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NCT Number: NCT06389305

CIK Cell Therapy for Relapsed or Refractory Acute B-Lymphoblastic Leukemia: Prognostic Impact on Patients With Early CAR-T Cell Dysfunction

This is a single-center, double-blind, randomized trial. Patients with relapsed or refractory acute B-lymphoblastic leukemia(r/r B-ALL) experiencing early functional exhaustion of CAR-T cells will be randomly allocated into three groups: the control cell group, the CIK treatment group, and the messenger RNA(mRNA)-CIK treatment group. The primary objective of the study is to evaluate the prognostic impact of CIK cell therapy on the early functional exhaustion of CAR-T cells in children and adolescent and young adult (AYA) with r/r B-ALL. The primary endpoint of the study is the event-free survival rate of these patient in the CIK cell therapy group.A total number of 213 subjects will be enrolled.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • A patient must meet all of the following to be enrolled:
  • A confirmed diagnosis of refractory or relapsed B-ALL (criteria reference: NCCN, 2024.4), where all patients meet the National Comprehensive Cancer Network(NCCN) guidelines for the diagnosis of acute lymphoblastic leukemia (hematopathological examination of bone marrow aspirate and biopsy tissue showing ≥20% lymphoblasts in the bone marrow, confirmed by comprehensive flow cytometry (FCM) immunotyping, minimal residual disease analysis, and G-banded metaphase chromosome karyotype analysis). Molecular characteristics can be described through methods such as interphase fluorescence in situ hybridization (FISH) testing, reverse transcription polymerase chain reaction (RT-PCR) testing, and next-generation sequencing (NGS) for comprehensive detection of fusion genes and pathogenic mutations. Determination can also be made by the World Health Organization's subtypes of acute lymphoblastic leukemia, as well as cytogenetic and clinical risk groups.
  • Loss of CAR-T cell activity within 6 months after previous CAR-T therapy and no relapse.
  • Age between 1 and 39 years old.
  • No severe allergic constitution.
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2.
  • Life expectancy, as judged by the investigator, of at least 60 days.
  • Patients with self-awareness between 8 and 39 years of age voluntarily sign an informed consent, and the legal representative (guardians) of child patients under 18 years of age voluntarily signs an informed consent.

Exclusion criteria

  • A patient with at least one of the following conditions will be excluded:
  • Received bendamustine treatment within the past 9 months;
  • Intracranial hypertension or impaired consciousness in the brain;
  • Symptomatic heart failure or severe arrhythmia;
  • Symptoms of severe respiratory failure;
  • With other types of malignant tumors;
  • Disseminated intravascular coagulation;
  • Serum creatinine and/or blood urea nitrogen ≥ 1.5 times the normal value;
  • Suffering from sepsis or other uncontrollable infections;
  • Uncontrollable diabetes;
  • Severe mental disorders;
  • Significant lesions in the brain as detected by head magnetic resonance imaging;
  • Leukemic cells in the cerebrospinal fluid >20 cells/μL;
  • Peripheral blood leukemic cell proportion >30%;
  • Have undergone organ transplantation;
  • Female patients (those with childbearing potential) are pregnant or lactating;
  • Active or uncontrollable infectious diseases, such as hepatitis (HBV, HCV), HIV, or syphilis.

Treatment and study plan

peripheral blood lymphocytes

Drug

autologous or allogeneic peripheral blood lymphocytes

CIK cell

Drug

autologous or allogeneic cytokine-induced killer (CIK) cells

Primary outcomes

  1. Event-free survival(EFS) in CIK infusion group

    Time frame: 2-year EFS rate

    EFS is defined as the time from CIK-cell infusion to the earliest relapse, death from any cause, or treatment failure

Secondary outcomes

  1. Progression-free survival(PFS) in CIK infusion group

    Time frame: 2-year PFS rate

    PFS is defined as the time from CIK-cell infusion until objective tumor progression or death depending on study protocol

  2. Duration of response(DOR) in CIK infusion group

    Time frame: from enrollment to the end of treatment at 15 years

    DOR is defined as the time interval from the earliest qualifying minimal residual disease-negative response [i.e. complete remission(CR),complete remission with partial hematological recovery(CRh), complete remission with incomplete hematological recovery(CRi), morphologic leukemia-free state(MLFS), or aplastic marrow (patients with blood and bone marrow disease), central nervous system(CNS) remission (patients with CNS disease) and complete resolution of the lymphomatous enlargement by CT or positron emission tomography(PET)-CT negative (for patients with a previous positive PET-CT) (patients with lymphomatous extramedullary disease)] to the date of relapse or death from any cause.

  3. Overall survival(OS) in CIK infusion group

    Time frame: from enrollment to the end of treatment at 15 years

    OS is defined as the time from CIK-cell infusion to death from any cause.

  4. EFS in mRNA-CIK infusion group

    Time frame: 2-year EFS rate

    EFS is defined as the time from mRNA-CIK-cell infusion to the earliest relapse, death from any cause, or treatment failure

Study contacts

Contact information is provided by the study sponsor or research team.

Tengyu Wang

CONTACT

[email protected]

86+18333186020

Sponsors and collaborators

Lead sponsor

Beijing GoBroad Hospital

Other

Registry information

Official study title

Cytokine-induced Killer(CIK) Cell Therapy and Its Impact on Early Functional Exhaustion of Chimeric Antigen Receptor-T(CAR-T) Cells in Relapsed or Refractory Acute B-Lymphoblastic Leukemia: A Prospective Study

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Apr 29, 2024
Registry last updated
Feb 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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