- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT03087929
Follow-up Trial of Rituximab Interferon Transplant Trial: Study Drug-Rituximab and Alpha Interferon
17 de março de 2017 atualizado por: Dr. Neil Berinstein, Sunnybrook Health Sciences Centre
Phase II Follow-up Trial of Rituximab Interferon Transplant Trial: Study Drug-Rituximab and Alpha Interferon
A previous phase II trial entitled Treatment of Follicular non-Hodgkin's Lymphoma with High Dose Therapy and Stem Cell Support Followed by Consolidative Immunotherapy with Rituximab and Alpha Interferon was conducted at the Odette Cancer Centre between 2005 and 2012.
The primary objectives of this previous trial was to assess progression free survival and overall survival.
Of the 36 patients in this trial, approximately 18 remain in remission.
In this new follow up trial, follow up data will prospectively be collected on patients who provide informed consent to do so.
Visão geral do estudo
Tipo de estudo
Observacional
Inscrição (Real)
12
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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Ontario
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Toronto, Ontario, Canadá, M4N 3M5
- Sunnybrook Health Sciences Centre, Odette Cancer Centre
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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 a 65 anos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Sim
Gêneros Elegíveis para o Estudo
Tudo
Método de amostragem
Amostra Não Probabilística
População do estudo
Twelve patients with low grade follicular lymphoma who consented to long term follow-up and were previously treated with high dose therapy and autologous stem cell transplant with rituximab and alpha interferon as part of the phase II trial Treatment of Follicular Non-Hodgkin's Lymphoma with High Dose Therapy and Stem Cell Support Followed by Consolidative Immunotherapy with Rituximab and Alpha Interferon.
Descrição
Inclusion Criteria:
- Patients with 1-2 relapses of WHO Classification follicle centre NHL grade 1-2/3. Patients must have achieved at least a PR to previous treatment.
- Central pathology review before registration
- Ann Arbor stage III or IV
- Measurable disease: defined as clinically or radiologically documented disease with at least one site bidimensionally measurable using clinical exam, CT or MRI performed in the 3 weeks prior to study enrollment.
- ECOG performance status of <2.
- Patients may have received not more than 1 prior course (4 infusions) of rituximab. Timing from last dose of rituximab must exceed 6 months prior to registration. Patients must have demonstrated at least a PR to rituximab if previously administered.
- Patient consent according to institutional and university human experimentation committee requirements
Adequate Renal, hepatic and hematopoietic function test unless the abnormal values are thought to be due to involvement with lymphoma as defined by:
- Hb> 85
- ANC >1000/mm3
- Platelets >100,000/mm3
- Serum/Total Bilirubin >=2 SI units
- AST/ALT <2x Upper Limit of Normal
Exclusion Criteria:
- Positive serology for HIV
- Uncontrolled Infection
- Pregnancy
- CNS Metastases
- History of Psychiatric Disorder
- Other Malignancy (except nonmelanoma skin cancer)
- Serious non-malignant disease (e.g., congestive heart failure, or active uncontrolled bacterial, viral, or fungal infections), or other conditions, which, in the opinion of the investigator and/or the sponsor, would compromise other protocol objectives.
- Major surgery, other than diagnostic surgery, within four weeks.
- Presence of anti-murine antibody (HAMA) reactivity. These laboratory results must be available prior to receiving treatment for those patients
- who have received prior murine proteins or patients who have allergies to murine proteins.
- New York Heart Association Class III or IV heart disease (see Appendix H, Clinical Evaluation of Functional Capacity of Patients with Heart Disease in Relation to Ordinary Physical Activity) or myocardial infarction within the past six months.
- Treatment with an investigational drug within 30 days or five half-lives (of the study drug with the longest half-life) prior to entry into the study, which ever is longer.
- Previous chemotherapy, immunotherapy, radiotherapy, or investigational therapy for the treatment of other malignancy except basal cell or squamous cell skin cancer or carcinoma in situ of the cervix within the last 5 years.
- History of allergic reactions to compounds chemically related to Rituximab.
- Refusal to practice contraception if of reproductive potential.
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
Coortes e Intervenções
Grupo / Coorte |
Intervenção / Tratamento |
|---|---|
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Treatment Arm
Patients who had previously undergone high dose therapy with stem cell support followed by consolidation with Rituximab and alpha-interferon as part of the trial Treatment of Follicular non-Hodgkin's Lymphoma with High Dose Therapy and Stem Cell Support Followed by Consolidative Immunotherapy with Rituximab and Alpha Interferon.
The patients in this arm have consented to long-term follow up.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Overall survival
Prazo: through study completion, up to 15 years
|
Number of months from date of enrollment to date of death or last follow-up, whichever comes first.
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through study completion, up to 15 years
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Progression-free survival
Prazo: through study completion, up to 15 years
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Number of months from date of enrollment to date of progression.
Progression is defined as a greater than or equal to 50% increase in the sum of the product of measurable lesions.
Appearance of new lesions will also constitute progressive disease.
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through study completion, up to 15 years
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Event-free survival
Prazo: through study completion, up to 15 years
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Number of months from date of enrollment to date of an event.
An event is defined as death, disease progression, transformation, or development of secondary malignancy.
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through study completion, up to 15 years
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Adverse events possibly or probably related to transplant
Prazo: through study completion, up to 15 years
|
Adverse events include second malignancies, myelodysplastic syndrome (MDS), hypogammaglobulinemia, and pulmonary fibrosis.
This outcome measurement is descriptive.
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through study completion, up to 15 years
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Minimal Residual Disease
Prazo: through study completion, up to 15 years
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This exploratory endpoint is used to evaluate the detection of recurrent lymphoma in peripheral blood DNA.
It is measured as real-time quantitative polymerase chain reaction (RQ-PCR) and is expressed as a percent of detection per 100,000 cells at each follow-up time point.
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through study completion, up to 15 years
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Investigadores
- Investigador principal: Neil Berinstein, MD, Sunnybrook Health Sciences Centre
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 (Real)
20 de setembro de 2013
Conclusão Primária (Real)
15 de março de 2017
Conclusão do estudo (Real)
15 de março de 2017
Datas de inscrição no estudo
Enviado pela primeira vez
10 de fevereiro de 2017
Enviado pela primeira vez que atendeu aos critérios de CQ
17 de março de 2017
Primeira postagem (Real)
23 de março de 2017
Atualizações de registro de estudo
Última Atualização Postada (Real)
23 de março de 2017
Última atualização enviada que atendeu aos critérios de controle de qualidade
17 de março de 2017
Última verificação
1 de março de 2017
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- Rituxan INF II
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
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 .