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Efficacy of UFT plus oral leucovorin in advanced colorectal cancer: a multicenter study.
Artigo em Inglês | IMSEAR | ID: sea-39643
ABSTRACT

PURPOSE:

To evaluate the efficacy and toxicity of UFT plus oral leucovorin in advanced colorectal cancer. MATERIAL AND

METHOD:

Twenty cases of advanced colorectal cancer were entered into the study. All patients must have histologic proof and have measurable disease. Prior to the treatment all patients should have normal baseline hematology and normal liver and renal function, ECOG Performance status < or = 2 and age 18-75 years. Chemotherapeutic drugs consisted of UFT 350 mg/m2/day divided into 3 doses (8 hours apart) plus oral leucovorin 15 mg every 8 hours. Duration of treatment was 21 days per each cycle. Treatment was recycled every 28 days.

RESULTS:

Four cases (22.2%) had partial responses and six cases (33.3%) had stable disease. Duration of response was 4(+)-7+ months. Toxicity was darkened skin, mild diarrhea and mild alopecia.

CONCLUSION:

UFT plus oral leucovorin was one of the active regimens in the treatment of advanced colorectal cancer.
Assuntos
Texto completo: DisponíveL Índice: IMSEAR (Sudeste Asiático) Assunto principal: Prognóstico / Uracila / Índice de Gravidade de Doença / Idoso / Feminino / Humanos / Masculino / Esquema de Medicação / Neoplasias Colorretais / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudo: Ensaio Clínico Controlado / Estudo prognóstico Idioma: Inglês Ano de publicação: 2000 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: IMSEAR (Sudeste Asiático) Assunto principal: Prognóstico / Uracila / Índice de Gravidade de Doença / Idoso / Feminino / Humanos / Masculino / Esquema de Medicação / Neoplasias Colorretais / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudo: Ensaio Clínico Controlado / Estudo prognóstico Idioma: Inglês Ano de publicação: 2000 Tipo de documento: Artigo