CD180 CART for Relapsed or Refractory CD180 Positive Hematologic Malignancies

Official title

CD180 CART Cell Injection in the Treatment of Relapsed or Refractory CD180 Positive Hematologic Malignancies: a Prospective, Single-arm, Single-center Clinical Study.

Overview

The objective of this study was to evaluate the safety and efficacy of CD180 CART cells in the treatment of patients with relapsed/refractory CD180-positive hematological malignancies. In this single-arm, open-label, single-center, Phase I clinical trial, two cohorts were set up: (1) relapsed and refractory AML cohort; and (2) relapsed and refractory B-ALL/LBL cohort. CD180 CART cells will be administered intravenously using a 3+3 dose escalation and rapid titration design, with CART dose groups of (1) 0.5×10\^6 CART cells/kg;(2)1×10\^6 CART cells/kg; and (3) 3×10\^6 CART cells/kg. Each cohort was planned to enroll 6-12 patients.

Detailed description

This study will utilize CD180 CART cells to treat CD180-positive relapsed or refractory hematological malignancies, especially AML and B-ALL/LBL patients. Two cohorts were established: (1) relapsed and refractory AML cohort; and (2) relapsed and refractory B-ALL/LBL cohort. A 3+3 dose escalation and rapid titration design was used to explore the maximum tolerated dose for each cohort. 3+3 dose escalation CART dose groups were (1) 0.5×10\^6 CART cells/kg; (2)1×10\^6 CART cells/kg;(3) 3×10\^6 CART cells/kg. A minimum of 6 and a maximum of 12 patients are expected to be enrolled in each cohort. Fludarabine and cyclophosphamide-based preconditioning should be performed within 1 week prior to CD180 CART infusion. CD180 CART can be infused on D-1 provided that the requirement of 24 hours after completion of preconditioning is met. The objective of the study was to evaluate the safety and efficacy of CD180 CART cells in the treatment of patients with relapsed/refractory CD180-positive hematological malignancies.

Interventions

• Biological CD180 CART
  Subjects screened to meet the requirements for CD180 CART use will enter clinical trials. Subjects were assessed at baseline. Fludarabine and cyclophosphamide based preconditioning should be performed within 1 week prior to CD180 CART infusion: fludarabine (Flu) 30mg/m2 ×3 days; cyclophosphamide (CTX) 500mg/m2 ×3 days. The investigator can adjust the pretreatment regimen appropriately according to the condition of the subject, such as increasing the dose of CTX to 600mg/m2 ×3 days, increasing th

Primary outcome measures

• Dose-limiting toxicity（DLT） [Time frame: 3 months after CD180 CART cells infusion]
• Number of adverse event of CD180 CART cells treatment [Time frame: Participants will be followed for the duration of the treatment, an expected average of 24 months.]

Secondary outcome measures (6)

• Response rate in 3 months [Time frame: within 3 months after CD180 CART cells infusion]
• Duration of remission (DOR) [Time frame: Participants will be followed for the duration of the treatment, an expected average of 24 months.]
• Event-free survival (EFS) [Time frame: Participants will be followed for the duration of the treatment, an expected average of 24 months.]
• Leukemia-free Survival (LFS) [Time frame: Participants will be followed for the duration of the treatment, an expected average of 24 months.]
• Proportion of patients receiving hematopoietic stem cell [Time frame: Participants will be followed for the duration of the treatment, an expected average of 24 months.]
• Overall survival (OS) [Time frame: Participants will be followed for the duration of the treatment, an expected average of 24 months.]

Eligibility criteria

Inclusion criteria

• Age ≥18 and <70 years, regardless of gender;
• B-ALL/LBL was diagnosed according to the criteria of NCCN Clinical Practice Guidelines for Acute Lymphocytic Leukemia (2020.v1) and B-cell Lymphoma Clinical Practice Guidelines (2020.v1);
• Patients diagnosed with AML with reference to the Guidelines for Diagnosis and Treatment of Adult Acute Myeloid Leukemia (2018 Edition) issued by the Health Commission;
• Cytology confirmed that the tumor cells were CD180 positive.
• Number of blasts in bone marrow ≥5% at screening (bone marrow morphology);
• Complies with the diagnosis of relapsed/refractory AML, including any of the following conditions according to China Guidelines for Diagnosis and Treatment of Relapsed/Refractory Acute Myeloid Leukemia (2021 Edition):

