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

Cancer Trials Ireland60 enrolled

Overview

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.

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.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Prostate Cancer

Interventions

Non-interventionalOTHER

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.

Protein expression analysisGENETIC

Proteomic profilingGENETIC

Eligibility

Sex: MALEMin age: 18 Years

Medical Language ↔ Plain English

Inclusion criteria: 1. Age 18 years or over. 2. Histologically confirmed invasive adenocarcinoma of the prostate (by TURP or TRUS). 3. Localised prostate cancer with a Gleason score 7 4. Short term hormonal treatment 4-8 months 5. Performance status of KPS ≥ 60 / WHO 0-2 6. Absence of distant metastases Exclusion criteria: 1. The patient has previously received treatment for prostate cancer other than TURP/ TRUS 2. The patient has had a bilateral orchidectomy 3. The patient has previously received hormonal treatment for prostate cancer 4. Evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the patient to participate in the trial. In the opinion of the investigator, any evidence of severe or uncontrolled systematic disease (e.g. unstable or uncompensated respiratory, cardiac, hepatic or renal disease 5. The patient has or had other co-existing malignancies within the past 5 years other than non- melanoma skin cancer 6. Treatment with non-approved or investigational drug within 30 days before day one of the trial

Locations (2)

Beacon Hospital

Dublin, Ireland

Saint Luke's Radiation Oncology Network

Dublin, Ireland

Outcomes

Primary Outcomes

Changes in serum and urine proteomic profiles

Time frame: Ongoing until patient progression

Prognostic and biochemical markers of early disease progression

Time frame: Ongoing until patient progression

Protein expression and temporal alterations

Time frame: Ongoing until patient progression

Molecular targets

Time frame: Ongoing until patient progression

Data from ClinicalTrials.gov

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