- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT00098527
FR901228 in Treating Patients With Refractory Stomach Cancer or Gastroesophageal Junction Cancer
A Phase 2 Study of Single Agent Depsipeptide (FK228) in Gastric and Esophageal Cancers
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
PRIMARY OBJECTIVES:
I. Determine the radiographic response rate (complete response and partial response) in patients with refractory adenocarcinoma of the stomach or gastroesophageal junction treated with FR901228 (depsipeptide).
SECONDARY OBJECTIVES:
I. Determine the median time to progression and progression-free survival of patients treated with this drug.
II. Determine the grade 3 and 4 toxic effects of this drug in these patients.
OUTLINE: This is an open-label, multicenter study.
Patients receive FR901228 (depsipeptide) IV over 4 hours on days 1, 8, and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
PROJECTED ACCRUAL: A total of 13-20 patients will be accrued for this study within 6.5-10 months.
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 2
Contactos y Ubicaciones
Ubicaciones de estudio
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North Carolina
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Durham, North Carolina, Estados Unidos, 27710
- Duke University Medical Center
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Histologically or cytologically confirmed adenocarcinoma of the stomach or gastroesophageal junction
Measurable disease
- At least 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques OR ≥ 10 mm by spiral CT scan
Refractory* to at least 1, but no more than 3, of the following first-line agents:
- Fluoropyrimidine (e.g., capecitabine or fluorouracil)
- Taxane (e.g., paclitaxel or docetaxel)
- Platinum (e.g., carboplatin, cisplatin, or oxaliplatin)
No known active brain metastases
- Treated brain metastases allowed provided metastases are stable off steroids for ≥ 30 days
- Performance status - ECOG 0-2
- Performance status - Karnofsky 60-100%
- At least 3 months
- WBC ≥ 3,000/mm^3
- Absolute neutrophil count ≥ 1,500/mm^3
- Platelet count ≥ 100,000/mm^3
- Bilirubin ≤ 1.5 times upper limit of normal (ULN)
- AST and ALT ≤ 2.5 times ULN (5 times ULN if liver metastases are present)
- Creatinine clearance ≥ 50 mL/min
- No congestive heart failure
- No New York Heart Association class III or IV heart disease
- No myocardial infarction within the past 6 months
- No ventricular arrhythmias requiring medication
- No angioplasty or vascular stenting within the past 3 months
- No unstable angina
- No left ventricular hypertrophy by EKG
- No known history of serious ventricular arrhythmia (e.g., ventricular tachycardia or ventricular fibrillation ≥ 3 beats in a row)
- QTc < 500 msec
- LVEF > 40% by MUGA or echocardiogram
- No other significant cardiac disease
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- Potassium ≥ 4.0 mmol/L (stable level with no change in supplementation within the past 2 weeks)
- Magnesium ≥ 2.0 mg/dL (stable level with no change in supplementation within the past 2 weeks)
- No history of allergic reaction attributed to compounds of similar chemical or biologic composition to study drug
- No ongoing or active infection
- No psychiatric illness or social situation that would preclude study compliance
- No other uncontrolled illness
- Prior biological agents allowed
- No concurrent prophylactic filgrastim (G-CSF)
- No concurrent biologic therapy
- More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and recovered
- No other concurrent chemotherapy
- More than 4 weeks since prior radiotherapy and recovered
- No concurrent radiotherapy
- Prior targeted agents allowed
- No other prior or concurrent cytotoxic agents
- No other concurrent investigational agents
- No other concurrent anticancer therapy
- No concurrent medications causing QTc prolongation
- No concurrent potassium supplementation > 40 mg/day or magnesium supplementation > 1 g/week
- No concurrent hydrochlorothiazide
- No concurrent combination antiretroviral therapy for HIV-positive patients
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Tratamiento (romidepsina)
Los pacientes reciben FR901228 (depsipéptido) IV durante 4 horas los días 1, 8 y 15.
Los cursos se repiten cada 28 días en ausencia de progresión de la enfermedad o toxicidad inaceptable.
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Estudios correlativos
Dado IV
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Radiographic response rate (complete response & partial response)
Periodo de tiempo: Not Provided
|
Not Provided
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Progression-free survival (PFS) according to RECIST
Periodo de tiempo: Up to more than 6 months
|
The median time to progression and median PFS for all eligible patients, along with their CIs, will be reported.
The Kaplan-Meier analysis approach may be used to summarize these time-to-event endpoints.
|
Up to more than 6 months
|
|
Frequency of treatment related grade 1-4 toxicities and cardiac toxicities as assessed by NCI Common Terminology Criteria for Adverse Events (CTCAE) version 3.0
Periodo de tiempo: Up to 12 months
|
Up to 12 months
|
|
|
Correlation of changes in gene expression profile in dermal granulation tissue pre- and post-treatment with gene expression profile
Periodo de tiempo: Not Provided
|
Not Provided
|
|
|
Correlation of wound vascular scores pre- and post-treatment with gene/protein changes
Periodo de tiempo: Not Provided
|
Not Provided
|
|
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Toxicity
Periodo de tiempo: Not Provided
|
Not Provided
|
|
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Changes in gene expression profile
Periodo de tiempo: At pre- and post-treatment
|
At pre- and post-treatment
|
|
|
Changes in levels of p21 and thymidine kinase expression, and tubulin acetylation using Western blotting
Periodo de tiempo: From baseline to 3 weeks
|
From baseline to 3 weeks
|
|
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Changes in gene expression profile in dermal granulation tissue
Periodo de tiempo: From baseline to up to 3 weeks
|
From baseline to up to 3 weeks
|
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Change in plasma and urine TGFB levels
Periodo de tiempo: At pre-and post-treatment
|
At pre-and post-treatment
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Herbert Hurwitz, Duke University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades del Sistema Digestivo
- Procesos Patológicos
- Neoplasias por tipo histológico
- Neoplasias
- Neoplasias por sitio
- Carcinoma
- Neoplasias Glandulares y Epiteliales
- Atributos de la enfermedad
- Neoplasias Gastrointestinales
- Neoplasias del Sistema Digestivo
- Enfermedades Gastrointestinales
- Neoplasias de Cabeza y Cuello
- Enfermedades esofágicas
- Reaparición
- Adenocarcinoma
- Neoplasias Esofágicas
- Agentes antineoplásicos
- Antibióticos, Antineoplásicos
- Romidepsina
Otros números de identificación del estudio
- NCI-2012-02637
- 6075-04-7R0
- DUMC-6075-04-7R0
- CDR0000398177
- NCI-6351
- U01CA099118 (Subvención/contrato del NIH de EE. UU.)
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