Hisada M, Garber J E, Fung C Y, Fraumeni J F, Li F P
Dana-Farber Cancer Institute, and Department of Epidemiology, Harvard School of Public Health, Boston, MA 02115, USA.
J Natl Cancer Inst. 1998 Apr 15;90(8):606-11. doi: 10.1093/jnci/90.8.606.
Li-Fraumeni syndrome is a dominantly inherited disorder characterized by early-onset breast cancer, sarcomas, and other cancers in children and young adults. Members of families with this syndrome also develop multiple primary cancers, but the frequency is unknown. To approach this issue, we quantified the incidence of second and third primary cancers in individuals from 24 Li-Fraumeni kindreds originally diagnosed with cancer during the period from 1968 through 1986.
The relative risk (RR) of subsequent cancers and 95% confidence intervals (CIs) were calculated by use of population-based incidence data from the Connecticut Cancer Registry. Kaplan-Meier analysis was used to determine the cumulative probability (+/- standard error) of subsequent cancers.
Among 200 Li-Fraumeni syndrome family members diagnosed with cancer, 30 (15%) developed a second cancer. Eight individuals (4%) had a third cancer, while four (2%) eventually developed a fourth cancer. Overall, the RR of occurrence of a second cancer was 5.3 (95% CI = 2.8-7.8), with a cumulative probability of second cancer occurrence of 57% (+/- 10%) at 30 years after diagnosis of a first cancer. RRs of second cancers occurring in families with this syndrome were 83.0 (95% CI = 36.9-187.6), 9.7 (95% CI = 4.9-19.2), and 1.5 (95% CI = 0.5-4.2) for individuals with a first cancer at ages 0-19 years, 20-44 years, and 45 years or more, respectively. Thirty (71%) of 42 subsequent cancers in this group were component cancers of Li-Fraumeni syndrome.
Compared with the general population, members of Li-Fraumeni syndrome families have an exceptionally high risk of developing multiple primary cancers. The excess risk of additional primary cancers is mainly for cancers that are characteristic of Li-Fraumeni syndrome, with the highest risk observed for survivors of childhood cancers. Cancer survivors in these families should be closely monitored for early manifestations of new cancers.
李-佛美尼综合征是一种常染色体显性遗传病,其特征为儿童和青年期的早发性乳腺癌、肉瘤及其他癌症。患有该综合征的家族成员也会发生多种原发性癌症,但其发生率尚不清楚。为探讨这一问题,我们对1968年至1986年期间最初被诊断患有癌症的24个李-佛美尼家族的个体中第二和第三种原发性癌症的发生率进行了量化。
利用康涅狄格癌症登记处基于人群的发病率数据计算后续癌症的相对风险(RR)及95%置信区间(CI)。采用Kaplan-Meier分析确定后续癌症的累积概率(±标准误)。
在200名被诊断患有癌症的李-佛美尼综合征家族成员中,30人(15%)发生了第二种癌症。8人(4%)发生了第三种癌症,4人(2%)最终发生了第四种癌症。总体而言,第二种癌症发生的RR为5.3(95%CI=2.8-7.8),在诊断第一种癌症后30年时第二种癌症发生的累积概率为57%(±10%)。对于首次患癌年龄在0至19岁、20至44岁和45岁及以上的个体,该综合征家族中第二种癌症发生的RR分别为83.0(95%CI=36.9-187.6)、9.7(95%CI=4.9-19.2)和1.5(95%CI=0.5-4.2)。该组42例后续癌症中有30例(71%)是李-佛美尼综合征的组成性癌症。
与一般人群相比,李-佛美尼综合征家族成员发生多种原发性癌症的风险极高。额外原发性癌症的超额风险主要针对李-佛美尼综合征特征性的癌症,儿童癌症幸存者的风险最高。这些家族中的癌症幸存者应密切监测新癌症的早期表现。