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Early Stage Prostate Cancer Cohort

11. April 2013 aktualisiert von: US Department of Veterans Affairs

CSP #719B - Prospective Cohort of Early Stage Prostate Cancer

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.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Detaillierte Beschreibung

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.

Studientyp

Beobachtungs

Einschreibung (Tatsächlich)

1116

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Arizona
      • Tucson, Arizona, Vereinigte Staaten, 85723
        • Southern Arizona VA Health Care System, Tucson
    • California
      • Long Beach, California, Vereinigte Staaten, 90822
        • VA Medical Center, Long Beach
    • District of Columbia
      • Washington, District of Columbia, Vereinigte Staaten, 20422
        • VA Medical Center, DC
    • Florida
      • Tampa, Florida, Vereinigte Staaten, 33612
        • James A. Haley Veterans Hospital, Tampa
    • Massachusetts
      • Boston, Massachusetts, Vereinigte Staaten, 02130
        • VA Medical Center, Jamaica Plain Campus
    • Missouri
      • Kansas City, Missouri, Vereinigte Staaten, 64128
        • VA Medical Center, Kansas City MO
      • St Louis, Missouri, Vereinigte Staaten, 63106
        • VA Medical Center, St Louis
    • New York
      • Northport, New York, Vereinigte Staaten, 11768
        • VA Medical Center, Northport
      • Syracuse, New York, Vereinigte Staaten, 13210
        • VA Medical Center, Syracuse
    • Pennsylvania
      • Pittsburgh, Pennsylvania, Vereinigte Staaten, 15240
        • VA Pittsburgh Health Care System
    • Texas
      • Houston, Texas, Vereinigte Staaten, 77030
        • Michael E. DeBakey VA Medical Center (152)
    • Virginia
      • Richmond, Virginia, Vereinigte Staaten, 23249
        • Hunter Holmes McGuire VA Medical Center
    • West Virginia
      • Huntington, West Virginia, Vereinigte Staaten, 25704
        • VA Medical Center, Huntington

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Männlich

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

We propose to establish an observational cohort of 1000 US male veterans from 10-12 VAMC with early stage prostate cancer with no known distant metastases.

Beschreibung

Inclusion Criteria:

  • US male veterans with early stage prostate cancer.

Exclusion Criteria:

  • Men will be excluded if they have prior history of other cancer within the last 5 years (with the exception of non-melanoma skin cancer) or other major illness that would preclude long-term participation.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Beobachtungsmodelle: Kohorte
  • Zeitperspektiven: Interessent

Kohorten und Interventionen

Gruppe / Kohorte
Gruppe 1

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
The primary endpoint of the study will be prostate cancer mortality.
Zeitfenster: approximately once a year
approximately once a year

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Studienstuhl: Michael J. Gaziano, MD MOH, VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Januar 2001

Primärer Abschluss (Tatsächlich)

1. Juni 2006

Studienabschluss (Tatsächlich)

1. Januar 2010

Studienanmeldedaten

Zuerst eingereicht

15. Februar 2001

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

16. Februar 2001

Zuerst gepostet (Schätzen)

19. Februar 2001

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

15. April 2013

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

11. April 2013

Zuletzt verifiziert

1. April 2013

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Andere Studien-ID-Nummern

  • 719B

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