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Relapsed and/or Refractory Non-Hodgkin Lymphoma Study (COMBOSTAT)

15 de setembro de 2017 atualizado por: The Methodist Hospital Research Institute

Phase II Study of Combination Vorinostat and Bortezomib in Patients With Relapsed and/or Refractory Non-Hodgkin Lymphoma

The purpose of this study is to determine the rate of response to the drugs bortezomib (Velcade) and vorinostat (Zolinza), when used in combination, in patients with relapsed (recurrent) and/or refractory (difficult to treat) non-Hodgkin Lymphoma, and to determine the safety and tolerability of this regimen.

Visão geral do estudo

Status

Retirado

Condições

Descrição detalhada

More selective and less toxic therapeutic strategies are needed to improve cure rates and prolong survival in patients with relapsed and/or refractory non-Hodgkin Lymphoma.

Amongst the multiple new pathways recently studied two have emerged as potentially important targets for new agents in lymphoma. These include the ubiquitin proteasome pathway and the biochemical reactions that control histone acetylation. The first two agents in each class to have been studied in lymphomas are: bortezomib and vorinostat. Bortezomib has been granted FDA approval for the treatment of mantle cell lymphoma and has established activity in a variety of B-cell lymphomas including follicular, marginal zone and diffuse large B-cell lymphoma. Vorinostat or SAHA (suberoylanilide hydroxamic acid) has been FDA approved for the treatment of refractory cutaneous T-cell lymphomas and has also shown activity in other lymphomas.

Synergistic activity between vorinostat and bortezomib has been observed in different cell lines. The proposed study will be a phase II trial of the combination of vorinostat and bortezomib at the recommended dose-schedule in patients with recurrent and/or refractory lymphomas, indolent and aggressive, and B or T.

Tipo de estudo

Intervencional

Estágio

  • Fase 2

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

Inclusion Criteria:

  • Histologically confirmed non-Hodgkin Lymphoma including small lymphocytic lymphoma, lymphoplasmacytic lymphoma, follicular center cell lymphoma, mantle cell lymphoma, marginal zone lymphoma, diffuse large B cell lymphoma, Burkitt's lymphoma, lymphoblastic lymphoma, anaplastic large cell lymphoma, nasal NK/T cell lymphoma, mycosis fungoides/Sezary syndrome, angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphomas not otherwise specified
  • Received 2 or > prior therapies, which may include hematopoietic cell transplant (HCT)
  • Received treatment with a nucleoside analog, or an alkylating agent, an anthracycline and/or in the case of B cell lymphomas, rituximab
  • Resistant disease to 2 regimens or resistant disease to at least 1 regimen after first relapse
  • Bi-dimensionally measurable disease documented within 30 days prior to enrollment. Bidimensionally measurable disease is defined as:

    • A lymph node or tumor mass that can be accurately measured in two dimensions by CT,MRI, medical photograph (skin or oral lesion), plain X-ray, PET scan or other conventional technique and a greatest diameter of 1 cm or >; or palpable lesions with both diameters > 2 cm (lesion measured in 2 largest perpendicular dimensions in millimeters)
    • For the purposes of this protocol, disease should be located in an area of no prior radiation therapy or a clear progression in an area that was previously irradiated
  • Adequate organ and marrow function obtained < or = to 14 days prior to enrollment as defined by a(n):

    • ANC > or = to 1,000/microliter
    • Platelet count > or = to 100,000/microliter, or > or = to 75,000/microliter if the bone marrow is involved
    • Hemoglobin level > or = to 9 g/dL
    • Total bilirubin < or = to 1.5 x institutional upper limit of normality (ULN).(If abnormal, direct bilirubin less than or equal to 1.5 x institutional ULN)
    • ALT or AST < or = to 2.5 x institutional ULN (< or = to 5 x institutional ULN if liver involvement with lymphoma)
    • Serum creatinine < or = to 1.5 x institutional ULN
  • Zubrod (ECOG) Performance Status of 0 or 1
  • Age > than or = to 18 years
  • Life expectancy > or = to 3 months as clinically determined by referring physician
  • Female patient is either post menopausal, free from menses for > 2 years, surgically sterilized or willing to use highly effective methods of contraception (i.e., a condom in conjunction with a diaphragm, or spermicidal jelly; or oral, injectable, or implanted birth control; or abstinence ) to prevent pregnancy throughout the study, starting with visit 1
  • Female patients of childbearing potential must have a negative serum pregnancy test (beta-HCG) within 72 hours of enrollment and should not be nursing due to the potential for congenital abnormalities and of harm to nursing infants due to this treatment regimen
  • Male patient agrees to use an adequate method of contraception (i.e., a condom if female partner uses a diaphragm, spermicidal jelly; or oral, injectable, or implanted birth control; or abstinence) for the duration of the study and for 12 weeks after the last dose
  • Patient must be able to swallow capsules
  • Signed and dated IRB/ethics committee-approved informed consent before any protocol specific screening procedures are performed
  • Both men and women of all races and ethnic groups are eligible for this trial

