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- Ensayo clínico NCT07575919
Targeted CD22/CD19 CAR-T Therapy for Consolidation in Standard-Risk B-ALL
An Exploratory Study on Targeted CD22/CD19 Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy for Enhanced Consolidation Therapy of Standard-risk B-cell Acute Lymphoblastic Leukemia
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Li-Ping Dou, Dr.
- Número de teléfono: +8613681207138
- Correo electrónico: lipingruirui@163.com
Ubicaciones de estudio
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Beijing Municipality
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Beijing, Beijing Municipality, Porcelana, 100853
- Reclutamiento
- Chinese PLA General Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Patients who have provided written informed consent and are willing and able to comply with study procedures, including scheduled visits, treatment, laboratory tests, and other study-related assessments.
- Patients with cytologically or histologically confirmed B-cell acute lymphoblastic leukemia/lymphoma (B-ALL/LBL) according to WHO 2022 criteria, with CD19-positive and/or CD22-positive disease. Patients must have achieved first morphological complete remission (CR1; bone marrow blasts <5%) after standard induction chemotherapy. Patients may or may not have achieved deep remission, defined as minimal residual disease (MRD) negativity assessed by flow cytometry and/or molecular methods (e.g., quantitative PCR or next-generation sequencing).
- Adult patients with standard-risk B-cell acute lymphoblastic leukemia , as defined by cytogenetic and molecular risk stratification and without high-risk features, who have achieved complete remission (CR) after treatment, received two cycles of long-course intensive consolidation chemotherapy, maintained sustained bone marrow MRD negativity by multiparameter flow cytometry (MFC) and sustained molecular MRD negativity by real-time quantitative polymerase chain reaction (RT-qPCR) or next-generation sequencing (NGS), are not considered to require allogeneic hematopoietic stem cell transplantation (allo-HSCT) for consolidation, and refuse or are ineligible to receive CD19/CD3 bispecific antibody therapy (e.g., blinatumomab), and are therefore planned to receive CAR-T cell immunotherapy as enhanced consolidation therapy followed by long-term maintenance treatment.
- Age between 18 and 85 years, regardless of sex.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
- Estimated life expectancy ≥3 months.
- Hemoglobin ≥60 g/L (transfusion allowed).
- Absolute neutrophil count ≥1,000/μL and platelet count ≥45,000/μL.
- Adequate organ function, defined as:
Total bilirubin ≤1.5 × upper limit of normal (ULN) (except Gilbert's syndrome); ALT and AST ≤2.5 × ULN; Serum creatinine ≤1.5 × ULN or creatinine clearance ≥60 mL/min (Cockcroft-Gault formula); Left ventricular ejection fraction (LVEF) ≥50%, no clinically significant arrhythmia, and no pericardial effusion; Baseline oxygen saturation >92% on room air; No clinically significant pleural effusion.
10. Subjects of reproductive potential must agree to use effective contraception from enrollment until at least 6 months after completion of the study. Subjects who are pregnant or suspected to be pregnant must notify the investigator immediately.
Exclusion Criteria:
Patients with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL), or with risk factors indicating the need for allogeneic hematopoietic stem cell transplantation, who are planned to receive allogeneic hematopoietic stem cell transplantation or CD19/CD3 bispecific antibody (blinatumomab) therapy and refuse CAR-T cell immunotherapy as consolidation treatment, including any of the following conditions:
① Early relapse within 6 months after achieving first complete remission;
② Primary refractory disease, defined as failure to achieve first morphological complete remission after two cycles of standard first-line induction chemotherapy;
③ Failure to achieve complete remission or relapse after first-line or multiple lines of salvage chemotherapy;
④ Relapse after allogeneic hematopoietic stem cell transplantation;
⑤ Persistent MRD positivity with a high risk of relapse.
- Prior treatment with any CAR-T cell therapy or other genetically modified T-cell therapies.
