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

Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01696981
Enrollment
154900
Registered
2012-10-02
Start date
1993-11-16
Completion date
2026-03-25
Last updated
2025-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colon Carcinoma, Rectal Carcinoma

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 colorectal cancer.

Detailed description

PRIMARY OBJECTIVES: I. To determine whether screening with flexible sigmoidoscopy (60-cm sigmoidoscope) can reduce mortality from colorectal cancer in women and men aged 55-74 at study 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 (Colorectal Screening): Participants undergo a colorectal examination with a flexible sigmoidoscope at baseline and year 5. 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 colorectal cancer (follow-up diagnostic procedures are through their own medical care environment). Participants diagnosed with colorectal 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 colorectal 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.

Interventions

Undergo questionnaire assessments

PROCEDURESigmoidoscopy

Undergo a flexible sigmoidoscopy

Sponsors

National Cancer Institute (NCI)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
55 Years to 74 Years
Healthy volunteers
No

Exclusion criteria

* Men and women 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 (men only) * Until October 1996, women with previous surgical removal of both ovaries were excluded from the trial. In order to increase the enrollment of women into the trial, beginning in October 1996, these women were no longer excluded for this reason. * 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. * Prior to April 1, 1999 women were excluded from the trial if they were currently taking or had taken Tamoxifen or Evista\\Raloxifene in the past 6 months. As of April 1999 based on a decision from the PLCO Ovary Subcommittee, women who have or are currently taking Tamoxifen or Evista\\Raloxifene are not excluded from participation. * 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

Design outcomes

Primary

MeasureTime frameDescription
Colorectal Cancer DeathsEvents through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.Colorectal cancer deaths confirmed in participants by a death review committee if available, otherwise by death certificate.
Colorectal Cancer Death RatesEvents through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.Colorectal 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

MeasureTime frameDescription
Colorectal Cancer IncidenceEvents through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.Colorectal cancer diagnoses confirmed by medical record abstraction.
Colorectal Cancer Incidence RatesEvents through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.Colorectal cancer diagnoses confirmed by medical record abstraction. Incidence rate (cumulative) defined as colorectal cancer diagnoses divided by person years at risk for colorectal cancer.
Deaths From All CausesEvents through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.Deaths from all causes were compared between the colorectal cancer screening arm and the usual care arm.
T0 (Baseline) FSG Screening ResultsT0 (at study entry)Flexible sigmoidoscopy (FSG) result
T3/T5 FSG Screening ResultT3 (three years after entry) or T5 (five years after entry)Flexible sigmoidoscopy (FSG) result
Complications of Diagnostic Evaluation Following a Positive Screening TestOne year from screening examinationNumber of participants who experienced complications during diagnostic work-up of a positive colorectal examination.
Death Rates From All CausesEvents through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.Deaths from all causes were compared between the colorectal cancer screening arm and the usual care arm. Rate is the number of deaths divided by person years of follow-up in the study.

Countries

United States

Participant flow

Recruitment details

Participants were enrolled between November 1993 and July 2001 at 10 study centers. Recruitment was done for all four outcomes of the study (prostate, lung, colorectal and ovarian).

Pre-assignment details

Participants signed a study informed consent prior to being randomized to a study arm.

Participants by arm

ArmCount
Control
Participants receive standard medical care. Participants complete a baseline questionnaire at entry and a dietary history questionnaire (DHQ) during study years 0-6.
77,455
Colorectal Screening
Participants undergo a colorectal examination with a flexible sigmoidoscope at baseline and year 5. Participants complete a Dietary Questionnaire (DQX) at baseline and a Dietary History Questionnaire (DHQ) at study years 3-6. An Annual Study Update (ASU) (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 colorectal cancers and all deaths that occur among both screened and control arm subjects during the trial.
77,445
Total154,900

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyCancer Before Rand. (Colo. Screening)020
Overall StudyDied Before ASU (Control)2780
Overall StudyDied Before Randomization38
Overall StudyRefused ASU (Control)9200
Overall StudyRefused Screen (Colorectal Screening)010,346

Baseline characteristics

CharacteristicColorectal ScreeningControlTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
27811 Participants27845 Participants55656 Participants
Age, Categorical
Between 18 and 65 years
49634 Participants49610 Participants99244 Participants
Age, Continuous62.6 years
STANDARD_DEVIATION 5.4
62.6 years
STANDARD_DEVIATION 5.4
62.6 years
STANDARD_DEVIATION 5.4
Region of Enrollment
United States
77445 participants77455 participants154900 participants
Sex: Female, Male
Female
39105 Participants39111 Participants78216 Participants
Sex: Female, Male
Male
38340 Participants38344 Participants76684 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
504 / 77,445
serious
Total, serious adverse events
0 / 77,445

Outcome results

Primary

Colorectal Cancer Death Rates

Colorectal 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 12.1 years.

