Anti-CD22 Chimeric Antigen Receptor (CAR)-Modified T Cell Therapy for Relapsed Refractory B-cell Malignancies

Acute Lymphoblastic Leukemia Clinical Trial

Official title:

Efficacy and Safety of Anti-CD22 CAR-T Therapy in Patients With Relapsed/Refractory B-cell Malignancies: a Single-center, Open-label, Single-arm Clinical Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04007978
• Other study ID #: WHUH-CART-CD22-01
• Status: Recruiting
• Phase: Phase 1
• Start date: August 5, 2019
• Est. completion date: December 30, 2022

Study information

• Verified date: August 2019
• Source: Wuhan Union Hospital, China
• Contact: Yu Hu, M.D., Ph.D
• Phone: 86-13986183871
• Email: dr_huyu[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a single-center, open-label, single-arm study to evaluate the safety and efficacy of anti-CD22 CAR-T cells in patients with relapsed or refractory B-cell Malignancies.

Description:

Chimeric antigen receptor (CAR)-modified T cells (CAR-T cells) have the capabilities to recognize tumor associated antigen and kill tumor cells specifically. CAR-T therapy showed great effect on patients with relapsed or refractory B-cell malignancies. CAR consists of single chain variable fragment (scFv) and activation domain of T cell. In preclinical study, the researchers constructed a third generation CAR containing CD137 and CD28 costimulatory domains.

This study aims to evaluate the safety and effectiveness of anti-CD22 CAR-T cells in patients with relapsed or refractory B-cell Malignancies.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: December 30, 2022
• Est. primary completion date: June 30, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 14 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Patient or his or her legal guardian voluntarily participates in and signs an informed consent form.

2. Male or female patients aged 14 to 70 years (including 14 and 70 years old).

3. Pathological and histological examination confirmed CD22+ B-cell malignancies, and patients met the following criteria for refractory or relapsed B-cell malignancies.

A.Refractory/relapsed B-cell lymphoblastic leukemia (Meeting one of the following)

i. Recurrence within 6 months after first remission.

ii. Primary refractory disease which cannnot achieve complete remission (CR) after 2 cycles of standardized chemotherapy regimen.

iii. Failure to achieve CR or relapse after one line or multiple lines of salvage chemotherapy.

iv. Not suitable for hematopoietic stem cell transplantation (HSCT), or abandon HSCT due to various restrictions, or relapse after HSCT.

B.Refractory/relapsed B-cell lymphoma (Meeting 1 of the first 4 items plus item 5)

i. Tumor shrinkage less than 50% or disease progression after 4 cycles of standard chemotherapy.

ii. Achieved CR after standard chemotherapy, but relapsed within 6 months.

iii. 2 or more relapses after CR.

iv. Not suitable for HSCT, or abandon HSCT due to various restrictions, or relapse after HSCT.

v. Subjects must have received adequate treatment in the past, including anti-CD20 monoclonal antibody and combination chemotherapy with anthracyclines.

4. B-cell malignancies include the following three types

A. B-cell acute lymphoblastic leukemia (B-ALL)

B. Indolent B-cell lymphoma (CLL, FL, MZL, LPL, HCL)

C. Invasive B-cell lymphoma (DLBCL, BL, MCL)

5. Having a measurable or evaluable lesion

A. Patients with lymphoma require a single lesion=15mm or 2 or more lesions=10mm.

B. Patients with leukemia require persistent positive or positive relapse of bone marrow MRD.

6. Patient's main organs functioning well

A. Liver function: ALT/AST < 3 times the upper limit of normal (ULN) and total bilirubin=34.2µmol/L

B. Renal function: Creatinine < 220µmol/L.

C. Pulmonary function: Indoor oxygen saturation=95%.

D. Cardiac Function: Left ventricular ejection fraction (LVEF) =40%.

7. The patients did not receive any antitumor treatments such as chemotherapy, radiotherapy and immunotherapy (such as immunosuppressive drugs) within 4 weeks before enrollment, and the toxicity related to previous treatments had returned to < 1 level at enrollment (except for low grade toxicity such as alopecia).

8. The patient's peripheral superficial venous blood flow smoothly, which can meet the needs of intravenous drip.

9. Patient ECOG score= 2, estimated survival time=3 months.

Exclusion Criteria:

1. Have a history of epilepsy or other central nervous system diseases.

2. Women who are pregnant (urine/blood pregnancy test positive) or lactating.

3. Male or female with a pregnancy plan in the next 1 year.

4. Patients cannot guarantee effective contraception (condom or contraceptives, etc.) within 1 year after enrollment.

5. Uncontrolled infectious disease within 4 weeks prior to enrollment.

6. Active hepatitis B/C virus infection.

7. HIV infected patients.

8. Suffering from a serious autoimmune disease or immunodeficiency disease.

9. The patient is allergic to macromolecular biopharmaceuticals such as antibodies or cytokines.

10. The patient participated in other clinical trials within 6 weeks prior to enrollment.

11. Systemic use of corticosteroids within 4 weeks prior to enrollment (except for patients with inhaled corticosteroids).

12. Suffering from mental diseases.

13. Patient has drug abuse/addiction.

14. According to the researcher's judgment, the patient has other unsuitable enrollment conditions.

Related Conditions & MeSH terms

• Acute Lymphoblastic Leukemia
• B Cell Lymphoma
• Leukemia, Lymphoid
• Lymphoma, B-Cell
• Precursor Cell Lymphoblastic Leukemia-Lymphoma

Intervention

Genetic:
• Third generation CAR-T cells
Patients receive CD22 CAR-T cells transduced with a lentiviral vector on day 0 in the absence of disease progression or unacceptable toxicity.

Locations

Country	Name	City	State
China	Union Hospital, Tongji Medical College, Huazhong University of Science and Technology	Wuhan	Hubei

Sponsors (2)

Lead Sponsor	Collaborator
Wuhan Union Hospital, China	Wuhan Bio-Raid Biotechnology Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with adverse events	Therapy-related adverse events were recorded and assessed according to the National Cancer Institute's Common Terminology Criteria for Adverse Events (CTCAE, Version 4.0).	3 years
Secondary	One-month remission rate	Response of B-ALL to CAR-T therapy was assessed on day 30 (±2), against the National Comprehensive Cancer Network (NCCN, Version 1.2015).	1 month
Secondary	Overall survival	OS was calculated from the first CAR-T cell infusion to death or last follow-up (censored).	3 years
Secondary	Event-free survival	EFS was calculated from the first CAR-T cell infusion to death, progression of the disease, relapse or gene recurrence, whichever came first, or last visit (censored).	3 years
Secondary	Relapse-free survival	RFS was calculated from the first CAR-T cell infusion to relapse or last visit (censored).	3 years
Secondary	Rate of anti-CD22 CAR-T cells in bone marrow cells and peripheral blood cells	In vivo (bone marrow and peripheral blood) rate of CAR-T cells were determined by means of flow cytometry.	3 years
Secondary	Quantity of anti-CD22 CAR-T cells in bone marrow cells and peripheral blood cells	In vivo (bone marrow and peripheral blood) quantity of CAR-T cells were determined by means of flow cytometry.	3 years
Secondary	Quantity of anti-CD22 CAR copies in bone marrow cells and peripheral blood cells	In vivo (bone marrow and peripheral blood) quantity of anti-CD22 CAR copies were determined by means of qPCR.	3 years