Abstract 204P
Background
Although neoadjuvant chemoradiotherapy followed by surgery is the standard treatment for esophageal cancer patients, most patients are unable to achieve pathological complete response with neoadjuvant therapy, resulting in poor outcomes. The aim of this study is to develop a method for selecting patients who can achieve pathological complete response through pre-neoadjuvant therapy chest-enhanced CT scans.
Methods
Two hundreds and one patients with esophageal cancer were enrolled and divided into a training set and a testing set in a 7:3 ratio. Radiomics features of intra-tumoral and peritumoral images were extracted from preoperative chest-enhanced CT scans of these patients. The features were dimensionally reduced in two steps. The selected intra-tumoral and peritumoral features, including marginal (with a distance of 0-3mm from the tumor) and adjacent (with a distance of 3-6mm from the tumor) ROI, were used to build models with four machine learning classifiers, including Support Vector Machine, XG-Boost, Random Forest and Naive Bayes. Models with satisfied accuracy and stability levels were considered to perform well. Finally, the performance of these well-performing models on the testing set was displayed using ROC curves.
Results
Among the 16 models, the best-performing models were the integrated (intra-tumoral and peritumoral features)-XGBoost and integrated-random forest models, which had average ROC AUCs of 0.906 and 0.918, respectively, with relative standard deviations (RSDs) of 6.26 and 6.89 in the training set. In the testing set, the AUCs were 0.845 and 0.871, respectively. There was no significant difference in the ROC curves between the two models. Table: 204P
The performance of the selected models on the testing set
Model | AUC (95% CI) | Specificity | Sensitivity |
Integrated-XGBoost | 0.845 (0.764, 0.928) | 0.864 | 0.777 |
Original-XGBoost | 0.759 (0.660, 0.857) | 0.900 | 0.592 |
Integrated-Random Forest | 0.871 (0.796, 0.946) | 0.682 | 0.933 |
Original-Random Forest | 0.795 (0.703, 0.887) | 0.825 | 0.673 |
Adjacent-Random Forest | 0.769 (0.671, 0.868) | 0.886 | 0.533 |
Integrated-Support Vector Machine | 0.719 (0.613, 0.825) | 0.795 | 0.622 |
Conclusions
The addition of peritumoral radiomics features to the radiomics analysis may improve the predictive performance of pathological response for esophageal cancer patients to neoadjuvant chemoradiotherapy.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
298P - Managing locally advanced cervical cancer: Insights from a tertiary care center and a 3-year follow-up on outcomes
Presenter: Ambedkar Yadala
Session: Poster Display
Resources:
Abstract
299P - Sexual dysfunction assessment in longterm survivors of carcinoma cervix using LENT SOMA scale
Presenter: Niharika Sethi
Session: Poster Display
Resources:
Abstract
300P - Assessing ovarian function in Vietnamese cervical cancer patients who underwent ovary transposition prior to pelvic radiation therapy
Presenter: Cuong Nguyen
Session: Poster Display
Resources:
Abstract
301P - Correlation between cervical cancer recurrence after radiation therapy and vaginal microbiome
Presenter: Xiaoxian Xu
Session: Poster Display
Resources:
Abstract
302P - Expression of ERCC4 gene and its correlation with clinical and pathological parameters in cervical cancer
Presenter: Himanshu Mishra
Session: Poster Display
Resources:
Abstract
303P - Prognostic value of body composition and systemic inflammatory markers in patients with locally advanced cervical cancer following chemoradiotherapy
Presenter: Hui Guo
Session: Poster Display
Resources:
Abstract
305P - A real-world multicenter cohort study of lenvatinib (LEN) plus pembrolizumab (PEM) in Japanese patients with endometrial cancer: Interim analysis of GOGO-EM4 study
Presenter: Yoshikazu Nagase
Session: Poster Display
Resources:
Abstract
306P - Adjuvant treatment and impact on relapse in stage IA uterine papillary serous and clear cell carcinomas: A single center retrospective study
Presenter: Sachin Khurana
Session: Poster Display
Resources:
Abstract
307P - Hormonal therapy vs combination chemotherapy in metastatic leiomyosarcomas: A systematic review
Presenter: Patricia Angel
Session: Poster Display
Resources:
Abstract
309P - Expression of estrogen receptor is a negative predictive biomarker for immunotherapy with lenvatinib plus pembrolizumab for advanced endometrial cancer with pMMR
Presenter: Hiroyuki Fujii
Session: Poster Display
Resources:
Abstract