An Open Label, Randomized, Controlled, Phase III, Multi-center, Clinical Trial Of PN401 With High Dose 5-Fluorouracil (5FU) Versus Gemcitabine For Treatment Of Patients With Advanced Pancreatic Cancer
Colección de datos
Enfermedades del Sistema Digestivo+5
+ Neoplasias del sistema digestivo
+ Enfermedades del Sistema Endocrino
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de febrero de 2001
Fecha en la que se inscribió al primer participante.OBJECTIVES: * Compare the survival of patients with unresectable locally advanced or metastatic pancreatic cancer treated with triacetyluridine and high-dose fluorouracil vs gemcitabine. * Compare the time to tumor progression, overall response rate, and response duration in patients treated with these regimens. * Compare the safety of these regimens in these patients. OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to disease stage (II or III vs IV). Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive high-dose fluorouracil (5-FU) IV over 30 minutes once weekly on weeks 1-3 followed by 1 week of rest. After each dose of 5-FU, patients receive oral triacetyluridine every 8 hours for a total of 8 doses. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity. * Arm II: Patients receive gemcitabine IV over 30 minutes once weekly on weeks 1-7 followed by 1 week of rest (course 1). Subsequent courses are given on weeks 1-3. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed for survival. PROJECTED ACCRUAL: A total of 260 patients (130 per treatment arm) will be accrued for this study within 30 months.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 250 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed adenocarcinoma of the pancreas * Unresectable locally advanced or metastatic disease * Stage II, III, or IV * Measurable or evaluable disease * No elevated tumor marker (CA 19-9) only * No clinically significant third-space fluid accumulation (e.g., ascites or pleural effusion) * No carcinoid, islet cell, or lymphoma of the pancreas * No prior or concurrent brain or leptomeningeal metastases PATIENT CHARACTERISTICS: Age: * 18 and over Performance status: * Karnofsky 70-100% Life expectancy: * At least 3 months Hematopoietic: * WBC at least 3,500/mm\^3 * Platelet count at least 100,000/mm\^3 * Hemoglobin at least 9.5 g/dL Hepatic: * Bilirubin no greater than 2.0 mg/dL * ALT or AST less than 3 times upper limit of normal (ULN) (5 times ULN if liver metastases present) * No uncontrolled hepatic dysfunction Renal: * Creatinine less than 2.0 mg/dL * No uncontrolled renal dysfunction Cardiovascular: * No uncontrolled cardiovascular disease requiring therapy, including the following: * Angina * Arrhythmias * Uncompensated cardiac failure * Myocardial infarction within the past 6 months Pulmonary: * No uncontrolled pulmonary dysfunction Gastrointestinal: * Able to take and/or retain oral medication * No uncontrolled malabsorption syndrome or any other condition that would interfere with intestinal absorption Other: * No known allergy to fluorouracil (5-FU), gemcitabine, triacetyluridine, or any of their components * No dihydropyrimidine-dehydrogenase deficiency * No active uncontrolled infection * No uncontrolled neurologic or psychiatric dysfunction * No other malignancy except previously resected basal cell cancer or curatively resected stage I or less cervical cancer that has been disease free for at least 5 years * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception * HIV negative PRIOR CONCURRENT THERAPY: Biologic therapy: * No concurrent biologic therapy (including immunotherapy) for cancer Chemotherapy: * No prior chemotherapy for cancer other than as a radiosensitizer * No prior 5-FU or gemcitabine other than as a radiosensitizer * No prior triacetyluridine * No other concurrent chemotherapy (including leucovorin calcium) for cancer Endocrine therapy: * No concurrent hormonal therapy for cancer * Concurrent megestrol, oral contraceptives, or postmenopausal estrogen replacement therapy allowed Radiotherapy: * Prior radiotherapy allowed * No concurrent radiotherapy Surgery: * See Disease Characteristics * Prior resection of pancreas allowed Other: * At least 30 days since prior investigational drug or therapeutic device * No other concurrent anticancer therapy * No other concurrent investigational drugs or devices * No concurrent drugs that would interact adversely with 5-FU or gemcitabine
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Objetivos del Estudio
Objetivos Primarios
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 29 ubicaciones
Comprehensive Cancer Center at University of Alabama at Birmingham
Birmingham, United StatesProvidence Saint Joseph Medical Center - Burbank
Burbank, United StatesCity of Hope Comprehensive Cancer Center
Duarte, United States