Improving the accuracy of prognosis for clinical stage I solid lung adenocarcinoma by radiomics models covering tumor per se and peritumoral changes on CT.

Liu, Kunfeng; Li, Kunwei; Wu, Tingfan; Liang, Mingzhu; Zhong, Yinghua; Yu, Xiangyang; Li, Xin; Xie, Chuanmiao et al. · Eur Radiol · 2022

retrospective_cohort · Level III

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Abstract

To assess methods to improve the accuracy of prognosis for clinical stage I solid lung adenocarcinoma using radiomics based on different volumes of interests (VOIs). This retrospective study included patients with postoperative clinical stage I solid lung adenocarcinoma from two hospitals, center 1 and center 2. Three databases were generated: dataset A (training set from center 1), dataset B (internal test set from center 1), and dataset C (external validation test from center 2). Disease-free survival (DFS) data were collected. CT radiomics models were constructed based on four VOIs: gross tumor volume (GTV), 3 mm external to the tumor border (peritumoral volume [PTV]<sub>0~+3</sub>), 6 mm crossing tumor border (PTV<sub>-3~+3</sub>), and 6 mm external to the tumor border (PTV<sub>0~+6</sub>). The area under the receiver operating characteristic curve (AUC) was used to compare the model accuracies. A total of 334 patients were included (204 and 130 from centers 1 and 2). The model using PTV<sub>-3~+3</sub> (AUC 0.81 [95% confidence interval {CI}: 0.75, 0.94], 0.81 [0.63, 0.90] for datasets B and C) outperformed the other three models, GTV (0.73 [0.58, 0.81], 0.73 [0.58, 0.83]), PTV<sub>0~+3</sub> (0.76 [0.52, 0.87], 0.75 [0.60, 0.83]), and PTV<sub>0~+6</sub> (0.72 [0.60, 0.81], 0.69 [0.59, 0.81]), in datasets B and C, all p < 0.05. A radiomics model based on a VOI of 6 mm crossing tumor border more accurately predicts prognosis of clinical stage I solid lung adenocarcinoma than that based on VOIs including overall tumor or external rims of 3 mm and 6 mm. • Radiomics is a useful approach to improve the accuracy of prognosis for stage I solid adenocarcinoma. • The radiomics model based on VOIs that includes 3 mm within and external to the tumor border (peritumoral volume [PTV]<sub>-3~+3</sub>) outperformed models that included either only the tumor itself or those that only included the peritumoral volume.

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