Xu Tao, Dillon Joseph S, Quelle Dawn E, Nash Sarah H, Cho Hyunkeun, O'Rorke Michael A
Department of Epidemiology, College of Public Health, University of Iowa, Iowa City, Iowa.
Holden Comprehensive Cancer Center, University of Iowa, Iowa City, Iowa.
Cancer Epidemiol Biomarkers Prev. 2025 Aug 1;34(8):1395-1404. doi: 10.1158/1055-9965.EPI-25-0155.
The incidence of neuroendocrine tumors (NET), which arise primarily in lung and gastroenteropancreatic (GEP) tissues, has increased dramatically in the past 50 years. However, the etiology of NETs remains inconclusive.
We conducted a nested case-control study using data from the All of Us Research Program (version 7; index dates: 2000-2022) to compare the odds of diagnosed GEP or lung NET in the presence or absence of various potential risk factors. One case was matched to five controls without cancer diagnoses by age at consent and sex. We used piecewise structural equation modeling to generate effect estimates.
Of 2,180 individuals (including 366 with NETs), most were non-Hispanic White (62.8%) and female (61.0%). Individuals with a family history of any cancer [OR, 1.43; 95% confidence interval (CI), 1.06-1.95; P = 0.021], a past diagnosis of type 2 diabetes (OR, 1.46; 95% CI, 1.09-1.96; P = 0.012), and any immune-mediated disease (OR, 1.40; 95% CI, 1.11-1.76; P = 0.004) had higher odds of developing GEP or lung NETs.
This study confirms prior evidence in less diverse cohorts that the risk of developing GEP or lung NETs is significantly associated with having a first-degree relative with any cancer or previous diagnosis of type 2 diabetes.
Our findings are the first to demonstrate that a preexisting diagnosis of any immune-mediated disease is a risk factor for developing NETs. Together, our findings suggest that NET development may be influenced by unmodifiable factors as well as modifiable conditions.
神经内分泌肿瘤(NET)主要起源于肺和胃肠胰(GEP)组织,在过去50年中其发病率急剧上升。然而,NET的病因仍无定论。
我们利用“我们所有人”研究计划(第7版;索引日期:2000 - 2022年)的数据进行了一项巢式病例对照研究,以比较存在或不存在各种潜在风险因素时被诊断为GEP或肺NET的几率。一名病例按同意时的年龄和性别与五名无癌症诊断的对照进行匹配。我们使用分段结构方程模型来生成效应估计值。
在2180名个体(包括366名患有NET的个体)中,大多数是非西班牙裔白人(62.8%)且为女性(61.0%)。有任何癌症家族史的个体[比值比(OR),1.43;95%置信区间(CI),1.06 - 1.95;P = 0.021]、既往诊断为2型糖尿病的个体(OR,1.46;95% CI,1.09 - 1.96;P = 0.012)以及任何免疫介导疾病的个体(OR,1.40;95% CI,1.11 - 1.76;P = 0.004)发生GEP或肺NET的几率更高。
本研究证实了在多样性较低的队列中的先前证据,即发生GEP或肺NET的风险与有任何癌症的一级亲属或先前诊断为2型糖尿病显著相关。
我们的研究结果首次表明,预先存在的任何免疫介导疾病的诊断是发生NET的一个风险因素。总之,我们的研究结果表明,NET的发生可能受到不可改变的因素以及可改变的状况的影响。