Safety and Efficacy of CT125A Cells for Treatment of Relapsed/Refractory CD5+ Hematopoietic Malignancies

Early Phase 1

• Conditions: Diffuse Large B-cell Lymphoma (DLBCL); Peripheral T-cell Lymphomas (PTCL); Mantle Cell Lymphoma (MCL); Chronic Lymphocytic Leukemia (CLL); Follicular Lymphoma (FL); CD5+ Relapsed/Refractory Hematopoietic Malignancies
• Interventions: Biological: CT125A cells; Drug: Cyclophosphamide, fludarabine

• Registration Number: NCT04767308
• Lead Sponsor: Huazhong University of Science and Technology

Brief Summary

Current treatments for relapsed/refractory hematopoietic malignancies such as B-cell lymphomas (BCLs) and peripheral T-cell lymphomas (PTCLs) are far from satisfactory. CD5 is widely expressed in multiple subtypes of BCLs and PTCLs but rarely found in normal tissues except certain types of lymphocytes. Chimeric antigen receptor (CAR) T cells against CD5 offer another potential therapeutic option for patients with relapsed/refractory CD5 positive hematopoietic malignancies. In the current study, the safety and efficacy of a novel CAR T cell therapy, termed CT125A cells, are evaluated in patients with relapsed/refractory CD5+ hematopoietic malignancies. The endogenous CD5 in CT125A cells is knocked out via CRISPR/Cas9 genome editing technology to prevent fratricide during CAR T cells manufacturing.

Detailed Description

Not available

Study Timeline

• Status Verified: 2021-02
• Study First Submitted: 2021-02-09
• Study First Submitted QC: 2021-02-19
• Last Update Submitted: 2021-02-19
• Study First Posted: 2021-02-23
• Last Update Posted: 2021-02-23
• Study Start: 2021-03
• Primary Completion: 2023-09
• Study Completion: 2023-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

1.Subjects with CD5 positive B-cell lymphomas must meet the diagnostic criteria from National Comprehensive Cancer Network (NCCN) guidelines for B-Cell Lymphomas (2020.V1) and have CD5 expression on lymphoma cells (results within 60 days before informed consent signing are acceptable if current clinical condition is not suitable for sampling, and the investigator will judge whether the test results from other hospitals are acceptable and whether they can be enrolled); according to Lugano 2014 criteria, patients with B-cell lymphomas have at least one measurable lesion with the longest diameter ≥ 1.5 cm or bone marrow involvement detected by flow cytometry .

Including:

1. Chronic lymphocytic leukemia/small lymphocytic lymphoma: any BTK inhibitor have been given for at least 6 months and the treatment has failed (SD or PD).
2. Mantle cell lymphoma (MCL): patients with MCL must have relapsed/refractory diseases after receiving at least one treatment regimen. Previous treatment must include chemotherapy with anthracyclines or bendamustine, anti-CD20 monoclonal antibody, and any BTK Inhibitor therapy.
3. Diffuse large B-cell lymphoma: patients with diffuse large B-cell lymphoma who have failed or relapsed after at least two lines of therapy (a standard chemotherapy and a rescue chemotherapy); and meet one of the following conditions: a. unable to receive autologous hematopoietic stem cell transplantation (autoHSCT); b. refuse to receive autoHSCT; c. relapse after autoHSCT.

2.Subjects with CD5 positive peripheral T-cell lymphomas (PTCLs) are diagnosed according to criteria from World Health Organization classification for tumors of the hematopoietic and lymphoid tissues (2016 Edition) and have CD5 expression on lymphoma cells (results within 60 days before informed consent signing are acceptable if current clinical condition is not suitable for sampling, and the investigator will judge whether the test results from other hospitals are acceptable and whether they can be enrolled); according to Lugano 2014 criteria, patients with T-cell lymphomas must have at least one measurable lesion with the longest diameter ≥ 1.5 cm and no bone marrow involvement confirmed by flow cytometry and gene rearrangement (TCR/IGH) tests (and PET-CT results, if any, that must indicate no increased bone marrow metabolism); patients must fail or relapse after at least one line of therapy; including but not limited to the following PTCLs:

1. Peripheral T cell lymphoma - not otherwise specified (PTCL-NOS)
2. Angioimmunoblastic lymphoma
3. ALK negative anaplastic large cell lymphoma
4. Extranodal NK/T cell lymphoma
5. Enteropathy-associated T-cell lymphoma
6. Large granular T lymphocyte leukemia
7. Adult T cell leukemia

3.Age ≥18 and ≤70 years old, regardless of gender.

