Etzel Carol J, Amos Christopher I, Spitz Margaret R
Department of Epidemiology, The University of Texas M D Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer Res. 2003 Dec 1;63(23):8531-5.
Studies of familial aggregation of cancer provide indirect evidence for the role of genetic predisposition to cancer. In an ongoing case-control study, we evaluated whether first-degree relatives of lung cancer cases are at increased risk of lung and other cancers. Smoking-related cancers were defined as cancers of the lung, bladder, head and neck, kidney, and pancreas. The 806 probands included in this analysis were patients referred to The University of Texas M. D. Anderson Cancer Center (Houston, TX). We identified 663 controls, matched to the cases on age (+/-5 years), sex, ethnicity, and smoking history, who were recruited from a local multispecialty physician practice in the Houston metropolitan area. Self-reported cancer family history data were available for 6430 first-degree relatives of the cases and 4936 first-degree relatives of the controls. An excess of cancer in relatives was evaluated by comparing the observed cancer cases among relatives of the cases with relatives of the controls. We conducted further analysis after stratifying on age of lung cancer onset (age at study registration for controls) and smoking status (never, former, or current) of the probands. We also conducted Cox regression analysis and compared time to cancer diagnosis among the relatives of the cases and controls adjusted for age and smoking status of proband and family members. Siblings [relative risk (RR) = 1.85; P = 0.003] of cases had a significant excess of lung cancer and an excess of smoking-related cancers (RR = 1.29; P = 0.01). We observed evidence of familial aggregation (RR = 1.71; P < 0.001) of lung cancer among relatives of late-onset lung cancer cases. From the Cox regression, we observed a moderate risk for development of lung (RR = 1.25; P = 0.09) and other smoking-related cancers (RR = 1.23; P = 0.05). After adjustment for smoking behavior of probands and their relatives, the risks of lung cancer (RR = 1.33; P = 0.03) and smoking-related cancers (RR = 1.28; P = 0.02) were statistically significant. We further stratified on age at onset and observed no evidence (P = 0.81) of familial aggregation of lung cancer among young onset (<or=55 years of age) lung cancer cases. We also did not observe evidence of familial aggregation (P = 0.88) of smoking-related cancers in the same group. There was no evidence of increased risk (P = 0.77) of lung cancer among relatives of never-smokers. These findings support the need for additional study in the characterization and identification of genetic factors that influence and modulate cancer susceptibility in humans.
癌症家族聚集性研究为癌症遗传易感性的作用提供了间接证据。在一项正在进行的病例对照研究中,我们评估了肺癌病例的一级亲属患肺癌及其他癌症的风险是否增加。与吸烟相关的癌症定义为肺癌、膀胱癌、头颈癌、肾癌和胰腺癌。本次分析纳入的806名先证者是转诊至德克萨斯大学MD安德森癌症中心(德克萨斯州休斯顿)的患者。我们确定了663名对照,根据年龄(±5岁)、性别、种族和吸烟史与病例进行匹配,这些对照是从休斯顿大都市地区当地的多专科医生诊所招募的。病例的6430名一级亲属和对照的4936名一级亲属可获得自我报告的癌症家族史数据。通过比较病例亲属和对照亲属中观察到的癌症病例,评估亲属中癌症的超额情况。我们在先证者的肺癌发病年龄(对照的研究登记年龄)和吸烟状况(从不、曾经或当前)分层后进行了进一步分析。我们还进行了Cox回归分析,并比较了病例和对照亲属中经先证者及家庭成员的年龄和吸烟状况调整后的癌症诊断时间。病例的兄弟姐妹患肺癌的比例显著过高(相对风险RR = 1.85;P = 0.003),与吸烟相关的癌症比例也过高(RR = 1.29;P = 0.01)。我们观察到晚发型肺癌病例的亲属中存在肺癌家族聚集性的证据(RR = 1.71;P < 0.001)。从Cox回归分析中,我们观察到患肺癌(RR = 1.25;P = 0.09)和其他与吸烟相关癌症(RR = 1.23;P = 0.05)的风险中等。在先证者及其亲属的吸烟行为调整后,肺癌(RR = 1.33;P = 0.03)和与吸烟相关癌症(RR = 1.28;P = 0.02)的风险具有统计学意义。我们进一步按发病年龄分层,未观察到年轻发病(≤55岁)肺癌病例中有肺癌家族聚集性的证据(P = 0.81)。在同一组中,我们也未观察到与吸烟相关癌症家族聚集性的证据(P = 0.88)。从不吸烟者的亲属中没有肺癌风险增加的证据(P = 0.77)。这些发现支持有必要进一步研究影响和调节人类癌症易感性的遗传因素的特征和识别。