Neoadjuvant Bev Plus DOF vs DOF in LAGC and Its Association With Circulating Tumor Cell
Primary Purpose
Locally Advanced Gastric Carcinoma
Status
Completed
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Bevacizumab
docetaxel oxaliplatin 5-FU CF
Gastrectomy
Sponsored by
About this trial
This is an interventional treatment trial for Locally Advanced Gastric Carcinoma
Eligibility Criteria
Inclusion Criteria:
- Histologically confirmed locally advanced adenocarcinoma of the stomach.
- Age of 18 to 70, Karnofsky score higher than 80.
- T3-4,N1-3,M0 (AJCC 7th), potentially resectable.
- No severe functional damage of major organ, normal blood cell, normal liver and kidney function.
Exclusion Criteria:
- Clinical findings of distant metastasis or Peritoneal carcinomatosis
- Prior systemic (chemo- or targeted) treatment. Prior radiotherapy to the upper abdomen
- Previous malignancy within 5 years, with the exception of adequately treated cervical carcinoma in situ or localized non-melanoma skin cancer
- Upper gastrointestinal bleeding
- Any contraindication to treatment with docetaxel, 5-fu or oxaliplatin
Sites / Locations
- First Affiliated Hospital, Chinese PLA General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
bevacizumab plus DOF
DOF
Arm Description
patients receive bev +DOF pre and post surgery up to total 6 cycles
patients receive DOF pre and post surgery up to total 6 cycles
Outcomes
Primary Outcome Measures
R0 resection rate
Secondary Outcome Measures
pCR rate
OS
DFS
ORR
safety of peroperative treatment and surgery
Full Information
NCT ID
NCT02048540
First Posted
January 25, 2014
Last Updated
April 23, 2014
Sponsor
Chinese PLA General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02048540
Brief Title
Neoadjuvant Bev Plus DOF vs DOF in LAGC and Its Association With Circulating Tumor Cell
Official Title
Phase 2 Study of Neoadjuvant Bevacizumab Plus DOF Versus DOF in Local Advanced Gastric Carcinoma and Its Association With Circulating Tumor Cell
Study Type
Interventional
2. Study Status
Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese PLA General Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background Local advanced gastric carcinoma (LAGC) is suggested to be potentially cured by R0 resection, and neoadjuvant chemotherapy can increase the R0 resection rate but not enough. Bevacizumab (Bev), an anti-tumor angiogenesis monoclonal antibody, combined with chemotherapy has been shown effective in advanced GC. In addition, CTC has been suggested as an indicator of the anti-tumor drugs' efficacy. Therefore, in this study, the investigators plan to evaluate the efficacy and safety of neoadjuvant Bev plus docetaxel/oxaliplatin/5-FU/CF (DOF) versus DOF in mainly gastric antrum LAGC, and to investigate whether CTC is an effectiveness indicator.
Methods 86 patients diagnosed as IIIb-IIIc GC have been enrolled and randomly assigned (1:1) to receive neoadjuvant Bev (5 mg/kg, d1) plus DOF (docetaxel, 75 mg/m2, iv, d1; oxaliplatin, 85 mg/m2, iv, d1; 5-FU, iv infusion 600 mg/m2 and iv injection 400mg/m2, d1-2; CF, 200 mg/m2, d1 and d2) or DOF each 3-week, up to 2-4 cycles preoperation, and another 2-4 cycles postoperation up to total 6 cycles. The primary endpoint is R0 resection rate. CTC was detected every 8 weeks. All patients signed the informed consent.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Locally Advanced Gastric Carcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
86 (Actual)
8. Arms, Groups, and Interventions
Arm Title
bevacizumab plus DOF
Arm Type
Experimental
Arm Description
patients receive bev +DOF pre and post surgery up to total 6 cycles
Arm Title
DOF
Arm Type
Active Comparator
Arm Description
patients receive DOF pre and post surgery up to total 6 cycles
Intervention Type
Biological
Intervention Name(s)
Bevacizumab
Intervention Description
Bev (5 mg/kg, d1) every 3 weeks, up to 2-4 cycles preoperation, and another 2-4 cycles postoperation up to total 6 cycles.
Intervention Type
Drug
Intervention Name(s)
docetaxel oxaliplatin 5-FU CF
Intervention Description
docetaxel, 75 mg/m2, iv, d1; oxaliplatin, 85 mg/m2, iv, d1; 5-FU, iv infusion 600 mg/m2 and iv injection 400mg/m2, d1-2; CF, 200 mg/m2, d1 and d2 each 3-week, up to 2-4 cycles preoperation, and another 2-4 cycles postoperation up to total 6 cycles.
Intervention Type
Procedure
Intervention Name(s)
Gastrectomy
Primary Outcome Measure Information:
Title
R0 resection rate
Time Frame
6-12 weeks after administration
Secondary Outcome Measure Information:
Title
pCR rate
Time Frame
Day 1 after surgery
Title
OS
Time Frame
3 years after surgery
Title
DFS
Time Frame
3 years after surgery
Title
ORR
Time Frame
6 weeks after administration
Title
safety of peroperative treatment and surgery
Time Frame
from first administration to 28 days after last administration
Other Pre-specified Outcome Measures:
Title
circulating tumor cell number change
Description
to investigate the circulating tumor cell number change before and after neoadjuvant therapy and whether it's an effectiveness and survival predictor in LAGC
Time Frame
6 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed locally advanced adenocarcinoma of the stomach.
Age of 18 to 70, Karnofsky score higher than 80.
T3-4,N1-3,M0 (AJCC 7th), potentially resectable.
No severe functional damage of major organ, normal blood cell, normal liver and kidney function.
Exclusion Criteria:
Clinical findings of distant metastasis or Peritoneal carcinomatosis
Prior systemic (chemo- or targeted) treatment. Prior radiotherapy to the upper abdomen
Previous malignancy within 5 years, with the exception of adequately treated cervical carcinoma in situ or localized non-melanoma skin cancer
Upper gastrointestinal bleeding
Any contraindication to treatment with docetaxel, 5-fu or oxaliplatin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nan Du, Phd
Organizational Affiliation
First Affiliated Hospital, Chinese PLA General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
First Affiliated Hospital, Chinese PLA General Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100048
Country
China
12. IPD Sharing Statement
Learn more about this trial
Neoadjuvant Bev Plus DOF vs DOF in LAGC and Its Association With Circulating Tumor Cell
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