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

NCT04828174 | Suspended Phase 1

• 1 other identifier: SHYSXY-202101-CART
• Study Type: interventional
• Target: 9
• Locations: 1 country
• Sites: 1

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

Conditions

Peripheral T Cell Lymphoma; Angioimmunoblastic T-cell Lymphoma; Anaplastic Lymphoma; Acute T Cell Leukemia; T-lymphoblastic Lymphoma

Outcome Measures

Primary Outcomes (1)

• Safety and Tolerability

  Safety measured by occurence of study related adverse effects defined by NCI CTCAE5.0

  28 days post infusion

Secondary Outcomes (5)

• CAR-T cell expansion and persistence

  2 years post infusion

• Total response rate (ORR) after administration

  3 months post infusion

• Duration of remission (DOR) after administration

  2 years post infusion

• Overall Survival (OS)after administration

  2 years post infusion

• Progression Free Survival (PFS) after infusion

  2 years after infusion

Study Arms (1)

anti-TRBC1 CAR-T cell

EXPERIMENTAL

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

Drug: anti-TRBC1 CAR-T cell therapy

Interventions

anti-TRBC1 CAR-T cell therapy DRUG

TRBC1 positve patients with relapsed or refractory T cell malignacy will receive CAR-T cell therapy targetting TRBC1

anti-TRBC1 CAR-T cell

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• (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:
• Patients who do not get a CR with ≥2 prior lines of therapy
• 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
• 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
• Patients who do not get a CR with ≥2 prior lines of therapy
• Relapsed patients failing to acheive a CR after 1 line salvage chemotherapy
• 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

You may not qualify if:

• 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;
• 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;
• 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;
• 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

Sponsors & Collaborators

• Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine: lead

Study Sites (1)

Xianmin Song

Shanghai, Shanghai Municipality, 200080, China

Location

MeSH Terms

Conditions

Lymphoma, T-Cell, Peripheral; Immunoblastic Lymphadenopathy; Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Condition Hierarchy (Ancestors)

Lymphoma, T-Cell; Lymphoma, Non-Hodgkin; Lymphoma; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Hemic and Lymphatic Diseases; Immunoproliferative Disorders; Immune System Diseases; Lymphadenopathy; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Leukemia, Lymphoid; Leukemia; Hematologic Diseases

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: principal investigator

Study Record Dates

• First Submitted: March 31, 2021
• First Posted: April 1, 2021
• Study Start: March 31, 2021
• Primary Completion: November 26, 2023
• Study Completion: November 26, 2023
• Last Updated: November 29, 2023

Record last verified: 2023-11

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)