A gene-based score for the risk stratification of stage IA lung adenocarcinoma

Respir Res. 2024 Jan 4;25(1):18. doi: 10.1186/s12931-023-02647-4.

Abstract

Objective: We aim to molecularly stratify stage IA lung adenocarcinoma (LUAD) for precision medicine.

Methods: Twelve multi-institution datasets (837 cases of IA) were used to classify the high- and low-risk types (based on survival status within 5 years), and the biological differences were compared. Then, a gene-based classifying score (IA score) was trained, tested and validated by several machine learning methods. Furthermore, we estimated the significance of the IA score in the prognostic assessment, chemotherapy prediction and risk stratification of stage IA LUAD. We also developed an R package for the clinical application. The SEER database (15708 IA samples) and TCGA Pan-Cancer (1881 stage I samples) database were used to verify clinical significance.

Results: Compared with the low-risk group, the high-risk group of stage IA LUAD has obvious enrichment of the malignant pathway and more driver mutations and copy number variations. The effect of the IA score on the classification of high- and low-risk stage IA LUAD was much better than that of classical clinicopathological factors (training set: AUC = 0.9, validation set: AUC = 0.7). The IA score can significantly predict the prognosis of stage IA LUAD and has a prognostic effect for stage I pancancer. The IA score can effectively predict chemotherapy sensitivity and occult metastasis or invasion in stage IA LUAD. The R package IAExpSuv has a good risk probability prediction effect for both groups and single stages of IA LUAD.

Conclusions: The IA score can effectively stratify the risk of stage IA LUAD, offering good assistance in precision medicine.

Keywords: IA score; IAExpSuv; LUAD; Prognosis; Risk stratification; Stage IA.

MeSH terms

  • Adenocarcinoma of Lung* / diagnosis
  • Adenocarcinoma of Lung* / genetics
  • DNA Copy Number Variations
  • Databases, Factual
  • Humans
  • Lung Neoplasms* / diagnosis
  • Lung Neoplasms* / genetics
  • Prognosis
  • Risk Assessment