口腔肿瘤患者风险分层和预后预测模型的建立和验证

Vishnu Priya Veeraraghavan , Shikhar Daniel , Ravikanth Manyam , Amarender Reddy , Santosh R. Patil
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引用次数: 0

摘要

背景:口腔鳞状细胞癌(OSCC)是一种发病率和死亡率很高的普遍恶性肿瘤,特别是在低收入和中等收入国家。尽管治疗取得了进步,但整合临床、组织病理学和分子数据的预后工具仍然不发达,限制了个性化的风险分层和生存预测。目的本研究旨在建立并验证一种结合临床、组织病理学和分子因素的OSCC总生存期(OS)和无进展生存期(PFS)的预测模型。方法对132例经组织病理学证实的OSCC患者进行回顾性分析。收集了人口统计学、临床(肿瘤分期、淋巴结受累)、组织病理学(肿瘤分级、神经周围浸润)和分子(HPV状态)变量的数据。采用逻辑回归和机器学习算法建立预测模型。采用自举法进行内部验证,采用受试者工作特征(ROC)曲线下面积、校准图和决策曲线分析(DCA)评估模型性能。结果该模型具有较强的预测能力,OS和PFS的ROC曲线下面积(AUC)分别为0.85和0.83。肿瘤分期、淋巴结受累和HPV状态被确定为生存的关键预测因素。Kaplan-Meier分析显示,在最初的24个月内,OS概率急剧下降,强调了早期干预的必要性。校正图显示预测结果与观测结果非常吻合,支持模型的可靠性。结论本研究建立了一个经验证的OSCC OS和PFS预测模型,具有较强的区分能力和校准能力。整合临床、组织病理学和分子数据,增强口腔肿瘤的个性化风险分层和治疗计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and validation of a prediction model for risk stratification and outcome prediction in oral oncology patients

Background

Oral squamous cell carcinoma (OSCC) is a prevalent malignancy with significant morbidity and mortality, particularly in low- and middle-income countries. Despite advancements in treatment, prognostic tools integrating clinical, histopathological, and molecular data remain underdeveloped, limiting personalized risk stratification and survival prediction.

Objective

This study aimed to develop and validate a prediction model for overall survival (OS) and progression-free survival (PFS) in OSCC, incorporating clinical, histopathological, and molecular factors.

Methods

A retrospective cohort of 132 patients with histopathologically confirmed OSCC was analyzed. Data on demographic, clinical (tumor stage, lymph node involvement), histopathological (tumor grade, perineural invasion), and molecular (HPV status) variables were collected. Logistic regression and machine learning algorithms were used to build the prediction model. Internal validation was conducted using bootstrapping, and model performance was assessed using the area under the receiver operating characteristic (ROC) curve, calibration plots, and decision curve analysis (DCA).

Results

The model demonstrated robust predictive performance, with an area under the ROC curve (AUC) of 0.85 for OS and 0.83 for PFS. Tumor stage, lymph node involvement, and HPV status were identified as key predictors of survival. Kaplan-Meier analysis showed steep declines in OS probabilities during the first 24 months, emphasizing the need for early interventions. Calibration plots indicated strong agreement between predicted and observed outcomes, supporting the model's reliability.

Conclusion

This study developed a validated prediction model for OS and PFS in OSCC, demonstrating high discriminatory ability and calibration. Integrating clinical, histopathological, and molecular data enhances personalized risk stratification and treatment planning in oral oncology.
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