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Poster display session: Basic science, Endocrine tumours, Gastrointestinal tumours - colorectal & non-colorectal, Head and neck cancer (excluding thyroid), Melanoma and other skin tumours, Neuroendocrine tumours, Thyroid cancer, Tumour biology & pathology

3060 - A model using computed tomography-based compactness to predict prognosis after multimodal treatment for esophageal squamous cell carcinoma

Date

21 Oct 2018

Session

Poster display session: Basic science, Endocrine tumours, Gastrointestinal tumours - colorectal & non-colorectal, Head and neck cancer (excluding thyroid), Melanoma and other skin tumours, Neuroendocrine tumours, Thyroid cancer, Tumour biology & pathology

Topics

Staging and Imaging

Tumour Site

Oesophageal Cancer

Presenters

Qifeng Wang

Citation

Annals of Oncology (2018) 29 (suppl_8): viii205-viii270. 10.1093/annonc/mdy282

Authors

Q. Wang1, B. Cao2, J. Chen3, T. Li4, J. Lang4, Z. Xiao5

Author affiliations

  • 1 Radiaition Oncology, Sichuan Cancer Hospital & Institution, Sichuan Cancer Center, School of Medicine, University of Electronic, Chengdu,610041, China., 610042 - Chengdu/CN
  • 2 Radiaition Oncology, Sichuan Cancer Hospital & Institution, Sichuan Cancer Center, School of Medicine, University of Electronic, Chengdu,610041, China., 610041 - Chengdu/CN
  • 3 Radiaition Oncology, Fujian Cancer Hospital & Fujian Medical University Cancer Hospital, Fuzhou, 350014, China, 310000 - Fuzhou/CN
  • 4 Department Of Radiotherapy, Sichuan Cancer Hospital&institute, 610042 - Chengdu/CN
  • 5 Radiaition Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China., 100021 - Beijing/CN
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Resources

Abstract 3060

Background

We aimed to establish a risk model using computed tomography-based compactness to predict overall survival (OS) and progression-free survival (PFS) after multimodal treatment for esophageal squamous cell carcinoma (ESCC).

Methods

We extracted pre-treatment CT-based tumor data (volume, surface area, and compactness) for 512 cases of ESCC that were treated at 3 centers. A risk model based on compactness was trained using Cox regression analyses of 83 cases, and then the model was validated using two independent cohorts (98 patients and 283 patients). The largest cohort (283 patients) was then evaluated using the risk model to predict response to radiotherapy with or without chemotherapy.

Results

In the three datasets, the pre-treatment compactness risk model provided good accuracy for predicting OS (P = 0.012, P = 0.022, and P = 0.003) and PFS (P < 0.001, P = 0.003, and P = 0.005). Patients in the low-risk group did not experience a significant OS benefit from concurrent chemoradiotherapy (P = 0.099). Furthermore, after pre-operation concurrent chemoradiotherapy, the OS outcomes were similar among patients in the low-risk group who did and did not achieve a pathological complete response (P = 0.127). Compactness was correlated with clinical T stage but was more accurate for predicting prognosis after treatment for ESCC, based on higher C-index values in all three datasets.

Conclusions

Our compactness-based risk model was effective for predicting OS and PFS after multimodal treatment for ESCC. Therefore, it may be useful for guiding personalized treatment.

Clinical trial identification

Legal entity responsible for the study

Sichuan Cancer Hospital.

Funding

This work was supported by the National Key Projects of Research and Development of China [grant number 2016YFC0904600], the National Natural Science Foundation of China [grant number 81272512], the Capital Clinical Characteristic Application Research of China [grant number Z121107001012004], and the Capital Health Research and Development of Special of China [grant number 2016-2-4021].

Editorial Acknowledgement

Michelle Doctorate/Evolutionary Biology/University of Exeter/Exeter, UK/2008.

Disclosure

All authors have declared no conflicts of interest.

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