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吸烟、NBS1 多态性与半贝叶斯调整危险比变异后肺癌和上呼吸消化道癌的生存

Tobacco smoking, NBS1 polymorphisms, and survival in lung and upper aerodigestive tract cancers with semi-Bayes adjustment for hazard ratio variation.

机构信息

Zhejiang Provincial CDC, Hangzhou, Zhejiang, People's Republic of China.

出版信息

Cancer Causes Control. 2014 Jan;25(1):11-23. doi: 10.1007/s10552-013-0303-0. Epub 2013 Oct 29.

DOI:10.1007/s10552-013-0303-0
PMID:24166361
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3889468/
Abstract

PURPOSE

Although single nucleotide polymorphisms (SNPs) of NBS1 have been associated with susceptibility to lung and upper aerodigestive tract (UADT) cancers, their relations to cancer survival and measures of effect are largely unknown.

METHODS

Using follow-up data from 611 lung cancer cases and 601 UADT cancer cases from a population-based case-control study in Los Angeles, we prospectively evaluated associations of tobacco smoking and 5 NBS1 SNPs with all-cause mortality. Mortality data were obtained from the Social Security Death Index. We used Cox regression to estimate adjusted hazard ratios (HR) for main effects and ratios of hazard ratios (RHR) derived from product terms to assess hazard ratio variations by each SNP. Bayesian methods were used to account for multiple comparisons.

RESULTS

We observed 406 (66 %) deaths in lung cancer cases and 247 (41 %) deaths in UADT cancer cases with median survival of 1.43 and 1.72 years, respectively. Ever tobacco smoking was positively associated with mortality for both cancers. We observed an upward dose-response association between smoking pack-years and mortality in UADT squamous cell carcinoma. The adjusted HR relating smoking to mortality in non-small cell lung cancer (NSCLC) was greater for cases with the GG genotype of NBS1 rs1061302 than for cases with AA/AG genotypes (semi-Bayes adjusted RHR = 1.97; 95 % limits = 1.14, 3.41).

CONCLUSIONS

A history of tobacco smoking at cancer diagnosis was associated with mortality among patients with lung cancer or UADT squamous cell carcinoma. The HR relating smoking to mortality appeared to vary with the NBS1 rs1061302 genotype among NSCLC cases.

摘要

目的

尽管 NBS1 的单核苷酸多态性 (SNP) 与肺癌和上呼吸消化道 (UADT) 癌症的易感性有关,但它们与癌症生存和效应衡量指标的关系在很大程度上尚不清楚。

方法

使用洛杉矶基于人群的病例对照研究中 611 例肺癌病例和 601 例 UADT 癌症病例的随访数据,我们前瞻性评估了吸烟和 5 个 NBS1 SNP 与全因死亡率的关系。死亡率数据来自社会保障死亡指数。我们使用 Cox 回归估计主要效应的调整危险比 (HR) 和乘积项得出的危险比比值 (RHR),以评估每个 SNP 的危险比变化。贝叶斯方法用于考虑多次比较。

结果

我们观察到肺癌病例中有 406 例(66%)死亡,UADT 癌症病例中有 247 例(41%)死亡,中位生存时间分别为 1.43 年和 1.72 年。吸烟与两种癌症的死亡率均呈正相关。我们观察到吸烟包年数与 UADT 鳞状细胞癌死亡率之间存在向上的剂量反应关系。NBS1 rs1061302 的 GG 基因型与 AA/AG 基因型相比,与非小细胞肺癌 (NSCLC) 死亡率相关的吸烟调整 HR 更大(半贝叶斯调整 RHR=1.97;95%可信区间=1.14,3.41)。

结论

癌症诊断时的吸烟史与肺癌或 UADT 鳞状细胞癌患者的死亡率有关。吸烟与死亡率之间的 HR 似乎因 NSCLC 病例中 NBS1 rs1061302 基因型而异。

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