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Comparison Study of Dendritic Cell Vaccine With and Without Cyclophosphamide to Treat Stage IV Melanoma Patients

5 de julho de 2013 atualizado por: Baylor Research Institute

Melanoma Peptide-Loaded Dendritic Cell Vaccine in HLA-A*0201 Patients With Stage IV Melanoma: A Phase II Randomized Trial to Compare Vaccination With and Without Cyclophosphamide Treatment.

The purpose of this study is to determine whether the combination of chemotherapy (Cyclophosphamide) and CD34-DC vaccines results in the improved rate of clinical responses for stage IV melanoma patients.

Visão geral do estudo

Descrição detalhada

Vaccination of patients with metastatic melanoma using ex vivo generated dendritic cells (DCs) loaded with tumor-associated antigen(s) have been shown to induce tumor-specific immunity against melanoma antigens measured by in vitro assays and, in some cases, tumor regression. At the present time, the numbers of recorded patients with metastatic melanoma who have been treated with DC vaccinations are too small to predict with certainty the future of overall therapeutic value of DC vaccinations in the management of patients with metastatic melanoma. The purpose of this study is to gather data on feasibility and efficacy of novel combination therapy of CPA and a DC vaccine outlined in this protocol to treat metastatic melanoma.

Tipo de estudo

Intervencional

Inscrição (Real)

9

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

    • Texas
      • Dallas, Texas, Estados Unidos, 75204
        • Baylor University Medical Center

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

21 anos a 75 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  1. Biopsy-proven metastatic melanoma, Stages M1a, M1b, M1c
  2. HLA-A*0201 phenotype
  3. Age: 21-75 years
  4. ECOG performance status 0-1
  5. Measurable metastatic melanoma lesions by physical examination or radiographs or scans.
  6. Adequate marrow function:

    • White count ≥ 4,000/microliter: Subjects who have recently completed chemotherapy will be allowed study entry with White count ≥ 3,500/microliter
    • Hemoglobin ≥ 10.0 gm: Subjects who have recently completed chemotherapy will be allowed study entry with Hemoglobin ≥ 9.0 gm.
    • Platelets ≥ 100,000/microliter
  7. Adequate hepatic function:

    • Bilirubin ≤ 1.5/mg/dL
    • Alkaline phosphatase ≤ 5 times the upper limit of normal
    • SGOT ≤ 5 times the upper limit of normal
    • SGPT ≤ 5 times the upper limit of normal
  8. Adequate renal function:

    • Serum creatinine ≤ 1.5/mg/dL
  9. No active CNS metastatic disease at screening.

    • Patients with a history of CNS melanoma lesions must have had lesions resected by surgery and/or gamma knife irradiation at least 3 months prior to study entry.
    • The total number of CNS lesions at diagnosis should not have exceeded 3.
  10. Written informed consent

Exclusion Criteria:

  1. Patients who have received > 8 cycles of cytotoxic chemotherapy or metastatic melanoma
  2. Patients who have received any chemotherapy < 4 weeks before the beginning of the trial
  3. Patients who have received interferon alpha (IFNα-2b) or sargramostim (GM-CSF) < 4 weeks before the beginning of the trial
  4. Patients who have received high-dose interleukin-2 (IL-2) < 4 weeks before the beginning of the trial
  5. Patients that have been diagnosed with more than 3 CNS melanoma lesions.
  6. Patients that have been diagnosed with more than 5 hepatic metastases or any hepatic metastasis > 5 cm.
  7. Baseline serum LDH > 1.1 times the upper limit of normal
  8. Patients who are HIV+ (HIV patients are often profoundly immunodeficient because of the viral infection and this additional parameter will interfere with the evaluation of DC induced immune responses in melanoma patients. Furthermore, the safety of collecting DCs, loading them with antigen and re-infusing these cells to HIV+ patients has not yet been determined.)
  9. Pregnancy (Pregnancy is associated with considerable immunosuppression 70 and this additional parameter will interfere with the evaluation of DC induced immune responses in melanoma patients. In addition, the safety and tolerability of cell body-loaded DC given subcutaneously is entirely unknown.)
  10. Patients who have received corticosteroids or other immunosuppressive agents < 4 weeks before beginning the trial
  11. Patients with active asthma and/or on treatment for asthma
  12. Patients with angina pectoris
  13. Patients with congestive heart failure
  14. Patients with a history of autoimmune disease including lupus erythematosus, rheumatoid arthritis or thyroiditis
  15. Patients with active infections including viral hepatitis
  16. Patients with a history of neoplastic disease other than melanoma < 5 years prior to entry on the trial except for patients with carcinomas in situ of the cervix and basal/squamous cell carcinomas of the skin. Patients who have any of these two types of cancer and melanoma can be included.

