Dendritic Cell-based Immunotherapy in Treatment Gastric Cancer

Gastric Cancer Clinical Trial

Official title:

Activated Autologous Dendritic Cells by Autologous Tumor Cell Membrane Proteins in Treatment of Gastric Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03410732
• Other study ID #: LAUDC 2017001
• Status: Recruiting
• Phase: Phase 2
• First received: January 16, 2018
• Last updated: January 24, 2018
• Start date: July 1, 2017
• Est. completion date: December 1, 2020

Study information

• Verified date: January 2018
• Source: LanZhou University
• Contact: Yumin Li, MD, PhD
• Phone: +8613893615421
• Email: liym[@]lzu.edu.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Study objectives are to investigate the efficacy and safety of activated autologous dendritic cells (DCs) in treatment of gastric cancer. DCs are activated by the proteins from autologous tumor cell membrane and cytokines in vitro. The efficacy endpoints include objective response, immune-cell response, recurrent rate after a radical surgery, progression-free survival and overall survival, and the safety endpoints include adverse events, laboratory tests, ECG, ECOG-PT, etc.

Description:

Study objectives are to investigate the efficacy and safety of activated autologous dendritic cells (DCs) in treatment of gastric cancer. The autologous DCs are collected and enriched from peripheral blood, and then are activated by the proteins from autologous tumor cell membrane and cytokines in vitro. The efficacy endpoints include objective response, immune-cell response, recurrent rate after a radical surgery, progression-free survival and overall survival, and the safety endpoints include adverse events, laboratory tests, ECG, ECOG-PT, etc. All patients will be followed up for at least 2 years after treatment.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 120
• Est. completion date: December 1, 2020
• Est. primary completion date: July 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Written informed consent given before any trial-specific procedure is initiated

2. Male or female, at least 18 years of age at the time of informed consent

3. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1

4. Life expectancy >3 months assessed during Screening

5. Documented (histologically- or cytologically-proven) gastric cancer that is can be radially removed

Exclusion Criteria:

1. Non-healing wounds on any part of the body

2. Active thrombosis, or a history of deep vein thrombosis or pulmonary embolism, within 1 month prior to surgery, unless adequately treated and stable

3. Active uncontrolled bleeding or a known bleeding diathesis

4. Significant cardiovascular disease or condition, including:

1. Congestive heart failure currently requiring therapy

2. Class III or IV cardiovascular disease according to the New York Heart Association's (NYHA) functional criteria (25)

3. Need for antiarrhythmic medical therapy for a ventricular arrhythmia

4. Severe conduction disturbance (e.g., 3rd degree heart block)

5. Unstable angina pectoris (last episode at least 6 months prior to surgery)

6. Uncontrolled hypertension (per the Investigator's discretion)

7. Myocardial infarction within 6 months prior to C1/D1

5. Abnormal hematologic, renal or hepatic function as defined by the following criteria:

1. Absolute neutrophil count (ANC) <1.5 ×109/L (1500/mm3)

2. Hemoglobin =9 g/dL

3. Platelet count <75 ×109/L (75,000/mm3)

4. Serum creatinine >1.5 × upper limit of normal (ULN) for the institution

5. Aspartate aminotransferase (AST) >3.5 × ULN for the institution or AST >5 × ULN for the institution in case of known liver metastases

6. Alanine aminotransferase (ALT) >3.5 × ULN for the institution or ALT >5 × ULN for the institution in case of known liver metastases

7. Total bilirubin >1.5 × ULN for the institution

8. Prothrombin time as assessed by International Normalized Ratio (INR) >1.5 × ULN for the institution*

9. Partial thromboplastin time (PTT) >1.5 × ULN for the institution*

6. Any of the following within 2 weeks prior to surgery:

1. Any serious or uncontrolled infection

2. Any infection requiring parenteral antibiotics

3. Unexplained fever >38.0 °C

7. Any other life-threatening illness, significant organ system dysfunction, or clinically significant laboratory abnormality, which in the opinion of the Investigator, would either compromise the patient's safety or interfere with the evaluation of the safety of the trial treatment

8. Any kind of disorder that compromises the ability of the patient to give written informed consent and/or to comply with trial procedures or is unwilling or unable to comply with trial requirements at the discretion of the Investigator

9. Breast feeding, or plans by the patient (or the patient's partner) to become pregnant during treatment or within 4 months after the end of treatment

Related Conditions & MeSH terms

• Gastric Cancer
• Stomach Neoplasms

Intervention

Biological:
• activated DCs
autologous dendritic cells are collected and enriched from 50 ml of peripheral blood, then activated by autologous tumor cell membrane proteins. Then the activated DCs are iv infused in 21 days after a radical surgery.

Procedure:
• radical surgery only
Only radical surgery is given to the control group

Locations

Country	Name	City	State
China	Lanzhou University Second Hospital	Lanzhou	Gansu

Sponsors (1)

Lead Sponsor	Collaborator
LanZhou University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	progression-free survival	Time to progression/death or censored time	3 years
Secondary	recurrent rate	the rate of cancer recurring after surgery	3 years
Secondary	overall survival rate	time to death or censored time	5 years
Secondary	immune-cells response	CD4/CD8 T lymphocyte percentage change	3 months
Secondary	Adverse event rate	Adverse event rate	3 months