Perioperatorio 5-FU y 5-FU/Leucovorina para cáncer de colon Dukes' B3 o C
Este estudio tiene como objetivo evaluar la efectividad del tratamiento con 5-FU perioperatorio y 5-FU/Leucovorin en la mejora de la tasa de supervivencia general a los 5 años en pacientes diagnosticados con cáncer de colon Dukes' B3 o C.
fluorouracil
+ leucovorin calcium
+ fluorouracil
Enfermedades del colon+9
+ Enfermedades del Sistema Digestivo
+ Neoplasias del sistema digestivo
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de octubre de 1993
Fecha en la que se inscribió al primer participante.OBJECTIVES: I. To determine if adjuvant therapy with one week of continuous 5-FU given within 24 hours of a curative colon resection followed by 6 months of 5-FU/leucovorin is effective in prolonging the disease-free survival and increasing overall survival in patients with Dukes' B3 or C colon cancer, when compared to patients who are treated with 5-FU/leucovorin only. II. 1. To determine if a week of perioperative continuous 5-FU affects disease-free survival and overall survival in patients with Dukes' B2 colon cancer. OUTLINE: This is an open-label, randomized phase III study. Patients undergo curative colon resection via laparotomy. Patients are randomized to 1 of 2 arms in a 1:1 ratio. Arm I (Perioperative 5-FU): Within 24 hours of the colon resection, patients receive perioperative 5-fluorouracil (5-FU) intravenously (IV) over 24 hours for 7 days. Arm II (No perioperative 5-FU): Patients receive no perioperative fluorouracil. After surgery, patients with stage I, stage IIA, or stage IV colon cancer are immediately removed from study. Patients with stage IIB, IIC, or III colon cancer are re-registered within 35 days postoperatively. Beginning 21-35 days after surgery, patients with stage IIC or III disease receive leucovorin calcium IV bolus immediately followed by 5-FU IV bolus on days 1-5. Courses repeat every 28 days for a total of 6 courses in the absence of disease progression or unacceptable toxicity. Patients with stage IIB disease do not receive adjuvant 5-FU and leucovorin calcium. Patients are followed every 3 months for 2 years, then every 6 months for 2 years, and then annually until 15 years. PROJECTED ACCRUAL: A total of 800-2,000 patients (at least 400 per treatment arm) will be accrued for this study over 2-3 years.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 859 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
Eligibility Criteria for Randomization: Inclusion Criteria: Adenocarcinoma of the colon documented by colonoscopy or barium enema Tumor either considered resectable or totally resected within 24 hours prior to study Randomization within 2 weeks prior to surgery or within 24 hours after surgery required Patients randomized after surgery must meet the following criteria: Complete resection performed with no evidence of residual disease or distant metastases Distal margin of tumor above the peritoneal reflection in area of rectum No free perforation Intestinal obstruction allowed Preliminary or complementary colostomy allowed Concurrent registration for E3293 strongly recommended Age 18 and over Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 Adequate organ function based on the following tests within 2 weeks prior to randomization White Blood Cell (WBC) at least 3,000/mm^3 Platelet count at least 100,000/mm^3 Bilirubin no greater than 2.0 mg/dL Creatinine no greater than 2.0 mg/dL No second malignancy within 5 years except: superficial non-melanomatous skin cancer and carcinoma in situ of the cervix Fertile patients must use adequate contraception Exclusion Criteria: Dual primary tumors Prior nonmalignant systemic disease that would preclude use of chemotherapy Pregnant or nursing Prior fluorouracil Other prior or concurrent chemotherapy for this malignancy Prior or concurrent radiotherapy for this malignancy Eligibility Criteria for Re-registration for Patients Randomized Pre-operatively: Must have pathologic classification of Dukes' B2, B3, or C disease by the contributing institution. Must be re-registered < 35 days after surgery. ECOG performance status of 0-2. Complete resection must have been performed with no evidence of residual disease or distant metastasis. Distal margin of the tumor must not extend below the peritoneal reflection in the area of the rectum. Single primary colon carcinoma without free perforation demonstrated. Patients with intestinal obstruction are eligible. Preliminary or complementary colostomy dose not preclude entry of a patient. Have WBC > 3000/mm^3, platelets > 100,000/mm^3, adequate renal (serum creatinine <= 2.0mg/dL) and hepatic function (bilirubin <= 2.0mg/dL), within one week prior to beginning adjuvant chemotherapy (For Dukes' B3 and C patients only). Eligibility Criteria for Re-registration for Patients Randomized Post-operatively: Must have pathologic classification of Dukes' B2, B3, or C disease by the contributing institution. Patient must be re-registered < 35 days after surgery. ECOG performance status of 0-2. Started perioperative 5-FU, if assigned, within 24 hours of surgery. Have WBC > 3000/mm^3, platelets > 100,000/mm^3, adequate renal (serum creatinine <= 2.0mg/dL) and hepatic function (bilirubin < =2.0mg/dL), within one week prior to beginning adjuvant chemotherapy (For Dukes' B3 and C patients only).
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.2 grupos de intervención están designados en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalGrupo II
Comparador ActivoObjetivos del Estudio
Objetivos Primarios
Objetivos Secundarios
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 una ubicación
Loyola University Medical Center
Maywood, United StatesAbrir Loyola University Medical Center en Google Maps