College of Medicine and Biological Information Engineering, Northeastern University, Shenyang, China.
Key Laboratory of Intelligent Computing in Medical Image, Ministry of Education, Northeastern University, Shenyang, China.
Cancer Imaging. 2023 Oct 22;23(1):101. doi: 10.1186/s40644-023-00620-4.
This study aims to establish nomograms to accurately predict the overall survival (OS) and progression-free survival (PFS) in patients with non-small cell lung cancer (NSCLC) who received chemotherapy alone as the first-line treatment.
In a training cohort of 121 NSCLC patients, radiomic features were extracted, selected from intra- and peri-tumoral regions, and used to build signatures (S1 and S2) using a Cox regression model. Deep learning features were obtained from three convolutional neural networks and utilized to build signatures (S3, S4, and S5) that were stratified into over- and under-expression subgroups for survival risk using X-tile. After univariate and multivariate Cox regression analyses, a nomogram incorporating the tumor, node, and metastasis (TNM) stages, radiomic signature, and deep learning signature was established to predict OS and PFS, respectively. The performance was validated using an independent cohort (61 patients).
TNM stages, S2 and S3 were identified as the significant prognosis factors for both OS and PFS; S2 (OS: (HR (95%), 2.26 (1.40-3.67); PFS: (HR (95%), 2.23 (1.36-3.65)) demonstrated the best ability in discriminating patients with over- and under-expression. For the OS nomogram, the C-index (95% CI) was 0.74 (0.70-0.79) and 0.72 (0.67-0.78) in the training and validation cohorts, respectively; for the PFS nomogram, the C-index (95% CI) was 0.71 (0.68-0.81) and 0.72 (0.66-0.79). The calibration curves for the 3- and 5-year OS and PFS were in acceptable agreement between the predicted and observed survival. The established nomogram presented a higher overall net benefit than the TNM stage for predicting both OS and PFS.
By integrating the TNM stage, CT radiomic signature, and deep learning signatures, the established nomograms can predict the individual prognosis of NSCLC patients who received chemotherapy. The integrated nomogram has the potential to improve the individualized treatment and precise management of NSCLC patients.
本研究旨在建立列线图,以准确预测接受单纯化疗作为一线治疗的非小细胞肺癌(NSCLC)患者的总生存期(OS)和无进展生存期(PFS)。
在 121 例 NSCLC 患者的训练队列中,提取了来自肿瘤内和肿瘤周围区域的放射组学特征,并使用 Cox 回归模型构建了特征(S1 和 S2)。从三个卷积神经网络中获得深度学习特征,并使用 X-tile 将其分层为表达过高和过低的亚组,以预测生存风险,从而构建特征(S3、S4 和 S5)。通过单因素和多因素 Cox 回归分析,建立了一个包含肿瘤、淋巴结和转移(TNM)分期、放射组学特征和深度学习特征的列线图,分别用于预测 OS 和 PFS。使用独立队列(61 例)验证了该模型的性能。
TNM 分期、S2 和 S3 被确定为 OS 和 PFS 的显著预后因素;S2(OS:(HR(95%),2.26(1.40-3.67);PFS:(HR(95%),2.23(1.36-3.65))在区分表达过高和过低的患者方面表现出最佳能力。对于 OS 列线图,训练队列和验证队列的 C 指数(95%CI)分别为 0.74(0.70-0.79)和 0.72(0.67-0.78);对于 PFS 列线图,C 指数(95%CI)分别为 0.71(0.68-0.81)和 0.72(0.66-0.79)。3 年和 5 年 OS 和 PFS 的校准曲线在预测生存与实际生存之间具有可接受的一致性。建立的列线图在预测 OS 和 PFS 方面均优于 TNM 分期,具有更高的整体净效益。
通过整合 TNM 分期、CT 放射组学特征和深度学习特征,建立的列线图可以预测接受化疗的 NSCLC 患者的个体预后。该综合列线图有可能改善 NSCLC 患者的个体化治疗和精确管理。