Anti-CD7 CAR-T Cell Therapy for Relapse and Refractory CD7 Positive T Cell Malignancies

Sponsor

Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine (Other)

Overall Status

Recruiting

CT.gov ID

NCT05290155

Collaborator

(none)

Enrollment

Location

Arm

22.9

Anticipated Duration (Months)

0.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of CAR T cell treatment targeting CD7 in patients with relapsed or refractory CD7 positive T-cell hematological maliganacies

Condition or Disease	Intervention/Treatment	Phase
T Lymphoblastic Leukemia/Lymphoma T-cell Acute Lymphoblastic Leukemia Peripheral T Cell Lymphoma Angioimmunoblastic T-cell Lymphoma Anaplastic Large Cell Lymphoma	Drug: anti-CD7 CAR-T cells	Phase 1

Detailed Description

This study is single-armed，open lable，dose escalation clinical trial.The main purpose is to evaluate the safety and efficacy of anti-CD7 CAR-T cells in relapsed/refractory patients with CD7 positive T cell malignancies,including T lymphoblastic lymphoma/leukemia ,T-cell non-Hodgkin lymphoma(peripheral T cell lymphoma,NOS,angioimmunoblastic T cell lymphoma and anaplastic large cell lymphoma).There will be three CAR T cell dose groups:0.510^6 cells per kilogram of body weight;110^{6 cells per kilogram of body weight，2 *10}6 ells per kilogram of body weight.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

4 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

The Safety and Clinical Efficacy of Human CD7 CAR-T Cell Therapy for Patients With Relapsed/Refractory CD7 Positive T Cell Hematological Maliganacies

Anticipated Study Start Date :

May 4, 2022

Anticipated Primary Completion Date :

Apr 1, 2023

Anticipated Study Completion Date :

Apr 1, 2024

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Anti-CD7 CAR T cells Administration with anti-CD7 CAR-T cells in the relapsed/refractory T cell hematological malignancy patients	Drug: anti-CD7 CAR-T cells Administration with anti-CD7 CAR-T cells in the relapsed/refractory T cell hematological malignancy patients

Arm

Intervention/Treatment

Experimental: Anti-CD7 CAR T cells

Administration with anti-CD7 CAR-T cells in the relapsed/refractory T cell hematological malignancy patients

Drug: anti-CD7 CAR-T cells

Administration with anti-CD7 CAR-T cells in the relapsed/refractory T cell hematological malignancy patients

Outcome Measures

Primary Outcome Measures

Incidence of Treatment-Emergent Adverse Events [28 days post infusion]
The occurence of study related adverse effects defined by NCI CTCAE5.0

Secondary Outcome Measures

CAR-T cell expansion [2 years post infusion]
Using flow cytometry to reveal cell surface expression of the CAR protein on T cells;and using quantitative polymerase chain reaction to detect DNA copies of the transgene irrespective of gene expression(per ug DNA) to evaluate anti-CD7 CAR-T cell expansion after infusion
CAR-T cell persistence [2 years post infusion]
Using flow cytometry to reveal cell surface expression of the CAR protein on T cells;and using quantitative polymerase chain reaction to detect DNA copies of the transgene irrespective of gene expression(per ug DNA) to evaluate anti-CD7 CAR-T cell persistence after infusion
Number of CD7+ lymphocytes of peripheral blood [2 years post infusion]
To evaluate CD7 positive cells of peripheral blood after infusion
Total response rate (ORR) after administration [3 months post infusion]
CR+CRi for T-ALL ;CR+PR for T cell lyphoma and T lymphoblastic lymphoma
Duration of remission (DOR) after administration [2 years post infusion]
Duration of remission (DOR) after administration
Overall survival(OS) after administration [2 years post infusion]
Overall Survival (OS)after administration
Progression Free Survival (PFS) after administration [2 years post infusion]
Progression Free Survival (PFS) after administration

