4.6 Article

Nomograms integrating CT radiomic and deep learning signatures to predict overall survival and progression-free survival in NSCLC patients treated with chemotherapy

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CANCER IMAGING
卷 23, 期 1, 页码 -

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BMC
DOI: 10.1186/s40644-023-00620-4

关键词

Nomogram; Overall survival; Progression-free survival; Lung cancer; Chemotherapy treatment; Radiomics

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The study aims to establish accurate prediction nomograms for overall survival (OS) and progression-free survival (PFS) in non-small cell lung cancer (NSCLC) patients who receive chemotherapy as the first-line treatment. By integrating TNM stage, CT radiomic signature, and deep learning signatures, the established nomograms have the potential to improve individualized treatment and precise management of NSCLC patients.
ObjectivesThis 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.Materials and methodsIn 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).ResultsTNM 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.ConclusionBy 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. Integrated nomograms aim to predict the chemotherapy prognosis of NSCLC patients.The 3- and 5-year overall survival and progression-free survival are predicted.CT peritumoral radiomic signature has the highest hazard ratio for the prognosis.Deep learning signature is a significant predictive factor of the prognosis.The integrated nomograms are noninvasive, low cost, and phenotypic.

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