Trends in uterine cancer incidence and mortality: insights from a natural history model.

IF 9.9 1区 医学 Q1 ONCOLOGY
William D Hazelton, Matthew Prest, Ling Chen, Kevin Rouse, Elena B Elkin, Jennifer S Ferris, Xiao Xu, Nina B Bickell, Chung Yin Kong, Stephanie Blank, Eric J Feuer, Goli Samimi, Brandy M Heckman-Stoddard, Tracy M Layne, Jason D Wright, Evan R Myers, Laura J Havrilesky
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引用次数: 0

Abstract

Background: Uterine cancer incidence and mortality are increasing, with concomitant disparities in outcomes between racial groups. Natural history modeling can evaluate risk factors, predict future trends, and simulate approaches to reducing mortality and disparities.

Methods: We designed a natural history model of uterine cancer using a multistage clonal expansion design. The model is informed by National Health and Nutrition Examination Surveys (NHANES), National Health Examination Surveys (NHES), age, period, birth cohort, and birth certificate data on reproductive histories (RH) and body mass index (BMI), and is fit and calibrated to Surveillance, Epidemiology, and End Results (SEER) data by race/ethnicity and histologic subgroup. We projected future incidence and estimated the degree of contribution of BMI, RH, and competing hysterectomy to excess uterine cancer incidence.

Results: The model accurately replicated SEER incidence for endometrioid (EM), non-endometrioid (non-EM), and sarcoma subgroups for non-Hispanic Black (NHB) and non-Hispanic White (NHW) patients. For EM, non-EM, and Sarcomas, BMI-attributable risks are greater for NHW than NHB; RH-attributable risks are greater for NHB. Between 2018 and 2050, EM incidence is projected to rise by 64.9% in NHB and17.5% in NHW; non-EM projected rise is 41.4% in NHB and 22.5% in NHW; sarcoma incidence projected increase is 36% in NHB and 29.2% in NHW.

Conclusions: Uterine cancer risk is substantially explained by RH and BMI, with differences observed between NHB and NHW and future projections indicating perpetuation of disparities. Lower rates of hysterectomy and rising obesity rates will likely contribute to continued increases in uterine cancer incidence.

子宫癌发病率和死亡率的趋势:来自自然历史模型的见解。
背景:子宫癌的发病率和死亡率正在上升,同时在不同种族间的预后也存在差异。自然历史建模可以评估风险因素,预测未来趋势,并模拟减少死亡率和差距的方法。方法:采用多期克隆扩增法建立子宫癌自然历史模型。该模型由国家健康和营养检查调查(NHANES)、国家健康检查调查(NHES)、年龄、时期、出生队列和生育史(RH)和体重指数(BMI)的出生证明数据提供信息,并根据种族/民族和组织学亚组适合和校准监测、流行病学和最终结果(SEER)数据。我们预测了未来的发病率,并估计了BMI、RH和竞争性子宫切除术对过量子宫癌发病率的贡献程度。结果:该模型准确地复制了非西班牙裔黑人(NHB)和非西班牙裔白人(NHW)患者的子宫内膜样(EM)、非子宫内膜样(non-EM)和肉瘤亚组的SEER发生率。对于EM、非EM和肉瘤,NHW的bmi归因风险大于NHB;NHB的rh归因风险更大。在2018年至2050年期间,新兴市场发病率预计将在高卫生保健国家上升64.9%,在高卫生保健国家上升17.5%;非新兴市场预计NHB增长41.4%,NHW增长22.5%;NHB组肉瘤发病率预计增加36%,NHW组增加29.2%。结论:子宫癌风险主要由RH和BMI解释,NHB和NHW之间存在差异,未来预测表明这种差异将持续存在。子宫切除术率的降低和肥胖率的上升可能会导致子宫癌发病率的持续上升。
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来源期刊
CiteScore
17.00
自引率
2.90%
发文量
203
审稿时长
4-8 weeks
期刊介绍: The Journal of the National Cancer Institute is a reputable publication that undergoes a peer-review process. It is available in both print (ISSN: 0027-8874) and online (ISSN: 1460-2105) formats, with 12 issues released annually. The journal's primary aim is to disseminate innovative and important discoveries in the field of cancer research, with specific emphasis on clinical, epidemiologic, behavioral, and health outcomes studies. Authors are encouraged to submit reviews, minireviews, and commentaries. The journal ensures that submitted manuscripts undergo a rigorous and expedited review to publish scientifically and medically significant findings in a timely manner.
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