XELOX Plus Apatinib vs XELOX as Post-operative Chemotherapy in Locally Advanced Gastric Signet Ring Carcinoma
Primary Purpose
Gastric Carcinoma
Status
Not yet recruiting
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Apatinib
XELOX
Sponsored by
About this trial
This is an interventional treatment trial for Gastric Carcinoma
Eligibility Criteria
Inclusion Criteria:
- 1. ≥ 18 and ≤ 70 years of age;
- 2. Eastern Cooperative Oncology Group Performance Status: 0-1;
- 3. Had been treated with Radical resection (D2, R0) of gastric cancer (Lymph node≥16);
- 4. Postoperative histological proven gastric signet-ring cell carcinoma(or contains signet-ring cell carcinoma);
- 5. Pathological stage:IIIA-IIIC(8th AJCC TNM);
- 6. Patients have adequate baseline organ and marrow function :hemoglobin≥9g/dL; absolute neutrophil count (ANC) ≥1,500/mm3; PLT(platelets)≥1000,000/mm3; total bilirubin ≤1.5×upper normal limit(ULN); AST ≤2.5 ×ULN, ALT ≤2.5 ×ULN; prothrombin time-international normalized ratio≤1.5, and APTT(activated partial thromboplastin time) was within normal range; creatine ≤ 1.5 x ULN;
- 7. The ECG(electrocardiography) was basically normal in the 4 weeks before the study, and there was no obvious clinical symptoms of heart disease;
- 8. sign informed consent.
Exclusion Criteria:
- 1. Patients with hypertension and uncontrolled hypertension with hypotensive drugs therapy ;
- 2. Patients with dysphagia, complete or incomplete digestive tract obstruction, gastrointestinal bleeding, perforation, etc;
- 3. Patients had bradycardia or a QT extension;
- 4. Patients had gastrointestinal fistula and lacerations after surgery;
- 5. Allergic to capecitabine or oxaliplatin, or metabolic disorders;
- 6. Patients accepted Preoperative chemotherapy, radiotherapy or targeted therapy;
- 7. Attending other drug clinical trials;
- 8. Patients with Serious liver disease (such as cirrhosis, etc.), kidney disease, respiratory disease or uncontrolled diabetes, hypertension and other chronic systemic diseases, heart disease with Clinical symptoms(such as congestive heart failure, coronary heart disease symptoms, drug is difficult to control arrhythmia, hypertension, or six months had a myocardial infarction attack, or cardiac insufficiency);
- 9. Patients with peripheral nervous system disorder or apparent mental disorders or had the history of central nervous system disorders;
- 10. Patients with serious infection(above CTCAE grade 2);
- 11. Patient with history of another malignant cancer within past 5 years(not including: cervical carcinoma in situ, non melanoma skin cancer and superficial bladder tumor );
- 12. Have the history of organ transplantation, Or have received systemic steroid therapy for a long time (note: short term user stopping medication >2 weeks can be included);
- 13. Pregnant or lactating women, women of child-bearing potential, unwilling to use adequate contraceptive protection during the process of the study;
- 14. Patients without legal capacity,or medical/ethical reasons may influence the study to continue.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
experimental group
active comparator
Arm Description
Drug:Apatinib with XELOX(Capecitabine and Oxaliplatin)
Drug:XELOX(Capecitabine and Oxaliplatin)
Outcomes
Primary Outcome Measures
Disease Free Survival(DFS)
Disease Free Survivalof the Participants
Secondary Outcome Measures
Overall Survival(OS)
Overall Survival of the Participants
Percentage of Participants With Adverse Events
Percentage of Participants With Adverse Events
Full Information
NCT ID
NCT03355612
First Posted
November 22, 2017
Last Updated
November 22, 2017
Sponsor
Tianjin Medical University Cancer Institute and Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03355612
Brief Title
XELOX Plus Apatinib vs XELOX as Post-operative Chemotherapy in Locally Advanced Gastric Signet Ring Carcinoma
Official Title
A Randomized, Multicenter, Controlled Study of XELOX (Oxaliplatin With Capecitabine) Combined With Apatinib Versus XELOX as Post-operative Chemotherapy in Locally Advanced Gastric Signet Ring Carcinoma With D2 Dissection.
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 20, 2017 (Anticipated)
Primary Completion Date
December 20, 2020 (Anticipated)
Study Completion Date
December 20, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tianjin Medical University Cancer Institute and Hospital
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
This is a randomized, multicenter, controlled study to compared the Efficacy and Safety of XELOX combined with Apatinib versus XELOX as post-operative chemotherapy in locally advanced gastric signet ring carcinoma with D2 dissection.
