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1.
Indian J Cancer ; 2014 Jan-Mar; 51(1): 5-9
Artículo en Inglés | IMSEAR | ID: sea-154271

RESUMEN

INTRODUCTION: Imatinib is a bcr‑abl tyrosine kinase inhibitor which has revolutionized the treatment for chronic myeloid leukemia (CML). Even though there is much data on CML chronic phase, there is limited data on imatinib‑naïve advanced phase CML. MATERIALS AND METHODS: We retrospectively analysed 90 patients with advanced phase CML (accelerated phase [AP]: 51 and blast crisis [BC]: 39), patients who received imatinib as frontline therapy. RESULTS: The median age of presentation in CML‑AP and CML‑BC were 32 years (12‑61) and 39 years (8‑59), respectively. Imatinib at 600 mg/day was initiated within 2 weeks of diagnosis. Median time to complete hematological response in both CML‑AP and CML‑BC was 3 months (CML‑AP: 1‑9 months and CML‑BC: 1‑14 months). At 6 months 30 (59%) CML‑AP and 15 (38%) CML‑BC patients achieved major cytogenetic response (MCyR), of them 24 (47%) and 10 (25.6%) being the complete cytogenetic response, respectively. At a median follow‑up of 41 months, the median overall survival in CML‑AP was 61 months, but in CML‑BC it was 14 months. The median progression‑free survival and event‑free survival were 30 months and 23 months in CML‑AP and 14 and 12 months in CML‑BC, respectively. On univariate analysis, performance status (PS), spleen size, and MCyR predicted survival in AP, whereas in BC, platelet count, PS, and early MCyR were predictive. Non‑hematologic and hematologic adverse events were observed in 80% and 60% of patients, respectively. Dose was reduced in 10% of patients for grade IV toxicity and interrupted in 30% for grade III toxicity. CONCLUSION: Front‑line imatinib is an option in advanced phases of CML especially in CML‑AP in low‑resource countries, where stem cell transplantation and alternate TKIs are not available.


Asunto(s)
Adolescente , Adulto , Antineoplásicos/uso terapéutico , Benzamidas/uso terapéutico , Crisis Blástica/tratamiento farmacológico , Crisis Blástica/mortalidad , Crisis Blástica/patología , Niño , Resistencia a Antineoplásicos/efectos de los fármacos , Femenino , Estudios de Seguimiento , Humanos , Leucemia Mielógena Crónica BCR-ABL Positiva/tratamiento farmacológico , Leucemia Mielógena Crónica BCR-ABL Positiva/mortalidad , Leucemia Mielógena Crónica BCR-ABL Positiva/patología , Masculino , Persona de Mediana Edad , Estadificación de Neoplasias , Piperazinas/uso terapéutico , Pronóstico , Pirimidinas/uso terapéutico , Inducción de Remisión , Estudios Retrospectivos , Tasa de Supervivencia , Adulto Joven
2.
Rev. méd. Chile ; 137(8): 1023-1030, ago. 2009. ilus, tab
Artículo en Español | LILACS | ID: lil-531992

RESUMEN

Background: Asymptomatic patients with severe coronary atherosclerosis may have a normal resting electrocardiogram and stress test. Aim: To assess the yield of Gated Single Photon Emission Computer Tomography (SPECT) for the screening of silent myocardial ischemia in type 2 diabetic patients. Material and methods: Electrocardiogram, stress test and gated-SPECT were performed on 102 type 2 diabetic patients aged 60 ± 8 years without cardiovascular symptoms. AH subjects were also subjected to a coronary angiography whose results were used as gold standard. Results: Gated-SPECT showed myocardial ischemia on 26.5 percent of studied patients. The sensibility, specifity accuracy, positive predictive value and negative predictive value were 92.3 percent, 96 percent, 95 percent, 88.8 percent, 97.3 percent, respectively. In four and six patients ischemia was detected on resting electrocardiogram and stress test, respectively. Eighty percent of patients with doubtful resting electrocardiogram results and 70 percent with a doubtful stress test had a silent myocardial ischemia detected by gated-SPECT There was a good agreement between the results of gated-SPECT and coronary angiography (k =0.873). Conclusions: Gated-SPECT was an useful tool for the screening of silent myocardial ischemia.


Asunto(s)
Femenino , Humanos , Masculino , Persona de Mediana Edad , /complicaciones , Isquemia Miocárdica , Tomografía Computarizada de Emisión de Fotón Único/normas , Electrocardiografía/métodos , Prueba de Esfuerzo , Isquemia Miocárdica/diagnóstico , Reproducibilidad de los Resultados
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