Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah; George E. Wahlen Department of Veterans Affairs Medical Center, Salt Lake City, Utah; Huntsman Cancer Institute, Salt Lake City, Utah.
Division of Thoracic Surgery, Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland.
J Thorac Oncol. 2019 Jul;14(7):1184-1191. doi: 10.1016/j.jtho.2019.04.019. Epub 2019 May 7.
Published risk estimates for diagnosis of lung cancer based on family history are typically focused on close relatives, rather than a more diverse or complete family history. This study provides estimates of relative risk (RR) for lung cancer based on comprehensive family history data obtained from a statewide cancer registry linked to a high-quality genealogy data resource that is extensive and deep. The risk estimates presented avoid common recall, recruitment, ascertainment biases, and are based on an individual's (proband's) lung cancer family history constellation (pattern of lung cancer affected relatives); numerous constellations are explored.
We used a population-based genealogic resource linked to a statewide electronic Surveillance Epidemiology and End Results program cancer registry to estimate RR for lung cancer for an individual based on their lung cancer family history. The family history data available for a proband included degree of relationship (first- to third-degree), paternal or maternal family lung cancer history, number of lung cancer-affected relatives, and age at diagnosis of affected relatives. More than 1.3 million probands with specific constellations of lung cancer were analyzed. To estimate RRs for lung cancer, the observed number of lung cancer cases among probands with a specific family history constellation was compared to the expected number using internal cohort-specific rates.
A total of 5048 lung cancer cases were identified. Significantly elevated RR was observed for any number of lung cancer-affected relatives among first-, second-, or third-degree relatives. RRs for lung cancer were significantly elevated for each additional lung cancer first-degree relative (FDR) ranging from RR = 2.57 (confidence interval [CI] 95%: 2.39, 2.76) for 1 or more FDR to RR = 4.24 (CI 95%: 1.56, 9.23) for 3 or more FDRs affected. In an absence of FDR family history, increased risk for lung cancer was significant for increasing numbers of affected second-degree relatives (SDRs) ranging from 1.41 (CI 95%: 1.30, 1.52) for 1 or more SDRs to 4.76 (CI 95%: 1.55, 11.11) for 4 or more SDRs. In the absence of affected FDRs and SDRs, there were significantly increased risks based on lung cancer-affected third-degree relatives (TDRs) ranging from 1.18 (CI 95%: 1.11, 1.24) for 1 or more affected TDRs to 1.55 (CI 95%: 1.03, 2.24) for 4 or more affected TDRs. RRs were significantly increased with earlier age at diagnosis of a FDR, and equivalent risks for maternal compared to paternal history were observed.
This study provides population-based estimates of lung cancer risk based on a proband's complete family history (lung cancer constellation). Many individuals at two to five or more times increased risk for lung cancer are identified. Estimates of RR for lung cancer based on family history are arguably relevant clinically. The constellation RR estimates presented could serve in individual decision-making to direct resource use for lung cancer screening, and could be pivotal in decision-making for screening, treatment, and post-treatment surveillance.
基于家族史的肺癌诊断风险估计通常集中于近亲,而不是更广泛或完整的家族史。本研究基于从全州癌症登记处与高质量家谱数据资源链接获得的综合家族史数据,提供了肺癌风险比(RR)的估计,该数据资源广泛而深入。所呈现的风险估计避免了常见的回忆、招募、确定偏倚,并基于个体(先证者)的肺癌家族史组合(肺癌受影响亲属的模式);探讨了许多组合。
我们使用基于人群的家谱资源与全州电子监测、流行病学和最终结果计划癌症登记处链接,根据个体的肺癌家族史来估计个体的肺癌 RR。先证者的家族史数据包括亲属关系程度(一级至三级)、父系或母系肺癌家族史、肺癌受影响亲属数量以及受影响亲属的诊断年龄。分析了超过 130 万个具有特定肺癌组合的先证者。为了估计肺癌的 RR,使用内部队列特定的比率比较特定家族史组合中先证者的观察肺癌病例数与预期病例数。
共确定了 5048 例肺癌病例。在一级、二级或三级亲属中,肺癌受影响亲属的数量越多,RR 显著升高。每个额外的肺癌一级亲属(FDR)的肺癌 RR 显著升高,范围从 1 个或多个 FDR 的 RR=2.57(95%置信区间[CI]:2.39,2.76)到 3 个或更多 FDR 受影响的 RR=4.24(95%CI:1.56,9.23)。在没有 FDR 家族史的情况下,肺癌风险随着受影响的二级亲属(SDR)数量的增加而显著增加,范围从 1 个或多个 SDR 的 RR=1.41(95%CI:1.30,1.52)到 4 个或更多 SDR 的 RR=4.76(95%CI:1.55,11.11)。在没有受影响的 FDR 和 SDR 的情况下,肺癌受影响的三级亲属(TDR)的风险显著增加,范围从 1 个或多个受影响的 TDR 的 RR=1.18(95%CI:1.11,1.24)到 4 个或更多受影响的 TDR 的 RR=1.55(95%CI:1.03,2.24)。FDR 的诊断年龄越早,RR 增加越显著,且母系家族史与父系家族史的风险相当。
本研究基于先证者的完整家族史(肺癌组合)提供了肺癌风险的基于人群的估计。确定了许多肺癌风险增加 2 至 5 倍或更多倍的个体。基于家族史的肺癌 RR 估计在临床上可能具有相关性。所呈现的 RR 估计可用于个体决策,以指导肺癌筛查的资源利用,并可能在筛查、治疗和治疗后监测的决策中发挥关键作用。