Stomach Neoplasms Clinical Trial
Official title:
The Randomized, Controlled, Multicenter Clinical Trial of Apatinib Plus CIK as the Third Line Therapy for Patients With Advanced Gastric Cancer
The purpose of this study is to evaluate the safety and efficacy of Apatinib combined with cytokine-induced killer cell (CIK) vs Apatinib as the third line therapy for patients with advanced gastric cancer.
Status | Active, not recruiting |
Enrollment | 80 |
Est. completion date | June 2033 |
Est. primary completion date | June 2030 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Patients who can accept curative operations 18-70 years old - Histologically confirmed with gastric cancer at stage ? - Patients who can accept oral drugs; - Eastern Cooperative Oncology Group (ECOG) performance status was 0 - 1. Exclusion Criteria: - Hemoglobin<8.0 g/dL,White blood cell <3 X 10^9/L;Platelet count <75 X 10^9/L; alanine aminotransferase, glutamic-oxalacetic transaminase, blood urine nitrogen and creatinine more than normal limits on 3.0 times - Known or suspected allergy to the investigational agent or any agent given in association with this trial - Pregnant or lactating patients - Known history of Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV) or TreponemaPallidun (TP) infection - Patients who are suffering from serious autoimmune disease - Patients who had used long time or are using immunosuppressant - Patients who had active infection - Patients who are suffering from serious organ dysfunction - Patients who are suffering from other cancer - Other situations that the researchers considered unsuitable for this study. |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
The First People's Hospital of Changzhou |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Adverse events | 1 months | Yes | |
Primary | Overall Survival(OS) | 3 months | No | |
Secondary | Disease-free survival | 3 months | No |
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