ArmMeasureValue (NUMBER)
ControlColorectal Cancer Death Rates3.9 Deaths per 10,000 PY
Colorectal ScreeningColorectal Cancer Death Rates2.9 Deaths per 10,000 PY
95% CI: [0.63, 0.87]Poisson regression
Primary

Colorectal Cancer Deaths

Colorectal 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 12.1 years.

ArmMeasureValue (NUMBER)
ControlColorectal Cancer Deaths341 Participants
Colorectal ScreeningColorectal Cancer Deaths252 Participants
Secondary

Colorectal Cancer Incidence

Colorectal cancer diagnoses confirmed by medical record abstraction.

Time frame: Events through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.

Population: All participants. An intention-to-treat analysis was performed.

ArmMeasureValue (NUMBER)
ControlColorectal Cancer Incidence1287 Participants
Colorectal ScreeningColorectal Cancer Incidence1012 Participants
Secondary

Colorectal Cancer Incidence Rates

Colorectal cancer diagnoses confirmed by medical record abstraction. Incidence rate (cumulative) defined as colorectal cancer diagnoses divided by person years at risk for colorectal cancer.

Time frame: Events through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.

Population: All participants. An intention-to-treat analysis was performed.

ArmMeasureValue (NUMBER)
ControlColorectal Cancer Incidence Rates15.2 Diagnoses per 10,000 PY
Colorectal ScreeningColorectal Cancer Incidence Rates11.9 Diagnoses per 10,000 PY
95% CI: [0.72, 0.85]Poisson regression
Secondary

Complications of Diagnostic Evaluation Following a Positive Screening Test

Number of participants who experienced complications during diagnostic work-up of a positive colorectal examination.

Time frame: One year from screening examination

Population: The units analyzed were positive screening exams with documented diagnostic follow-up. If a participant received 2 positive screens with documented follow-up after each one, he would be counted 2 times in the number of units analyzed.

ArmMeasureGroupValue (NUMBER)
ControlComplications of Diagnostic Evaluation Following a Positive Screening TestWhen DE Led to Colorectal Cancer Diagnosis58 Positive screens w/ complications
ControlComplications of Diagnostic Evaluation Following a Positive Screening TestWhen DE Did Not Lead to Colorectal Cancer Diag279 Positive screens w/ complications
Secondary

Death Rates From All Causes

Deaths from all causes were compared between the colorectal 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; median follow-up 12.1 years.

Population: All participants. An intention-to-treat analysis was performed.

ArmMeasureValue (NUMBER)
ControlDeath Rates From All Causes127.0 Deaths per 10,000 PY
Colorectal ScreeningDeath Rates From All Causes124.3 Deaths per 10,000 PY
95% CI: [0.95, 1]Poisson regression
Secondary

Deaths From All Causes

Deaths from all causes were compared between the colorectal cancer screening arm and the usual care arm.

Time frame: Events through 13 years of follow-up or through December 31, 2009; median follow-up 12.1 years.

Population: All participants. An intention-to-treat analysis was performed.

ArmMeasureValue (NUMBER)
ControlDeaths From All Causes11064 Participants
Colorectal ScreeningDeaths From All Causes10835 Participants
Secondary

T0 (Baseline) FSG Screening Results

Flexible sigmoidoscopy (FSG) result

Time frame: T0 (at study entry)

Population: All participants in the Colorectal Screening arm who had an FSG at T0 were analyzed.

ArmMeasureGroupValue (NUMBER)
ControlT0 (Baseline) FSG Screening ResultsNegative42403 Participants
ControlT0 (Baseline) FSG Screening ResultsPositive15154 Participants
ControlT0 (Baseline) FSG Screening ResultsInadequate screen7096 Participants
Secondary

T3/T5 FSG Screening Result

Flexible sigmoidoscopy (FSG) result

Time frame: T3 (three years after entry) or T5 (five years after entry)

Population: All participants in the Colorectal Screening arm who had an FSG at T0 or T3 were analyzed.

ArmMeasureGroupValue (NUMBER)
ControlT3/T5 FSG Screening ResultPositive9818 Participants
ControlT3/T5 FSG Screening ResultInadequate screen5346 Participants
ControlT3/T5 FSG Screening ResultNegative26694 Participants

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026