Detailed Description
The purpose of this study is to prove that as for disease free survival time, and safety, Apatinib with XELOX(Oxaliplatin with Capecitabine) has a better effect over that of XELOX adjunct therapy group for postoperative chemotherapy of locally advanced gastric signet ring carcinoma with D2 dissection.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Carcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
456 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
experimental group
Arm Type
Experimental
Arm Description
Drug:Apatinib with XELOX(Capecitabine and Oxaliplatin)
Arm Title
active comparator
Arm Type
Active Comparator
Arm Description
Drug:XELOX(Capecitabine and Oxaliplatin)
Intervention Type
Drug
Intervention Name(s)
Apatinib
Other Intervention Name(s)
YN968D1
Intervention Description
Apatinib: 500 mg, qd, po, last 180 days
Intervention Type
Drug
Intervention Name(s)
XELOX
Other Intervention Name(s)
Capecitabine and Oxaliplatin
Intervention Description
Capecitabine:1000 mg/m2 bid d1-14 q3w, Oxaliplatin:130 mg/m2 d1 q3w
Primary Outcome Measure Information:
Title
Disease Free Survival(DFS)
Description
Disease Free Survivalof the Participants
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Overall Survival(OS)
Description
Overall Survival of the Participants
Time Frame
8 years
Title
Percentage of Participants With Adverse Events
Description
Percentage of Participants With Adverse Events
Time Frame
5 years
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:
1. ≥ 18 and ≤ 70 years of age;
2. Eastern Cooperative Oncology Group Performance Status: 0-1;
3. Had been treated with Radical resection (D2, R0) of gastric cancer (Lymph node≥16);
4. Postoperative histological proven gastric signet-ring cell carcinoma(or contains signet-ring cell carcinoma);
5. Pathological stage:IIIA-IIIC(8th AJCC TNM);
6. Patients have adequate baseline organ and marrow function :hemoglobin≥9g/dL; absolute neutrophil count (ANC) ≥1,500/mm3; PLT(platelets)≥1000,000/mm3; total bilirubin ≤1.5×upper normal limit(ULN); AST ≤2.5 ×ULN, ALT ≤2.5 ×ULN; prothrombin time-international normalized ratio≤1.5, and APTT(activated partial thromboplastin time) was within normal range; creatine ≤ 1.5 x ULN;
7. The ECG(electrocardiography) was basically normal in the 4 weeks before the study, and there was no obvious clinical symptoms of heart disease;
8. sign informed consent.
Exclusion Criteria:
1. Patients with hypertension and uncontrolled hypertension with hypotensive drugs therapy ;
2. Patients with dysphagia, complete or incomplete digestive tract obstruction, gastrointestinal bleeding, perforation, etc;
3. Patients had bradycardia or a QT extension;
4. Patients had gastrointestinal fistula and lacerations after surgery;
5. Allergic to capecitabine or oxaliplatin, or metabolic disorders;
6. Patients accepted Preoperative chemotherapy, radiotherapy or targeted therapy;
7. Attending other drug clinical trials;
8. Patients with Serious liver disease (such as cirrhosis, etc.), kidney disease, respiratory disease or uncontrolled diabetes, hypertension and other chronic systemic diseases, heart disease with Clinical symptoms(such as congestive heart failure, coronary heart disease symptoms, drug is difficult to control arrhythmia, hypertension, or six months had a myocardial infarction attack, or cardiac insufficiency);
9. Patients with peripheral nervous system disorder or apparent mental disorders or had the history of central nervous system disorders;
10. Patients with serious infection(above CTCAE grade 2);
11. Patient with history of another malignant cancer within past 5 years(not including: cervical carcinoma in situ, non melanoma skin cancer and superficial bladder tumor );
12. Have the history of organ transplantation, Or have received systemic steroid therapy for a long time (note: short term user stopping medication >2 weeks can be included);
13. Pregnant or lactating women, women of child-bearing potential, unwilling to use adequate contraceptive protection during the process of the study;
14. Patients without legal capacity,or medical/ethical reasons may influence the study to continue.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Han Liang, Master
Phone
(022)23340123
Ext
1063
Email
tjlianghan@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Mingzhi Cai, Master
Phone
13821389052
Email
tsaimingzhi@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Han Liang, Master
Organizational Affiliation
Tianjin Medical University Cancer Institute and Hospital
Official's Role
Study Chair
12. IPD Sharing Statement
Learn more about this trial
XELOX Plus Apatinib vs XELOX as Post-operative Chemotherapy in Locally Advanced Gastric Signet Ring Carcinoma
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