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N/A
18 Years
N/A
Open (Enrolling)
Both
Esophageal Carcinoma

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Trial Information


Inclusion Criteria:



- cytologically or histologically confirmed locally advanced esophageal carcinoma

- Age: > 18

- Karnofsky performance status ≥ 70

- At least one measurable tumor lesions according to the RECIST criteria.

- 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

- Informed consent signed

Exclusion Criteria:

- Patients with metastatic disease in the central nervous system (CNS).

- Patients who are pregnant or nursing.

- Patients with poor bone marrow, liver and kidney functions, which would make
chemotherapy intolerable

- Patients with contraindication for irradiation: complete obstruction of esophagus,
deep esophageal ulcer, fistula to mediastinum, or haematemesis

- coexisted morbidities that investigators believed not suitable for chemoradiation

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

the quality of life

Outcome Time Frame:

initial assessment, months 1, 3, 6 and 12

Safety Issue:

No

Authority:

China:State Food and Drug Administraion

Study ID:

JR-01

NCT ID:

NCT01691625

Start Date:

September 2012

Completion Date:

September 2017

Related Keywords:

  • Esophageal Carcinoma
  • Locally advanced esophageal carcinoma
  • DC-CIK
  • Immunotherapy
  • Carcinoma
  • Esophageal Diseases
  • Esophageal Neoplasms

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