incidence ratios (SIRs) were used to measure the risk. Among the 1327 offspring bone cancers, only two parent-offspring pairs and one sibling pair were noted with concordant bone cancer but the SIRs were not significant. Significant associations were observed in specific histological types or specific age groups, some of which may be chance findings arising from multiple comparisons. However, the risk of early-onset (< 25 years) osteosarcoma in offspring was significantly increased when mothers presented with breast cancer (1.7) and melanoma (2.9), suggesting that Li-Fraumeni syndrome could partly explain this familial aggregation. Other associations, such as childhood osteosarcoma with parental liver cancer, Ewing's sarcoma with kidney cancer and giant cell sarcoma with maternal breast cancer, were novel findings and may be related to other familial diseases.
我们使用瑞典全国性的家庭癌症数据库,通过父母或同胞先证者来研究后代特定组织学类型骨癌的家族风险。采用调整后的标准化发病率比(SIRs)来衡量风险。在1327例后代骨癌中,仅发现两对父母-子女对和一对同胞对患有一致性骨癌,但SIRs无统计学意义。在特定组织学类型或特定年龄组中观察到显著关联,其中一些可能是多次比较产生的偶然发现。然而,当母亲患有乳腺癌(1.7)和黑色素瘤(2.9)时,后代早发型(<25岁)骨肉瘤的风险显著增加,这表明李-弗劳梅尼综合征可能部分解释了这种家族聚集现象。其他关联,如儿童骨肉瘤与父母肝癌、尤因肉瘤与肾癌以及巨细胞肉瘤与母亲乳腺癌,均为新发现,可能与其他家族性疾病有关。