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Oncotarget ; 5(11): 3607-10, 2014 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-25003820

RESUMEN

Erdheim-Chester disease (ECD) is a rare histiocytosis with a high prevalence of BRAF V600E mutation (>50% of patients). Patients with BRAF-mutant ECD can respond to BRAF inhibitors. Unfortunately, the lack of adequate archival tissue often precludes BRAF testing. We hypothesized that cell-free DNA (cfDNA) from plasma or urine can offer an alternative source of biologic material for testing. We tested for BRAF V600E mutation in cfDNA from the plasma and urine of 6 ECD patients. In patients with available archival tissue, the result of BRAF mutation analysis was concordant with plasma and urine cfDNA results in all 3 patients (100% agreement, kappa 1.00). In all 6 patients, BRAF mutation analysis of plasma and urine cfDNA was concordant in 5 of 6 patients (83% agreement, kappa 0.67). Testing for BRAF V600E mutation in plasma and urine cfDNA should be further investigated as an alternative to archival tissue mutation analysis.


Asunto(s)
ADN/sangre , Enfermedad de Erdheim-Chester/enzimología , Enfermedad de Erdheim-Chester/genética , Mutación , Proteínas Proto-Oncogénicas B-raf/genética , Adulto , Anciano , ADN/genética , Análisis Mutacional de ADN , Enfermedad de Erdheim-Chester/sangre , Enfermedad de Erdheim-Chester/orina , Femenino , Humanos , Masculino , Persona de Mediana Edad , Pronóstico , Estudios Prospectivos , Proteínas Proto-Oncogénicas B-raf/sangre , Proteínas Proto-Oncogénicas B-raf/orina
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