Transrectal Tumour Oxygen - US Army

Sponsor
University Health Network, Toronto (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT00160979
Collaborator
U.S. Army Medical Research and Development Command (U.S. Fed), Princess Margaret Hospital, Canada (Other)
195
1
1
324
0.6

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Pre-treatment tumour oxygen measurements
Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
195 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
A Study of Transrectal Tumour Oxygen Measurements in Patients With Clinically Localized Prostate Cancer
Study Start Date :
Jan 1, 2001
Anticipated Primary Completion Date :
Jan 1, 2028
Anticipated Study Completion Date :
Jan 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: hypoxia and RT in prostate cancer

Procedure: Pre-treatment tumour oxygen measurements
Pre-treatment tumour oxygen measurements

Outcome Measures

Primary Outcome Measures

  1. 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. [after follow-up is completed]

  2. 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. [after follow up is completed]

Secondary Outcome Measures

  1. To evaluate oxygen levels in clinically localized prostate cancer prior to treatment. [after follow-up is completed]

  2. To determine the relationship between pre-treatment tumor oxygen levels and the subsequent development of metastases and androgen-resistant prostate cancer. [after follow is completed]

  3. To determine whether androgen ablation overcomes any adverse effect of hypoxia on outcome. [after follow up is completed]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Princess Margaret Hospital Toronto Ontario Canada M5G 2M9

Sponsors and Collaborators

  • University Health Network, Toronto
  • U.S. Army Medical Research and Development Command
  • Princess Margaret Hospital, Canada

Investigators

  • Principal Investigator: Michael Milosevic, MD, Princess Margaret Hospital, Canada

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Health Network, Toronto
ClinicalTrials.gov Identifier:
NCT00160979
Other Study ID Numbers:
  • UHN REB 00-0443-C
  • US Army DAMD17-01-1-0111
First Posted:
Sep 12, 2005
Last Update Posted:
Oct 6, 2021
Last Verified:
Oct 1, 2021
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 6, 2021