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A Study of Panobinostat (LBH589) as Second-Line Therapy in Patients With Chronic Graft-Versus-Host Disease

11 de fevereiro de 2013 atualizado por: SCRI Development Innovations, LLC

A Phase II Study of Panobinostat (LBH589) as Second-Line Therapy in Patients With Chronic Graft-Versus-Host Disease

There is a clear need for effective, steroid-sparing agents for the management of chronic graft-versus-host disease (GVHD). Thus, agents like Histone deacetylase (HDAC) inhibitors, with the potential of decreasing pro-inflammatory events leading to GVHD without affecting graft-versus-leukemia (GVL), may have a central role in the prevention and treatment of GVHD.

This study will look at the efficacy of panobinostat (LBH589), an HDAC inhibitor, in the treatment of patients with chronic GVHD who have failed corticosteroids. In this group of patients, effective steroid-sparing options are limited and are usually associated with profound immunosuppression and decreased GVL effect.

Visão geral do estudo

Descrição detalhada

Chronic GVHD is an autoimmune, inflammatory disorder that occurs in the majority of patients who experience acute GVHD. Long-term corticosteroids are still standard therapy for chronic GVHD. Corticosteroids are associated with high morbidity and non-relapse mortality. In addition, corticosteroids are broadly immunosuppressive and can also decrease the GVL effect and increase the incidence of relapse. There is a clear need for effective, steroid-sparing agents for the management of chronic GVHD. Thus, agents like HDAC inhibitors, with the potential of decreasing pro-inflammatory events leading to GVHD without affecting GVL, may have a central role in the prevention and treatment of GVHD.

This study will look at the efficacy of panobinostat (LBH589), an HDAC inhibitor, in the treatment of patients with chronic GVHD who have failed corticosteroids. In this group of patients, effective steroid-sparing options are limited and are usually associated with profound immunosuppression and decreased GVL effect.

Tipo de estudo

Intervencional

Estágio

  • Fase 2

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

    • Tennessee
      • Nashville, Tennessee, Estados Unidos, 37023
        • Tennessee Oncology, PLLC

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:

  1. Chronic GvHD following allogeneic HSCT of any source (bone marrow, peripheral blood, or cord blood stem cells), from any donor type (related, unrelated, or mismatched) and with any type of malignancy. Chronic GvHD will be defined according to NIH Consensus Criteria.
  2. Patients must have had inadequate response to treatment with steroids and calcineurin inhibitors. Patients must have been treated with an initial dose of at least 1 mg/kg/day of methylprednisolone (MP) or equivalent in combination with tacrolimus or cyclosporine and must fulfill the definition of steroid refractoriness or resistance. Steroid refractoriness or resistance will be defined as:

    1. Lack of any response after 1 month of treatment with MP, including 15 days of at least 0.5 mg/kg/day.
    2. Worsening of existing GvHD or new organ involvement at any time following one week of initiation of MP at 1 mg/kg/day.
    3. Reflare or worsening of GvHD at any time during steroid taper.
    4. Patients should not have received any drug or treatment for chronic GvHD other than steroids and calcineurin inhibitors (i.e., cyclosporine or tacrolimus).
  3. Patient must not have evidence of primary disease relapse.
  4. An ECOG (Eastern Cooperative Oncology Group) performance status of ≤2
  5. Baseline MUGA or ECHO must demonstrate left ventricular ejection fraction (LVEF) ≥40%.
  6. No uncontrolled arrhythmias or symptoms of heart disease.
  7. FEV1, FVC, and DLCO ≥40%.
  8. Laboratory values as follows:

