- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07754682
Immunoglobulin Replacement Therapy (IgRT) Versus Antibiotic Prophylaxis (PA) in Patients Treated by CD19-targeted Chimeric Antigen Receptor (CAR)T Cells for a B Cell Acute Lymphoblastic Leukemia or a B Cell Lymphoma (PREV-CART)
A Multicentric Phase III Randomized Clinical Trial Open-label, Comparing Immunoglobulin Replacement Therapy (IgRT) and Antibiotic Prophylaxis (AP) in Patients Treated by CD19-targeted Chimeric Antigen Receptor (CAR)T Cells for a B Cell Acute Lymphoblastic Leukemia or a B Cell Lymphoma
B cell (CD19) targeted chimeric antigen receptor modified T Cells (CAR-T) has transformed treatment of relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL) or B-cell lymphoma (BCL).
Because patients receiving CAR-T often present uncontrolled disease and have undergone several lines of treatment, they may be deeply immuno-depressed and prone to infections. Hypogammaglobulinemia were reported in 74% of patients preCAR-T cells infusion (Hill JA, et al. Blood Rev. 2019 Nov). CART cells also results in depletion of normal CD19+ B cells and hypogammaglobulinemia as an on-target, off tumor toxicity.
Because CAR-T cells can persist for years, patients are exposed to infectious complications secondary to long-term Bcell aplasia and severe hypogammaglobulinemia (<4g/l). Data from patients who received rituximab (CD20-specific monoclonal antibody) show that patients with severe hypogammaglobulinemia experienced recurrent bronchitis, sinusitis, pneumonia, and rarely, enteroviral meningoencephalitis. In patients receiving CAR T-cells, infection density is 0.55-0.67 infections/100 days3,5 at risk after the first month with a majority of respiratory and ENT (earsnose-throat) infections. To prevent infections, anti-bacterial prophylaxis (AP) based on local guidelines is often used in patients treated by CAR-T cells, with the risk of subsequent resistance. Otherwise, intravenous immunoglobulin replacement therapy (IgRT) is authorized by the French authorities for patients with secondary antibody deficiencies who developed severe or recurrent infections after appropriate antimicrobial therapy, if IgG levels <4g/l. However, although IgRT as primary prophylaxis (PP) have no approval, they are used as PP after CAR T-cells by many centers, with no data supporting such a strategy. The benefit of IgRT over AP as a primary prophylaxis in the setting of CD19 CAR-T cells therapy should be demonstrated given its burden for patients and care, as well as its cost and the risk of Ig shortage. Therefore, this multi-centric prospective randomized openlabel study aims to assess the benefits of IgRT versus AP as PP in patients with secondary antibody deficiencies.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 3
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Jérôme Lambert, MD PhD
- Número de teléfono: +33 +33 1 42 49 97 42
- Correo electrónico: jerome.lambert@u-paris.fr
Copia de seguridad de contactos de estudio
- Nombre: Florence Rabian, MD
- Número de teléfono: +33 +33 1 42 38 51 27
- Correo electrónico: florence.rabian@aphp.fr
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age 16-80 years at inclusion
- B-cell acute lymphoblastic leukemia or a B-cell lymphoma
- With gamma globulins <4g/L at the time of screening
- Receiving CD19-targeted autologous CAR-T cells (with AMM in their indication)
- Patients with childbearing potential* should have reliable contraception for the all duration of the study and another 12 months after CAR-T infusion.
- Contraceptive measures for concerned patients
- Informed consent signed by patient or legal representatives
Exclusion Criteria:
- Any medical history of intolerance to intravenous immunoglobulin
- With renal failure calculated glomerular filtrate rate <30 mL / min;
- With hepatic failure or hepatitis or bilirubin> 3 times the upper limit of normal, Serum ALT/AST >=5N
- With existing serious acute infection
- Contraindication to immunoglobulin or to prophylactic antibiotherapy administered in this clinical trial
- No health insurance coverage
- Females who are pregnant or breastfeeding
- Participation in another interventional study or being
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Immunoglobulin Replacement therapy
|
IgRT 0.4g/Kg IV every 4 weeks for 12 months
|
|
Comparador activo: Antibiotic prophylaxis
|
PA following each center's guidelines, for 12 months
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Occurrence of recurrent infections
Periodo de tiempo: At 12 months
|
Defined by at least 2 episodes requiring a curative systemic antibiotic treatment
|
At 12 months
|
|
Occurrence of a severe infection
Periodo de tiempo: At 12 months
|
Defined by the need of hospitalization
|
At 12 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Cumulative hazard of severe infections
Periodo de tiempo: Up to 12 months
|
requiring hospitalization
|
Up to 12 months
|
|
Infection-free survival rate
Periodo de tiempo: Up to 12 months
|
Up to 12 months
|
|
|
Occurrence of COVID19 infection
Periodo de tiempo: Up to 12 months
|
Up to 12 months
|
|
|
Cumulative incidence of readmissions due to infectious episode after hospital discharge following the infusion of CART cells
Periodo de tiempo: Up to 12 months
|
Up to 12 months
|
|
|
Incidence of adverse events due to IgRT and/or PA
Periodo de tiempo: Up to 12 months
|
Up to 12 months
|
|
|
Dosage of immune markers
Periodo de tiempo: Up to 12 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts, at lymphodepletion
|
Up to 12 months
|
|
Dosage of immune markers
Periodo de tiempo: At 1 month
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 1 month
|
|
Dosage of immune markers
Periodo de tiempo: At 3 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 3 months
|
|
Dosage of immune markers
Periodo de tiempo: At 6 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 6 months
|
|
Dosage of immune markers
Periodo de tiempo: At 9 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 9 months
|
|
Dosage of immune markers
Periodo de tiempo: At 12 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 12 months
|
|
Quality of life assessment
Periodo de tiempo: At 3 months
|
EQ5D5L : standardized measure of health-related quality of life assessing five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.