Exclusion Criteria:

  • Prior investigational therapy within 3 weeks of enrollment. Investigational therapy is defined as treatment that is not approved for any indication
  • CNS metastases, as indicated by clinical symptoms,cerebral edema, requirement for corticosteroids and/or progressive growth (treated CNS metastases must be stable for greater than 2 weeks prior to enrollment)
  • Active second malignancy that requires treatment or that would interfere with assessment of response
  • Prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer with < 5 years of documented disease-free status
  • Treatment with the following within the timeframe specified prior to enrollment:

    • Chemotherapy, radiotherapy, immunotherapy (active (such as vaccines) or passive (such as monoclonal antibodies or immunotoxins)) or major surgery < or = to 3 weeks;
    • Nitrosourea, or mitomycin < or = to 6 weeks
    • Radioimmunotherapy (e.g. Bexxar or Zevalin) < or = to 12 weeks
    • Concurrent enzyme-inducing anticonvulsant agents or valproic acid in last 4 weeks
    • Prior bortezomib or any other proteasome inhibitor
    • Prior vorinostat or any other histone deacetylase inhibitor
    • Concurrent systemic corticosteroids (<10 mg/day of prednisone or equivalent for adrenal insufficiency or acute allergic reactions allowed)
  • Uncontrolled current illness including, but not limited to:

    • Clinically or laboratory determined active infection
    • Clinically limiting congestive heart failure or ejection fraction (EF) <45%
    • Clinically unstable angina pectoris (or myocardial infarction within 6 months of Day 1)
    • Clinically significant cardiac arrhythmia
    • Limiting pulmonary hypertension
    • Pre-existing neuropathy ≥ grade 2
    • Patients with pleural effusions, ascites or peripheral edema grade 2 or >
  • HIV
  • Active viral hepatitis
  • Major surgery or significant traumatic injury within 21 days prior to enrollment (this does not apply to placement of a venous access device)
  • Hypersensitivity to any of the components in vorinostat or bortezomib or agents containing boron or mannitol
  • Significant psychiatric illness/social situations that would limit compliance with study medication and requirements of the study as determined by study MD
  • Significant medical illness or abnormal laboratory finding that would, in the investigator's judgment, increase the subject's risk by participating in this study

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: Não randomizado
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Combination Vorinostat + Bortezomib
Six cycle combination therapy with vorinostat and bortezomib.
Patients will be treated with oral vorinostat on days 1 through 14 followed by a 7-day rest period, for a 21-day treatment cycle for up to 6 cycles in the absence of disease progression or unacceptable toxicity. The patients will receive once-daily oral vorinostat (400 mg) with bortezomib 1.3 mg/m2 as an IV push on days 1, 4, 8, 11.
Outros nomes:
  • vorinostat (Zolinza)
  • bortezomib (Velcade)

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Determine the response rate of this regimen in this patient population.
Prazo: 6 cycles
6 cycles

Medidas de resultados secundários

Medida de resultado
Prazo
Determine the progression free survival of this regimen in this patient population.
Prazo: entire length of study
entire length of study
Determine the safety and tolerability of this regimen in this patient population.
Prazo: throughout course of study
throughout course of study
To correlate response rate and progression free survival with pre-treatment and post-treatment NFkB, TRAIL, cyclin D1, histone acetylation, EBV related proteins, and CTA expression.
Prazo: 6 cycles
6 cycles

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Hector A Preti, M.D., The Methodist Hospital Research Institute

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 junho de 2010

Conclusão Primária (Real)

1 de maio de 2012

Conclusão do estudo (Real)

1 de maio de 2012

Datas de inscrição no estudo

Enviado pela primeira vez

3 de fevereiro de 2009

Enviado pela primeira vez que atendeu aos critérios de CQ

4 de fevereiro de 2009

Primeira postagem (Estimativa)

5 de fevereiro de 2009

Atualizações de registro de estudo

Última Atualização Postada (Real)

19 de setembro de 2017

Última atualização enviada que atendeu aos critérios de controle de qualidade

15 de setembro de 2017

Última verificação

1 de setembro de 2017

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Descrição do plano IPD

To be determined

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 .

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