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Neoadjuvant Chemotherapy for the Treatment of Resectable Locally Advanced Colon Cancer

Primary Purpose

Colon Cancer

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Postoperative chemotherapy
Neoadjuvant chemotherapy
Sponsored by
The First Affiliated Hospital with Nanjing Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colon Cancer focused on measuring locally advanced colon cancer, neoadjuvant chemotherapy

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients suitable for curative surgery between 18 to 80 years old;
  • American Society of Anesthesiologists(ASA) grade I-III;
  • Pathological diagnosis of adenocarcinoma;
  • Tumor located between the cecum and sigmoid colon;
  • Enhanced CT scan of chest, abdominal and pelvic cavity: preoperative assessment of tumor stage is T3-T4 N0 or T any N+ (according to the National Comprehensive Cancer Network(NCCN) clinical practice guidelines in oncology: colon cancer version 2.2015);there is no distant metastasis;
  • Informed consent;
  • No preoperative chemoradiotherapy;
  • No history of familial adenomatous polyposis, ulcerative colitis or Crohn's disease.

Exclusion Criteria:

  • Pregnant patient;
  • History of psychiatric disease;
  • Use of systemic steroids;
  • Simultaneous multiple primary colorectal cancer;
  • Preoperative imaging examination results show:

    1. distant metastasis;
    2. unable to perform R0 resection;
  • Postoperative pathology of T1-T2 N0;
  • History of any other malignant tumor in recent 5 years;
  • Patients need emergency operation: mechanic ileus, perforation.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Postoperative chemotherapy

    Neoadjuvant chemotherapy

    Arm Description

    Patients receive 6 months of chemotherapy after surgery.

    Patients receive 3-4 cycles of chemotherapy before surgery. Preoperative and postoperative chemotherapy will be given for a total of 6 months.

    Outcomes

    Primary Outcome Measures

    disease-free survival

    Secondary Outcome Measures

    overall survival
    recurrence-free survival
    local recurrence rate
    length of postoperative hospital stay
    Length of postoperative hospital stay is defined as a duration between surgery and first discharge. An expected average is 10 days.
    early complication rate
    Early complication is defined as a complication that occurred between the finish of the surgery and postoperative day 30. Complications includes anastomotic leakage, anastomotic bleeding, chyle leakage, wound infection, pulmonary embolism, myocardial infarction et al.The Clavien-Dindo Classification of Surgical Complications will be applied to access the degree of severity of postoperative complications.
    operative time
    number of lymph nodes retrieved

    Full Information

    First Posted
    August 24, 2016
    Last Updated
    August 28, 2016
    Sponsor
    The First Affiliated Hospital with Nanjing Medical University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02882269
    Brief Title
    Neoadjuvant Chemotherapy for the Treatment of Resectable Locally Advanced Colon Cancer
    Official Title
    A Randomized Controlled Clinical Trial to Investigate the Effect of Neoadjuvant Chemotherapy for the Treatment of Resectable Locally Advanced Colon Cancer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 2016 (undefined)
    Primary Completion Date
    December 2021 (Anticipated)
    Study Completion Date
    December 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    The First Affiliated Hospital with Nanjing Medical University

