- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio 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.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 3
Contactos e Locais
Contato de estudo
- Nome: Jérôme Lambert, MD PhD
- Número de telefone: +33 +33 1 42 49 97 42
- E-mail: jerome.lambert@u-paris.fr
Estude backup de contato
- Nome: Florence Rabian, MD
- Número de telefone: +33 +33 1 42 38 51 27
- E-mail: florence.rabian@aphp.fr
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Prevenção
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Immunoglobulin Replacement therapy
|
IgRT 0.4g/Kg IV every 4 weeks for 12 months
|
|
Comparador Ativo: Antibiotic prophylaxis
|
PA following each center's guidelines, for 12 months
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Occurrence of recurrent infections
Prazo: At 12 months
|
Defined by at least 2 episodes requiring a curative systemic antibiotic treatment
|
At 12 months
|
|
Occurrence of a severe infection
Prazo: At 12 months
|
Defined by the need of hospitalization
|
At 12 months
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Cumulative hazard of severe infections
Prazo: Up to 12 months
|
requiring hospitalization
|
Up to 12 months
|
|
Infection-free survival rate
Prazo: Up to 12 months
|
Up to 12 months
|
|
|
Occurrence of COVID19 infection
Prazo: 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
Prazo: Up to 12 months
|
Up to 12 months
|
|
|
Incidence of adverse events due to IgRT and/or PA
Prazo: Up to 12 months
|
Up to 12 months
|
|
|
Dosage of immune markers
Prazo: Up to 12 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts, at lymphodepletion
|
Up to 12 months
|
|
Dosage of immune markers
Prazo: At 1 month
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 1 month
|
|
Dosage of immune markers
Prazo: At 3 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 3 months
|
|
Dosage of immune markers
Prazo: At 6 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 6 months
|
|
Dosage of immune markers
Prazo: At 9 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 9 months
|
|
Dosage of immune markers
Prazo: At 12 months
|
IgA, IgG, IgM, CD19/CD4/CD8 lymphocytes counts
|
At 12 months
|
|
Quality of life assessment
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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)
Prazo: Up to 12 months
|
Up to 12 months
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
- Neoplasias
- Doenças do sistema imunológico
- Infecções
- Doenças Virais
- Neoplasias por Tipo Histológico
- Infecções por vírus de DNA
- Doenças Linfáticas
- Distúrbios Linfoproliferativos
- Distúrbios imunoproliferativos
- Linfoma Não-Hodgkin
- Linfoma
- Infecções pelo vírus Epstein-Barr
- Infecções Herpesviridae
- Infecções por Vírus Tumorais
- Doenças hemic e linfáticas
- Linfoma de Células B
- Linfoma de Burkitt
- Aminoácidos, peptídeos e proteínas
- Proteínas
- Terapêutica
- Terapia medicamentosa
- Imunoproteínas
- Proteínas sanguíneas
- Globulinas de soro
- Globulins
- Quimioprevenção
- Premedicação
- Imunoglobulinas
- Profilaxia antibiótica
Outros números de identificação do estudo
- APHP241013
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