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Multi-omics and Multi-VOIs to predict esophageal fistula in esophageal cancer patients treated with radiotherapy

  • Wei Guo,
  • Bing Li,
  • Wencai Xu,
  • Chen Cheng,
  • Chengyu Qiu,
  • Sai-kit Sam,
  • Jiang Zhang,
  • Xinzhi Teng,
  • Lingguang Meng,
  • Xiaoli Zheng,
  • Yuan Wang,
  • Zhaoyang Lou,
  • Ronghu Mao,
  • Hongchang Lei,
  • Yuanpeng Zhang,
  • Ta Zhou,
  • Aijia Li,
  • Jing Cai,
  • Hong Ge

摘要

Objective

This study aimed to develop a prediction model for esophageal fistula (EF) in esophageal cancer (EC) patients treated with intensity-modulated radiation therapy (IMRT), by integrating multi-omics features from multiple volumes of interest (VOIs).

Methods

We retrospectively analyzed pretreatment planning computed tomographic (CT) images, three-dimensional dose distributions, and clinical factors of 287 EC patients. Nine groups of features from different combination of omics [Radiomics (R), Dosiomics (D), and RD (the combination of R and D)], and VOIs [esophagus (ESO), gross tumor volume (GTV), and EG (the combination of ESO and GTV)] were extracted and separately selected by unsupervised (analysis of variance (ANOVA) and Pearson correlation test) and supervised (Student T test) approaches. The final model performance was evaluated using five metrics: average area under the receiver-operator-characteristics curve (AUC), accuracy, precision, recall, and F1 score.

Results

For multi-omics using RD features, the model performance in EG model shows: AUC, 0.817 ± 0.031; 95% CI 0.805, 0.825; p < 0.001, which is better than single VOI (ESO or GTV).

Conclusion

Integrating multi-omics features from multi-VOIs enables better prediction of EF in EC patients treated with IMRT. The incorporation of dosiomics features can enhance the model performance of the prediction.