Intraperitoneal Infusion of EpCAM CAR-T Cell in Advanced Gastric Cancer With Peritoneal Metastasis (WCH-GC-CART)

Sponsor
Jian-Kun Hu (Other)
Overall Status
Recruiting
CT.gov ID
NCT03563326
Collaborator
(none)
40
1
2
52
0.8

Study Details

Study Description

Brief Summary

To investigate the safety and efficacy of intraperitoneal infusion of EpCAM CAR-T cell in advanced gastric cancer with peritoneal metastasis by a prospective nonrandomized controlled trial.

Condition or Disease Intervention/Treatment Phase
  • Biological: CAR-T cells targeting EpCAM
  • Biological: Chemotherapy
Phase 1

Detailed Description

Chimeric antigen receptor modified T (CAR-T) cells have the capability in targeting and recognizing tumor antigen, and can specifically recognize, bind and kill tumor cells with positive antigen. Through local drug delivery, CAR-T cells have successfully achieved remarkable effect to treat solid tumors. Gastric cancer is one of the most frequent malignant tumors with high mortality, especially in China. Peritoneal metastasis is one of the common routes of metastasis. Once peritoneal metastasis occurred, patients should be categorized as clinical pathological stage IV with extremely poor prognosis, and the effect of routine treatments would be unsatisfactory. Epithelial cell adhesion molecule (EpCAM) is highly expressed in gastric cancer cells and closely associated with the poor prognosis of patients. In our previous pre-clinical research researches, the investigators have obtained CAR-T cells targeting EpCAM (EpCAM CAR-T), and finished the preparations of cells which could be used in clinical practice. Based on our previous works, the investigators aim to investigate the safety and efficacy of peritoneal infusion of EpCAM CAR-T cell in advanced gastric cancer with peritoneal metastasis by a prospective nonrandomized controlled trial. The results of this clinical trial are expected to provide the new treatment strategy for gastric cancer patients with peritoneal metastasis.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Clinical Trial of Intraperitoneal CAR-T Cells Infusion for the Treatment of Advanced Gastric Cancer With Peritoneal Metastasis
Actual Study Start Date :
Aug 30, 2018
Anticipated Primary Completion Date :
Dec 31, 2019
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: CAR-T cell and chemotherapy

Biological: CAR-T cells targeting EpCAM Chemotherapy: determined by medical Oncologist

Biological: CAR-T cells targeting EpCAM
Biological: CAR-T cells targeting EpCAM

Biological: Chemotherapy
Chemotherapy: determined by medical Oncologist

Active Comparator: chemotherapy

Chemotherapy: determined by medical Oncologist

Biological: Chemotherapy
Chemotherapy: determined by medical Oncologist

Outcome Measures

Primary Outcome Measures

  1. EpCAM CAR-T cells treatment related adverse events [4 weeks]

    Adverse events after receiving EpCAM CAR-T cells treatment, according to NCI-CTCAE v4.0.

Secondary Outcome Measures

  1. Overall survival outcome [2 years]

    2-year overall survival rate

  2. Metabolism kinetics of CAR-T cells [2 years]

    The level of CAR-T cells will be tested regularly by Real-time Quantitative Polymerase Chain Reaction Detecting System(qPCR) or Flow cytometry.

  3. Progress free survival outcome [2 years]

    2-year progress free survival

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients with EpCAM positive gastric cancer who have peritoneal metastasis at first visit; Patients with highly suspected or previous proven peritoneal metastasis by biopsy, CT, digital rectal examination, etc. who failed to the routine therapies like chemotherapy;

  2. Age between 18 and 75;

  3. Estimated survival time is longer than 3 months;

  4. Eastern Cooperative Oncology Group (ECOG)scores 0-2;

  5. Hemoglobin≥90g/L, ANC≥1.5×109/L, PLT≥80×109/L;

  6. Negative pregnancy test for child-bearing period; both male and female patients should agree to apply effective contraceptive methods in the period of treatment and one year after treatment;

  7. Both patients and families totally understand the objectives and risks of the treatments and sign the informed consent.

Exclusion Criteria:
  1. Comorbidity with other diseases treated by immunosuppressive drugs or steroids therapy systematically;

  2. Uncontrolled active infection;

  3. HIV positive;

  4. Active hepatic B or C virus infection, active tuberculosis;

  5. Pregnant or lactation female;

  6. Disagree to apply effective contraceptive methods in the period of treatment and one year after treatment;

  7. Positive cytology examination alone.

Contacts and Locations

Locations

Site City State Country Postal Code
1 West China Hospital, Sichuan University Chengdu Sichuan China 610041

Sponsors and Collaborators

  • Jian-Kun Hu

Investigators

  • Principal Investigator: Jian-Kun Hu, M.D. Ph.D., West China Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jian-Kun Hu, Vice director of Gastrointestinal Surgery department, West China Hospital; Director of Institute of Gastric Cancer, State Key Laboratory of Biotherapy, West China Hospital, West China Hospital
ClinicalTrials.gov Identifier:
NCT03563326
Other Study ID Numbers:
  • WCH-GC-CART
First Posted:
Jun 20, 2018
Last Update Posted:
Sep 17, 2018
Last Verified:
Sep 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jian-Kun Hu, Vice director of Gastrointestinal Surgery department, West China Hospital; Director of Institute of Gastric Cancer, State Key Laboratory of Biotherapy, West China Hospital, West China Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 17, 2018