Department of Radiology, The First Affiliated Hospital of Fujian Medical University, 20 Cha-Zhong Road, Fuzhou, 350005, Fujian, China.
Shanghai Key Laboratory of Magnetic Resonance, School of Physics and Electronic Science, East China Normal University, 3663 North Zhangshan Road, Shanghai, 200062, China.
Sci Rep. 2023 Sep 20;13(1):15586. doi: 10.1038/s41598-023-42916-2.
Early acquired resistance (EAR) to epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in lung adenocarcinomas before radiographic advance cannot be perceived by the naked eye. This study aimed to discover and validate a CT radiomic model to precisely identify the EAR. Training cohort (n = 67) and internal test cohort (n = 29) were from the First Affiliated Hospital of Fujian Medical University, and external test cohort (n = 29) was from the Second Affiliated Hospital of Xiamen Medical College. Follow-up CT images at three different times of each patient were collected: (1) baseline images before EGFR-TKIs therapy; (2) first follow-up images after EGFR-TKIs therapy (FFT); (3) EAR images, which were the last follow-up images before radiographic advance. The features extracted from FFT and EAR were used to construct the classic radiomic model. The delta features which were calculated by subtracting the baseline from either FFT or EAR were used to construct the delta radiomic model. The classic radiomic model achieved AUC 0.682 and 0.641 in training and internal test cohorts, respectively. The delta radiomic model achieved AUC 0.730 and 0.704 in training and internal test cohorts, respectively. Over the external test cohort, the delta radiomic model achieved AUC 0.661. The decision curve analysis showed that when threshold of the probability of the EAR to the EGFR-TKIs was between 0.3 and 0.82, the proposed model was more benefit than treating all patients. Based on two central studies, the delta radiomic model derived from the follow-up non-enhanced CT images can help clinicians to identify the EAR to EGFR-TKIs in lung adenocarcinomas before radiographic advance and optimize clinical outcomes.
早期获得性耐药(EAR)在影像学进展前无法用肉眼察觉肺腺癌表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)。本研究旨在发现和验证 CT 放射组学模型,以准确识别 EAR。训练队列(n=67)和内部测试队列(n=29)来自福建医科大学附属第一医院,外部测试队列(n=29)来自厦门医学院第二附属医院。每位患者的三个不同时间点采集了随访 CT 图像:(1)EGFR-TKIs 治疗前的基线图像;(2)EGFR-TKIs 治疗后的第一次随访图像(FFT);(3)EAR 图像,即影像学进展前的最后一次随访图像。从 FFT 和 EAR 中提取的特征用于构建经典放射组学模型。通过从 FFT 或 EAR 中减去基线计算出的 delta 特征用于构建 delta 放射组学模型。经典放射组学模型在训练和内部测试队列中的 AUC 分别为 0.682 和 0.641。Delta 放射组学模型在训练和内部测试队列中的 AUC 分别为 0.730 和 0.704。在外部测试队列中,Delta 放射组学模型的 AUC 为 0.661。决策曲线分析表明,当 EAR 对 EGFR-TKIs 的概率阈值在 0.3 到 0.82 之间时,该模型比治疗所有患者更有利。基于两项中心研究,从随访非增强 CT 图像中得出的 delta 放射组学模型可以帮助临床医生在影像学进展前识别肺腺癌对 EGFR-TKIs 的 EAR,并优化临床结果。