    • white blood cell ≥2500/mm³;
    • absolute neutrophil count (ANC) ≥1,000/mm³;
    • hemoglobin ≥9.5 g%;
    • platelets ≥50,000/mm³;
    • total bilirubin <3 x upper limits of normal;
    • aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤5 × the institutional upper limit of normal (ULN);
    • creatinine <1.5 × ULN or creatinine clearance ≥ 50 ml/min;
    • serum potassium ≥ LLN;
    • serum sodium ≥ LLN;
    • serum calcium WNL;
    • serum phosphorus WNL;
    • serum magnesium WNL;
  9. Patients with elevated alkaline phosphatase due to bone metastasis may be enrolled.
  10. TSH and free T4 within normal limits (clinically euthyroid patients are permitted to receive thyroid supplements to treat underlying hypothyroidism).
  11. Age ≥ 18 years, male or female.
  12. Ability to understand and willingness to sign a written informed consent document.

Exclusion Criteria:

  1. Prior HDAC, DAC, HSP90 inhibitors or valproic acid for the treatment of cancer.
  2. Patients who will need valproic acid for any medical condition during the study or ≤5 days prior to first panobinostat treatment.
  3. Use of prior immunosuppressants other than steroids and calcineurin inhibitors(i.e. cyclosporine or tacrolimus).
  4. Chronic active hepatitis or cirrhosis.
  5. Impaired cardiac function including any of the following:

    • Patients with congenital long QT syndrome;
    • Patients with history or presence of sustained ventricular tachyarrhythmias;
    • Patients with any history of ventricular fibrillation or Torsades de Pointes;
    • Patients with bradycardia defined as HR <50 bpm. Patients with pacemakers are eligible if HR ≥50 bpm.
    • Patients with myocardial infarction or unstable angina ≤6 months prior to starting study drug;
    • Right bundle branch block plus left anterior hemiblock (bifasicular block);
    • Screening ECG with QTc >450 msec;
    • Congestive heart failure (CHF) > New York Heart Association (NYHA) Class II (see Appendix D).
  6. Concomitant use of drugs with a risk of causing Torsades de Pointes (see Appendix A).
  7. Other concurrent severe and/or uncontrolled medical conditions.
  8. Any condition that impairs patient's ability to swallow whole pills or gastrointestinal (GI) tract disease that involves an inability to take oral medication, malabsorption syndrome, a requirement for intravenous (IV)

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
Experimental: 1
Systemic Therapy
20 mg PO three times weekly
Outros nomes:
  • Panobinostat
1 mg/kg/day PO continuously
Outros nomes:
  • Medrol, Depo-Medrol

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
To assess the response rate to panobinostat of patients with cGvHD inadequately treated with steroids and calcineurin inhibitors.
Prazo: 30 months
30 months

Medidas de resultados secundários

Medida de resultado
Prazo
To evaluate the safety and tolerability of panobinostat in patients with cGvHD.
Prazo: 30 months
30 months
To assess the steroid-sparing capacity of panobinostat (as proportion of patients able to discontinue steroids while receiving, or following therapy with, panobinostat).
Prazo: 30 months
30 months
To assess changes in quality of life (QOL) after treatment with panobinostat.
Prazo: 30 months
30 months
To analyze survival at 6 and 12 months after initiation of panobinostat.
Prazo: 30 months
30 months
To evaluate the relapse rate of the underlying malignancy as well as the occurrence of second malignancies at 6 and 12 months after initiation of panobinostat.
Prazo: 30 months
30 months

Colaboradores e Investigadores

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

Colaboradores

Investigadores

  • Cadeira de estudo: Daniel R Couriel, M.D., SCRI Development Innovations, LLC

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 de inscrição no estudo

Enviado pela primeira vez

7 de dezembro de 2009

Enviado pela primeira vez que atendeu aos critérios de CQ

8 de dezembro de 2009

Primeira postagem (Estimativa)

9 de dezembro de 2009

Atualizações de registro de estudo

Última Atualização Postada (Estimativa)

13 de fevereiro de 2013

Última atualização enviada que atendeu aos critérios de controle de qualidade

11 de fevereiro de 2013

Última verificação

1 de fevereiro de 2013

Mais Informações

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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