Colon Carcinoma, Rectal Carcinoma
Conditions
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
Undergo a flexible sigmoidoscopy
Sponsors
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| Colorectal Cancer Deaths | Events 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 Rates | Events 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
| Measure | Time frame | Description |
|---|---|---|
| Colorectal Cancer Incidence | Events 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 Rates | Events 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 Causes | Events 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 Results | T0 (at study entry) | Flexible sigmoidoscopy (FSG) result |
| T3/T5 FSG Screening Result | T3 (three years after entry) or T5 (five years after entry) | Flexible sigmoidoscopy (FSG) result |
| Complications of Diagnostic Evaluation Following a Positive Screening Test | One year from screening examination | Number of participants who experienced complications during diagnostic work-up of a positive colorectal examination. |
| Death Rates From All Causes | Events 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
| Arm | Count |
|---|---|
| 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 |
| Total | 154,900 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Cancer Before Rand. (Colo. Screening) | 0 | 20 |
| Overall Study | Died Before ASU (Control) | 278 | 0 |
| Overall Study | Died Before Randomization | 3 | 8 |
| Overall Study | Refused ASU (Control) | 920 | 0 |
| Overall Study | Refused Screen (Colorectal Screening) | 0 | 10,346 |
Baseline characteristics
| Characteristic | Colorectal Screening | Control | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 27811 Participants | 27845 Participants | 55656 Participants |
| Age, Categorical Between 18 and 65 years | 49634 Participants | 49610 Participants | 99244 Participants |
| Age, Continuous | 62.6 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 participants | 77455 participants | 154900 participants |
| Sex: Female, Male Female | 39105 Participants | 39111 Participants | 78216 Participants |
| Sex: Female, Male Male | 38340 Participants | 38344 Participants | 76684 Participants |
Adverse events
| Event type | EG000 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
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.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Control | Colorectal Cancer Death Rates | 3.9 Deaths per 10,000 PY |
| Colorectal Screening | Colorectal Cancer Death Rates | 2.9 Deaths per 10,000 PY |
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.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Control | Colorectal Cancer Deaths | 341 Participants |
| Colorectal Screening | Colorectal Cancer Deaths | 252 Participants |
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.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Control | Colorectal Cancer Incidence | 1287 Participants |
| Colorectal Screening | Colorectal Cancer Incidence | 1012 Participants |
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.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Control | Colorectal Cancer Incidence Rates | 15.2 Diagnoses per 10,000 PY |
| Colorectal Screening | Colorectal Cancer Incidence Rates | 11.9 Diagnoses per 10,000 PY |
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.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Control | Complications of Diagnostic Evaluation Following a Positive Screening Test | When DE Led to Colorectal Cancer Diagnosis | 58 Positive screens w/ complications |
| Control | Complications of Diagnostic Evaluation Following a Positive Screening Test | When DE Did Not Lead to Colorectal Cancer Diag | 279 Positive screens w/ complications |
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.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Control | Death Rates From All Causes | 127.0 Deaths per 10,000 PY |
| Colorectal Screening | Death Rates From All Causes | 124.3 Deaths per 10,000 PY |
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.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Control | Deaths From All Causes | 11064 Participants |
| Colorectal Screening | Deaths From All Causes | 10835 Participants |
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.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Control | T0 (Baseline) FSG Screening Results | Negative | 42403 Participants |
| Control | T0 (Baseline) FSG Screening Results | Positive | 15154 Participants |
| Control | T0 (Baseline) FSG Screening Results | Inadequate screen | 7096 Participants |
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.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Control | T3/T5 FSG Screening Result | Positive | 9818 Participants |
| Control | T3/T5 FSG Screening Result | Inadequate screen | 5346 Participants |
| Control | T3/T5 FSG Screening Result | Negative | 26694 Participants |