4.Expected life expectancy ≥12 weeks.

5.Serum total bilirubin ≤ 37.2 μmol/L (Gilbert syndrome patients ≤ 3.0 ULN, direct bilirubin ≤ 1.5 ULN), estimated glomerular filtration rate eGFR (CKD-EPI) ≥ 30 ml/min/1.73m2, alanine aminotransferase and aspartate aminotransferase less than 2.5 times the upper limit of normal range.

6.ECOG score 0-1 points.

7.Echocardiography suggests left ventricular ejection fraction (LVEF) ≥50%; blood oxygen saturation >91%.

8.After signing the informed consent form, subjects and their partners must be willing to use effective and reliable method of contraception, devices or medicines, within one year after CAR T cell infusion (excluding contraception safety periods). A negative pregnancy test must be obtained for female subjects.

Subjects must provide written informed consent before the study begin.

Exclusion Criteria

Subjects who meet any of the following criteria will be excluded:

1. History of allergies to any of the ingredients in cell products.
2. Patients with acute GVHD judged to be grade II-Ⅳ by Glucksberg criteria or grade B-D by IBMTR index; acute or chronic GVHD patients who need systemic treatment within four weeks before enrollment.
3. Injected with live vaccines within 4 weeks before enrollment.
4. Central nervous system diseases not associated with lymphoma CNS invasion (such as cerebral aneurysm, epilepsy, stroke, senile dementia, psychosis, etc.). Lymphoma CNS invasion or digestive tract invasion is not considered as an exclusion criterion, but whether to be enrolled in the group is determined by the investigator.
5. Severe active infection (except simple urinary tract infection and bacterial pharyngitis), or currently receiving intravenous antibiotic treatment. However, preventive antibiotics, antiviral and antifungal infection treatments are permitted.
6. Hepatitis B surface antigen (HBsAg) positive or hepatitis B core antibody (HBcAb) positive and peripheral blood hepatitis B virus (HBV) DNA > 100 IU/mL.
7. Hepatitis C virus (HCV) antibody positive and peripheral blood hepatitis C virus (HCV) RNA positive.
8. Subjects with other acquired and congenital immunodeficiency diseases, including but not limited to human immunodeficiency virus (HIV) antibody positive; subjects with cytomegalovirus (CMV) DNA > 400 copy/mL; subjects with syphilis test positive.
9. Cardiac insufficiency of grade III or IV according to the New York Heart Association (NYHA) cardiac function classification criteria.
10. History of other primary cancers, except for the following conditions:

1)Non-melanoma skin cancer with complete resection, such as basal cell carcinoma; 2)Cured carcinoma in situ such as cervical cancer, bladder cancer or breast cancer; 3)No recurrence of other primary cancers has been found for more than 5 years after treatment.

11.History of solid organ transplantation.

12.Subjects with previous autoimmune diseases (mainly abnormality of cellular immunity), immunodeficiency or subjects requiring immunosuppressive therapy.

13.Received other interventional clinical trial treatment within 3 months before signing ICF.

14.Pregnant or lactating women.

15.Suffer from mental illness or disturbance of consciousness or central nervous system disease.

16.The toxicity of previous treatment has not been relieved to baseline or ≤2 (NCI-CTCAE v5.0, except for hair loss).

17.Drug use:

1. Steroid drugs: therapeutic dose of steroids used within 72 hours before CAR-T cell infusion, but physiological doses of steroid supplementation are allowed (<12mg/m2/day of hydrocortisone or its equivalent dose);
2. Systemic anti-tumor therapy is not ended at least 2 weeks or 5 drug half-lives before apheresis (except for BTK inhibitors in CLL); interval between apheresis and immune checkpoint inhibitor treatment is less than 3 drug half-lives.

18.Active lung infection.

19.Contraindications for peripheral blood apheresis.