The EQ-5D-5L index score typically ranges from values below 0 (health states considered worse than death) to 1.0 (full health), depending on the country-specific value set.
Higher scores indicate better health-related quality of life.
|
At 3 months
|
|
Quality of life assessment
Periodo de tiempo: At 6 months
|
EQ5D5L : standardized measure of health-related quality of life assessing five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.
The EQ-5D-5L index score typically ranges from values below 0 (health states considered worse than death) to 1.0 (full health), depending on the country-specific value set.
Higher scores indicate better health-related quality of life.
|
At 6 months
|
|
Quality of life assessment
Periodo de tiempo: At 9 months
|
EQ5D5L : standardized measure of health-related quality of life assessing five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.
The EQ-5D-5L index score typically ranges from values below 0 (health states considered worse than death) to 1.0 (full health), depending on the country-specific value set.
Higher scores indicate better health-related quality of life.
|
At 9 months
|
|
Quality of life assessment
Periodo de tiempo: At 12 months
|
EQ5D5L : standardized measure of health-related quality of life assessing five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.
The EQ-5D-5L index score typically ranges from values below 0 (health states considered worse than death) to 1.0 (full health), depending on the country-specific value set.
Higher scores indicate better health-related quality of life.
|
At 12 months
|
|
Quality of life assessment
Periodo de tiempo: At 3 months
|
EORTC QLQ-C30 : cancer-specific questionnaire designed to assess health-related quality of life in patients with cancer.
Scores are linearly transformed to a 0-100 scale.
For the Global Health Status/Quality of Life scale and the functional scales, higher scores indicate better quality of life and functioning.
For symptom scales, higher scores indicate greater symptom burden and poorer health status.
|
At 3 months
|
|
Quality of life assessment
Periodo de tiempo: At 6 months
|
EORTC QLQ-C30 : cancer-specific questionnaire designed to assess health-related quality of life in patients with cancer.
Scores are linearly transformed to a 0-100 scale.
For the Global Health Status/Quality of Life scale and the functional scales, higher scores indicate better quality of life and functioning.
For symptom scales, higher scores indicate greater symptom burden and poorer health status.
|
At 6 months
|
|
Quality of life assessment
Periodo de tiempo: At 9 months
|
EORTC QLQ-C30 : cancer-specific questionnaire designed to assess health-related quality of life in patients with cancer.
Scores are linearly transformed to a 0-100 scale.
For the Global Health Status/Quality of Life scale and the functional scales, higher scores indicate better quality of life and functioning.
For symptom scales, higher scores indicate greater symptom burden and poorer health status.
|
At 9 months
|
|
Quality of life assessment
Periodo de tiempo: At 12 months
|
EORTC QLQ-C30 : cancer-specific questionnaire designed to assess health-related quality of life in patients with cancer.
Scores are linearly transformed to a 0-100 scale.
For the Global Health Status/Quality of Life scale and the functional scales, higher scores indicate better quality of life and functioning.
For symptom scales, higher scores indicate greater symptom burden and poorer health status.
|
At 12 months
|
|
Incremental Cost-Effectiveness Ratio (ICER)
Periodo de tiempo: Up to 12 months
|
Up to 12 months
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
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
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
- Infecciones por el virus de Epstein-Barr
- Infecciones por herpesviridae
- Infecciones por virus tumorales
- Enfermedades hemic y linfáticas
- Linfoma de células B
- Linfoma de Burkitt
- Aminoácidos, péptidos y proteínas
- Proteínas
- Terapéutica
- Terapia con drogas
- Inmunoproteínas
- Proteínas de la sangre
- Globulinas séricas
- Globulinas
- Quimioprevención
- Premedicación
- Inmunoglobulinas
- Profilaxis antibiótica
Otros números de identificación del estudio
- APHP241013
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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