Absolute risk prediction for esophageal squamous cell carcinoma adaptable to regional disease burden across diverse regions.

IF 3.7 3区 医学 Q2 ONCOLOGY
Mengfei Liu, Yi Huang, Hongrui Tian, Chuanhai Guo, Zhen Liu, Anxiang Liu, Haijun Yang, Fenglei Li, Liping Duan, Lin Shen, Qi Wu, Chao Shi, Yaqi Pan, Fangfang Liu, Ying Liu, Huanyu Chen, Zhe Hu, Hong Cai, Zhonghu He, Yang Ke
{"title":"Absolute risk prediction for esophageal squamous cell carcinoma adaptable to regional disease burden across diverse regions.","authors":"Mengfei Liu, Yi Huang, Hongrui Tian, Chuanhai Guo, Zhen Liu, Anxiang Liu, Haijun Yang, Fenglei Li, Liping Duan, Lin Shen, Qi Wu, Chao Shi, Yaqi Pan, Fangfang Liu, Ying Liu, Huanyu Chen, Zhe Hu, Hong Cai, Zhonghu He, Yang Ke","doi":"10.1158/1055-9965.EPI-24-1465","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Esophageal squamous cell carcinoma (ESCC) exhibits a long latency period and has a significant geographical disparity in incidence, which underscores the need for models predicting the long-term absolute risk adaptable to regional disease burden.</p><p><strong>Methods: </strong>31,883 participants in a large-scale population-based screening trial (Hua County, China) were enrolled to develop the model. Severe dysplasia and above (SDA) identified at screening or follow-up were defined as the outcome. We calculated the absolute risk in three steps: 1) constructing a relative risk model using logistic regression, 2) calculating the age-specific baseline hazard, and 3) adjusting for the competing risk of all-cause death excluding ESCC. Flexible incidence rate parameters were integrated into the model to ensure its relevance across diverse regions worldwide.</p><p><strong>Results: </strong>A total of 295 SDAs were detected. The relative risk model consisted of old age, male gender, irregular meal pattern, preference for hot or hard food, BMI of less than 22 kg/m2, and ESCC family history. The area under the receiver operating characteristic curve was 0.753 (95% CI: 0.749-0.757). The averaged 5-year and 10-year absolute risk were 0.53% and 1.30% among participants. Based on our model, we developed an online calculator incorporated flexible incidence rate parameters, demonstrating ideal risk stratification tailored to regions with varying disease burdens (https://pkugenetics.shinyapps.io/escc_risk_prediction/).</p><p><strong>Conclusions: </strong>We developed an absolute risk model to predict individualized long-term risk of ESCC, accounting for local disease burden.</p><p><strong>Impact: </strong>This model has the potential to mitigate the global burden of ESCC by enabling targeted screening and personalized prevention strategies.</p>","PeriodicalId":9458,"journal":{"name":"Cancer Epidemiology Biomarkers & Prevention","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Epidemiology Biomarkers & Prevention","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1158/1055-9965.EPI-24-1465","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Esophageal squamous cell carcinoma (ESCC) exhibits a long latency period and has a significant geographical disparity in incidence, which underscores the need for models predicting the long-term absolute risk adaptable to regional disease burden.

Methods: 31,883 participants in a large-scale population-based screening trial (Hua County, China) were enrolled to develop the model. Severe dysplasia and above (SDA) identified at screening or follow-up were defined as the outcome. We calculated the absolute risk in three steps: 1) constructing a relative risk model using logistic regression, 2) calculating the age-specific baseline hazard, and 3) adjusting for the competing risk of all-cause death excluding ESCC. Flexible incidence rate parameters were integrated into the model to ensure its relevance across diverse regions worldwide.

Results: A total of 295 SDAs were detected. The relative risk model consisted of old age, male gender, irregular meal pattern, preference for hot or hard food, BMI of less than 22 kg/m2, and ESCC family history. The area under the receiver operating characteristic curve was 0.753 (95% CI: 0.749-0.757). The averaged 5-year and 10-year absolute risk were 0.53% and 1.30% among participants. Based on our model, we developed an online calculator incorporated flexible incidence rate parameters, demonstrating ideal risk stratification tailored to regions with varying disease burdens (https://pkugenetics.shinyapps.io/escc_risk_prediction/).

Conclusions: We developed an absolute risk model to predict individualized long-term risk of ESCC, accounting for local disease burden.

Impact: This model has the potential to mitigate the global burden of ESCC by enabling targeted screening and personalized prevention strategies.

背景:食管鳞状细胞癌(ESCC)潜伏期较长,且发病率存在显著的地域差异,因此需要建立适应地区疾病负担的长期绝对风险预测模型。筛查或随访中发现的严重发育不良及以上(SDA)被定义为结果。我们分三步计算绝对风险:1)使用逻辑回归构建相对风险模型;2)计算年龄特异性基线危险度;3)调整排除 ESCC 的全因死亡竞争风险。该模型中纳入了灵活的发病率参数,以确保其适用于全球不同地区:结果:共检测到 295 例 SDA。相对风险模型包括:年龄大、性别为男性、进餐不规律、偏好热食或硬食、体重指数小于 22 kg/m2,以及 ESCC 家族史。接受者操作特征曲线下的面积为 0.753(95% CI:0.749-0.757)。参与者的 5 年和 10 年平均绝对风险分别为 0.53% 和 1.30%。根据我们的模型,我们开发了一个在线计算器,其中纳入了灵活的发病率参数,为疾病负担不同的地区量身定制了理想的风险分层 (https://pkugenetics.shinyapps.io/escc_risk_prediction/)。结论:我们开发了一个绝对风险模型来预测个体化的 ESCC 长期风险,同时考虑到当地的疾病负担:影响:这一模型通过有针对性的筛查和个性化的预防策略,有可能减轻 ESCC 的全球负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Cancer Epidemiology Biomarkers & Prevention
Cancer Epidemiology Biomarkers & Prevention 医学-公共卫生、环境卫生与职业卫生
CiteScore
6.50
自引率
2.60%
发文量
538
审稿时长
1.6 months
期刊介绍: Cancer Epidemiology, Biomarkers & Prevention publishes original peer-reviewed, population-based research on cancer etiology, prevention, surveillance, and survivorship. The following topics are of special interest: descriptive, analytical, and molecular epidemiology; biomarkers including assay development, validation, and application; chemoprevention and other types of prevention research in the context of descriptive and observational studies; the role of behavioral factors in cancer etiology and prevention; survivorship studies; risk factors; implementation science and cancer care delivery; and the science of cancer health disparities. Besides welcoming manuscripts that address individual subjects in any of the relevant disciplines, CEBP editors encourage the submission of manuscripts with a transdisciplinary approach.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信