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TerminatedNCT00078897Updated Sep 24, 2019Results posted

Selenium for Prevention of Adenomatous Colorectal Polyps

A Phase 3 interventional study of Selenium in Colorectal Cancer, Adenomatous Colorectal Polyps and Precancerous Condition, sponsored by University of Arizona. Terminated at 7 sites in United States. Open to participants aged 40 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-09-24.

Sponsored by University of Arizona · Phase 3, Interventional, and Prevention

Why this study was terminated
Concluded - Terminated by PI
Phase
Phase 3
Study type
Interventional
Enrollment
1,621
Allocation
Randomized
Ages
40 Years to 80 Years
Sex
All
01

Study summary

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. Selenium may be effective in preventing the recurrence of adenomatous colorectal polyps.

PURPOSE: This randomized phase III trial is studying selenium to see how well it works in preventing the recurrence of polyps in patients with adenomatous colorectal polyps.

Read the detailed description

OBJECTIVES:

Primary

  • Compare the effects of selenium vs placebo on the recurrence of adenomatous colorectal polyps, in terms of histologic type, degree of dysplasia, number, size, and location, in patients with adenomatous colorectal polyps.
  • Compare the type, incidence, and outcome of side effects in patients treated with these regimens.
  • Determine patient adherence to long-term treatment with these regimens.

Secondary

  • Determine the effects of regimen modification by baseline blood selenium level, low-dose aspirin, selenoprotein genetic marker polymorphisms (e.g., GPx-1, GPx-2, and SEP15)
  • Determine the effects of low-dose aspirin (81 mg/day) modification by ornithine decarboxylase promoter genotype, and toxicity by slow-metabolizer genotypes of the cytochrome p450 2C9 and UT1A6 loci in these patients.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to use of low-dose (≤ 81 mg/day) aspirin (yes vs no). Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive oral selenium once daily.
  • Arm II: Patients receive oral placebo once daily. In both arms, treatment continues for up to 5 years* in the absence of disease progression or unacceptable toxicity.

Patients undergo follow-up colonoscopy approximately 5 years* after baseline colonoscopy.

NOTE: Some patients will continue participation for up to 7 and a half years

PROJECTED ACCRUAL: A total of 1,600 patients with an adenoma will be randomized to this study, followed by a second group of randomization of 200 patients with at least one advanced adenoma (at baseline) for a substudy. Total planned randomizations = 1,800 participants.

02

Conditions studied

  • Colorectal Cancer
  • Adenomatous Colorectal Polyps
  • Precancerous Condition

Keywords

  • colon cancer
  • rectal cancer
  • colorectal cancer
  • adenomatous polyp
03

In context

Colorectal Neoplasms

5,599 studies on the registry are indexed under Colorectal Neoplasms; 1,459 are open to participants now.

This study's enrollment of 1,621 is above the median of 77 across 4,123 interventional studies indexed under Colorectal Neoplasms.

Browse Colorectal Neoplasms studies →

Lead sponsor

University of Arizona is the lead sponsor of 466 studies on the registry; 87 are open to participants now.

Of its 47 completed or terminated interventional studies of FDA-regulated products, 29 (62%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histologically confirmed colorectal adenomatous polyps
  • Meets the following criteria by colonoscopy (performed within the past 6 months):

    • Cecum was totally visualized or reached
    • At least 90% visualization of colon surface area
    • Removed at least 1 adenomatous polyp of at least 3 mm in size during procedure (For the Advanced Adenoma Sub-study: Removal of at least 1 advanced colorectal adenomatous polyp during procedure. An adenoma is considered advanced if it is 10 mm or greater in size, and/or has villous histology and/or shows high grade dysplasia)
    • Removed no more than 10 adenomatous polyps of any size by endoscopy
    • All other neoplastic and non-neoplastic colon polyps must have been completely removed (except for diminutive [less than 3 mm] sessile rectal polyps)
    • For the sub-study, at least 1 advanced adenomatous polyp defined as 10 mm or greater in size and/or has villous histology and/or shows high grade dysplasia
  • No prior diagnosis of any of the following:

    • Colorectal cancer
    • Familial adenomatous polyposis
    • Ulcerative colitis
    • Crohn's disease
    • Hereditary non-polyposis colon cancer (HNPCC), defined as:

      • Histologically confirmed colorectal cancer in at least 3 relatives, 1 of whom is a first-degree relative of the other 2
      • Disease occurrence in at least 2 consecutive generations
      • Colorectal cancer diagnosis in at least 1 family member who is less than 50 years of age