Other Outcome Measures

Immunogenicity of CAR-T cells [2 years post infusion]
Using flow cytometry to detect whether anti-car antibodies are contained in serum of patients receiving CAR-T cells infusion,and to evaluate the number of participants with antibodies

Eligibility Criteria

Criteria

Ages Eligible for Study:

14 Years to 70 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion criteria

Fourteen to 70 Years Old, Male and female;
Expected survival > 12 weeks; ECOG score 0-2;
Confirmed diagnosis of acute T cell leukemia and screened for CD7 positive,including following conditions:a. Patients who do not get a CR with ≥2 prior induction therapy

Those who achieves CR, but have a early relapse(<12months),or a late relapse (>=12months) failing to acheive a CR after re-induction chemotherapy c. For any Patiens failed ASCT/allo-SCT

Relapsed and refractory patients with diagnosis of CD7 positive T cell lymphoma have had≥2 prior lines of therapy,who do not acheive at least a PR, or have a relapse including:a. Peripheral T cell lymphoma NOS, or b.Angioimmunoblastic T cell lymphoma,or c. Anaplastic large cell lymphoma c.Disease can be assessed(BM or CT scan)
Confirmed T lymphoblatic lymphoma：a. Patients who do not get a PR with ≥2 induction chemotherapy or a CR with ≥ 4 induction chemotherapy b. Relapsed patients failing to acheive a CR after 1 line salvage chemotherapy c. For any Patiens failed ASCT/allo-SCT d.Disease can be assessed(BM or CT scan)
The venous access required for collection can be established and mononuclear cell collection can be determined by the investigators;
Liver, kidney and cardiopulmonary functions meet the following requirements: a. Ccr≥60mL/min(Cockcroft Gault) b. Left ventricular ejection fraction >50%; c.Baseline oxygen saturation>92%; d. Total bilirubin ≤ 1.5×ULN; e. ALT and AST≤ 3×ULN;
Able to understand and sign the Informed Consent

Exclusion Criteria:

Malignant tumors other than T cell malignancies within 5 years prior to screening, in addition to adequately treated cervical carcinoma in situ, basal cell or squamous cell skin cancer, localized prostate cancer after radical resection, and ductal carcinoma in situ after radical resection;
Uncontrolled infection including bacteral or virus or fugal disease;patients with positive HBsAg or HBcAb and positive peripheral blood HBV DNA titer detection ;HCV antibody positive and peripheral blood HCV RNA positive; HIV antibody positive; syphilis positive;
Any instability of systemic disease, including but not limited to unstable angina, cerebrovascular accident, or transient cerebral ischemic (within 6 months prior to screening),myocardial infarction (within 6 months prior to screening), congestive heart failure (New York heart association (NYHA) classification ≥ III), need drug therapy of severe arrhythmia,liver, kidney, or metabolic disease;
Any uncontrolled disease may affect entry
Current or history of CNS involvement by malignancy.Known history or presence of clinically relevant central nervous system (CNS) pathology.Patients with a known history or prior diagnosis other immunologic or inflammatory disease affecting the CNS (such as epilepsy)
Patients who are receiving systemic steroid treatment and requiring long-term systemic steroid treatment during the treatment as determined by the investigator before screening (except inhalation or topical use); And subjects treated with systemic steroids (except inhalation or topical use) within 72h prior to cell transfusion;
Subjects treated with anti-PD1 or anti-PDL1 therapies within 3months before enrollment
Pregnant or lactating woman, and female subject who plans to have a pregnancy within 1 year after cell transfusion, or male subject whose partner plans to have a pr egnancy within 1 year after cell transfusion;
Active or uncontrollable infection requiring systemic therapy Received CAR-T treatment or other gene therapies before enrollment;
Kown be allergic to anti-TRBC1 CAR-T cells or drugs(Fludarabine or Cyclophophamide)
The investigators consider other conditions unsuitable for enrollment.
Patients who may not be able to sign the Informed Consent due to disease,or who do not understand or unwillingness or inability to comply with research requirements