Known history of HIV infection, active hepatitis B virus (HBV) infection, or any uncontrolled active systemic infection requiring intravenous antibiotics.
(Active HBV infection is defined as: HBV DNA ≥2000 IU/mL, ALT ≥2×ULN, and exclusion of other causes of hepatitis.)
Non-disease-related hepatic or renal dysfunction defined as:
ALT or AST >3×ULN; Total bilirubin >2×ULN; Creatinine clearance <30 mL/min.
- History of significant cardiovascular disease within 12 months prior to enrollment, including myocardial infarction, coronary intervention, unstable angina, or clinically significant arrhythmia.
- Other severe or uncontrolled medical conditions that may interfere with study participation or outcomes, including but not limited to uncontrolled diabetes, severe gastrointestinal disease, severe cardiopulmonary disease, autoimmune disease, immunodeficiency, or uncontrolled infections.
- History of severe immediate hypersensitivity reactions to study-related drugs, aminoglycosides, or biologic agents.
- Pregnant or breastfeeding women.
- Patients who are unable or unwilling to comply with study procedures or follow-up, or who have poor adherence as judged by the investigator.
- History of other malignancies unless disease-free for at least 3 years without active treatment (except for adequately treated non-melanoma skin cancer or carcinoma in situ).
- Receipt of live vaccines within 6 weeks prior to initiation of lymphodepleting chemotherapy.
- Major surgery within 14 days prior to enrollment or planned major surgery during the study period.
- Any other condition that, in the investigator's judgment, may increase risk, interfere with study results, or make the patient unsuitable for the study.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: CD22/CD19 Dual-Target CAR-T Cell Therapy
Patients will receive CD22/CD19 dual-target CAR-T cell therapy following lymphodepleting chemotherapy.
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Autologous CD22/CD19 dual-target chimeric antigen receptor T cells
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
2-year Event-Free Survival Rate (EFSR)
Periodo de tiempo: 2 years after CAR-T cell infusion
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The 2-year event-free survival rate after CD22/CD19 CAR-T cell therapy used as enhanced consolidation treatment in high-risk B-cell acute lymphoblastic leukemia.
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2 years after CAR-T cell infusion
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Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Overall Survival (OS)
Periodo de tiempo: Up to 2 years after CAR-T cell infusion
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Up to 2 years after CAR-T cell infusion
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Progression-Free Survival (PFS)
Periodo de tiempo: Up to 2 years after CAR-T cell infusion
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Up to 2 years after CAR-T cell infusion
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Time to Progression (TTP)
Periodo de tiempo: Up to 2 years after CAR-T cell infusion
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Up to 2 years after CAR-T cell infusion
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Disease-Free Survival (DFS)
Periodo de tiempo: Up to 2 years after CAR-T cell infusion
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Up to 2 years after CAR-T cell infusion
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Duration of Response (DOR)
Periodo de tiempo: Up to 2 years after CAR-T cell infusion
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Up to 2 years after CAR-T cell infusion
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Relapse Rate
Periodo de tiempo: Up to 2 years after CAR-T cell infusion
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Up to 2 years after CAR-T cell infusion
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Mortality Rate
Periodo de tiempo: Up to 2 years after CAR-T cell infusion
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Up to 2 years after CAR-T cell infusion
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Neoplasias
- Enfermedades del sistema inmunológico
- Infecciones
- Enfermedades virales
- Neoplasias por tipo histológico
- Infecciones por virus de ADN
- Enfermedades linfáticas
- Trastornos linfoproliferativos
- Trastornos inmunoproliferativos
- Linfoma No Hodgkin
- Linfoma de células B
- Linfoma
- Infecciones por el virus de Epstein-Barr
- Infecciones por herpesviridae
- Infecciones por virus tumorales
- Enfermedades hemic y linfáticas
- Linfoma de Burkitt
Otros números de identificación del estudio
- S2025-1061-02
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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