Jung Hyun Ae, Lee Daehwan, Park Boram, Lee Kiwon, Lee Ho Yun, Kim Tae Jung, Jeon Yeong Jeong, Lee Junghee, Park Seong Yong, Cho Jong Ho, Choi Yong Soo, Park Sehhoon, Sun Jong-Mu, Lee Se-Hoon, Ahn Jin Seok, Ahn Myung-Ju, Kim Hong Kwan
Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Spidercore Inc, Daejeon, Republic of Korea.
JCO Precis Oncol. 2025 Jul;9:e2500172. doi: 10.1200/PO-25-00172. Epub 2025 Jul 23.
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.
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.
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).
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.
早期非小细胞肺癌(NSCLC)的监测方案并非取决于复发的个体风险因素。本研究旨在利用临床实践中的综合数据开发一种用于实际纵向监测的深度学习模型。
开发了一种带有变压器的多模态深度学习模型,用于使用基线临床、病理和分子数据以及监测期间收集的纵向实验室和放射学数据进行实时复发预测。纳入了2008年1月至2022年9月间接受根治性手术的NSCLC患者(I至III期)。主要结局是预测监测点后1年内的复发情况。本研究展示了风险评分(RADAR评分)的及时提供、确定的阈值以及相应的AUC。
共纳入14177例患者(I期10262例,II期2380例,III期1703例)。该模型纳入了基线时的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读数据。I期患者的平均基线RADAR评分为0.324(标准差[SD],0.256),II期为0.660(SD,0.210),III期为0.824(SD,0.140)。所有阶段预测监测点后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)。
这项初步研究引入了一种深度学习模型,该模型使用常规临床实践中的多模态数据来预测早期NSCLC的复发。它展示了向临床医生及时提供RADAR风险评分以进行复发预测,可能指导风险适应性监测策略和积极的辅助全身治疗。