A Clinical Research of CAR T Cells Targeting CEA Positive Colorectal Cancer (CRC)

NCT ID: NCT04513431

Last Updated: 2020-08-14

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-08-30
• Study Completion Date: 2023-08-30

Brief Summary

The main purpose of this research is to verify the safety of CEA targeted chimeric antigen receptor T cells and to determine the proper dosage of CAR T cells infused.

Detailed Description

Chimeric antigen receptor (CAR)-modified T cells have demonstrated great successes in treating even late stage cluster of differentiation antigen 19 (CD19) positive B cell malignancies. But it has few studies in solid tumors. The carcino-embryonic antigen(CEA) is widely expressed in cancers like gastric cancer, lung cancer, pancreatic cancer, breast cancer and colorectal cancer. To confirm if CAR T cells still function in solid tumors, we have developed anti-CEA CAR-modified T cells. Preclinical studies have demonstrated effective killing of CEA target cells. In this study, the CEA CARs, will be evaluated in CEA positive gastric cancer. The primary goal is to confirm its adverse effects including cytokine storm response and any other adverse effects. In addition, tumor targeting and disease status after treatment will also be evaluated.

Conditions

Stage III Colorectal Cancer; Colorectal Cancer Liver Metastasis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Colorectal cancer

Colorectal cancer treated with T cells modified with Anti-CEA-CAR T.

Group Type: EXPERIMENTAL

Anti-CEA-CAR T

Intervention Type: BIOLOGICAL

T cells modified with CEA targeted chimeric antigen receptor.

Interventions

Anti-CEA-CAR T

T cells modified with CEA targeted chimeric antigen receptor.

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

1. CEA positive T4/N2 high-risk stage-Ⅲ colorectal cancer after surgery or patients with colorectal cancer liver metastasis after R0 surgery;

2. Patients whose serum CEA ≥11 ng/mL;

3. Life expectancy ≥ 3 months;

4. PS score 0-2, KPS score ≥60;

5. >3 CTC/7.5 mL blood sample;

6. Patients who plan to use XELOX chemotherapy after surgery;

7. Patients must have adequate organ function , such as NYHA heart function classification grade III or higher, no severe anemia, hypoxia; liver function: total bilirubin ≤ 1.5 × ULN (total bilirubin ≤ 3 × ULN when liver metastasis), ALT≤2.5×ULN, AST≤2.5×ULN (ALT or/and AST≤5×ULN when liver metastasis); renal function: blood creatinine ≤1.5 × ULN and creatinine clearance ≥50 mL/min, only when blood creatinine ≤ Calculate the creatinine clearance rate when 1.5 × ULN;

8. Sufficient peripheral blood can be obtained through peripheral veins without contraindications to apheresis;

9. Patients of childbearing age have no birth plans and take effective contraceptive measures during the study period and within 1 year after the study.

Exclusion Criteria

1. Patients who have a history of severe central nervous system disease;

2. Other organ metastases except liver;

3. Patients who have non malignant diseases, including autoimmune diseases, primary immunodeficiency diseases or obstructive or restrictive respiratory diseases;

4. Patients received car-t or other gene modified T cell therapy previously;

5. Patients who plan to use other targeted anti-tumor drugs;

6. Patients who participated in other clinical studies within 30 days before screening or planned to participate in other clinical studies during the study period;

7. Patients who have syphilis or HIV / HBV / HCV / HPV / EBV / CMV infection ; HBV-DNA copy number ≥ 1 × 10 ^ 5 copies / ml is required for HBV seropositive patients;

8. Patients who have uncontrollable systemic infectious diseases;

9. Patients who have multiple malignant tumor;

10. Patients who received or may need Chinese herbal medicine, systemic glucocorticoid or other immunosuppressants within 2 weeks before enrollment;

11. Patient who are pregnancy and lactating;

12. Patients who have severe gastroduodenal ulcer, ulcerative colitis and other intestinal inflammation;

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

HuaDao (Shanghai) Biomedical Co., Ltd.

OTHER

Sponsor Role: collaborator

Ruijin Hospital

OTHER

Sponsor Role: lead

Responsible Party

Mei Wang

Director of Oncology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Ren Zhao, Medical PhD

Role: PRINCIPAL_INVESTIGATOR

Ruijin Hospital

Mei Wang, Medical PhD

Role: PRINCIPAL_INVESTIGATOR

Ruijin Hospital

Chen xianze, Medical PhD

Role: STUDY_CHAIR

Ruijin Hospital

Liu Kun, Medical PhD

Role: STUDY_CHAIR

Ruijin Hospital

Shi Yiqing, Medical PhD

Role: STUDY_CHAIR

Ruijin Hospital

Wang Chen, Medical PhD

Role: STUDY_CHAIR

Ruijin Hospital

He Qianyun, Medical PhD

Role: STUDY_CHAIR

Ruijin Hospital

Mao Dongliang, Medical PhD

Role: STUDY_CHAIR

Ruijin Hospital

Central Contacts

Mei Wang, Medical PhD

Role: CONTACT

13601810867@163.com

+86-13601810867

Lin Tian, Medical PhD

Role: CONTACT

lin.tian@huadaocart.com

13651760950

Other Identifiers

RJBY_anti-CEA CAR-T_CRC01

Identifier Type: -

Identifier Source: org_study_id