头颈部癌症风险预测模型的开发和外部验证。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-06-08 DOI:10.1002/hed.27834
Craig D. L. Smith BSc, Alex D. McMahon PhD, Donald M. Lyall PhD, Mariel Goulart MSc, Gareth J. Inman PhD, Al Ross PhD, Mark Gormley PhD, Tom Dudding PhD, Gary J. Macfarlane PhD, Max Robinson PhD, Lorenzo Richiardi PhD, Diego Serraino PhD, Jerry Polesel PhD, Cristina Canova PhD, Wolfgang Ahrens PhD, Claire M. Healy PhD, Pagona Lagiou PhD, Ivana Holcatova PhD, Laia Alemany PhD, Ariana Znoar PhD, Tim Waterboer PhD, Paul Brennan PhD, Shama Virani PhD, David I. Conway PhD
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引用次数: 0

摘要

背景:头颈癌(HNC)的发病率呈上升趋势,通常在晚期才确诊,预后较差。风险预测工具在预防和早期发现方面具有潜在作用:方法:采用 IARC-ARCAGE 欧洲病例对照研究作为模型开发数据集。通过多变量逻辑回归分析,利用行为和人口学预测因素建立了临床 HNC 风险预测模型。该模型随后在英国生物库队列中进行了外部验证。使用辨别度和校准度检验了模型的性能:该模型的开发使用了 1926 例 HNC 病例和 2043 例对照。包括社会人口学、吸烟和饮酒变量在内的开发数据集模型具有适度的区分度,曲线下面积(AUC)值为 0.75(95% CI,0.74-0.77);校准斜率(0.75)和测试表明校准效果良好。384 616 名英国生物库参与者(其中有 1177 个 HNC 病例)可用于模型的外部验证。经外部验证,该模型的AUC为0.62(95% CI,0.61-0.64):我们利用 ARCAGE 和英国生物库研究分别开发了一个 HNC 风险预测模型,并进行了外部验证。该模型在开发人群中表现一般,在验证数据集中表现尚可。人口统计学和风险行为是预测 HNC 的有力因素,该模型可能是初级牙科保健中促进预防和确定牙科检查召回间隔的有用工具。未来加入 HPV 血清学或遗传因素可进一步提高个体风险预测能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Development and external validation of a head and neck cancer risk prediction model

Background

Head and neck cancer (HNC) incidence is on the rise, often diagnosed at late stage and associated with poor prognoses. Risk prediction tools have a potential role in prevention and early detection.

Methods

The IARC-ARCAGE European case–control study was used as the model development dataset. A clinical HNC risk prediction model using behavioral and demographic predictors was developed via multivariable logistic regression analyses. The model was then externally validated in the UK Biobank cohort. Model performance was tested using discrimination and calibration metrics.

Results

1926 HNC cases and 2043 controls were used for the development of the model. The development dataset model including sociodemographic, smoking, and alcohol variables had moderate discrimination, with an area under curve (AUC) value of 0.75 (95% CI, 0.74–0.77); the calibration slope (0.75) and tests were suggestive of good calibration. 384 616 UK Biobank participants (with 1177 HNC cases) were available for external validation of the model. Upon external validation, the model had an AUC of 0.62 (95% CI, 0.61–0.64).

Conclusion

We developed and externally validated a HNC risk prediction model using the ARCAGE and UK Biobank studies, respectively. This model had moderate performance in the development population and acceptable performance in the validation dataset. Demographics and risk behaviors are strong predictors of HNC, and this model may be a helpful tool in primary dental care settings to promote prevention and determine recall intervals for dental examination. Future addition of HPV serology or genetic factors could further enhance individual risk prediction.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
期刊最新文献
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