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    A randomized controlled clinical trial to compare the short and long outcomes of Neoadjuvant chemotherapy with postoperative chemotherapy in patients with resectable locally advanced colon cancer
    Detailed Description
    For resectable locally advanced colon cancer, the preferred treatment is colectomy with en bloc removal of the regional lymph nodes followed by chemotherapy of about 6 months. However, surgery may postpone the administration of chemotherapy due to postoperative complications such as anastomosis leakage, abdominal infection, thus leads to a poor survival. Some scholars suggested that for patients with locally advanced colon cancer, chemotherapy given before surgery might shrink or downstage tumor, facilitate surgery and promote a better oncological outcome. Whether adjuvant chemotherapy benefits these patients with better outcome still remains controversial. In this study, eligible patients will be randomly allocated to receive either adjuvant chemotherapy or not. For patients receiving adjuvant chemotherapy, surgery will be performed 3-4 weeks later. Preoperative and postoperative chemotherapy will be given for a total of about 6 months. For patients receiving no preoperative chemotherapy, chemotherapy will be given for about 6 months postoperatively. The recommended chemotherapy regimes includes FOLFOX, CapeOX, FOLFIRI, Capecitabine monotherapy. Patients will be followed up every 3 months for 2 year, every 6 months for 3 years postoperatively.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Colon Cancer
    Keywords
    locally advanced colon cancer, neoadjuvant chemotherapy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2, Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    400 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Postoperative chemotherapy
    Arm Type
    Active Comparator
    Arm Description
    Patients receive 6 months of chemotherapy after surgery.
    Arm Title
    Neoadjuvant chemotherapy
    Arm Type
    Experimental
    Arm Description
    Patients receive 3-4 cycles of chemotherapy before surgery. Preoperative and postoperative chemotherapy will be given for a total of 6 months.
    Intervention Type
    Drug
    Intervention Name(s)
    Postoperative chemotherapy
    Other Intervention Name(s)
    drug combination (FOLFOX, CapeOX or FOLFIRI) or Capecitabine monotherapy
    Intervention Description
    Locally advanced colon cancer patients will receive surgery first, followed by 6 months of chemotherapy. The recommended chemotherapy regimes includes FOLFOX, CapeOX, FOLFIRI, Capecitabine monotherapy.
    Intervention Type
    Drug
    Intervention Name(s)
    Neoadjuvant chemotherapy
    Other Intervention Name(s)
    drug combination (FOLFOX, CapeOX or FOLFIRI) or Capecitabine monotherapy
    Intervention Description
    Neoadjuvant chemotherapy will be given to locally advanced colon cancer patients for 3-4 cycles. Surgery will be performed between 3 to 4 weeks subsequent to the last cycle of chemotherapy. After surgery, additional chemotherapy will be given. Preoperative and postoperative chemotherapy will be given for a total of 6 months. The recommended chemotherapy regimes includes FOLFOX, CapeOX, FOLFIRI, Capecitabine monotherapy.
    Primary Outcome Measure Information:
    Title
    disease-free survival
    Time Frame
    3 years
    Secondary Outcome Measure Information:
    Title
    overall survival
    Time Frame
    3 years
    Title
    recurrence-free survival
    Time Frame
    3 years
    Title
    local recurrence rate
    Time Frame
    3 years
    Title
    length of postoperative hospital stay
    Description
    Length of postoperative hospital stay is defined as a duration between surgery and first discharge. An expected average is 10 days.
    Time Frame
    30 days
    Title
    early complication rate
    Description
    Early complication is defined as a complication that occurred between the finish of the surgery and postoperative day 30. Complications includes anastomotic leakage, anastomotic bleeding, chyle leakage, wound infection, pulmonary embolism, myocardial infarction et al.The Clavien-Dindo Classification of Surgical Complications will be applied to access the degree of severity of postoperative complications.
    Time Frame
    30 days
    Title
    operative time
    Time Frame
    1 day
    Title
    number of lymph nodes retrieved
    Time Frame
    1 day

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients suitable for curative surgery between 18 to 80 years old; American Society of Anesthesiologists(ASA) grade I-III; Pathological diagnosis of adenocarcinoma; Tumor located between the cecum and sigmoid colon; Enhanced CT scan of chest, abdominal and pelvic cavity: preoperative assessment of tumor stage is T3-T4 N0 or T any N+ (according to the National Comprehensive Cancer Network(NCCN) clinical practice guidelines in oncology: colon cancer version 2.2015);there is no distant metastasis; Informed consent; No preoperative chemoradiotherapy; No history of familial adenomatous polyposis, ulcerative colitis or Crohn's disease. Exclusion Criteria: Pregnant patient; History of psychiatric disease; Use of systemic steroids; Simultaneous multiple primary colorectal cancer; Preoperative imaging examination results show: distant metastasis; unable to perform R0 resection; Postoperative pathology of T1-T2 N0; History of any other malignant tumor in recent 5 years; Patients need emergency operation: mechanic ileus, perforation.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yueming Sun, PhD
    Phone
    02568136026
    Email
    jssym@vip.sina.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Fumin Zhang, Professor
    Organizational Affiliation
    Ethics Committee of the First Affiliated Hospital, Nanjing Medical University, Jiangsu Province Hospital
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Neoadjuvant Chemotherapy for the Treatment of Resectable Locally Advanced Colon Cancer

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