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Alanosine in Treating Patients With Cancer

0 criterios cumplidosConsulta de un vistazo cómo tu perfil cumple con cada criterio de elegibilidad.
Qué se está evaluando

L-alanosine

Medicamento
Quiénes están siendo reclutados

Lung Cancer
+1

+ Malignant Mesothelioma
+ Pancreatic Cancer
A partir de 13 años
Cómo está diseñado el estudio

Estudio de Tratamiento

Fase 2
Intervencional
Inicio del estudio: marzo de 2003

Resumen

Patrocinador PrincipalMemorial Sloan Kettering Cancer Center
Última actualización: 26 de junio de 2013
Extraido de una base de datos validada por el gobierno.Reclamar como socio
Fecha de inicio: 1 de marzo de 2003Fecha en la que se inscribió al primer participante.

RATIONALE: Drugs used in chemotherapy such as alanosine use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: This phase II trial is studying how well alanosine works in treating patients with soft tissue sarcoma, sarcoma of the bone, mesothelioma, non-small cell lung cancer, or pancreatic cancer. OBJECTIVES: * Determine the response rates in patients with methylthioadenosine phosphorylase (MTAP)-deficient cancer when treated with alanosine. * Determine the time to response and duration of response in patients treated with this drug. * Determine the progression-free survival of patients treated with this drug. * Determine the pharmacodynamic activity of this drug in these patients, based on special imaging to measure tumor adenosine triphosphate depletion. * Determine the pharmacokinetic activity of this drug in these patients. * Determine the safety and tolerability of this drug in these patients. OUTLINE: This is a nonrandomized, open-label, multicenter study. Patients receive alanosine IV continuously on days 1-5. Treatment repeats every 21 days for up to 9 courses in the absence of disease progression or unacceptable toxicity. Patients are followed at 28 days. PROJECTED ACCRUAL: A total of 50-145 patients (10-29 per tumor type) will be accrued for this study.

Título OficialA Phase II, Open-Label, Non-Randomized, Multicenter, Single Agent Study of Intravenous SDX-102 for the Treatment of Patients With MTAP-Deficient Cancer 
Patrocinador PrincipalMemorial Sloan Kettering Cancer Center
Última actualización: 26 de junio de 2013
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño
Estudio de Tratamiento
Estos estudios prueban nuevas formas de tratar una enfermedad, condición o problema de salud. El objetivo es determinar si un nuevo medicamento, terapia o enfoque funciona mejor o tiene menos efectos secundarios que las opciones existentes.

Cómo se mantiene la confidencialidad de las intervenciones asignadas a los participantes
Todos los involucrados en el estudio saben qué tratamiento se está administrando. Esto se utiliza cuando no es posible o necesario ocultar los detalles del tratamiento a los participantes o investigadores.

Otras formas de enmascarar la información
Simple ciego
: Los participantes no saben qué tratamiento están recibiendo, pero los investigadores sí.

Doble ciego
: Ni los participantes ni los investigadores saben qué tratamiento se está administrando.

Triple ciego
: Participantes, investigadores y evaluadores de resultados no saben qué tratamiento se está administrando.

Cuádruple ciego
: Participantes, investigadores, evaluadores de resultados y personal de atención no saben qué tratamiento se está administrando.

Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios
Cualquier sexoSexo biológico de los participantes elegibles para inscribirse.
A partir de 13 añosRango de edades de los participantes que pueden unirse al estudio.
Voluntarios sanos no permitidosIndica si personas sanas, sin la condición que se estudia, pueden participar.
Condiciones
Patología
Lung Cancer
Malignant Mesothelioma
Pancreatic Cancer
Sarcoma
Criterios

DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed malignancy of any of the following types: * Soft-tissue sarcoma * High grade * Chemotherapy naïve or progressive or metastatic after no more than 2 prior cytotoxic treatment regimens (not including adjuvant therapy) * Sarcoma of the bone (including osteosarcoma\* and chondrosarcoma) * High grade * Progressive or recurrent after no more than 2 prior cytotoxic treatment regimens * No newly diagnosed or chemotherapy naïve disease NOTE: \*Prior treatment with cisplatin and doxorubicin required * Mesothelioma * Unresectable * Chemotherapy naïve or progressive after no more than 1 prior cytotoxic chemotherapy regimen * Not amenable to curative treatment with surgery * Evidence of gross unresectability includes, but is not limited to, direct extension into the chest wall, mediastinal or hilar lymphadenopathy, pulmonary or cardiac function that is inadequate to tolerate resection, and sarcomatoid or mixed histology * Non-small cell lung cancer * Stage III with malignant pleural or pericardial effusion, stage IV, or progressive after no more than 2 prior cytotoxic chemotherapy regimens * No newly diagnosed or chemotherapy naïve disease * Pancreatic cancer * Stage IV adenocarcinoma after no more than 1 prior cytotoxic treatment regimen * No newly diagnosed or chemotherapy naïve disease * No Ewing's sarcoma of the soft tissue or bone * Documented absence of methylthioadenosine phosphorylase on fixed tumor specimens * Measurable disease * For all tumor types, at least 1 lesion measurable by MRI or CT scan * Chest x-ray allowed only for clearly defined lesions surrounded by aerated lung * Soft tissue component of bone disease considered measurable provided it can be measured by MRI or CT scan * Must be outside of a previously irradiated area * No uncontrolled CNS metastases of primary tumor under study * Patients with brain metastases are eligible only if the brain metastases have been treated with prior radiotherapy and/or surgery, are neurologically stable with no progressing symptoms, and are off steroids and anticonvulsants PATIENT CHARACTERISTICS: Age * 18 and over (13 and over for osteosarcoma only) Performance status * WHO 0-2 Life expectancy * At least 3 months Hematopoietic * Absolute granulocyte count at least 1,500/mm\^3 * Platelet count at least 100,000/mm\^3 Hepatic * Bilirubin no greater than 1.5 times upper limit of normal (ULN) * Alkaline phosphatase no greater than 2.5 times ULN * AST and ALT no greater than 2.5 times ULN (5 times ULN if liver metastases are present) Renal * Creatinine no greater than 1.5 times ULN Other * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective barrier contraception during and for 4 weeks after study treatment * No premalignant bony lesions (e.g., Paget's disease) * No other concurrent active malignancy except completely excised nonmelanoma skin cancer or carcinoma in situ of the cervix or bladder * No serious infection * No medical or psychiatric condition that would preclude the achievement of the study objectives PRIOR CONCURRENT THERAPY: Biologic therapy * Not specified Chemotherapy * See Disease Characteristics * More than 42 days since prior nitrosoureas or mitomycin Endocrine therapy * See Disease Characteristics Radiotherapy * See Disease Characteristics * At least 28 days since prior brain radiotherapy * More than 28 days since prior radiotherapy to more than 50% of the bone marrow Surgery * See Disease Characteristics * At least 28 days since prior thoracic or other major surgery Other * Recovered from prior therapy * More than 28 days since prior cytotoxic agents * More than 28 days since prior anticancer investigational agents * No other concurrent anti-tumor treatment



Centros del Estudio

Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.
Este estudio tiene 12 ubicaciones
Suspendido
University of Alabama at Birmingham Comprehensive Cancer CenterBirmingham, United StatesVer ubicación
Suspendido
Arizona Cancer Center at University of Arizona Health Sciences CenterTucson, United States
Suspendido
Wilshire Oncology Medical Group, Incorporated - La VerneLa Verne, United States
Suspendido
Cedars-Sinai Comprehensive Cancer Center at Cedars-Sinai Medical CenterLos Angeles, United States

Completado12 Centros de Estudio