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Screening for Prostate Cancer in Older Patients (PLCO Screening Trial)

Primary Purpose

Prostate Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Laboratory Biomarker Analysis
Medical Examination
Screening Questionnaire Administration
Sponsored by
National Cancer Institute (NCI)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Prostate Carcinoma

Eligibility Criteria

55 Years - 74 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Exclusion Criteria: Men who at the time of randomization are less than 55 or greater than or equal to 75 years of age Individuals undergoing treatment for cancer at this time, excluding basal-cell and squamous-cell skin cancer Individuals with known prior cancer of the colon, rectum, lung, prostate This includes primary or metastatic PLCO cancers Individuals with previous surgical removal of the entire colon, one lung, or the entire prostate Individuals who are participating in another cancer screening or cancer primary prevention trial Males who have taken Proscar/Propecia/finasteride in the past 6 months NOTE: Individuals who are already enrolled in the trial when their physician prescribes finasteride are not prevented from taking this medication. As a result, these participants will continue to be screened and followed just as those participants who are not on finasteride. NOTE: Men who are taking Tamoxifen are not excluded from any part of the PLCO Screening Trial. Individuals who are unwilling or unable to sign the informed consent form Males who have had more than one PSA blood test in the past three years Individuals who have had a colonoscopy, sigmoidoscopy, or barium enema in the past three years

Sites / Locations

  • National Institutes of Health Clinical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control

Prostate Screening

Arm Description

Participants receive standard medical care. Participants complete a DHQ at baseline.

Participants undergo blood sample collection for PSA analysis at baseline and annually for 5 years. Serum that is not used in the study will be stored in an NCI biorepository. Participants also undergo a DRE at baseline and annually for 3 years. Participants complete a DQX at baseline and DHQ at year 3. An ADU (previously referred to as the PSH questionnaire) is mailed to each participant annually for 13 years to identify all prevalent and incident prostate cancers as all deaths that occur among both screened and control subjects during the trial.

Outcomes

Primary Outcome Measures

Prostate Cancer Deaths
Prostate cancer deaths confirmed in participants by a death review committee if available, otherwise by death certificate.
Prostate Cancer Death Rates
Prostate cancer deaths confirmed in participants by a death review committee if available, otherwise by death certificate. Rate is the number of deaths divided by person years of follow-up in the study.

Secondary Outcome Measures

Deaths From All Causes
Deaths from all causes were compared between the prostate cancer screening arm and the usual care arm.
Death Rates From All Causes
Deaths from all causes were compared between the prostate cancer screening arm and the usual care arm. Rate is the number of deaths divided by person years of follow-up in the study.
Prostate Cancer Incidence
Prostate cancer diagnoses confirmed by medical record abstraction. Incidence rate (cumulative) defined as prostate cancer diagnoses divided by person years at risk for prostate cancer.
Prostate Cancer Incidence Rates
Prostate cancer diagnoses confirmed by medical record abstraction. Incidence rate (cumulative) defined as prostate cancer diagnoses divided by person years at risk for prostate cancer.
Complications of Diagnostic Evaluation (DE) Following a Positive Screening Test
Number of positive screens with complications
T0 (Baseline) PSA Screening Results
Prostate-Specific Antigen (PSA) result.
T0 (Baseline) DRE Screening Results
Digital Rectal Examination (DRE) result.
T1 PSA Screening Results
Prostate-Specific Antigen (PSA) result.
T1 DRE Screening Results
Digital Rectal Examination (DRE) result.
T2 PSA Screening Results
Prostate-Specific Antigen (PSA) result.
T2 DRE Screening Results
Digital Rectal Examination (DRE) results
T3 PSA Screening Results
Prostate-Specific Antigen (PSA) result
T3 DRE Screening Results
Digital Rectal examination (DRE) result
T4 PSA Screening Result
Prostate-Specific Antigen (PSA) result
T5 PSA Screening Results
Prostate-Specific Antigen (PSA) result.

