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Apapitatin Combined With SOX for Palliative Adjuvant Chemotherapy in Patients With Advanced Gallbladder Carcinoma

Primary Purpose

Gallbladder Carcinoma

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Apatinib
Tegafur
Sponsored by
Eastern Hepatobiliary Surgery Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gallbladder Carcinoma

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. ages 18 to 75
  2. UICC/AJCC gallbladder TNM staging (The eighth edition), Ⅲ B - ⅣB (excluding M1) postoperative pathological diagnosis of gallbladder carcinoma;Patients confirmed to have undergone R1/R2 cholecystectomy or palliative surgery;
  3. The primary treatment is surgical resection or potentially resectable cholecystic carcinoma without other treatment
  4. ECOG performance status ≤1
  5. The liver and kidney function meets the following conditions: BIL<3 normal value upper limit (ULN);ALT and AST< 2.5 xULN;Serum Cr≤ 1xULN,Clearance rate of endogenous creatinine>50ml/min(Cockcroft-Gault);
  6. Other test rooms meet the following requirements:

    Hemoglobin ≥ 90 g/L (no blood transfusion within 14 days);Neutrophilic granulocyte count > 1.5x109 /L;The platelet count ≥ 80 x 10 ^ 9/L;

  7. Estimated life expectancy > 3 months.
  8. Before the enrollment, the heart function is good. There is no episode of myocardial infarction within half a year. For example, if you have hypertension or coronary heart disease, you should ensure that it is within the controllable range.
  9. Patient able and willing to provide written informed consent and to comply with the study protocol and Good compliance, with follow-up.

Exclusion Criteria:

  1. Non gallbladder carcinoma
  2. Significant clinical bleeding symptoms or a clear tendency to bleed occurred within the first month of randomization, such as cough/hemoptysis of 2.5ml or more, gastrointestinal bleeding, esophagogastric varices at risk of bleeding, hemorrhagic gastric ulcer, etc.
  3. Other topical treatments during the study (including intraperitoneal chemotherapy, radiotherapy, etc.)
  4. Pregnant or lactating women;
  5. Those who suffer from high blood pressure and cannot be treated to the normal range by antihypertensive drugs;
  6. HIV infection or the presence of AIDS-related diseases, or severe acute and chronic diseases;
  7. Have grade II or higher myocardial ischemia or myocardial infarction、Poorly controlled arrhythmia;
  8. Severe active infections;
  9. There are secondary malignant tumors or other tumors within 3 years before the start of the study and there is metastasis of the brain or meninges.
  10. Researchers believe that their compliance is poor
  11. There are contraindications for Apatinib and S-1

Sites / Locations

  • xiao qing xiao qing JiangRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Apatinib with SOX(Tegafur,Oxaliplatin)

SOX( Tegafur,Oxaliplatin)

Arm Description

Patients 3-4 weeks after surgery, the SOX regimen was given palliative adjuvant chemotherapy for 6-8 cycles, then followed by the second cycle combined with the treatment of apatinib mesylate and the monotherapy maintenance of apatinib mesylate

3-4 weeks after operation, 6-8 cycles of adjuvant chemotherapy with simple SOX protocol were given.

Outcomes

Primary Outcome Measures

PFS
progression-free survival

Secondary Outcome Measures

Full Information

First Posted
October 7, 2018
Last Updated
October 9, 2018
Sponsor
Eastern Hepatobiliary Surgery Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03702491
Brief Title
Apapitatin Combined With SOX for Palliative Adjuvant Chemotherapy in Patients With Advanced Gallbladder Carcinoma
Official Title
A Single-center Open, Randomized, Controlled Study to Compare the Apapitatin Combined With SOX and SOX for Palliative Adjuvant Chemotherapy in Patients With Advanced Gallbladder Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
August 10, 2018 (Actual)
Primary Completion Date
August 10, 2020 (Anticipated)
Study Completion Date
August 10, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Eastern Hepatobiliary Surgery 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
A Single-center Open, Randomized, Controlled Study to Compare the Apapitatin Mesylate Combined With SOX Regimen and SOX Regimen for Palliative Adjuvant Chemotherapy in Patients With Advanced Gallbladder Carcinoma
Detailed Description
The aim of the study is to observe and evaluate the progression-free survival time (PFS), overall survival time (OS) and safety of patients with advanced Gallbladder Carcinoma treated with apatinib mesylate combined with SOX