• Primary refractory patients who did not achieve CR after two cycles of standard induction chemotherapy;
• CR after consolidation chemotherapy, relapse within 12 months;
• Relapse 12 months after remission but ineffective after conventional chemotherapy;
• 2 or more relapses;
• Relapse after hematopoietic stem cell transplantation.
• Meet the diagnosis of relapsed/refractory B-ALL/LBL, including any of the following:

• Primary refractory patients who have not achieved complete response after two cycles of standard chemotherapy, or patients who have not achieved complete response after multi-line rescue chemotherapy;
• Relapse within <12 months after complete remission or ≥12 months after complete remission and fail to achieve complete remission induced by 1 or more cycles of standard treatment;
• Relapse after hematopoietic stem cell transplantation or relapse after CAR-T therapy at the same target;
• Complies with diagnosis of other relapsed/refractory CD180 positive hematologic malignancies
• Creatine clearance >60ml/min (Cockcroft and Gault formula); serum total bilirubin ≤3 times the upper limit of normal, serum ALT and AST ≤5 times the upper limit of normal range for patients without liver invasion;
• Echocardiography showing left ventricular ejection fraction (LVEF) ≥50%;
• Pulse oxygen saturation ≥92%;
• The estimated survival time is more than 3 months;
• ECOG score 0-2;
• Subjects or their legal guardians voluntarily participate in this trial and sign the informed consent form.

Exclusion criteria

Subjects who met any of the following criteria were excluded from the study:

• acute promyelocytic leukemia (APL);
• Presence of a genetic syndrome such as Fanconi's anemia, Kostmann's syndrome, Shwachman syndrome or any other known syndrome of bone marrow failure;
• Patients with uncontrolled active central nervous system leukemia (CNSL), i.e. cerebrospinal fluid grades CNS 2 and CNS 3;
• Patients who have received anti-tumor therapy before infusion should be excluded if any of the following conditions are met:

• Systemic chemotherapy (except for pretreatment) within 1 week;
• For those who have received monoclonal antibody therapy, the last time of monoclonal antibody infusion is less than 5 half-lives or 4 weeks (whichever is shorter) at screening;
• Received donor lymphocyte infusion (DLI) within 6 weeks;
• Presence of uncontrolled, serious, active infection at screening;
• Patients with a history of serious heart disease, including: severe cardiac insufficiency (subjects with cardiac insufficiency of Class III or IV according to the New York Heart Association (NYHA) cardiac function classification standard), myocardial infarction within 12 months or cardiac angioplasty or stenting, unstable angina pectoris, ECG indicating significant QT interval prolongation (>480ms) or serious arrhythmia judged by the investigator;
• Previous craniocerebral trauma, disturbance of consciousness, epilepsy, cerebral ischemia, cerebral vascular hemorrhagic disease and other medical history, and within six months of the need for drug treatment;
• Patients with hepatitis B surface antigen (HBsAg) greater than 10E6 IU/mL, hepatitis C virus (HCV) antibody positive, human immunodeficiency virus (HIV) antibody positive, syphilis antibody test positive, EBER positive or EBV copy number greater than the upper limit of normal at screening;
• Patients who must use steroid hormones during CAR-T infusion (except for local or inhaled steroid hormones); subjects who are receiving systemic steroid therapy before screening and need long-term systemic steroid therapy during treatment according to the investigator's judgment (except for inhaled or local use);
• Subjects with autoimmune diseases requiring treatment, immunodeficient subjects, or subjects requiring immunosuppressive treatment;
• Patients with acute graft-versus-host disease (GvHD) or moderate-to-severe chronic GvHD within 4 weeks prior to screening;
• Patients with a history of allergy to any component of cell products;
• Pregnant, lactating females, and subjects (male or female) of childbearing potential who are unable to use effective contraception within 1 year after cell infusion; male subjects who plan to become pregnant within 1 year after cell infusion; female subjects or partners who plan to become pregnant within 1 year after cell infusion;
• Any condition that, in the opinion of the investigator, may increase the risk to the subject or interfere with the results of the trial.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• Institute of Hematology & Blood Diseases Hospital — Tianjin

Identifiers

NCT: NCT07106749 · IIT2025076

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