Full Information

First Posted
November 1, 1999
Last Updated
June 30, 2022
Sponsor
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00002540
Brief Title
Screening for Prostate Cancer in Older Patients (PLCO Screening Trial)
Official Title
Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
November 16, 1993 (Actual)
Primary Completion Date
May 21, 2012 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

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

4. Oversight

5. Study Description

Brief Summary
This clinical trial studies whether screening methods used to diagnose cancer of the prostate, lung, colon, rectum, or ovaries can reduce deaths from these cancers. Screening tests may help doctors find cancer cells early and plan better treatment for prostate cancer.
Detailed Description
PRIMARY OBJECTIVES: I. To determine whether screening with digital rectal examination (DRE) plus serum prostate-specific antigen (PSA) can reduce mortality from prostate cancer in men aged 55-74 at entry. SECONDARY OBJECTIVES: I. To assess screening variables, other than mortality, for each of the interventions including sensitivity, specificity, and positive predictive value. II. To assess the incidence, stage, and survival of cancer cases. III. To investigate the mortality predictive value of biologic and/or prognostic characterizations of tumor tissue as intermediate endpoints. IV. To conduct biomolecular and genetic research into factors associated with cancer carcinogenesis and promotion, as well as the early detection of these factors. OUTLINE: Participants in the overall PLCO study are stratified by screening center, gender, and age (55-59 vs 60-64 vs 65-69 vs 70-74). Participants are randomized to 1 of 2 arms (control vs screening). ARM I (Control): Participants receive standard medical care. Participants complete a Diet History Questionnaire (DHQ) at baseline. ARM II (Prostate Screening): Participants undergo blood sample collection for PSA analysis at baseline and annually for 5 years. Serum that is not used in the study will be stored in an NCI biorepository. Participants also undergo a DRE at baseline and annually for 3 years. A scheduling and tracking procedure is implemented to ensure regular attendance at repeat screens for participants screened negative or for those who are designated suspicious or positive at screening but for whom subsequent diagnostic procedures do not reveal prostate cancer (follow-up diagnostic procedures are through their own medical care environment). Participants diagnosed with prostate cancer via a screening test are referred for treatment in accordance with current accepted practice for appropriate stage of disease, patient age, and medical condition; a procedure is provided for contact with qualified medical personnel to insure appropriate therapy. Participants complete a Dietary Questionnaire (DQX) at baseline and DHQ at year 3. An Annual Study Update (ADU) (previously referred to as the Periodic Survey of Health [PSH] questionnaire) is mailed to each participant annually for 13 years to identify all prevalent and incident prostate cancers as all deaths that occur among both screened and control subjects during the trial. After completion of screening, participants are followed up for at least 13 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Carcinoma

