Screening for Prostate Cancer in Older Patients (PLCO Screening Trial)
Prostate Carcinoma
About this trial
This is an interventional screening trial for Prostate Carcinoma
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
Sites / Locations
- National Institutes of Health Clinical Center
Arms of the Study
Arm 1
Arm 2
No Intervention
Active Comparator
Control
Prostate Screening
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.