Anti-TRBC1 CAR-T Cell Therapy in Patients With TRBC1 Positive T Cell Malignancies

Phase 1

Suspended

• Conditions: Peripheral T Cell Lymphoma; Angioimmunoblastic T-cell Lymphoma; Anaplastic Lymphoma; Acute T Cell Leukemia; T-lymphoblastic Lymphoma
• Interventions: Drug: anti-TRBC1 CAR-T cell therapy

• Registration Number: NCT04828174
• Lead Sponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of CAR T cell treatment targeting TRBC1 in patients with relapsed or refractory TRBC1 positive T-cell hematological maliganacies

Detailed Description

Not available

Study Timeline

• Study Start: 2021-03-31
• Study First Submitted: 2021-03-31
• Study First Submitted QC: 2021-03-31
• Study First Posted: 2021-04-01
• Status Verified: 2023-11
• Primary Completion: 2023-11-26
• Study Completion: 2023-11-26
• Last Update Submitted: 2023-11-26
• Last Update Posted: 2023-11-29

Recruitment & Eligibility

• Status: SUSPENDED
• Sex: All
• Target Recruitment: 9

Inclusion Criteria

(1)18 to 70 Years Old, Male and female; (2) Expected survival > 12 weeks; (3) ECOG score 0-2; (4) Confirmed diagnosis of acute T cell leukemia and screened for TRBC1 positive, including following conditions:

1. Patients who do not get a CR with ≥2 prior lines of therapy
2. Those who achieves CR, but have a early relapse(<12months),or a late relapse (>=12months) failing to acheive a CR after 1 line salvage chemotherapy
3. For any Patiens failed ASCT/allo-SCT (5) Relapsed and refractory patients with diagnosis of T cell lymphoma have had≥2 prior lines of therapy,including:

a. Peripheral T cell lymphoma NOS, or b. Angioimmunoblastic T cell lymphoma, or c. Anaplastic large cell lymphoma (6) Confirmed T lymphoblatic lymphoma

1. Patients who do not get a CR with ≥2 prior lines of therapy
2. Relapsed patients failing to acheive a CR after 1 line salvage chemotherapy
3. For any Patiens failed ASCT/allo-SCT (7) The venous access required for collection can be established and mononuclear cell collection can be determined by the investigators; (8) 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; (9) Able to understand and sign the In

Exclusion Criteria

1. Malignant tumors other than acute lymphoblastic leukemia 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;
2. Uncontrolled infection;patients with positive HBsAg or HBcAb and peripheral blood HBV DNA titer detection ≥ 1 × 10^2 copy number / L; HCV antibody positive and peripheral blood HCV RNA positive; HIV antibody positive; CMV DNA positive; syphilis positive;
3. 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;
4. Any uncontrolled disease may affect entry
5. 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)
6. 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;
7. 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;
8. Active or uncontrollable infection requiring systemic therapy
9. Received CAR-T treatment or other gene therapies before enrollment;
10. Kown be allergic to anti-TRBC1 CAR-T cells or drugs(Fludarabine or Cyclophophamide)
11. The investigators consider other conditions unsuitable for enrollment.
12. 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
anti-TRBC1 CAR-T cell	anti-TRBC1 CAR-T cell therapy	Administration with anti-TRBC1 CAR-T cells in the relapsed/refractory T cell hematological malignancy patients.

Primary Outcome Measures

Name	Time	Method
Safety and Tolerability	28 days post infusion	Safety measured by occurence of study related adverse effects defined by NCI CTCAE5.0

Secondary Outcome Measures

Name	Time	Method
CAR-T cell expansion and persistence	2 years post infusion	To evaluate anti-TRBC1 CAR-T cell expansion and persistence after infusion
Progression Free Survival (PFS) after infusion	2 years after infusion	Progression Free Survival (PFS) after infusion
Overall Survival (OS)after administration	2 years post infusion	Overall Survival (OS)after administration
Total response rate (ORR) after administration	3 months post infusion	CR+CRi for T-ALL CR+PR for T cell lyphoma
Duration of remission (DOR) after administration	2 years post infusion	Duration of remission (DOR) after administration

Trial Locations

Locations (1)

Xianmin Song; 🇨🇳 Shanghai, Shanghai, China