About this trial
This multicenter, prospective observational cohort study has the potential to optimize individualized chemoradiotherapy regimen for early-stage esophageal cancer patients who have received endoscopic submucosal dissection.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
1. Esophageal cancer patients who are pathologically confirmed as pT1a-MM stage or pT1b stage after endoscopic submucosal dissection; 2. No definite contraindications for chemo-radiotherapy; 3. Informed consent has been signed; 4. Refused surgery after endoscopic submucosal dissection.
Disqualifiers
1. Severe heart, brain, lung disease or renal dysfunction; 2. Previous history of other malignancies; 3. Prior radiation or chemotherapy 4. Researchers consider it inappropriate to participate in this experiment
Trial population
Esophageal cancer patients, and pathologic-comfirmed pT1a-MM stage or pT1b stage
Trial design
Cohort
Prospective
Treatments tested in this trial
chemo-radiation
Radiationdifferent Chemo-radiotherapy regimen
Treatment groups
Trial outcomes
Primary outcomes
Incidence of toxic events
esophageal stenosis, radiation pneumonitis, etc
Secondary outcomes
3-year overall survival
the time from randomization until death from any cause
3-year local-regional recurrence free survival
the time from randomization until local-regional recurrence
Sponsors and contacts
Click on the lead sponsor to view all of their trials.