- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT00714181
Hydroxychloroquine and Temozolomide in Treating Patients With Metastatic or Unresectable Solid Tumors
A Phase I Study of Hydroxychloroquine in Combination With Temozolomide in Patients With Advanced Solid Tumors
RATIONALE: Drugs used in chemotherapy, such as hydroxychloroquine and temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells.
PURPOSE: This phase I trial is studying the side effects and best dose of hydroxychloroquine when given together with temozolomide in treating patients with metastatic or unresectable solid tumors.
Descripción general del estudio
Estado
Intervención / Tratamiento
- Otro: estudio farmacológico
- Droga: temozolomida
- Otro: análisis de biomarcadores de laboratorio
- Otro: técnica de inmunoenzimas
- Otro: cromatografía líquida de alta resolución
- Otro: espectrometría de masas
- Otro: método de tinción inmunohistoquímica
- Genético: transferencia occidental
- Genético: Ensayo de marcaje de extremos de mella dUTP mediado por TdT
- Droga: hidroxicloroquina
- Otro: microscopio de electrones
Descripción detallada
OBJECTIVES:
Primary
- To determine the maximum tolerated dose (MTD) of hydroxychloroquine (HCQ) when administered in combination with temozolomide (TMZ) in patients with metastatic or unresectable solid tumors.
Secondary
- To determine the toxicity and toxicity rate of HCQ when administered at the MTD in combination with TMZ in these patients.
Tertiary
- To construct a population pharmacokinetic (PK) model using a limited sampling of whole blood to determine the drug exposure of HCQ and HCQ metabolites in these patients.
- To measure changes in autophagic vesicle accumulation by immunoblotting against the autophagy marker LC3 in protein lysates prepared from peripheral blood mononuclear cells (PBMC) collected from patients treated with HCQ and TMZ.
- To measure changes in median number of autophagic vesicles by electron microscopy in PBMC collected from patients treated with HCQ and TMZ.
- To assess tumor changes in LC3 and caspase 3 cleavage by western blotting.
- To assess tumor cell death characteristics by immunohistochemical methods (Ki67, TUNEL staining, cleaved caspase 3).
- To evaluate autophagy by electron microscopy.
- To define associations between changes in LC3 levels from baseline in PBMC with HCQ exposure.
- To measure the levels of HMGB1 in the serum of patients treated with HCQ and TMZ.
OUTLINE: This is a dose-escalation study of hydroxychloroquine (HCQ).
Patients receive oral HCQ alone once or twice daily for 14 days. Patients then receive oral HCQ once or twice daily on days 1-28 and oral temozolomide once daily on days 1-7 and 15-21. Treatment with HCQ and temozolomide repeats every 28 days in the absence of disease progression or unacceptable toxicity.
Patients undergo blood sample collection periodically for pharmacodynamic and pharmacokinetic correlative studies. Autophagic vesicles in blood samples are quantified by immunoblotting against the autophagy protein LC3 and by electron microscopy. Pharmacokinetics are analyzed by high-performance liquid chromatography with tandem mass spectrometry. Patients with tumors amenable to biopsy also undergo serial biopsies. Tumor tissue samples are assessed for tumor cell apoptosis and proliferation using Ki67 and TUNEL staining and for the number of autophagic vesicles and nuclear changes characteristic of apoptotic, autophagic, or necrotic cell death by western blotting and electron microscopy.
After completion of study treatment, patients are followed periodically.
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, Estados Unidos, 19104-4283
- Abramson Cancer Center of the University of Pennsylvania
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
DISEASE CHARACTERISTICS:
Histologically or cytologically confirmed solid tumor
- Metastatic or unresectable disease
- Refractory to standard therapy or no standard therapy exists
- Measurable disease by RECIST criteria
- Brain metastases allowed provided patient completed radiotherapy (if radiotherapy was clinically indicated at the time of diagnosis) AND discontinued steroids prior to study enrollment
PATIENT CHARACTERISTICS:
- ECOG performance status 0-1
- WBC ≥ 3,000/mm³
- Absolute granulocyte count ≥ 1,500/mm³
- Platelet count ≥ 100,000/mm³
- Serum creatinine ≤ 2.0 times upper limit of normal (ULN)
- Total bilirubin ≤ 1.5 times ULN (< 3.0 times ULN in the presence of Gilbert's disease)
- AST and ALT ≤ 2.5 times ULN (≤ 5.0 times ULN in the presence of liver metastases)
- aPTT normal
- INR ≤ 1.5 (if on anticoagulation, INR must be < 1.5 prior to starting anticoagulation)
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- HIV negative
- No porphyria
- No psoriasis, unless the disease is well controlled and patient is under the care of a specialist who agrees to monitor the patient for exacerbations
- No previously documented macular degeneration or diabetic retinopathy
No concurrent serious illness including, but not limited to, any of the following:
- Ongoing or active infection requiring parenteral antibiotics
- Clinically significant cardiovascular disease (e.g., uncontrolled hypertension, myocardial infarction, or unstable angina)
- New York Heart Association class II-IV congestive heart failure
- Serious cardiac arrhythmia requiring medication
- Peripheral vascular disease ≥ grade 2 within the past year
- Psychiatric illness/social situation that would limit compliance with study requirements
- No other concurrent malignancies, other than basal cell skin cancer, squamous cell skin cancer, carcinoma in situ of the cervix, or ductal or lobular carcinoma in situ of the breast
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- Recovered from all prior therapy
The following prior therapy is allowed in the adjuvant or metastatic disease setting:
- Immunotherapy (interferon, aldesleukin, or sargramostim [GM-CSF])
- Chemotherapy, either as a single-agent or as combination therapy
- Vaccine therapy
- Targeted or biological therapy
- Chloroquine derivatives
- At least 4 weeks since prior active immunotherapy (aldesleukin, interferon, or ipilimumab)
- At least 4 weeks since prior chemotherapy
- At least 2 weeks since prior oral targeted therapies
- More than 4 weeks since prior and no other concurrent investigational anticancer therapy (except for vaccines)
- No prior temozolomide
Prior radiotherapy allowed
- If radiotherapy has been administered to a lesion, there must be radiographic evidence of progression of that lesion in order for that lesion to constitute measurable disease or to be included in the measured target lesions
- No concurrent cytochrome P450 enzyme-inducing antiepileptic drugs (phenytoin, carbamazepine, phenobarbital, primidone, or oxcarbazepine), rifampin, or Hypericum perforatum (St. John's wort)
- No other concurrent anticancer therapy
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Enmascaramiento: Ninguno (etiqueta abierta)
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
|---|
|
Maximum tolerated dose of hydroxychloroquine
|
Medidas de resultado secundarias
Medida de resultado |
|---|
|
Toxicity rates
|
|
Pharmacodynamic and pharmacokinetic correlative endpoints
|
Colaboradores e Investigadores
Colaboradores
Investigadores
- Investigador principal: Ravi Amaravadi, MD, Abramson Cancer Center of the University of Pennsylvania
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (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
Palabras clave
Términos MeSH relevantes adicionales
- Neoplasias
- Mecanismos moleculares de acción farmacológica
- Agentes antiinfecciosos
- Inhibidores de enzimas
- Agentes antirreumáticos
- Agentes antineoplásicos
- Agentes antineoplásicos, alquilantes
- Agentes alquilantes
- Agentes antiprotozoarios
- Agentes antiparasitarios
- Antipalúdicos
- Temozolomida
- Hidroxicloroquina
Otros números de identificación del estudio
- CDR0000600329
- UPCC-12907
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .