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Se estima que 20 millones de hombres son examinados para detectar el cáncer de próstata en los EE.UU. cada año, y más de 1 millón son posteriormente remitidos para biopsia. La decisión de la biopsia de glándula de próstata de un paciente se realiza con base en un examen rectal digital (DRE) y las pruebas de sangre, como PSA (antígeno prostático específico). El diagnóstico del cáncer de próstata puede ser difícil en algunos pacientes, particularmente entre aquellos que tienen valores intermedios de PSA (4-10 ng / ml) con normalidad DRE. En estos casos, los urólogos deben decidir si se debe realizar una biopsia o colocar al paciente en un programa de vigilancia activa (manejo expectante). Ya que el 75% de las biopsias de próstata primario no muestran cáncer, evitar procedimientos innecesarios evita también el dolor del paciente y el gasto, y favorece la auséncia de posibles complicaciones relacionadas con el procedimiento, tales como la hemorragia y la sepsis (una infección grave, a veces mortal de la sangre). Además, las biopsias no siempre detecta el cáncer de próstata cuando está presente.

Aun cuando el cáncer de próstata es diagnosticado definitivamente, la clasificación clínica de la biopsia y la puntuación Gleason no se correlaciona necesariamente con la estadificación patológica. Aproximadamente el 50% de los hombres cuya enfermedad se cree que está localizado en la próstata antes de la cirugía en realidad tienen la extensión del tumor más allá de la prostate1, y una minoría significativa ya ha desarrollado la enfermedad metastásica. Determinar cuáles tumores son agresivos basados ​​en la biopsia y el puntaje de Gleason es particularmente difícil, con puntuaciones de Gleason intermedio de 6-7. En concreto, dentro de esta "zona gris" para las puntuaciones de Gleason, la capacidad de predecir agresividad de la enfermedad (como la extensión extracapsular, invasión de vesículas seminales y ganglios linfáticos) es limitada, incluso cuando los resultados de la biopsia de próstata son acoplados con otros parámetros clínicos como la física examen y PSA levels. las importantes necesidades clínicas een la detección de cáncer de próstata y la evaluación de riesgos son la fuerza impulsora detrás de los esfuerzos Metabolon para desarrollar mejores diagnósticos en esta área.

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La prueba de detección de cáncer de próstata Metabolon se basa en la detección de una firma metabólica única de la pastilla, donde se centrifúga una pequeña muestra de orina tomada después de la DRE. Esta prueba de alta precisión se puede realizar antes de la biopsia primaria (para informar a la decisión de realizar una biopsia), en el momento de la biopsia, o después de una primera biopsia negativa (para informar a la decisión de realizar una segunda biopsia). La prueba también se puede utilizar durante el proceso de manejo expectante. Porque la prueba Metabolon es no invasiva, que proporciona información clínica adicional para guiar el médico la toma de decisiones y mejorar el manejo del paciente y reducir al mínimo el riesgo para el paciente y el costo agregado de una biopsia innecesaria.

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La biopsia es el estándar de oro para el diagnóstico de cáncer de próstata, y el estudio histopatológico de la biopsia del paciente es uno de los factores utilizados para determinar si el cáncer se encuentra en una etapa temprana o avanzada. La prueba de Metabolon  hace la medición de un grupo de metabolitos en el tejido de la biopsia de próstata que le permite al médico determinar con mayor precisión si el tumor del paciente es agresivo. Esta prueba se realiza en el líquido en que biopsias centrales de próstatas se sumergen antes de su procesamiento por el patólogo. Proceso patentado de Metabolon para la extracción de metabolito de la biopsia de los núcleos no pone en peligro el tejido de la biopsia o alterar la morfología de los tejidos. La prueba de evaluación de biopsia de próstata Prostarix ™ proporciona información valiosa acerca de los médicos de la agresividad del cáncer de próstata de sus pacientes, lo que permite una mejor toma de decisiones en el manejo clínico de la enfermedad del paciente.

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