用于实时预测早期非小细胞肺癌复发的深度学习模型:一种多模式方法(RADAR CARE Study)。

IF 5.6 2区 医学 Q1 ONCOLOGY
JCO precision oncology Pub Date : 2025-07-01 Epub Date: 2025-07-23 DOI:10.1200/PO-25-00172
Hyun Ae Jung, Daehwan Lee, Boram Park, Kiwon Lee, Ho Yun Lee, Tae Jung Kim, Yeong Jeong Jeon, Junghee Lee, Seong Yong Park, Jong Ho Cho, Yong Soo Choi, Sehhoon Park, Jong-Mu Sun, Se-Hoon Lee, Jin Seok Ahn, Myung-Ju Ahn, Hong Kwan Kim
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引用次数: 0

摘要

目的:早期非小细胞肺癌(NSCLC)的监测方案不取决于复发的个体化危险因素。本研究旨在利用临床实践的综合数据,开发一种用于实际纵向监测的深度学习模型。方法:利用监测期间收集的基线临床、病理和分子数据以及纵向实验室和放射学数据,开发了一个多模态深度学习模型,用于实时复发预测。在2008年1月至2022年9月期间接受手术治疗的非小细胞肺癌(I至III期)患者被纳入研究。主要观察指标为预测监测后1年内的复发情况。本研究展示了及时提供风险评分(RADAR评分)和确定的阈值以及相应的AUC。结果:共有14177例患者入组(10262例I期,2380例II期,1703例III期)。该模型在基线时纳入了64个临床-病理-分子因素,以及纵向实验室和计算机断层扫描成像解释数据。平均基线RADAR评分I期0.324(标准差[SD], 0.256), II期0.660 (SD, 0.210), III期0.824 (SD, 0.140)。所有分期预测1年内复发的AUC为0.854,敏感性为86.0%,特异性为71.3% (I期AUC = 0.872, II期AUC = 0.737, III期AUC = 0.724)。结论:该试点研究引入了一种深度学习模型,该模型使用来自常规临床实践的多模态数据来预测早期非小细胞肺癌的复发。该研究表明,RADAR风险评分可及时为临床医生提供复发预测,潜在地指导适应风险的监测策略和积极的辅助全身治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep-Learning Model for Real-Time Prediction of Recurrence in Early-Stage Non-Small Cell Lung Cancer: A Multimodal Approach (RADAR CARE Study).

Purpose: The surveillance protocol for early-stage non-small cell lung cancer (NSCLC) is not contingent upon individualized risk factors for recurrence. This study aimed to use comprehensive data from clinical practice to develop a deep-learning model for practical longitudinal monitoring.

Methods: A multimodal deep-learning model with transformers was developed for real-time recurrence prediction using baseline clinical, pathological, and molecular data with longitudinal laboratory and radiologic data collected during surveillance. Patients with NSCLC (stage I to III) who underwent surgery with curative intent between January 2008 and September 2022 were included. The primary outcome was predicting recurrence within 1 year after the monitoring point. This study demonstrates the timely provision of risk scores (RADAR score) and determined thresholds and the corresponding AUC.

Results: A total of 14,177 patients were enrolled (10,262 with stage I, 2,380 with stage II, and 1,703 with stage III). The model incorporated 64 clinical-pathological-molecular factors at baseline, along with longitudinal laboratory and computed tomography imaging interpretation data. The mean baseline RADAR score was 0.324 (standard deviation [SD], 0.256) in stage I, 0.660 (SD, 0.210) in stage II, and 0.824 (SD, 0.140) in stage III. The AUC for predicting relapse within 1 year of the monitoring point was 0.854 across all stages, with a sensitivity of 86.0% and a specificity of 71.3% (AUC = 0.872 in stage I, AUC = 0.737 in stage II, and AUC = 0.724 in stage III).

Conclusion: This pilot study introduces a deep-learning model that uses multimodal data from routine clinical practice to predict relapses in early-stage NSCLC. It demonstrates the timely provision of RADAR risk scores to clinicians for recurrence prediction, potentially guiding risk-adapted surveillance strategies and aggressive adjuvant systemic treatment.

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CiteScore
9.10
自引率
4.30%
发文量
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