esophageal cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. histopathologically proven invasive esophageal cancer 2. clinical stage I without indicationf of ESD/EMR or clinical stages II - IV 3. PS: 0-2 4. written informed consent 5. WBC: 4000-12000/mm3, Neu > 2000/mm3, Plt > 100,000/mm3, Hb > 9.0g/dL, Tbil < 1.5mg/dL, GOT/GPT < 76/72U/L, Cre < 1.2mg/dL, PaO2 > 70mmHg
Exclusion criteria
Exclusion criteria: 1. having serious complications 2. having synchronism overlap cancer 3. having metastasis to other organs 4. with a history of radiation for the same lesion 5. with a history of chemothrapy 6. having administration contraindication of nedaplatin/5-FU 7. having drug hypersensitivity 8. A woman with the possibility (intention) of the pregnancy, a pregnant woman 9. charging doctor regards as inadequacy because of medical, psychologically, or other factors
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Isolated lymph node relapse rate | — |
Secondary
| Measure | Time frame |
|---|---|
| Complete response rate, progression free survival time, and frequency and degree of toxicity | — |
Countries
Japan
Contacts
University of Tokyo Hospital Department of Radiology