Comparación del hyper-CVAD con un régimen institucional en el tratamiento de la leucemia linfoblástica aguda del adulto en un hospital de México

  • Ramos-Peñafiel C
  • Cabrera-García Á
  • Rozen-Fuller E
  • et al.
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Abstract

In order to assess the mortality and toxicity of the Hyper-CVAD protocol used as first-line treatment of acute lymphoblastic leukemia, a retrospective cohort study was performed in patients less than 40 years of age from March to September 2011 treated with Hyper-CVAD regimen. Mortality and toxicity was compared with the results of patients treated with the institutional HGMLAL07 regimen between 2009-2012. 18 patients were included; the median age was 26 years old. Complete remissions (67.7% versus 81.9%) as well as one-year (40% versus 62%) and 2 year survival rates (18% versus 34%) were lower with the Hyper-CVAD regimen. By selecting only patients younger than 35 years, the effectiveness of Hyper-CVAD was also lower. In our experience and because of its high cost and toxicity, the Hyper-CVAD regimen should be limited to patients with relapsed or refractory leukemia.

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Ramos-Peñafiel, C. O., Cabrera-García, Á., Rozen-Fuller, E., González-León, G., Balderas, C., Kassack-Ipiña, J. J., … Collazo-Jaloma, J. (2014). Comparación del hyper-CVAD con un régimen institucional en el tratamiento de la leucemia linfoblástica aguda del adulto en un hospital de México. Revista Peruana de Medicina Experimental y Salud Pública, 31(3). https://doi.org/10.17843/rpmesp.2014.313.91

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