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Evaluate Risk Factors which Predict the Transformation of Early Stage to Clinically Aggressive Prostate Cancer

This study is currently recruiting patients.

Sponsored by: Department of Veterans Affairs
Information provided by: Department of Veterans Affairs

Purpose

Environmental factors such as diet and cigarette smoking may play a role in predicting the progression of early stage prostate cancer to advance disease. The goal of this project is to establish an observational cohort of patients with early stage prostate cancer who elect not to undergo radical prostatectomy or radiation therapy to evaluate risk factors which predict the transformation of early stage to clinically aggressive disease.

Condition
Prostate Cancer

MedlinePlus related topics:  Prostate Cancer

Study Type: Observational
Study Design: Natural History, Longitudinal, Defined Population, Prospective Study

Official Title: Study #719B - Prospective Cohort of Early Stage Prostate Cancer

Further Study Details: 

Expected Total Enrollment:  1000

Study start: January 2001;  Study completion: January 2005

Primary Objective: Evaluate risk factors which predict the transformation of early stage to clinically aggressive disease.

Intervention: None

Study Abstract: Environmental factors such as diet and cigarette smoking may play a role in predicting the progression of early stage prostate cancer to advance disease. The goal of this project is to establish an observational cohort of patients with early stage prostate cancer who elect not to undergo radical prostatectomy or radiation therapy to evaluate risk factors which predict the transformation of early stage to clinically aggressive disease. A total of 1,000 US male veterans with early stage prostate cancer will be recruited to participate in the study. In order to maximize African-American participation, VA medical centers that serve large minority populations will be utilized for recruitment. Eligible participants must have an early stage prostate cancer diagnosis (T0-T2) with no known involved lymph nodes or metastases, and no prior history of cancer (with the exception of nonmelanoma skin cancer) or other major illness that would preclude long term participation. Individuals willing to participate will be administered a lifestyle questionnaire and a dietary assessment. The lifestyle survey ascertains baseline demographics, mode of cancer diagnosis, medical history, smoking, family history of prostate cancer, alcohol use, level of physical activity, and other potential risk factors for prostate cancer progression. Nutritional parameters will be measured through a self-administered, semi-quantitative food frequency questionnaire. A blood specimen will also be collected for genetic and biochemical research. Participants will be followed annually with additional lifestyle and dietary questionnaires. Both surveys are currently being tested through a pilot project in a population of prostate cancer survivors to assess the feasibility of collecting diet and lifestyle data in veterans and to refine the study methods and recruitment strategies (the current versions of the surveys are included). A pilot study is being conducted to test different survey types and mailing techniques. The results from the pilot project will help improve the survey methodology and refine the survey research tools to accurately assess dietary and lifestyle factors. Lifestyle surveys have been created to ascertain baseline demographics and potential risk factors for prostate cancer survival and progression. Two versions have been generated to test participant response to varying survey lengths (a short form vs. a long form). The initial mailing of the lifestyle and dietary surveys was directed to 836 veterans diagnosed with prostate cancer in the Boston VA Healthcare Network (ICD-9 code in patient treatment files). Surveys were sent to 132 African-American veterans, 342 white veterans, and 362 veterans with no known race. An Access database has been developed to track survey response and blood collection sites have been established in VA health facilities in the Boston area. A phone tracking system has been established to answer participants questions about the survey. A total of 251 (30%) of the veterans completed the surveys and 72% agreed to provide blood samples. The response rate was 11% for African-Americans, 28% for whites, and 27% for unknown race. Follow-up mailings are currently being sent to veterans who didn’t respond to the initial survey request. A telephone survey is being designed to target African-American non-responders to improve survey response in this cohort. Prostate cancer is the most commonly diagnosed cancer in men and the second most common cause of cancer deaths among men in the United States. Counseling patients with early stage disease about treatment options is extremely difficult since the relative benefit of different approaches is not known. The evidence to date indicates that there is no clear benefit with invasive intervention over watchful waiting. In addition, little is known about risk factors which predict the transformation of early stage prostate cancer to clinically aggressive disease. This is of particular concern in the VA since more than a third of all veterans are over age 65. The ability to differentiate individuals with early stage prostate cancer from those with disease that will become clinically aggressive would have enormous benefits. It would help allay the anxiety of those with indolent disease and potentially reduce the morbidity and mortality of those with disease likely to become clinically aggressive.

Eligibility

Genders Eligible for Study:  Male

Criteria

US male veterans with early stage prostate cancer.

Location and Contact Information


Arizona
      Southern Arizona VAHCS, Tucson,  Arizona,  85723,  United States; Recruiting
Maria Bishop, MD  520-792-1450  Ext. 11807    maria.bishop@med.va.gov 

California
      Long Beach VAHCS, Long Beach,  California,  90822,  United States; Recruiting
Padmini Iyer, MD  562-826-5748  Ext. 5526    padmini.iyer@med.va.gov 

District of Columbia
      Washington D.C. VAMC, Washington,  District of Columbia,  20422,  United States; Recruiting
Steven Krasnow, MD  202-745-8179    steven.krasnow@med.va.gov 

Florida
      Tampa (James A Haley) VAMC, Tampa,  Florida,  33612,  United States; Recruiting
Raul Salup, MD  813-972-7579    raslup@gte.net 

Missouri
      Kansas City VAMC, Kansas City,  Missouri,  64128,  United States; Recruiting
Peter J VanVeldhuizen, MD  816-861-4700  Ext. 6775    vanveldhuizen.peter@kasas-city.va.gov 

      St. Louis VAMC (John Cochran Division), St. Louis,  Missouri,  63106,  United States; Recruiting
Melvin Blanchard, MD  314-652-4100    melvin.blanchard@med.va.gov 

New York
      Syracuse VAMC, Syracuse,  New York,  13210,  United States; Terminated

      Northport VAMC, Northport,  New York,  11768,  United States; Recruiting
Mohammad H Zarrabi, MD, MACP  631-261-4400  Ext. 2568    mohammad.zarrabi@med.va.gov 

Pennsylvania
      Pittsburgh VAMC, Pittsburgh,  Pennsylvania,  15240,  United States; Recruiting
Thomas R Hakala, MD  412-688-6209    hakalatr@msx.upmc.edu 

Texas
      Houston VAMC, Houston,  Texas,  77030,  United States; Recruiting
Terry Hayes, MD, PHD  713-794-7368    thayes@bcm.tmc.edu 

Virginia
      Richmond (McGuire) VAMC, Richmond,  Virginia,  23249,  United States; Recruiting
Michael Godschalk, MD  804-675-5088    michael.godschalk@med.va.gov 

West Virginia
      Huntington VA Medical Center, Huntington,  West Virginia,  25704,  United States; Recruiting
Sandra Prunty, RN, PhD  304-429-6775  Ext. 3530    sandra.prunty@med.va.gov 

More Information

Study ID Numbers:  719B
Record last reviewed:  January 2004
Record first received:  February 15, 2001
ClinicalTrials.gov Identifier:  NCT00011349
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2004-11-09
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