20. Subjects considered unsuitable for enrollment by the investigator for other reasons after careful consideration.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Arm 1	Cyclophosphamide, fludarabine	The tolerability and safety of CT125A cells will be assessed according to the "3+3" dose escalation design. There will be three dose levels, 1×10\^6, 2×10\^6, and 3×10\^6, CAR+T cells/kg. For each level, 1-3 subjects will be enrolled. If no dose limited toxicity (DLT) occurs, next level will be assessed for DLT. If DLT occurs in one subject, 3 more subjects will be enrolled in this cohort for the evaluation of DLT. If DLT occurs in ≤ 1/6 subjects, next level will be assessed for DLT. If DLT occurs in ≥ 2 subjects, no more subjects will be enrolled in this cohort and dose escalation will be canceled. For each cohort, following subjects can only receive CT125A infusion at least 14 days after the first subject received CT125A infusion. If DLT occurs in 2 subjects at Dose Level 1, whether to explore a lower dose will be determined by the investigator. After dose escalation phase is completed, the dose for extension phase will be determined based on safety and PK data.
Arm 1	CT125A cells	The tolerability and safety of CT125A cells will be assessed according to the "3+3" dose escalation design. There will be three dose levels, 1×10\^6, 2×10\^6, and 3×10\^6, CAR+T cells/kg. For each level, 1-3 subjects will be enrolled. If no dose limited toxicity (DLT) occurs, next level will be assessed for DLT. If DLT occurs in one subject, 3 more subjects will be enrolled in this cohort for the evaluation of DLT. If DLT occurs in ≤ 1/6 subjects, next level will be assessed for DLT. If DLT occurs in ≥ 2 subjects, no more subjects will be enrolled in this cohort and dose escalation will be canceled. For each cohort, following subjects can only receive CT125A infusion at least 14 days after the first subject received CT125A infusion. If DLT occurs in 2 subjects at Dose Level 1, whether to explore a lower dose will be determined by the investigator. After dose escalation phase is completed, the dose for extension phase will be determined based on safety and PK data.

Primary Outcome Measures

Name	Time	Method
Incidence and types of dose limited toxicities (DLTs) following infusion of CT125A chimeric antigen receptor (CAR) T cells	28 days after CAR T cell infusion	Incidence and types of dose limited toxicities (DLTs) after administration of CT125A cells in patients with relapsed/refractory CD5+ hematopoietic malignancies will be recorded at 3 dose levels to investigate the maximum tolerated dose of CT125A. DLT is defined as the following adverse events that occur during the first 28 days after CT125A infusion and are definitely or probably related to CT125A cells: 1) Cytokine release syndrome equal or greater than grade 4 lasting longer than 3 days graded by ASTCT 2019 consensus; 2) Grade 4 immune effector cell-associated neurotoxicity syndrome graded by ASTCT 2019 consensus; 3) Grade 4 hematological toxicity lasting longer than 28 days except for T cell aplasia; 4) Non-hematological toxicity equal or greater than grade 3 lasting longer than 7 days or Grade 4 non-hematological toxicity lasting longer than 3 days.
Incidence and severity of adverse events (AEs) following infusion of CT125A chimeric antigen receptor (CAR) T cells	2 years after CAR T cell infusion	Incidence of adverse events (AEs) after administration of each dose of CT125A cells in patients with relapsed/refractory CD5+ hematopoietic malignancies will be recorded and the severity of AEs will be graded according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 except that cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome will be graded according to the consensus by ASTCT in 2019. AE is defined as any untoward medical occurrence in a patient after CAR T cell infusion and which does not necessarily have a causal relationship with this treatment.

Secondary Outcome Measures

Name	Time	Method
Overall response rate (ORR) at 4th week and 12th week	12 weeks after CAR T cell infusion	At 4 weeks and 12 weeks after CT125A infusion, the response rate of subjects that are evaluated as complete response (CR) and partial response (PR) according to Lugano 2014 criteria will be measured
Time to first response after CT125A cells infusion	2 years after CAR T cell infusion	The number of days elapsed between the time when subjects receive CT125A infusion and the time when the response is first evaluated as partial response (PR) or complete response (CR) will be measured
Time to complete response (CR) after CT125A infusion	2 years after CAR T cell infusion	The number of days elapsed between the time when subjects receive CT125A infusion and the time when the response is first evaluated as complete response (CR) will be measured