- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT01793025
Mismatched Donor Cells to Treat Acute Myeloid Leukemia (ATAC-AML-01)
28 de agosto de 2017 atualizado por: Elizabeth Krakow, Maisonneuve-Rosemont Hospital
Adoptive Transfer of Alloreactive Cells to Treat Patients With Poor-Prognosis Acute Myeloid Leukemia-01
The purpose of this study is to assess the safety and efficacy of infusing immune cells from a donor as treatment for patients with acute myeloid leukemia that is resistant to chemotherapy or who have experienced relapse.
Unlike standard bone marrow or stem cell transplantation which uses donors who are well 'matched' to the patient, this study uses donors whose immune cells are not compatible with the patient.
With standard stem cell or bone marrow transplantation, the well-matched immune cells will attack the leukemia but they also attack the patient's organs (a situation called graft-versus-host disease, which can persist in the long term).
Our hypothesis is that the mismatched donor cells will fight the leukemia but will then be eliminated from the patient's body, so long-term side effects like graft-versus-host disease should not occur.
Visão geral do estudo
Status
Desconhecido
Condições
Intervenção / Tratamento
Descrição detalhada
The ATAC cell therapy product contains unselected, non-mobilized peripheral blood mononuclear cells from related donors who are mismatched to the recipients at 3 or more (out of 6) HLA loci.
Cohorts of 3 patients will be treated at each of four pre-specified dose levels (T cells per kg recipient weight).
One ATAC infusion is administered 24-48 hours following re-induction chemotherapy (for relapsed or primary refractory AML patients not in remission).
In situations where ATAC infusion is not available immediately following re-induction chemotherapy and patients nonetheless achieve complete remission, one ATAC infusion is given 24-48 hours after consolidation chemotherapy.
Tipo de estudo
Intervencional
Inscrição (Antecipado)
12
Estágio
- Fase 1
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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Quebec
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Montreal, Quebec, Canadá, H1T 3M4
- Recrutamento
- Hopital Maisonneuve-Rosemont
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
18 anos e mais velhos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Descrição
Recipient Inclusion Criteria:
- Age ≥ 18 years (no upper age limit, but physician discretion is advised)
- AML that is refractory to 2 courses of induction therapy (that together constitute the 'first-line' therapy) or that has relapsed after a period of morphologic complete remission or morphologic remission with incomplete blood count recovery (CRi)
- Candidacy for intense induction chemotherapy (ECOG 0-2, adequate renal, liver and cardiac function, absence of uncontrolled infections)
- Availability of parents, siblings or children who are HLA haploidentical (and not homozygous for the shared haplotype), who are deemed suitable donors after medical evaluation, and who complete peripheral blood mononuclear cell collection
- No history of autologous or allogeneic stem cell transplant, purine analog chemotherapy or cyclophosphamide, or total body irradiation
- Ability to comprehend the investigational nature of the study and provide informed consent
Recipient Exclusion Criteria:
- Acute promyelocytic leukemia (including those with non-classical rearrangements of RARα)
- History of severe myelodysplastic syndrome clearly preceding the diagnosis of AML (i.e., red cell transfusion dependence or erythropoietin dependence over a 4-month period, or in the absence of a clear cause, any of the following: hemoglobin consistently below 9 g/dL or platelets below 50 x 10^9/L or ANC below 1000/uL on 2 or more occasions 2 weeks apart, or use of G-CSF to maintain the ANC threshold in the absence of infection, in the 3 months preceding the diagnosis of AML). Exception: If ATAC therapy is being considered as a bridge to stem cell transplantation in patients with an available standard transplant donor (familial, unrelated, or cord blood), this exclusion criterion does not apply.
