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Annexin A3 (ANXA3) as Protein-Based Marker for Non-Invasive Molecular Diagnostics of Prostate Carcinoma
This study is ongoing, but not recruiting participants.
Sponsors and Collaborators: ProteoSys AG
Charite University, Berlin, Germany
University Hospital Tuebingen
Medical Centre, Ludwigshafen, Germany
Medical University Innsbruck
Information provided by: ProteoSys AG
ClinicalTrials.gov Identifier: NCT00400894
  Purpose

Emerging from a differential proteomic study of sample pairs of prostate cancer and benign tissue, annexin A3 (ANXA3) was chosen as a potential novel biomarker for the early and non-invasive diagnosis of prostate cancer. We wanted to show or investigate, that:

  • ANXA3 can be detected in urine after standard digital rectal examination.
  • ANXA3 has better specificities than tPSA, in particular in the grey zone of PSA
  • ANXA3 can help avoid unnecessary biopsies
  • ANXA3 can in the long run replace PSA as a marker

Condition
Prostate Cancer
Benign Prostatic Hyperplasia
Prostatic Intraepithelial Neoplasia

MedlinePlus related topics: Cancer Prostate Cancer Urine and Urination
U.S. FDA Resources
Study Type: Observational
Study Design: Screening, Longitudinal, Defined Population, Retrospective/Prospective Study
Official Title: Annexin A3 (ANXA3) as Protein-Based Marker for Non-Invasive Molecular Diagnostics of Prostate Carcinoma

Further study details as provided by ProteoSys AG:

Estimated Enrollment: 750
Study Start Date: September 2005
Estimated Study Completion Date: September 2006
Detailed Description:

The aim of this multi centre and double-blinded study was to investigate specificities and sensitivities of early detection of prostate cancer with a new protein biomarker, annexin A3, using urine after digital rectal examination/massage (exprimate urine) in direct comparison to the corresponding measurements of the gold standard, total PSA. The material obtained by this non-invasive procedure was moreover used to determine appropriate cut-off values and optimal fractions (e.g. after centrifugation) and calibrations for quantitative measurements of this novel marker.

Patients (500-750) were (and are) continuously recruited from four clinical centres in Germany (Berlin, Tübingen, Ludwigshafen) and Austria (Innsbruck). The major aspect was:

• Can annexin A3 provide a better specificity than tPSA, in particular in the grey zone of PSA (2-10 ng/ml) and can annexin A3 thus contribute to a significant reduction of invasive transrectal biopsies?

  Eligibility

Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients with a histological confirmation of adenocarcinoma of the prostate
  • Patients with benign prostatic hyperplasia (confirmed by histology of lance biopsies or TUR-P)

Exclusion Criteria:

  • Patients with rectal extirpation
  • Patients with renal or bladder tumors
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00400894

Sponsors and Collaborators
ProteoSys AG
Charite University, Berlin, Germany
University Hospital Tuebingen
Medical Centre, Ludwigshafen, Germany
Medical University Innsbruck
Investigators
Principal Investigator: Martin Schostak, PD Dr. University Medical Centre Charité, Berlin, Germany
Study Director: André Schrattenholz, Prof. Dr. ProteoSys AG, Mainz, Germany
  More Information

Publications:
Publications indexed to this study:
Study ID Numbers: EA 4/033/06
Study First Received: November 16, 2006
Last Updated: February 2, 2007
ClinicalTrials.gov Identifier: NCT00400894  
Health Authority: Germany: Ethics Commission

Keywords provided by ProteoSys AG:
prostate cancer
annexin A3
early detection
exprimate urine

Study placed in the following topic categories:
Prostatic Intraepithelial Neoplasia
Hyperplasia
Prostatic Diseases
Genital Neoplasms, Male
Prostatic Hyperplasia
Carcinoma in Situ
Urogenital Neoplasms
Genital Diseases, Male
Prostatic Neoplasms
Neoplasms, Glandular and Epithelial
Carcinoma

Additional relevant MeSH terms:
Neoplasms
Neoplasms by Histologic Type
Neoplasms by Site
Pathologic Processes

ClinicalTrials.gov processed this record on January 16, 2009