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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
Fudan University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophageal Squamous Cell Carcinoma

Eligibility Criteria

18 Years - 18 Years (Adult)All SexesAccepts Healthy Volunteers

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

    First Posted
    September 4, 2017
    Last Updated
    October 18, 2017
    Sponsor
    Fudan University
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    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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