search
Back to results

Transrectal Tumour Oxygen - US Army

Primary Purpose

Prostatic Neoplasms

Status
Active
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Pre-treatment tumour oxygen measurements
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostatic Neoplasms

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria: A histologic diagnosis of adenocarcinoma of the prostate A decision to treat using high-dose conformal radiotherapy, with or without neoadjuvant and concurrent androgen ablation Clinical stage T2a or T2b, N0, M0 (UICC 1997 68) No hormonal or cytotoxic anti-cancer therapy prior to study entry ECOG performance status of 2 or less Ability to understand the English language Signed informed consent Exclusion Criteria: Patients with prior or active malignancy within 5 years of the diagnosis of prostate cancer, except non-melanoma skin cancer

Sites / Locations

  • Princess Margaret Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

hypoxia and RT in prostate cancer

Arm Description

Outcomes

Primary Outcome Measures

To determine the relationship between pre-treatment prostate cancer oxygen levels and long-term disease control following treatment with radiotherapy, and the independent prognostic effect of oxygen measurements.
To determine the relationship between pre-treatment tumor oxygen levels and mutations of the p53 gene, and the impact of this interaction on patient outcome.

Secondary Outcome Measures

To evaluate oxygen levels in clinically localized prostate cancer prior to treatment.
To determine the relationship between pre-treatment tumor oxygen levels and the subsequent development of metastases and androgen-resistant prostate cancer.
To determine whether androgen ablation overcomes any adverse effect of hypoxia on outcome.

Full Information

First Posted
September 8, 2005
Last Updated
April 5, 2023
Sponsor
University Health Network, Toronto
Collaborators
U.S. Army Medical Research and Development Command, Princess Margaret Hospital, Canada
search

1. Study Identification

Unique Protocol Identification Number
NCT00160979
Brief Title
Transrectal Tumour Oxygen - US Army
Official Title
A Study of Transrectal Tumour Oxygen Measurements in Patients With Clinically Localized Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2001 (undefined)
Primary Completion Date
January 2028 (Anticipated)
Study Completion Date
January 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
U.S. Army Medical Research and Development Command, Princess Margaret Hospital, Canada

4. Oversight

5. Study Description

Brief Summary
Prostate cancer is now the most commonly diagnosed tumor among men in the United States. Most patients have tumors that are confined to the prostate gland at diagnosis and are suitable for treatment with surgery or radiotherapy (RT) that is aimed at curing the disease. Nevertheless, despite recent improvements in these treatments, a large number of men continue to die of prostate cancer. These patients often have spread of tumor to other areas of the body, and are treated with hormones that produce initial tumor shrinkage. However, over time the tumor learns to grow despite continued hormonal treatment. Effective therapy for patients with hormone-resistant prostate cancer is lacking and patients often deteriorate quickly and die. Thus, there is a need for better treatment that cures prostate cancer at an early stage, and a better understanding of the biology of prostate cancer specifically with respect to factors that determine the effectiveness of RT, the spread of tumor and the development of hormone-resistant disease. Low levels of oxygen (hypoxia) are known to exist in many human tumors, and studies have shown that hypoxic tumors are less likely to be cured by RT. In addition, hypoxia may lead to lower cure rates following surgery, spread of cancer to other areas of the body, and changes in the genetic characteristics of the cancer cells that cause them to behave more aggressively. The importance of hypoxia in prostate cancer has not previously been evaluated. The aims of this study are to determine how often hypoxia occurs in early prostate cancer and whether hypoxia influences the success of RT, tumor spread beyond the prostate to bones and other organs and the development of hormone-resistant disease. Patients will have tumor oxygen levels measured using a special fine-needle electrode system prior to beginning treatment with either RT or the combination of hormones plus RT. The measurements will be made through the rectum using ultrasound to position and guide the electrode. A biopsy of the tumor will be obtained at the site of the measurements, and this will be used to determine how oxygen influences changes in the genetic character of prostate cancer cells. A total of 195 patients will be evaluated in this way over 3 years. This study will provide unique information about the behavior of prostate cancer, which may help explain why currently available treatments including surgery, RT and hormones fail to cure patients. Assuming that this study shows hypoxia to be important in prostate cancer, future work will focus on new anti-hypoxia treatments to be used in combination with surgery or RT with the aim of overcoming this obstacle and improving cure rates.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatic Neoplasms

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
195 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
hypoxia and RT in prostate cancer
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Pre-treatment tumour oxygen measurements
Intervention Description
Pre-treatment tumour oxygen measurements
Primary Outcome Measure Information:
Title
To determine the relationship between pre-treatment prostate cancer oxygen levels and long-term disease control following treatment with radiotherapy, and the independent prognostic effect of oxygen measurements.
Time Frame
after follow-up is completed
Title
To determine the relationship between pre-treatment tumor oxygen levels and mutations of the p53 gene, and the impact of this interaction on patient outcome.
Time Frame
after follow up is completed
Secondary Outcome Measure Information:
Title
To evaluate oxygen levels in clinically localized prostate cancer prior to treatment.
Time Frame
after follow-up is completed
Title
To determine the relationship between pre-treatment tumor oxygen levels and the subsequent development of metastases and androgen-resistant prostate cancer.
Time Frame
after follow is completed
Title
To determine whether androgen ablation overcomes any adverse effect of hypoxia on outcome.
Time Frame
after follow up is completed

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A histologic diagnosis of adenocarcinoma of the prostate A decision to treat using high-dose conformal radiotherapy, with or without neoadjuvant and concurrent androgen ablation Clinical stage T2a or T2b, N0, M0 (UICC 1997 68) No hormonal or cytotoxic anti-cancer therapy prior to study entry ECOG performance status of 2 or less Ability to understand the English language Signed informed consent Exclusion Criteria: Patients with prior or active malignancy within 5 years of the diagnosis of prostate cancer, except non-melanoma skin cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Milosevic, MD
Organizational Affiliation
Princess Margaret Hospital, Canada
Official's Role
Principal Investigator
Facility Information:
Facility Name
Princess Margaret Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2M9
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Transrectal Tumour Oxygen - US Army

We'll reach out to this number within 24 hrs