Study of Validated Biomarkers in Urine for Patients with Adenocarcinoma of the Prostate

Overview

Información sobre este estudio

The purpose of this study is to assess the accuracy of DNA marker candidates (individually and in combination) assayed from urine and prostatic fluid (collected following digital prostate massage) for detection of prostate cancer.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Patient has a histology diagnosis of prostatic carcinoma/adenocarcinoma with a Gleason score.
  • Patient has an elevated PSA, palpable prostate nodule, abnormal imaging finding or worrisome PSA velocity where prostate biopsy is planned.
  • Male, age ≥ 18 years old.

Exclusion Criteria:

  • Patients has a history of bladder cancer.
  • Patient has had biopsy (within the last 6 weeks).
  • Patient has had surgery to completely remove current target pathology.
  • The current target pathology is a recurrence.
  • Patient has had a transplant.
  • Patient has received chemotherapy class drugs (e.g. Docetaxal, Methotrexate) or therapeutic radiation.
  • Patient has had anti-androgen (Flutamide, Androcur, Casodex, Nilandron) or LHRH (Lupron, Zoladex) therapy.
  • Patient has transurethral instrumentation (cystoscopy, placement of urinary catheter) within the past week.
  • Patient has chronic indwelling urinary catheter.
  • Patient has prior focal ablation (e.g. HIFU or cryoablation) of prostate cancer.
  • Patient has had a urinary tract infection within 14 days of collection.
  • Patient has ejaculated within 2 days of sample collection.

 

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

John Kisiel, M.D.

Abierto para la inscripción

Contact information:

Anna Gonser CCRP

(507) 538-4883

Gonser.Anna@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20446373

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