About this trial
Magnetic resonance imaging (MRI) with functional features of diffusion weighted imaging (DWI) are advancing imaging technologies that have potential to overcome limitations of conventional staging methods, radiation treatment planning and the assessment of tumor response in esophageal or esophagogastric cancer. This study aimed to explore the value of MRI for the prediction of tumor response to chemoradiotherapy and accurate target volume delineation as compared to CT simulation for patients with unresectable or potentially resectable esophageal or esophagogastric cancer undergoing chemoradiotherapy. The average CT texture features are also extracted before and during treatment to establish a model to predict the prognosis or side effects (e.g. radiation pneumonitis or esophagitis) of patients.
Eligibility criteria
Qualifiers
Histologically confirmed squamous cell carcinoma, adenocarcinoma of the esophageal or esophagogastric junction
Unresectable or potentially resectable tumor (cT3-4N0-1M0-M1a, according to AJCC 6th) based on standard primary staging by EUS and CT
Age>18 years
No distant metastasis other than supraclavicular lymph nodes
Disqualifiers
Contraindication for MRI scanning
Patients with other cancer history except cervical carcinoma in situ and non-malignant melanoma skin cancer
Pregnant or lactating females
Contraindication for radiotherapy or chemotherapy
Trial design
Treatments tested in this trial
- MRI and CT
- Ratiotherapy
- Paclitaxel, platinum-based drug