Abstract
Objectives
To determine the integrative value of clinical, hematological, and computed tomography (CT) radiomic features in survival prediction for locally advanced non-small cell lung cancer (LA-NSCLC) patients.
Methods
Radiomic features and clinical and hematological features of 118 LA-NSCLC cases were firstly extracted and analyzed in this study. Then, stable and prognostic radiomic features were automatically selected using the consensus clustering method with either Cox proportional hazard (CPH) model or random survival forest (RSF) analysis. Predictive radiomic, clinical, and hematological parameters were subsequently fitted into a final prognostic model using both the CPH model and the RSF model. A multimodality nomogram was then established from the fitting model and was cross-validated. Finally, calibration curves were generated with the predicted versus actual survival status.
Results
Radiomic features selected by clustering combined with CPH were found to be more predictive, with a C-index of 0.699 in comparison to 0.648 by clustering combined with RSF. Based on multivariate CPH model, our integrative nomogram achieved a C-index of 0.792 and retained 0.743 in the cross-validation analysis, outperforming radiomic, clinical, or hematological model alone. The calibration curve showed agreement between predicted and actual values for the 1-year and 2-year survival prediction. Interestingly, the selected important radiomic features were significantly correlated with levels of platelet, platelet/lymphocyte ratio (PLR), and lymphocyte/monocyte ratio (LMR) (p values all < 0.05).
Conclusions
The integrative nomogram incorporated CT radiomic, clinical, and hematological features improved survival prediction in LA-NSCLC patients, which would offer a feasible and practical reference for individualized management of these patients.
Key Points
• An integrative nomogram incorporated CT radiomic, clinical, and hematological features was constructed and cross-validated to predict prognosis of LA-NSCLC patients.
• The integrative nomogram outperformed radiomic, clinical, or hematological model alone.
• This nomogram has value to permit non-invasive, comprehensive, and dynamical evaluation of the phenotypes of LA-NSCLC and can provide a feasible and practical reference for individualized management of LA-NSCLC patients.
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Abbreviations
- CCRT:
-
Concurrent chemotherapy and radiotherapy
- C-index:
-
Concordance index
- CPH:
-
Cox proportional hazard
- CT:
-
Computed tomography
- GLCM:
-
Gray-level co-occurrence matrix
- GLSZM:
-
Gray-level size zone matrix
- GTV:
-
Gross tumor volume
- LA-NSCLC:
-
Locally advanced non-small cell lung cancer
- LMR:
-
Lymphocyte/monocyte ratio
- NLR:
-
Neutrophil/lymphocyte ratio
- PLR:
-
Platelet/lymphocyte ratio
- RECIST:
-
Response Evaluation Criteria in Solid Tumors
- RSF:
-
Random survival forest
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Funding
This work was supported by China Scholarship Fund, the Project of Postdoctoral Science Foundation of China (Grant Nos. 2016M590640 and 2016M592199), the Project of Postdoctoral Innovation of Shandong Province (Grant No. 201501010), National Health and Family Planning Commission of China (201402011), and National Natural Science Foundation of China (81472812).
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The scientific guarantor of this publication is Jinming Yu.
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Wang, L., Dong, T., Xin, B. et al. Integrative nomogram of CT imaging, clinical, and hematological features for survival prediction of patients with locally advanced non-small cell lung cancer. Eur Radiol 29, 2958–2967 (2019). https://doi.org/10.1007/s00330-018-5949-2
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DOI: https://doi.org/10.1007/s00330-018-5949-2