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1.
Br J Cancer ; 96(9): 1358-67, 2007 May 07.
Artículo en Inglés | MEDLINE | ID: mdl-17426706

RESUMEN

Gemcitabine (GEM)-based chemotherapy is regarded as the standard treatment of pancreatic adenocarcinoma, but yields a very limited disease control. Very few studies have investigated salvage chemotherapy after failure of GEM or GEM-containing chemotherapy and preclinical studies attempting to widen the therapeutic armamentarium, not including GEM, are warranted. MIA PaCa2, CFPAC-1 and Capan-1 pancreatic cancer cell lines were treated with GEM, fluouracil (5-FU), docetaxel (DCT), oxaliplatin (OXP), irinotecan (CPT-11), pemetrexed (PMX) and raltitrexed (RTX) as single agent. Pemetrexed, inducing apoptosis with IC50s under the Cmax in the three lines tested, appeared the most effective drug as single agent. Based on these results, schedule- and concentration-dependent drug interactions (assessed using the combination index) of PMX/GEM, PMX/DCT and PMX-CPT-11 were evaluated. The combinatory study clearly indicated the PMX and CPT-11 combination as the most active against pancreatic cancer. To confirm the efficacy of PMX-CPT-11 combination, we extended the study to a panel of 10 pancreatic cancer cell lines using clinically relevant concentrations (PMX 10 microM; CPT-11 1 microm). In eight of 10 lines, the PMX-CPT-11 treatment significantly reduced cell recovery and increased both the subG1 and caspase 3/7 fraction. After a 5-day wash out period, an increased fraction of subG1 and caspase3/7 persisted in PMX-CPT-11-pretreated cell lines and a significant reduction in the clonogenicity capacity was evident. Finally, in vivo, the PMX/CPT-11 combination showed the ability to inhibit xenograft tumours growth as second-line therapy after GEM treatment. The PMX and CPT-11 combination displays a strong schedule-independent synergistic cytotoxic activity against pancreatic cancer, providing experimental basis for its clinical testing as salvage chemotherapy in pancreatic cancer patients.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/farmacocinética , Camptotecina/análogos & derivados , Glutamatos/farmacología , Guanina/análogos & derivados , Neoplasias Pancreáticas/tratamiento farmacológico , Animales , Protocolos de Quimioterapia Combinada Antineoplásica/farmacología , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Apoptosis/efectos de los fármacos , Camptotecina/farmacocinética , Camptotecina/farmacología , Camptotecina/toxicidad , Ciclo Celular/efectos de los fármacos , Línea Celular Tumoral , Esquema de Medicación , Femenino , Glutamatos/farmacocinética , Glutamatos/toxicidad , Guanina/farmacocinética , Guanina/farmacología , Guanina/toxicidad , Humanos , Irinotecán , Ratones , Ratones Desnudos , Neoplasias Pancreáticas/patología , Pemetrexed , Trasplante Heterólogo
2.
Ann Ophthalmol ; 23(8): 312-7, 1991 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-1952642

RESUMEN

We present the case of a 29-year-old woman with the rare combination of lupus anticoagulant and bilateral optic disc edema. The linked etiopathologic problems are discussed to provide a proper clinical and ophthalmologic definition.


Asunto(s)
Inhibidor de Coagulación del Lupus/sangre , Papiledema/sangre , Corticoesteroides/uso terapéutico , Adulto , Enfermedades Autoinmunes/sangre , Femenino , Angiografía con Fluoresceína , Fondo de Ojo , Humanos , Papiledema/tratamiento farmacológico , Agudeza Visual , Campos Visuales
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