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: Randomizado
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: DC Vaccine & Cyclophosphamide

Patients will receive a fixed dose of about ≥15x106 viable dendritic cells per injection. Patients will receive a total of 8 doses of the vaccination with each individual dose being administered at weeks: 0, 2, 4, 6, 10, 14, 18 and 22. Responses will be evaluated and patients with SD, PR or CR may receive 4 more vaccine at 36, 48, 72 and 96 weeks, if there is vaccine available. The vaccine will be injected subcutaneously, in 3 separate injection sites (3.3.ml per site) in the upper and lower extremities.

Patients will receive either CPA 300mg/m2 for injections administered intravenously over a 2-hour infusion in the outpatient clinic 24 hours prior to DC vaccinations # 1, 3, 5, 6 and 7.

Patients will receive a fixed dose of about ≥15x106 viable dendritic cells per injection. Patients will receive a total of 8 doses of the vaccination with each individual dose being administered at weeks: 0, 2, 4, 6, 10, 14, 18 and 22. Responses will be evaluated and patients with SD, PR or CR may receive 4 more vaccine at 36, 48, 72 and 96 weeks, if there is vaccine available. The vaccine will be injected subcutaneously, in 3 separate injection sites (3.3.ml per site) in the upper and lower extremities.

Patients will receive either CPA 300mg/m2 for injections administered intravenously over a 2-hour infusion in the outpatient clinic 24 hours prior to DC vaccinations # 1, 3, 5, 6 and 7.

Outros nomes:
  • Cyclophosphamide (CPA)
  • DC Vaccine ( Dendritic cell vaccine)
Comparador de Placebo: DC Vaccine & Placebo

Patients will receive a fixed dose of about ≥15x106 viable dendritic cells per injection. Patients will receive a total of 8 doses of the vaccination with each individual dose being administered at weeks: 0, 2, 4, 6, 10, 14, 18 and 22. Responses will be evaluated and patients with SD, PR or CR may receive 4 more vaccine at 36, 48, 72 and 96 weeks, if there is vaccine available. The vaccine will be injected subcutaneously, in 3 separate injection sites (3.3.ml per site) in the upper and lower extremities.

Patients will receive saline for injections administered intravenously over a 2-hour infusion in the outpatient clinic 24 hours prior to DC vaccinations # 1, 3, 5, 6 and 7.

Patients will receive a fixed dose of about ≥15x106 viable dendritic cells per injection. Patients will receive a total of 8 doses of the vaccination with each individual dose being administered at weeks: 0, 2, 4, 6, 10, 14, 18 and 22. Responses will be evaluated and patients with SD, PR or CR may receive 4 more vaccine at 36, 48, 72 and 96 weeks, if there is vaccine available. The vaccine will be injected subcutaneously, in 3 separate injection sites (3.3.ml per site) in the upper and lower extremities.

Patients will receive saline for injections administered intravenously over a 2-hour infusion in the outpatient clinic 24 hours prior to DC vaccinations # 1, 3, 5, 6 and 7.

Outros nomes:
  • Vacina DC - Vacina de Células Dendríticas

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Induction of melanoma-specific CD8+T Cell Immunity.
Prazo: 2 years
2 years

Medidas de resultados secundários

Medida de resultado
Prazo
Rate of objective clinical responses.
Prazo: 2 years
2 years

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Joseph Fay, M.D., Baylor Institute for Immunology Research: Baylor University Medical Center

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 2008

Conclusão Primária (Real)

1 de abril de 2011

Conclusão do estudo (Real)

1 de julho de 2012

Datas de inscrição no estudo

Enviado pela primeira vez

23 de julho de 2008

Enviado pela primeira vez que atendeu aos critérios de CQ

24 de julho de 2008

Primeira postagem (Estimativa)

25 de julho de 2008

Atualizações de registro de estudo

Última Atualização Postada (Estimativa)

8 de julho de 2013

Última atualização enviada que atendeu aos critérios de controle de qualidade

5 de julho de 2013

Última verificação

1 de julho 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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