Adjuvant Radiotherapy for Esophageal Squamous Cell Carcinoma With Positive Circumstantial Resection Margin
Primary Purpose
Esophageal Squamous Cell Carcinoma, Positive Circumferential Resection Margin
Status
Not yet recruiting
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
radiation
Sponsored by
About this trial
This is an interventional treatment trial for Esophageal Squamous Cell Carcinoma
Eligibility Criteria
Inclusion Criteria:
Patients with esophageal cancer who received R0 operations in Fudan University Shanghai Cancer Center and postoperative pathology: squamous cell cancer,positive Circumferential Resection Margin(CRM)+
- KPS≥70 before radiotherapy;
- Did not receive neoadjuvant or adjuvant treatment;
- No clear recurrent or metastatic lesions before radiotherapy;
- Intensity modulated radiation therapy(IMRT) is accepted;
- Regular follow-up.
Exclusion Criteria:
- Exploratory thoracotomy or palliative surgery;
- No clear recurrent or metastatic sites;
- Recurrence or metastasis is not certain;
- death of no definite cause.
- Irregular follow-up;
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
surgery plus radiation
surgery alone
Arm Description
adjuvant radiotherapy is developed in this arm
No adjuvant radiotherapy,that is surgery alone is developed in this arm
Outcomes
Primary Outcome Measures
Disease-free survival time
including survival time from randomization to locoregional recurrence and to distal metastasis
Secondary Outcome Measures
overall survival time
survival time from randomization to death
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03273647
Brief Title
Adjuvant Radiotherapy for Esophageal Squamous Cell Carcinoma With Positive Circumstantial Resection Margin
Official Title
Adjuvant Radiotherapy for T3N0M0 Esophageal Squamous Cell Carcinoma With Positive Circumstantial Resection Margin(a Randomized Controlled Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 1, 2017 (Anticipated)
Primary Completion Date
December 1, 2019 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The purpose of this study is to determine the efficacy of adjuvant radiotherapy for esophageal squamous cell carcinoma with positive circumstantial resection margin.
Detailed Description
Although preoperative chemoradiation therapy followed by surgery is the most common approach for patients with resectable esophageal cancer, the considerable number of esophageal cancer patients received operation as the first treatment modality. Accordingly, postoperative treatments have been playing an important role because of the poor survival rates of the patients who have been treated with resection alone. The existing data shows that the 5-yeal survival rate of stage T2-3N0M0(UICC 7th edition) of thoracic esophageal squamous cell carcinoma(TESCC) after surgery is about 50% ,and locoregional lymph nodes metastases is responsible for the main cause of failure while distal metastases account for relatively less ratio. Therefore, the subclinical residual tumor is affirmative even if the early disease has been undergone curable excision and local adjuvant treatment may be essential. In rectal cancer, the involvement of the circumferential resection margin (CRM) is one of the key factors for local recurrence and poor prognosis,based on reports in which CRM with < 1mm was found to be prognostically significant, whereas the clinical and prognostic significance of the CRM involvement in EC has been investigated only in a few series showing conflicting results, as some studies suggest a significant influence of CRM. There is lack of clear evidence for prophylactic radiation therapy in positive Circumferential Resection Margin(CRM) patients of TESCC now. In view of this, the randomized controlled trial will determine the clinical efficacy and toxicity of adjuvant radiotherapy in positive Circumferential Resection Margin(CRM) for thoracic esophageal squamous cell carcinoma.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Squamous Cell Carcinoma, Positive Circumferential Resection Margin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
surgery plus radiation
Arm Type
Experimental
Arm Description
adjuvant radiotherapy is developed in this arm
Arm Title
surgery alone
Arm Type
No Intervention
Arm Description
No adjuvant radiotherapy,that is surgery alone is developed in this arm
Intervention Type
Radiation
Intervention Name(s)
radiation
Intervention Description
A total dose of 40Gy will be delivered in 20 fractions at 2.0Gy/fraction, 5 fractions per week in 4 weeks.
The CTV encompassed the bilateral supraclavicular region, all mediastinal lymph nodes, the anastomosis site, and the left gastric and Celiac nodes.
Primary Outcome Measure Information:
Title
Disease-free survival time
Description
including survival time from randomization to locoregional recurrence and to distal metastasis
Time Frame
up to 3 years
Secondary Outcome Measure Information:
Title
overall survival time
Description
survival time from randomization to death
Time Frame
up to 3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients with esophageal cancer who received R0 operations in Fudan University Shanghai Cancer Center and postoperative pathology: squamous cell cancer,positive Circumferential Resection Margin(CRM)+
KPS≥70 before radiotherapy;
Did not receive neoadjuvant or adjuvant treatment;
No clear recurrent or metastatic lesions before radiotherapy;
Intensity modulated radiation therapy(IMRT) is accepted;
Regular follow-up.
Exclusion Criteria:
Exploratory thoracotomy or palliative surgery;
No clear recurrent or metastatic sites;
Recurrence or metastasis is not certain;
death of no definite cause.
Irregular follow-up;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiaqing Xiang, MD
Phone
+86 13901992249
Email
j.q.xiang@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yiliang Zhang, MD
Phone
+86 18017317284
Email
ilya616@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiaqing Xiang, MD
Organizational Affiliation
professor of Department of Thoracic Surgery, Fudan University Shanghai Cancer Center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Adjuvant Radiotherapy for Esophageal Squamous Cell Carcinoma With Positive Circumstantial Resection Margin
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