A Phase II Study Of Docetaxel And Capecitabine In Patients With Measurable Metastatic Adenocarcinoma Of The Stomach And Gastroesophageal Junction
capecitabine
+ docetaxel
Enfermedades del Sistema Digestivo+8
+ Neoplasias del sistema digestivo
+ Enfermedades del esófago
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de septiembre de 2003
Fecha en la que se inscribió al primer participante.OBJECTIVES: * Determine the objective tumor response rate in patients with metastatic gastric or gastroesophageal junction adenocarcinoma treated with docetaxel and capecitabine. * Determine the time to progression in patients treated with this regimen. * Determine the overall survival in patients treated with this regimen. * Determine the toxic effects of this regimen in these patients. * Determine whether interleukin-1 polymorphisms are present among patients who have weight loss vs no weight loss, and their relationship to a poor prognosis. * Assess the quality of life and swallowing uniscale during chemotherapy in these patients. OUTLINE: Patients receive docetaxel IV over 1 hour on day 1 and oral capecitabine twice daily on days 1-14. Courses repeat every 21 days for up to 2 years in the absence of disease progression or unacceptable toxicity. Quality of life is assessed at baseline, at each tumor measurement, and at the end of treatment. Patients are followed every 3 months until disease progression and then every 6 months until 3 years from registration.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 46 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 stomach or gastroesophageal junction * Deemed unresectable and not a candidate for potentially curative treatment (e.g., surgical resection or combined modality therapy) * At least 4 weeks since prior abdominal exploration with resection (3 weeks without resection) * No other more conventional forms of therapy available with a reasonable chance of cure or significant palliation * Measurable disease\* * The following are not considered measurable disease: * Bone lesions * Leptomeningeal disease * Ascites * Pleural/pericardial effusion * Lymphangitis cutis/pulmonis * Abdominal masses that are not confirmed and followed by imaging * Cystic lesions NOTE: \*Patients having only lesions measuring ≥ 1 cm to \< 2 cm must use spiral CT scan for all tumor assessments. * No untreated or treated but symptomatic CNS metastases PATIENT CHARACTERISTICS: Age * 18 and over Performance status * ECOG 0-2 Life expectancy * At least 12 weeks Hematopoietic * Absolute neutrophil count at least 1,500/mm\^3 * Platelet count at least 100,000/mm\^3 Hepatic * Bilirubin no greater than upper limit of normal (ULN) * AST no greater than 2.5 times ULN if alkaline phosphatase is less than ULN OR * Alkaline phosphatase no greater than 4 times ULN if AST less than ULN Renal * Creatinine normal * Creatinine clearance at least 60 mL/min Cardiovascular * No New York Heart Association class III or IV heart disease Other * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception * Ability to swallow capecitabine * No prior anaphylactic reaction to any taxane * No prior severe reaction to fluoropyrimidine * No prior poor tolerance to capecitabine * No known sensitivity or poor tolerance to fluorouracil * No known dihydropyrimidine dehydrogenase deficiency * No uncontrolled infection * No uncontrolled seizure disorder * No chronic debilitating disease * No peripheral neuropathy of any etiology greater than grade 1 * No diabetes mellitus * No other malignancy within the past 5 years except adequately treated basal cell or squamous cell carcinoma or adequately treated noninvasive carcinoma PRIOR CONCURRENT THERAPY: Biologic therapy * No prior immunotherapy or biologic therapy for recurrent or metastatic disease * No concurrent biologic therapy Chemotherapy * No prior chemotherapy for recurrent or metastatic disease except for the following: * Adjuvant chemotherapy after complete resection of the original tumor * Neoadjuvant chemotherapy followed by surgical resection of the original tumor * No other concurrent chemotherapy Endocrine therapy * Not specified Radiotherapy * No prior radiotherapy except for the following: * Adjuvant radiotherapy after complete resection of the original tumor * Neoadjuvant radiotherapy followed by surgical resection of the original tumor * No prior radiotherapy to 25% or more of the bone marrow * More than 4 weeks since prior radiotherapy * No concurrent radiotherapy Surgery * See Disease Characteristics * No prior organ allograft Other * No concurrent brivudine or sorivudine
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Un solo grupo de intervención está designado en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalObjetivos 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 28 ubicaciones
Cancer Center of Kansas, PA - Chanute
Chanute, United StatesAbrir Cancer Center of Kansas, PA - Chanute en Google MapsCancer Center of Kansas, PA - Dodge City
Dodge City, United StatesCancer Center of Kansas, PA - El Dorado
El Dorado, United StatesCancer Center of Kansas, PA - Kingman
Kingman, United States