- Grade 2-3/3 fibrosis in the diagnostic bone marrow biopsy
- DLCO < 40% predicted
- Left ventricular ejection fraction < 40% (evaluated by ECHO or MUGA)
- AST/SGOT > 2.5 x ULN
- Bilirubin > 1.5 x ULN
- Creatinine > 1.5 x ULN
- Creatinine clearance < 50 mL/min
- HIV positive
- Major anticipated illness or organ failure incompatible with survival from chemotherapy
- Concurrent second primary cancer or a prior malignancy that required cytotoxic treatment within the past 12 months, other than cervical carcinoma in-situ or prostate cancer in-situ
- Severe psychiatric illness or mental deficiency sufficiently severe as to make compliance with the treatment unlikely and informed consent impossible
- Any congenital or acquired immunodeficiency that would possibly permit permanent engraftment of donor cells
- Receiving systemic steroid therapy or systemic immunosuppression such as cyclosporine or TNF-inhibitors
- Prior or concurrent receipt of any marketed or investigational agent deemed on an ad hoc basis to cause immunomodulation, pose a threat of permanent engraftment or increase the risk of GVHD.
Donor inclusion criteria:
- Mismatched family donor (incompatibility at 3 loci HLA-A, B and DR of the unshared haplotype, or higher-order incompatibility)
- Age ≥ 16 and ≤ 80 years
- Fit to undergo apheresis (normal blood counts, normotensive and no history of stroke).
- Donor has been tested negative for HIV-1, HIV-2, hepatitis B virus (HBV, surface and core antigen), hepatitis C virus, human T-lymphotropic virus types I/II, and Treponema pallidum (syphilis).
- ECOG performance status of 2 or less.
- Adequate veins for leukapheresis or agree to placement of a temporary central venous catheter.
- Donor must provide written informed consent.
- Where multiple equally-suitable donors are available, sex mismatched donors will be preferred.
Donor exclusion criteria:
- Medically uncontrolled coronary heart disease
- Myocardial infarction within the last 3 months
- History of seizure
- History of stroke
- History of malignancy (except basal cell or squamous carcinoma of the skin, or positive PAP smear and subsequent negative follow-up)
- Presence of a transmissible disease (such as HIV seropositivity)
- Presence of a major illness or a suspected systemic dysfunction
- Presence of an an active inflammatory or autoimmune disorder
- Female donors who are pregnant or nursing
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: ATAC Therapy
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Unselected peripheral blood mononuclear cells given 24-48 hours after induction or consolidation chemotherapy
Outros nomes:
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Safety
Prazo: 60 days (up to 2 years)
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Maximum tolerated cell dose: Dose at which < 33% of patients experienced dose-limiting toxicity.
If no DLT occurs, then dose titration will stop at a pre-specified number of T cells/kg.
Four dose-level cohorts are planned.
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60 days (up to 2 years)
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Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
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Treatment-related mortality
Prazo: Continuous up to 2 years
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Continuous up to 2 years
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Non-relapse mortality
Prazo: Continuous up to 2 years
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Continuous up to 2 years
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Incidence of graft-versus-host disease
Prazo: Continuous up to 2 years
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Continuous up to 2 years
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Duration of cytopenias
Prazo: Monitored continuously from ATAC infusion until peripheral blood count recovery or maximum 2 years (whichever is earlier)
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Monitored continuously from ATAC infusion until peripheral blood count recovery or maximum 2 years (whichever is earlier)
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Overall survival
Prazo: Continuous up to 2 years
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Continuous up to 2 years
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Complete and incomplete remissions (CR, CRi)
Prazo: Day 60 post cell infusion
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Day 60 post cell infusion
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Relapse-free survival
Prazo: Continuous up to 2 years
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Continuous up to 2 years
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Investigadores
- Cadeira de estudo: Jean-Sébastien Delisle, MD,PhD, Hôpital Maisonneuve-Rosemont and Université de Montréal
- Investigador principal: Elizabeth Krakow, MD, Hôpital Maisonneuve-Rosemont and Université de Montréal
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo
1 de setembro de 2012
Conclusão Primária (Antecipado)
1 de dezembro de 2018
Conclusão do estudo (Antecipado)
1 de dezembro de 2018
Datas de inscrição no estudo
Enviado pela primeira vez
10 de fevereiro de 2013
Enviado pela primeira vez que atendeu aos critérios de CQ
13 de fevereiro de 2013
Primeira postagem (Estimativa)
15 de fevereiro de 2013
Atualizações de registro de estudo
Última Atualização Postada (Real)
30 de agosto de 2017
Última atualização enviada que atendeu aos critérios de controle de qualidade
28 de agosto de 2017
Última verificação
1 de agosto de 2017
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- ATAC-AML-01
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .