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
About this trial
This is an interventional treatment trial for Colon Cancer focused on measuring locally advanced colon cancer, neoadjuvant chemotherapy
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.
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
NCT ID
NCT02882269
First Posted
August 24, 2016
Last Updated
August 28, 2016
Sponsor
The First Affiliated Hospital with Nanjing Medical University
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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