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临床试验/NCT01391572
NCT01391572Unknown2 期

A Randomized Phase II Trial Estimating The Optimal Radiation Volume Of Postsurgical Radiation For Patients With Locoregionally Advanced Thoracic Esophageal Squamous Cell Carcinoma

Fudan University1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2011年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
300
试验地点
1
主要终点
Survival

研究概览

简要总结

A randomized phase II trial to estimate the optimal radiation volume of postsurgical radiation for patients with locoregionally advanced thoracic esophageal squamous cell carcinoma (T3-4, any N, M0).

详细描述

Patient Population:

Thoracic esophageal squamous cell carcinoma after esophagectomy with at least 15 lymph nodes removed for adequate nodal staging.

T3-4, any N, M0.

Scheme:

After esophagectomy, patients are firstly stratified by 2 factors: (1)number of lymph node metastasis (<3 or >=3) and (2)tumor resection status (R1 resection or R2 resection).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 and ≤70
  • Performance status 0-1
  • Weight is not less than 90% of it before operation
  • Registration within 8 weeks after esophagectomy
  • Histologically proven primary thoracic esophageal squamous cell carcinoma
  • R0 resection and number of lymph nodes dissected ≥15 after esophagectomy
  • Pathological stage of T3-4N0-3M0
  • Chest and abdominal contrast enhanced CT within 6 weeks prior to registration(PET/CT scan is selective)
  • Without supraclavicular nodes and abdominal regions nodes existed after surgery
  • Without neo-adjuvant chemotherapy and radiotherapy
  • WBC≥ 4.0X109/L ,Absolute neutrophil count (ANC) ≥ 2.0X109/L
  • Platelets ≥ 100X109/L
  • Hemoglobin ≥ 90g/L(without blood transfusion)
  • AST (SGOT)/ALT (SGPT) ≤ 2.5 x upper limit of normal, Bilirubin ≤ 1.5 x upper limit of normal
  • Creatinine ≤ 1.5 x upper limit of normal
  • Sign study-specific informed consent prior to study entry

排除标准

  • Multiple primary esophageal tumors
  • Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 2 years (For example, carcinoma in situ of the breast, oral cavity, or cervix are all permissible).
  • Severe, active comorbidity, defined as follows:
  • 3.1 Unstable angina and/or congestive heart failure requiring hospitalization within the last 3 months 3.2 Transmural myocardial infarction within the last 6 months 3.3 Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration 3.4 Chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration 3.5 Acquired immune deficiency syndrome (AIDS) based upon current CDC definition; note, however, that HIV testing is not required for entry into this protocol. The need to exclude patients with AIDS from this protocol is necessary because the treatments involved in this protocol may be significantly immunosuppressive.
  • Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception.
  • Prior systemic chemotherapy, prior radiation therapy or prior target drug therapy

研究组 & 干预措施

A

Experimental

After esophagectomy, patients in Arm A will receive Large field radiation (tumor bed + ENI (elective nodal irradiation)) + Sequential chemotherapy

干预措施: enlarge irradiation volume (Radiation)

A

Experimental

After esophagectomy, patients in Arm A will receive Large field radiation (tumor bed + ENI (elective nodal irradiation)) + Sequential chemotherapy

干预措施: cisplatin (Drug)

A

Experimental

After esophagectomy, patients in Arm A will receive Large field radiation (tumor bed + ENI (elective nodal irradiation)) + Sequential chemotherapy

干预措施: fluorouracil (Drug)

B

Active Comparator

After esophagectomy, patients in Arm B will receive small field radiation (tumor bed only) + Sequential chemotherapy

干预措施: Small volume radiation (Radiation)

B

Active Comparator

After esophagectomy, patients in Arm B will receive small field radiation (tumor bed only) + Sequential chemotherapy

干预措施: cisplatin (Drug)

B

Active Comparator

After esophagectomy, patients in Arm B will receive small field radiation (tumor bed only) + Sequential chemotherapy

干预措施: fluorouracil (Drug)

结局指标

主要结局

Survival

To evaluate if the survival outcome of postsurgical radiation with a small target volume involved tumor bed only is not worse than a large volume (tumor bed and elective nodes) for patients with locoregionally advanced thoracic esophageal squamous cell carcinoma.

次要结局

  • Safety and Tolerability
  • Failure pattern

研究者

申办方类型
Other

研究点 (1)

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