Clinical Study on CAR-T Targeting Igβ Targets in Refractory Relapsed Non-Hodgkin's Lymphoma
Study Details
Study Description
Brief Summary
Aim of this study will evaluate the safety, tolerability and preliminary efficacy of chimeric antigen receptor T cells (CAR-T) targeting Igβ targets in patients with Igβ-positive refractory relapsed non-Hodgkin's lymphoma.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
Non-Hodgkin's lymphoma is a group of malignant neoplasms of the lymphatic system originating from B or T cells, of which 60-70% of patients have B-cell-derived lymphoma (B-NHL). Although rituximab in combination with chemotherapy has significantly improved the prognosis of B-cell lymphoma, some patients still have primary resistance or relapse. In recent years, breakthroughs have been made in the treatment of B-cell tumors with Chimeric Antigen Receptor-Modified T Cells (CART), the investigators therefore constructed CAR-T cells targeting Igβ to investigate the safety and efficacy of CAR-T cells with this target for the treatment of r/r B-NHL.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Chimeric Antigen Receptor T Cells (CAR-T) Targeting Igβ Targets Chimeric antigen receptor T cells targeting Igβ targets (CAR-T) |
Drug: Chimeric Antigen Receptor T Cells (CAR-T) Targeting Igβ Targets
Dose escalation studies:3 dose groups in total: expect 3-6 cases in each group, and dose set at 1×106/kg，3×106/kg，6×106/kg.
Dose extension study:3 cases (1 dose group).
Other Names:
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Outcome Measures
Primary Outcome Measures
- DLT [Measured from start of treatment until 28 days after last dose]
DLT occurring within 28 days of the last dose.
- Adverse events profile [Measured from start of treatment until 28 days after last dose]
Number of participants with adverse events. Frequencies of toxicities based on the NCI Common Terminology Criteria for Adverse Events (CTCAE), version 5.0 will be tabulated.
Secondary Outcome Measures
- Objective Response Rate [up to 3 months]
Proportion of CR and PR subjects will be assessed at 3 months post-infusion.
- Duration of Response [up to 12 months]
Duration of overall response will be assessed from the first chimeric antigen receptor T cells (CAR-T) targeting Igβ targets given to progression, death or last follow-up.
- Progression-free survival [up to 12 months]
To measure the duration of response to chimeric antigen receptor T cells (CAR-T) targeting Igβ targets over a follow-up period of 12 months.
- Overall Survival [up to 12 months]
OS will be assessed from the first chimeric antigen receptor T cells (CAR-T) targeting Igβ targets given to death or last follow-up.
- Peak Plasma Concentration [Measured from start of treatment until 28 days after last dose]
the peak amplification of Igβ-CART in peripheral blood.
- Time to Peak Amplification [Measured from start of treatment until 28 days after last dose]
the time to peak amplification of Igβ-CART in peripheral blood.
- AUC0-28 [Measured from start of treatment until 28 days after last dose]
the area under the curve (AUC0-28) obtained by plotting the number of CAR-T cells in serum against the visit time from 0 to 28 days after reinfusion.
- PD [Measured from start of treatment until 28 days after last dose]
Pharmacodynamics is the peripheral blood B-cell ratio.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Voluntary signing of informed consent and good compliance.
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Age ≥ 6 years.
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Previously treated with 2 or more lines of therapy.
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Has a measurable target lesion.
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ECOG 0-1#.
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Have appropriate organ function, subject to the following criteria (except for abnormal liver function due to tumor infiltration): AST≤3 times upper limit of normal#ALT≤3 times upper limit of normal# TB≤2 times ULN, unless combined with Gilbert's syndrome #Patients with Gilbert's syndrome with TB≤ 3 times ULN and DB≤ 1.5 times ULN can be include # Scr ≤1.5 times ULN or CCr≥60 ml/min# Lung function≤Level 1; dyspnea(CTCAE v5.0),and blood oxygen saturation without oxygen absorption> 91%# INR≤1.5 times ULN# aPTT≤1.5 times ULN.
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negative blood/urine pregnancy test in women of childbearing age within 7 days prior to cell infusion, and any male and female patients of childbearing potential must agree to use an effective method of contraception throughout the study and for at least six months after the study treatment is administered.
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Pass the T-cell amplification test.
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Have adequate venous access to single or venous blood and no other contraindications to leukocyte isolation.
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Estimated survival time ≥3 months.
Exclusion Criteria:
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Prior malignancy (other than Relapsed Refractory B-cell Non-Hodgkin's Lymphoma), except for cured malignant tumors with no active lesions for 3 years; Adequate treatment of inactive lesions in non-melanoma skin cancer, malignant tonsilloma or carcinoma in situ.
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Have used immunosuppressants or hormones within 2 weeks prior to signing informed consent, or plan to have to use immunosuppressants or high-dose hormones (e.g. prednisone >15mg) after signing informed consent, specifically systemic treatment, excluding treatment with topical or inhaled corticosteroids.
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The presence of bacterial, fungal, viral, mycoplasma or other types of infection that, in the judgment of the investigator, are difficult to control.
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HIV, Syphilis or COVID-19 infection.
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Active hepatitis B or active hepatitis C.
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Previous or current CNS disease other than this disease, such as seizures, cerebrovascular ischaemia/hemorrhage, dementia, cerebellar disease or any CNS-related autoimmune disease.
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A history of cardiac angioplasty or stent placement within 12 months prior to signing the informed consent form, or a history of myocardial infarction, unstable angina or other clinically significant heart disease.
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Patients with primary immunodeficiency.
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Have had a severe tachyphylaxis to any of the drugs to be used in this study.
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Live vaccination within 6 weeks prior to screening.
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Pregnant or breasting-feeding women.
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Active autoimmune diseases.
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Active acute or chronic graft-versus-host disease (GVHD) at the time of signing the informed consent form.
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Received an allogeneic hematopoietic stem cell transplant within 6 months prior to signing the informed consent form.
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Participated in an investigational clinical trial of any other drug within 30 days prior to signing the informed consent form.
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Conditions deemed by the researcher to be inappropriate for participation in this clinical trial.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The First Affiliated Hospital of Soochow University | Suzhou | Jiangsu | China | 215000 |
Sponsors and Collaborators
- The First Affiliated Hospital of Soochow University
Investigators
- Study Chair: Depei Wu, M.D, The First Affiliated Hospital of Soochow University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- R/R B-NHL 02