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- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT00112476
Temsirolimus and Bryostatin 1 in Treating Patients With Unresectable or Metastatic Solid Tumors
A Phase I Study of Intravenous CCI-779 in Combination With Bryostatin-1 in Solid Tumors (10038414)
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
PRIMARY OBJECTIVES:
I. Determine the maximum tolerated dose and recommended phase II dose of temsirolimus when given together with bryostatin 1 in patients with unresectable or metastatic solid tumors.
II. Determine the dose-limiting toxic effects of this regimen in these patients.
SECONDARY OBJECTIVES:
I. Correlate the extent and duration of inhibition of p70^S6kinase phosphorylation in peripheral blood mononuclear cells with tumor growth or reduction in these patients.
II. Correlate the phosphorylation total and phospho-AKT and total and phospho ribosomal S6 protein (indicators of mTOR activation) with antitumor effects of this regimen in these patients.
III. Correlate tumor expression of phospho-ERK1 and -ERK2 with antitumor effects of this regimen in these patients.
IV. Determine the pharmacokinetics of this regimen in these patients.
OUTLINE: This is a dose-escalation study of temsirolimus.
Patients receive bryostatin 1 IV over 1 hour on days 1, 8, 15, and 22 and temsirolimus IV over 30 minutes once on days 8, 15, and 22 during course 1. On subsequent courses patients receive bryostatin 1 and temsirolimus once on days 1, 8, and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Cohorts of 3-6 patients receive escalating doses of temsirolimus until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.
Tipo de estudo
Inscrição (Real)
Estágio
- Fase 1
Contactos e Locais
Locais de estudo
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Pennsylvania
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Philadelphia, Pennsylvania, Estados Unidos, 19111-2497
- Fox Chase Cancer Center
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
Histologically confirmed solid tumor, including melanoma or renal cell carcinoma
Metastatic or unresectable disease
- Must have evidence of residual, recurrent, or metastatic disease by radiography
Measurable disease
- At least 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques (CT scan, MRI, or x-ray) OR ≥ 10 mm by spiral CT scan
- Must show clear evidence of disease progression within the lesion if the only site of measurable disease is within a previously irradiated volume
- Standard curative or palliative measures do not exist OR are no longer effective
- No history of or known brain metastases
- Performance status - ECOG 0-1
- At least 3 months
- WBC ≥ 3,000/mm^3
- Absolute neutrophil count ≥ 1,500/mm^3
- Platelet count ≥ 100,000/mm^3
- AST and ALT ≤ 2.5 times upper limit of normal (ULN)
- Bilirubin normal
- Creatinine ≤ 1.5 times ULN
- Creatinine clearance ≥ 50 mL/min
- No symptomatic congestive heart failure
- No unstable angina pectoris
- No cardiac arrhythmia
- Fasting cholesterol ≤ 350 mg/dL*
- Triglycerides ≤ 400 mg/dL*
- Not pregnant or nursing
- Negative pregnancy test
- Fertile female patients must use effective contraception for ≥ 1 month before, during, and for ≥ 3 months after completion of study treatment (during and for ≥ 3 months after completion of study treatment for male patients)
- No history of allergic reaction attributed to compounds of similar chemical or biological composition to study drugs
- No ongoing or active bacterial or viral infection
- No psychiatric illness or social situation that would preclude study compliance
- No dementia or altered mental status that would preclude giving informed consent
- No other uncontrolled illnesses
- More than 3 weeks since prior immunotherapy
- Prior biological therapy (e.g., interferon or interleukin 2, vaccine, antibody-based and tyrosine kinase inhibitors) allowed
- No concurrent prophylactic hematopoietic colony-stimulating factors except for epoetin alfa
- No prior cytotoxic chemotherapy
- No prior bryostatin 1, temsirolimus, everolimus, or AP23573 for this malignancy
- More than 3 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin)
- No concurrent steroids except for topical or inhaled use
- No other concurrent experimental agents
- No prior radiotherapy to > 25% of bone marrow
- More than 3 weeks since prior radiotherapy
More than 3 weeks since prior major surgery, including nephrectomy
- Minor surgical procedures allowed
- Recovered from prior therapy
- More than 3 weeks since prior other anticancer investigational agents
- Concurrent CYP3A4 inducers or inhibitors allowed provided patient has been on a stable dose for ≥ 1 week before study entry
- No concurrent combination antiretroviral therapy for HIV-positive patients
- No other concurrent antineoplastic agents or therapies
Plano de estudo
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: Treatment (bryostatin, temsirolimus)
Patients receive bryostatin 1 IV over 1 hour on days 1, 8, 15, and 22 and temsirolimus IV over 30 minutes once on days 8, 15, and 22 during course 1.
On subsequent courses patients receive bryostatin 1 and temsirolimus once on days 1, 8, and 15.
Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
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Dado IV
Outros nomes:
Dado IV
Outros nomes:
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
MTD of CCI-779 and Bryostatin-1 administered in combination, graded according to NCI Common Toxicity Criteria, Version 3.0
Prazo: 28 days
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A dose-limiting toxicity is defined as a toxicity that is >= grade 3 and drug-related.
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28 days
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
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Changes in sum of RECIST measurements
Prazo: Baseline up to 30 days after completion of study treatment
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Baseline up to 30 days after completion of study treatment
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AKT activity, measured by immunohistochemistry (IHC), classified as none, weak, moderate, or strong
Prazo: Up to 30 days after completion of study treatment
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Up to 30 days after completion of study treatment
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Gary Hudes, Fox Chase Cancer Center
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
- Processos Patológicos
- Neoplasias por Tipo Histológico
- Neoplasias
- Neoplasias Urológicas
- Neoplasias urogenitais
- Neoplasias por local
- Doenças renais
- Doenças Urológicas
- Adenocarcinoma
- Carcinoma
- Neoplasias Glandulares e Epiteliais
- Atributos da doença
- Tumores Neuroectodérmicos
- Neoplasias, Células Germinativas e Embrionárias
- Neoplasias, Tecido Nervoso
- Neoplasias Renais
- Tumores Neuroendócrinos
- Nevos e Melanomas
- Carcinoma de Células Renais
- Recorrência
- Melanoma
- Efeitos Fisiológicos das Drogas
- Agentes Anti-Infecciosos
- Agentes Antineoplásicos
- Agentes imunossupressores
- Fatores imunológicos
- Agentes antibacterianos
- Adjuvantes Imunológicos
- Antibióticos, Antineoplásicos
- Antifúngicos
- Sirolimo
- Briostatina 1
Outros números de identificação do estudo
- NCI-2011-01382
- 04-037
- FCCC-04037
- NCI-5785
- CDR0000432955
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