Esophageal Cancer Clinical Trial
Official title:
Adoptive Cellular Therapy and Radiation Therapy After Surgery in Treating Patients With Esophageal Cancer
NCT number | NCT01691664 |
Other study ID # | JR-02 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | September 2012 |
Est. completion date | June 2022 |
Cytokine-induced killer (CIK) cells show cytolytic activity against tumor. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining Radiation therapy with adoptive cellular therapy after surgery may be more effective than uses radiation therapy alone in treating esophageal cancer.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | June 2022 |
Est. primary completion date | December 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - cytologically or histologically confirmed esophageal carcinoma - Tumor extension beyond muscularis propria and/or nodal involvement without evidence of M1 disease - Prior en bloc resection, with curative intent, of all known tumor - No metastatic disease - Age: > 18 - Karnofsky performance status = 70 - At least 3 weeks since prior surgery - Normal functions of heart, lung, liver, kidney and bone marrow - Blood exams qualified for chemotherapy, which included hemoglobulin =9 g/dl, neutrophil =1.5×109/L and platelet (PLT) =100×109/L, creatinine =1.5 UNL - All patients must be evaluated by a radiation oncologist prior to enrollment to ensure patient is appropriate for radiotherapy - Informed consent signed Exclusion Criteria: - Patients with metastatic disease. - Patients who are pregnant or nursing. - Patients with poor bone marrow, liver and kidney functions, which would make radiation therapy intolerable - Patients with contraindication for irradiation: complete obstruction of esophagus, deep esophageal ulcer, fistula to mediastinum, or haematemesis |
Country | Name | City | State |
---|---|---|---|
China | Beijing Shijitan Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Capital Medical University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Immunological assessment | Initial assessment, months 1,3,6and 12 | ||
Primary | Disease free survival | 4 years | ||
Secondary | quality of life | Initial assessment ? months 1,3,6 and 12 |
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