Clinical Trials Directory

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UnknownNCT00955435

Study of Blood and Urine Samples in Patients With Newly Diagnosed Localized Prostate Cancer Treated With Hormone Therapy and Radiation Therapy. ICORG 06-15

Proteomic Analysis of the Combined Hormonal Therapy and Radiation Therapy for Localized Prostate Cancer

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (actual)
Sponsor
Cancer Trials Ireland · Network
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Studying samples of blood and urine from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how patients will respond to treatment. PURPOSE: This clinical trial is studying blood and urine samples in patients with newly diagnosed localized prostate cancer treated with hormone therapy and radiation therapy.

Detailed description

OBJECTIVES: * Detect changes in serum and urine proteomic profiles that predict outcome in patients with newly diagnosed localized prostate cancer treated with hormonal therapy and radiotherapy. * Identify prognostic and biochemical markers of early disease progression in patients treated with this regimen. * Identify unique protein expression and temporal alterations, in these profiles, that facilitate understanding of the factors predicting relapse or toxicity. * Identify molecular signatures that allow identification of targets for therapeutic intervention. OUTLINE: This is a multicenter study. Patients receive induction hormones\* (bicalutimide and releasing-hormone agonist) for approximately 4 months prior to starting radiotherapy (per standard treatment). Patients then receive radiotherapy consisting of 74 Gy up to a maximum of 81 Gy to the prostate gland per standard treatment.NOTE: \* Patients receiving short-term hormonal treatment for 4-8 months are eligible to participate in the trial. Blood and urine samples are collected at baseline, and periodically during and after induction therapy for proteomic analysis. After completion of study therapy, patients are followed up periodically for 5 years and yearly thereafter for the duration of the trial.

Conditions

Interventions

TypeNameDescription
OTHERNon-interventionalPatients receive induction hormones\* (bicalutimide and releasing-hormone agonist) for approximately 4 months prior to starting radiotherapy per standard treatment. Patients then receive radiotherapy consisting of 74 Gy up to a maximum of 81 Gy to the prostate gland per standard treatment.
GENETICProtein expression analysis
GENETICProteomic profiling
OTHERLaboratory biomarker analysis

Timeline

Start date
2006-02-01
First posted
2009-08-10
Last updated
2021-02-18

Locations

2 sites across 1 country: Ireland

Source: ClinicalTrials.gov record NCT00955435. Inclusion in this directory is not an endorsement.