4.6 Article

Integrating additional factors into the TNM staging for cutaneous melanoma by machine learning

Journal

PLOS ONE
Volume 16, Issue 9, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0257949

Keywords

-

Funding

  1. grant Using Dendrograms to Create Prognostic Systems for Cancer - John P. Murtha Cancer Center Research Program
  2. grant Creating Prognostic Systems for Cancer - John P. Murtha Cancer Center Research Program
  3. grant Four Diamonds Fund from Penn State University - Penn State University

Ask authors/readers for more resources

This study introduces machine learning as a novel tool to integrate additional prognostic factors into the TNM staging system for more accurate risk classification and survival prediction in patients with cutaneous melanoma. By utilizing the Ensemble Algorithm for Clustering Cancer Data (EACCD), a more advanced prognostic system was developed that improved patient stratification and survival prediction accuracy. The integration of additional factors separated favorable from unfavorable clinical outcomes, enhancing cohort selection for clinical trials and treatment management.
Background Integrating additional factors into the TNM staging system is needed for more accurate risk classification and survival prediction for patients with cutaneous melanoma. In the present study, we introduce machine learning as a novel tool that incorporates additional prognostic factors to improve the current TNM staging system. Methods and findings Cancer-specific survival data for cutaneous melanoma with at least a 5 years follow-up were extracted from the Surveillance, Epidemiology, and End Results Program of the National Cancer Institute and split into the training set (40,781 cases) and validation set (5,390 cases). Five factors were studied: the primary tumor (T), regional lymph nodes (N), distant metastasis (M), age (A), and sex (S). The Ensemble Algorithm for Clustering Cancer Data (EACCD) was applied to the training set to generate prognostic groups. Utilizing only T, N, and M, a basic prognostic system was built where patients were stratified into 10 prognostic groups with well-separated survival curves, similar to 10 AJCC stages. These 10 groups had a significantly higher accuracy in survival prediction than 10 stages (C-index = 0.7682 vs 0.7643; increase in C-index = 0.0039, 95% CI = (0.0032, 0.0047); p-value = 7.2x10(-23)). Nevertheless, a positive association remained between the EACCD grouping and the AJCC staging (Spearman's rank correlation coefficient = 0.8316; p-value = 4.5x10(-13)). With additional information from A and S, a more advanced prognostic system was established using the training data that stratified patients into 10 groups and further improved the prediction accuracy (C-index = 0.7865 vs 0.7643; increase in C-index = 0.0222, 95% CI = (0.0191, 0.0254); p-value = 8.8x10(-43) ). Both internal validation using the training set and temporal validation using the validation set showed good stratification and a high predictive accuracy of the prognostic systems. Conclusions The EACCD allows additional factors to be integrated into the TNM to create a prognostic system that improves patient stratification and survival prediction for cutaneous melanoma. This integration separates favorable from unfavorable clinical outcomes for patients and improves both cohort selection for clinical trials and treatment management.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available