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
76685 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants receive standard medical care. Participants complete a DHQ at baseline.
Arm Title
Prostate Screening
Arm Type
Active Comparator
Arm Description
Participants undergo blood sample collection for PSA analysis at baseline and annually for 5 years. Serum that is not used in the study will be stored in an NCI biorepository. Participants also undergo a DRE at baseline and annually for 3 years. Participants complete a DQX at baseline and DHQ at year 3. An ADU (previously referred to as the PSH questionnaire) is mailed to each participant annually for 13 years to identify all prevalent and incident prostate cancers as all deaths that occur among both screened and control subjects during the trial.
Intervention Type
Other
Intervention Name(s)
Laboratory Biomarker Analysis
Intervention Description
Correlative studies
Intervention Type
Procedure
Intervention Name(s)
Medical Examination
Other Intervention Name(s)
Exam, Examination, Health Assessment, Medical Assessment, Medical Exam, Medical Inspection
Intervention Description
Undergo DRE
Intervention Type
Other
Intervention Name(s)
Screening Questionnaire Administration
Intervention Description
Undergo questionnaire assessments
Primary Outcome Measure Information:
Title
Prostate Cancer Deaths
Description
Prostate cancer deaths confirmed in participants by a death review committee if available, otherwise by death certificate.
Time Frame
Events through 13 years of follow-up or through December 31, 2009; median follow-up 12.0 years.
Title
Prostate Cancer Death Rates
Description
Prostate cancer deaths confirmed in participants by a death review committee if available, otherwise by death certificate. Rate is the number of deaths divided by person years of follow-up in the study.
Time Frame
Events through 13 years of follow-up or through December 31, 2009; median follow-up 12.0 years.
Secondary Outcome Measure Information:
Title
Deaths From All Causes
Description
Deaths from all causes were compared between the prostate cancer screening arm and the usual care arm.
Time Frame
Events through 13 years of follow-up or through December 31, 2009.
Title
Death Rates From All Causes
Description
Deaths from all causes were compared between the prostate cancer screening arm and the usual care arm. Rate is the number of deaths divided by person years of follow-up in the study.
Time Frame
Events through 13 years of follow-up or through December 31, 2009.
Title
Prostate Cancer Incidence
Description
Prostate cancer diagnoses confirmed by medical record abstraction. Incidence rate (cumulative) defined as prostate cancer diagnoses divided by person years at risk for prostate cancer.
Time Frame
Events through 13 years of follow-up or through December 31, 2009; median follow-up 12.0 years.
Title
Prostate Cancer Incidence Rates
Description
Prostate cancer diagnoses confirmed by medical record abstraction. Incidence rate (cumulative) defined as prostate cancer diagnoses divided by person years at risk for prostate cancer.
Time Frame
Events through 13 years of follow-up or through December 31, 2009; median follow-up 12.0 years.
Title
Complications of Diagnostic Evaluation (DE) Following a Positive Screening Test
Description
Number of positive screens with complications
Time Frame
One year from screening examination
Title
T0 (Baseline) PSA Screening Results
Description
Prostate-Specific Antigen (PSA) result.
Time Frame
T0 (at study entry)
Title
T0 (Baseline) DRE Screening Results
Description
Digital Rectal Examination (DRE) result.
Time Frame
T0 (at study entry)
Title
T1 PSA Screening Results
Description
Prostate-Specific Antigen (PSA) result.
Time Frame
T1 (one year after entry)
Title
T1 DRE Screening Results
Description
Digital Rectal Examination (DRE) result.
Time Frame
T1 (one year after entry)
Title
T2 PSA Screening Results
Description
Prostate-Specific Antigen (PSA) result.
Time Frame
T2 (two years after entry)
Title
T2 DRE Screening Results
Description
Digital Rectal Examination (DRE) results
Time Frame
T2 (two years after entry)
Title
T3 PSA Screening Results
Description
Prostate-Specific Antigen (PSA) result
Time Frame
T3 (three years after entry)
Title
T3 DRE Screening Results
Description
Digital Rectal examination (DRE) result
Time Frame
T3 (three years after entry)
Title
T4 PSA Screening Result
Description
Prostate-Specific Antigen (PSA) result
Time Frame
T4 (four years after entry)
Title
T5 PSA Screening Results
Description
Prostate-Specific Antigen (PSA) result.
Time Frame
T5 (five years after entry)

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Exclusion Criteria: Men who at the time of randomization are less than 55 or greater than or equal to 75 years of age Individuals undergoing treatment for cancer at this time, excluding basal-cell and squamous-cell skin cancer Individuals with known prior cancer of the colon, rectum, lung, prostate This includes primary or metastatic PLCO cancers Individuals with previous surgical removal of the entire colon, one lung, or the entire prostate Individuals who are participating in another cancer screening or cancer primary prevention trial Males who have taken Proscar/Propecia/finasteride in the past 6 months NOTE: Individuals who are already enrolled in the trial when their physician prescribes finasteride are not prevented from taking this medication. As a result, these participants will continue to be screened and followed just as those participants who are not on finasteride. NOTE: Men who are taking Tamoxifen are not excluded from any part of the PLCO Screening Trial. Individuals who are unwilling or unable to sign the informed consent form Males who have had more than one PSA blood test in the past three years Individuals who have had a colonoscopy, sigmoidoscopy, or barium enema in the past three years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine D Berg
Organizational Affiliation
National Cancer Institute (NCI)
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institutes of Health Clinical Center
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

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Screening for Prostate Cancer in Older Patients (PLCO Screening Trial)

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