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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
Tianjin Medical University Cancer Institute and Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Carcinoma

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    November 22, 2017
    Last Updated
    November 22, 2017
    Sponsor
    Tianjin Medical University Cancer Institute and Hospital
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    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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