Esophageal Cancer
Conditions
Keywords
Esophageal Cancer, Chemoradiotherapy, VEGF, Thalidomide
Brief summary
The purpose of this study is to down-regulate VEGF expression in esophageal cancer patients by thalidomide, so to improve their chemoradiotherapy effect. Patients with esophageal cancer receiving chemoradiotherapy were divided into different sub-group according to dynamic change of their VEGF level,and those showed increased or unchanged VEGF were added thalidomide at random. Efficacy and side effect of thalidomide combined with chemoradiotherapy were evaluated, and at the same time, activity of thalidomide on esophageal cancer and its clinical safely were assessed.
Detailed description
Radiotherapy:Patients will be conducted CT simulation, and three-dimensional conformal radiation therapy (3DCRT) was performed. 1.8-2.0 Gy/fraction, 5 fractions a week, with a total dose of 60-72Gy will be delivered for all patients by 6-MV-X-ray of linear accelerator. Chemotherapy: Patients will be concurrently administered with irradiation every 4 weeks with PT regimen (cis-platinum of 25 mg/m2/d, d1-4; PTX(paclitaxel)of 135mg/m2/d, d1) for 4 cycles. For the first 2-cycles of chemotherapy they will be concurrently given with irradiation and the remained 2 cycles, after irradiation. Administration of thalidomide: Determine serum VEGF level of the esophageal cancer patients 3-4 weeks after the beginning of radiotherapy, those whose VEGF level, compared with that before radiotherapy, increased or unchanged will be divided into two groups: one is given thalidomide concurrent with the following chemoradiotherapy, 100mg/d at bedtime for the initial week, and if no moderate above side effect occurred 200mg/d from the next week till the end of chemoradiotherapy; the other received concurrent chemoradiotherapy only. VEGF determination: Peripheral venous blood samples will be taken in one week before, 3-4 weeks during, and in one week after radiotherapy respectively. The serum VEGF will be determined by the double antibody sandwich ELISA.
Interventions
OTHERchemoradiotherapy
Patients only receive concurrent chemoradiotherapy if their serum VEGF level decrease.
DRUGthalidomide
Patients will be given thalidomide combined with concurrent chemoradiotherapy if their serum VEGF level increase or unchanged.
OTHERwithout thalidomide
Patients only receive concurrent chemoradiotherapy if their serum VEGF level increase or unchanged
Sponsors
Changzhou No.2 People's Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
Yes
Inclusion criteria
* cytologically or histologically confirmed esophageal carcinoma * age of 20 -80 * Karnofsky performance status ≥ 70 * no treatments prior to enrollment * at least one measurable lesion on CT, MRI or esophageal barium exam * 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
* prior treatments of chemotherapy or irradiation * poor bone marrow, liver and kidney functions, which would make chemotherapy intolerable * contraindication for irradiation: complete obstruction of esophagus, deep esophageal ulcer, fistula to mediastinum, or haematemesis * participating in other clinical trials * pregnancy, breast feeding, or not adopting birth control * drug or alcohol addiction, uncontrolled epileptic seizure, or psychotic with no ability of self control * coexisted morbidities that investigators believed not suitable for chemoradiation
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Treatment efficacy | 3 months after completion of treatment | Treatment efficacy were evaluated by the indexes as Locoregional tumor response. Locoregional tumor response will be evaluated 3 months after completion of treatment according to Response Evaluation Criteria in Solid Tumors (RECIST). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival (OS) | 1 year and 3 years after completion of treatment | Overall survival (OS) will be evaluated 1 year and 3 years after completion of treatment using Kaplan-Meier model. |
| Local progression-free survival (LPFS) | 1 year and 3 years after completion of treatment | 1 year and 3 years after completion of treatment using Kaplan-Meier model. |
| Safety | 1 week after completion of treatment | All patients are to be estimated Quality Of Life(such as dizzy, somnolence, queasiness and vomit,anaphylaxis incidence) ,acute radiation reactions such as acute radiation esophagitis and tracheitis incidence(evaluated by the Radiation Therapy Oncology Group (RTOG) toxicity criteria),complete blood cell count(such as leukocyte, neutrophil,hemoglobulin, platelet level), serum biochemistry(such as creatinine level). |
Countries
China
Contacts
Primary ContactSun Suping, M.D.,PhD.
Outcome results
None listed