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Isoflavones and Radiation Therapy in Treating Patients With Localized Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
soy protein isolate
radiation therapy
Sponsored by
Barbara Ann Karmanos Cancer Institute
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring stage I prostate cancer, stage II prostate cancer

Eligibility Criteria

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

DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the prostate that is localized to the prostate gland Must be scheduled to receive curative radiotherapy for prostate cancer Not eligible for a higher priority study at the Karmanos Cancer Institute PATIENT CHARACTERISTICS: Performance status 0-3 Life expectancy Not specified Hematopoietic Not specified Hepatic Not specified Renal Not specified Other No organ function restrictions PRIOR CONCURRENT THERAPY: Chemotherapy No prior chemotherapy Endocrine therapy No prior hormonal therapy Radiotherapy See Disease Characteristics Other No other concurrent micronutrient supplements, herbs, or vitamins except 1 daily multivitamin

Sites / Locations

  • Barbara Ann Karmanos Cancer Institute

Outcomes

Primary Outcome Measures

Oxidative DNA damage at 3 and 6 months

Secondary Outcome Measures

Quality of life as measured by questionnaire at 3 and 6 months
Toxicity as measured by number and grade of adverse events weekly during radiation and at 3 and 6 months
Response as measured by prostate-specific antigen and clinical assessment at 3 and 6 months
Isoflavone serum level at 3 and 6 months

Full Information

First Posted
October 20, 2005
Last Updated
April 3, 2013
Sponsor
Barbara Ann Karmanos Cancer Institute
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00243048
Brief Title
Isoflavones and Radiation Therapy in Treating Patients With Localized Prostate Cancer
Official Title
Phase II Randomized Study of Soy Isoflavones in Patients With Localized Prostate Cancer Treated With Radiation Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
May 2002 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
October 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Barbara Ann Karmanos Cancer Institute
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: Eating a diet high in soy foods may slow the progression of some types of cancer. Isoflavones are compounds found in soy food that may slow the growth of prostate cancer cells and prevent further development of prostate cancer. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving isoflavones together with radiation therapy may be an effective treatment for prostate cancer. PURPOSE: This randomized phase II trial is studying the side effects and how well giving isoflavones together with radiation therapy works in treating patients with localized prostate cancer.
Detailed Description
OBJECTIVES: Determine the effect of soy protein isolate (isoflavones) and radiotherapy on the modulation of biomarkers in patients with localized prostate cancer. Determine the toxicity of this regimen in these patients. Determine the effect of this regimen on the quality of life of these patients. OUTLINE: This is a randomized, placebo-controlled study. Patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive oral soy protein isolate (isoflavones) twice daily for 6 months in the absence of disease progression or unacceptable toxicity. Arm II: Patients receive an oral placebo twice daily for 6 months in the absence of disease progression or unacceptable toxicity. In both arms, patients also undergo radiotherapy while receiving isoflavones or placebo. Quality of life is assessed periodically. PROJECTED ACCRUAL: A total of 70 patients will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
stage I prostate cancer, stage II prostate cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Dietary Supplement
Intervention Name(s)
soy protein isolate
Intervention Type
Radiation
Intervention Name(s)
radiation therapy
Primary Outcome Measure Information:
Title
Oxidative DNA damage at 3 and 6 months
Secondary Outcome Measure Information:
Title
Quality of life as measured by questionnaire at 3 and 6 months
Title
Toxicity as measured by number and grade of adverse events weekly during radiation and at 3 and 6 months
Title
Response as measured by prostate-specific antigen and clinical assessment at 3 and 6 months
Title
Isoflavone serum level at 3 and 6 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the prostate that is localized to the prostate gland Must be scheduled to receive curative radiotherapy for prostate cancer Not eligible for a higher priority study at the Karmanos Cancer Institute PATIENT CHARACTERISTICS: Performance status 0-3 Life expectancy Not specified Hematopoietic Not specified Hepatic Not specified Renal Not specified Other No organ function restrictions PRIOR CONCURRENT THERAPY: Chemotherapy No prior chemotherapy Endocrine therapy No prior hormonal therapy Radiotherapy See Disease Characteristics Other No other concurrent micronutrient supplements, herbs, or vitamins except 1 daily multivitamin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Omer Kucuk, MD
Organizational Affiliation
Barbara Ann Karmanos Cancer Institute
Official's Role
Study Chair
Facility Information:
Facility Name
Barbara Ann Karmanos Cancer Institute
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201-1379
Country
United States

12. IPD Sharing Statement

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Isoflavones and Radiation Therapy in Treating Patients With Localized Prostate Cancer

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