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gallbladder Carcinoma

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Apatinib with SOX(Tegafur,Oxaliplatin)
Arm Type
Experimental
Arm Description
Patients 3-4 weeks after surgery, the SOX regimen was given palliative adjuvant chemotherapy for 6-8 cycles, then followed by the second cycle combined with the treatment of apatinib mesylate and the monotherapy maintenance of apatinib mesylate
Arm Title
SOX( Tegafur,Oxaliplatin)
Arm Type
Active Comparator
Arm Description
3-4 weeks after operation, 6-8 cycles of adjuvant chemotherapy with simple SOX protocol were given.
Intervention Type
Drug
Intervention Name(s)
Apatinib
Other Intervention Name(s)
Tegafur, Oxaliplatin
Intervention Description
Three to four weeks after surgery, the SOX regimen was given palliative adjuvant chemotherapy for 6-8 cycles, then followed by the second cycle combined with the treatment of apatinib mesylate and the monotherapy maintenance of apatinib mesylate
Intervention Type
Drug
Intervention Name(s)
Tegafur
Other Intervention Name(s)
Oxaliplatin
Intervention Description
3-4 weeks after operation, 6-8 cycles of adjuvant chemotherapy with simple SOX protocol were given.
Primary Outcome Measure Information:
Title
PFS
Description
progression-free survival
Time Frame
12 month after first treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ages 18 to 75 UICC/AJCC gallbladder TNM staging (The eighth edition), Ⅲ B - ⅣB (excluding M1) postoperative pathological diagnosis of gallbladder carcinoma;Patients confirmed to have undergone R1/R2 cholecystectomy or palliative surgery; The primary treatment is surgical resection or potentially resectable cholecystic carcinoma without other treatment ECOG performance status ≤1 The liver and kidney function meets the following conditions: BIL<3 normal value upper limit (ULN);ALT and AST< 2.5 xULN;Serum Cr≤ 1xULN,Clearance rate of endogenous creatinine>50ml/min(Cockcroft-Gault); Other test rooms meet the following requirements: Hemoglobin ≥ 90 g/L (no blood transfusion within 14 days);Neutrophilic granulocyte count > 1.5x109 /L;The platelet count ≥ 80 x 10 ^ 9/L; Estimated life expectancy > 3 months. Before the enrollment, the heart function is good. There is no episode of myocardial infarction within half a year. For example, if you have hypertension or coronary heart disease, you should ensure that it is within the controllable range. Patient able and willing to provide written informed consent and to comply with the study protocol and Good compliance, with follow-up. Exclusion Criteria: Non gallbladder carcinoma Significant clinical bleeding symptoms or a clear tendency to bleed occurred within the first month of randomization, such as cough/hemoptysis of 2.5ml or more, gastrointestinal bleeding, esophagogastric varices at risk of bleeding, hemorrhagic gastric ulcer, etc. Other topical treatments during the study (including intraperitoneal chemotherapy, radiotherapy, etc.) Pregnant or lactating women; Those who suffer from high blood pressure and cannot be treated to the normal range by antihypertensive drugs; HIV infection or the presence of AIDS-related diseases, or severe acute and chronic diseases; Have grade II or higher myocardial ischemia or myocardial infarction、Poorly controlled arrhythmia; Severe active infections; There are secondary malignant tumors or other tumors within 3 years before the start of the study and there is metastasis of the brain or meninges. Researchers believe that their compliance is poor There are contraindications for Apatinib and S-1
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
xiao qing Jiang, professor
Phone
13801603438
Ext
13801603438
Email
Jxq1225@sina.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
xiao qing Jiang, professor
Organizational Affiliation
700 Moyu Road North, Jiading District,Eastern Hepatobiliary Surgery Hospital, Shanghai, China
Official's Role
Principal Investigator
Facility Information:
Facility Name
xiao qing xiao qing Jiang
City
Shanghai
State/Province
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
xiao q xiao qing Jiang
Phone
13801603438
Ext
13801603438
Email
Jxq1225@sina.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Apapitatin Combined With SOX for Palliative Adjuvant Chemotherapy in Patients With Advanced Gallbladder Carcinoma

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