Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster session 09

817P - A machine learning algorithm utilizing clinicopathologic parameters for extranodal natural killer/T cell lymphoma

Date

14 Sep 2024

Session

Poster session 09

Presenters

Shuo Li

Citation

Annals of Oncology (2024) 35 (suppl_2): S596-S612. 10.1016/annonc/annonc1593

Authors

S. Li1, L. Gao2, Y. Zhong1, H. Hong3, J. Yun4, Y. Huang1

Author affiliations

  • 1 Department Of Pathology, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, 510060 - Guangzhou/CN
  • 2 Department Of Pathology, West China School of Medicine/West China Hospital of Sichuan University, 610041 - Chengdu/CN
  • 3 Department Of Medical Oncology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, 610000 - Chengdu/CN
  • 4 Department Of Pathology, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou/CN

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 817P

Background

Current clinical prediction indexes lack the requisite accuracy for extranodal natural killer/T-cell lymphoma (ENKTL) following non-anthracycline-based therapy. This study addresses this gap by introducing and validating a machine learning (ML) algorithm based on clinicopathologic parameters to effectively stratify risk among ENKTL patients.

Methods

Data from 977 patients with ENKTL from 3 cohorts of China were analyzed. 15 ML algorithms were trained and validated for overall survival (OS) prediction in 644 patients from Sun Yat-sen University Cancer Center. The optimization of hyperparameters was conducted through an exhaustive ten-fold cross-validation grid search. External validations were performed in two external cohorts (N=187 from West China Hospital, and N=146 from Sichuan Cancer Hospital, respectively). Evaluation of model performance included Harrell’s c-index, receiver operating characteristic (ROC) curve, calibration curve, and decision curve analysis.

Results

Among the 15 ML algorithms tested, Gradient Boosting Machine (GBM) demonstrated superior performance. The ENKTL-ML score, generated by GBM, incorporated 13 clinicopathologic parameters. In external validation cohorts, the c-indexes for the ENKTL-ML score were 0.84 (95% confidence interval [CI]: 0.81, 0.88) and 0.83 (0.72, 0.94), respectively. The area under ROC curves for 5-year OS were ≥ 0.81. The ENKTL-ML score outperformed existing indexes in discriminatory ability and treatment recommendations. Notably, it effectively stratified patients into low-, intermediate-, and high-risk groups with distinctive survival outcomes. The ENKTL-ML score demonstrated the ability to differentiate low-risk patients from those at stage I. Adding anti-PD-1 immunotherapy as first-line treatment significantly improved survival in the high-risk group, with no substantial benefit observed in low/intermediate-risk patients. An online calculator for the ENKTL-ML score is accessible online.

Conclusions

The ENKTL-ML score serves as an innovative machine learning tool, facilitating risk stratification and aiding clinicians in decision-making for ENKTL patient management.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Y. Huang.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.