Clinical trial · Interventional
CIK Cell Therapy for Relapsed or Refractory Acute B-Lymphoblastic Leukemia: Prognostic Impact on Patients With Early CAR-T Cell Dysfunction
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
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Acute Lymphoblastic Leukemia, in Relapse | Acute Lymphoblastic Leukemia | CURATED_BROADER | 0.78 |
| B-cell Acute Lymphoblastic Leukemia | B Acute Lymphoblastic Leukemia | ALIAS | 0.90 |
| Refractory Acute Lymphoid Leukemia | Acute Lymphoblastic Leukemia | CURATED_BROADER | 0.78 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CIK cell | Drug | — | UNRESOLVED |
| peripheral blood lymphocytes | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- PLACEBO_COMPARATOR
- label
- peripheral blood lymphocytes
- interventionNames
- Drug: peripheral blood lymphocytes
- type
- EXPERIMENTAL
- label
- CIK cells
- interventionNames
- Drug: CIK cell
Primary outcomes (1)
- measure
- Event-free survival(EFS) in CIK infusion group
- timeFrame
- 2-year EFS rate
- description
- EFS is defined as the time from CIK-cell infusion to the earliest relapse, death from any cause, or treatment failure
Secondary outcomes (4)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 1 Year
- Maximum age
- 39 Years
Show eligibility criteria text
Inclusion Criteria: * A patient must meet all of the following to be enrolled: 1. 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. 2. Loss of CAR-T cell activity within 6 months after previous CAR-T therapy and no relapse. 3. Age between 1 and 39 years old. 4. No severe allergic constitution. 5. Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2. 6. Life expectancy, as judged by the investigator, of at least 60 days. 7. 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: 1. Received bendamustine treatment within the past 9 months; 2. Intracranial hypertension or impaired consciousness in the brain; 3. Symptomatic heart failure or severe arrhythmia; 4. Symptoms of severe respiratory failure; 5. With other types of malignant tumors; 6. Disseminated intravascular coagulation; 7. Serum creatinine and/or blood urea nitrogen ≥ 1.5 times the normal value; 8. Suffering from sepsis or other uncontrollable infections; 9. Uncontrollable diabetes; 10. Severe mental disorders; 11. Significant lesions in the brain as detected by head magnetic resonance imaging; 12. Leukemic cells in the cerebrospinal fluid \>20 cells/μL; 13. Peripheral blood leukemic cell proportion \>30%; 14. Have undergone organ transplantation; 15. Female patients (those with childbearing potential) are pregnant or lactating; 16. Active or uncontrollable infectious diseases, such as hepatitis (HBV, HCV), HIV, or syphilis.
References
Publications (0)
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