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1.
Int J Clin Oncol ; 12(2): 125-30, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17443280

RESUMO

BACKGROUND: The efficacy of individual chemotherapy based on chemosensitivity has scarcely been studied. METHODS: We examined the chemosensitivites for four anticancer agents - 1-(4-amino-2-methyl-5-pyrimidinyl) methyl-3 (2-chloroethyl)-3-nitrosourea hydrochloride (ACNU), carboplatin, cisplatin, and etoposide - of 43 malignant astrocytic tumors (21 anaplastic astrocytomas and 22 glioblastomas) by using a collagen gel matrix assay, and we also determined the survival periods of the tumor-bearing patients. The chemosensitivity was evaluated in terms of the growth inhibition rate, using 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl-tetrazolium bromide (MTT) method. RESULTS: For the anaplastic astrocytomas, the mean growth inhibitory rate was 33.2% with cisplatin, 37.2% with carboplatin, 28.0% with ACNU, and 24.8% with etoposide. For the glioblastomas, these rates were 36.9%, 42.3%, 23.2%, and 34.8%, respectively. The median overall and progression-free survivals of anaplastic astrocytoma-bearing patients who had undergone chemotherapy with two anticancer drugs, both of which showed significant anticancer activity (growth inhibitory rate >30%) were significantly longer than those of the patients who had been treated with two drugs, one or both of which did not show significant anticancer activity. On the other hand, there was no significant difference in the overall or the progression-free survivals in the two corresponding groups of glioblastoma-bearing patients. CONCLUSION: The collagen gel matrix assay is clinically useful to determine in vitro chemosensitivity that reflects in vivo chemosensitivity. Individual chemotherapy for malignant astrocytic tumors, based on chemosensitivity data, could contribute to longer survival, particularly in anaplastic astrocytoma-bearing patients.


Assuntos
Antineoplásicos/uso terapêutico , Astrocitoma/tratamento farmacológico , Astrocitoma/patologia , Carboplatina/uso terapêutico , Cisplatino/uso terapêutico , Colágeno , Etoposídeo/uso terapêutico , Nimustina/uso terapêutico , Adulto , Idoso , Neoplasias do Sistema Nervoso Central/tratamento farmacológico , Progressão da Doença , Intervalo Livre de Doença , Ensaios de Seleção de Medicamentos Antitumorais , Feminino , Espuma de Fibrina , Seguimentos , Glioblastoma/tratamento farmacológico , Glioblastoma/patologia , Humanos , Japão , Avaliação de Estado de Karnofsky , Masculino , Pessoa de Meia-Idade , Sensibilidade e Especificidade , Análise de Sobrevida , Adesivos Teciduais , Resultado do Tratamento , Carga Tumoral/efeitos dos fármacos , Células Tumorais Cultivadas/efeitos dos fármacos
2.
Neurol Med Chir (Tokyo) ; 44(6): 311-6, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15253547

RESUMO

A 30-year-old female presented with a rare case of isolated recurrence of granulocytic sarcoma manifesting as extra- and intracranial masses 16 months after successful treatment of acute myeloblastic leukemia (M-2). She presented with a swelling located on her forehead that had appeared just after hitting her forehead, and never diminished in size. The mass was elastic hard and not freely mobile. Computed tomography and magnetic resonance imaging demonstrated enhanced masses in the right frontal extra- and intracranial region with no bone destruction. There was no evidence of relapse in the bone marrow. Needle aspiration biopsy of the subscalpal mass was performed. Fluorescence in situ hybridization revealed AML1/MTG8 fusion gene associated with t(8; 21). Two courses of systemic chemotherapy with high-dose cytarabine and total neural axis irradiation resulted in complete remission.


Assuntos
Neoplasias Encefálicas/patologia , Sarcoma Mieloide/patologia , Adulto , Antineoplásicos/uso terapêutico , Biópsia por Agulha , Lesões Encefálicas/complicações , Neoplasias Encefálicas/etiologia , Subunidade alfa 2 de Fator de Ligação ao Core , Citarabina/uso terapêutico , Proteínas de Ligação a DNA/genética , Feminino , Humanos , Hibridização in Situ Fluorescente , Leucemia Mieloide Aguda/etiologia , Leucemia Mieloide Aguda/genética , Leucemia Mieloide Aguda/patologia , Imageamento por Ressonância Magnética , Proteínas Proto-Oncogênicas/genética , Proteína 1 Parceira de Translocação de RUNX1 , Sarcoma Mieloide/tratamento farmacológico , Sarcoma Mieloide/etiologia , Fatores de Transcrição/genética
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