        • Patients with a family history of colorectal cancer but who are not diagnosed with HNPCC are allowed
  • No more than 1 prior segmental colon resection

PATIENT CHARACTERISTICS:

Age

  • 40 to 80

Performance status

  • SWOG 0-1

Life expectancy

  • Not specified

Hematopoietic

  • Hemoglobin > 11 g/dL
  • WBC 3,000 - 11,000/mm\^3

Hepatic

  • AST and ALT \< 2 times upper limit of normal
  • Bilirubin \< 2.0 mg/dL

Renal

  • Creatinine \< 1.9 mg/dL

Cardiovascular

  • No unstable* cardiac disease despite medication (e.g., diuretics or digitalis)
  • No uncontrolled hypertension (i.e., systolic blood pressure ≥ 170 mm Hg and/or diastolic blood pressure ≥ 110 mm Hg) despite medication NOTE: *Unstable defined as unable to walk across the room without chest pain or shortness of breath

Other

  • Not pregnant or nursing
  • Fertile patients must use effective contraception for at least 2 months before and during study treatment
  • Resident of a clinical center metropolitan area or obtaining regular health care in a clinical metropolitan area for at least 6 months out of the year
  • Must be able to swallow pills
  • No unexpected weight loss of 10% or more within the past 6 months
  • No prior rheumatoid arthritis
  • No poorly controlled diabetes mellitus despite medication, defined as:

    • Blood sugar level ≥ 200 mg/dL on more than half of the readings taken within the past month
  • No invasive malignancy within the past 5 years that required medical excision, radiotherapy, or chemotherapy except basal cell or squamous cell carcinoma

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • No concurrent drugs that regulate the immune system

Chemotherapy

  • No concurrent chemotherapy

Endocrine therapy

  • Not specified

Radiotherapy

  • No concurrent radiotherapy

Surgery

  • See Disease Characteristics

Other

  • Prior enrollment in another adenoma prevention study allowed
  • Concurrent routine aspirin (≤ 81 mg/day) allowed
  • No regular use of non-steroidal anti-inflammatory drugs (NSAIDs)
  • No concurrent enrollment in another research study using pharmacological cancer drugs, a cyclo-oxygenase-2 inhibitor, or selenium
  • No other concurrent selenium unless dosage is ≤ 50 µg/day
05

Study design

Phase
Phase 3
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
1,621 participants (actual)

Study arms

  • Active comparator
    Selenium

    Participants receive oral selenium 200 mcg once daily.

    Drug: Selenium

  • Placebo comparator
    Placebo

    Participants receive oral placebo once daily.

    Drug: Selenium

Interventions

  • DrugSelenium

    Participants will be randomized either to selenium or placebo, taking the randomized intervention for 3 to 5 years, depending on when their recommended follow up colonoscopy is scheduled.

    Also known as: SelenoExcell

06

What researchers measure

Primary outcomes

  1. Number of Recurrent Adenomas at Surveillance Colonoscopy

    Detection of metachronous colorectal adenomas during follow-up, by treatment, in the original cohort. Surveillance colonoscopy is recommended 3 to 5 years after removal of colorectal adenoma(s). Participants will remain on the study intervention until their surveillance colonoscopy. Surveillance colonoscopy is determined by participants' GI physician.

    Time frame: 3 to 5 years after baseline colonoscopy

  2. Median Selenium Blood Levels at One Year.

    Adequate adherence to long-term selenium treatment as measured by blood selenium levels (ng/mL) at one year.

    Time frame: One year

07

Results

Posted Sep 24, 2019

Participant flow

Participants were recruited through clinical centers in Arizona, Colorado, Texas, and New York following ambulatory colonoscopies. Eligible participants were between age 40 and 80 years and had undergone colonoscopic removal of one or more colorectal adenomas 3 mm or larger within six months prior to random assignment.

Participant flow — Overall Study
MilestoneSeleniumPlacebo
Started809812
Completed685689
Not completed124123

Outcome measures

PrimaryNumber of Recurrent Adenomas at Surveillance Colonoscopy

Detection of metachronous colorectal adenomas during follow-up, by treatment, in the original cohort. Surveillance colonoscopy is recommended 3 to 5 years after removal of colorectal adenoma(s). Participants will remain on the study intervention until their surveillance colonoscopy. Surveillance colonoscopy is determined by participants' GI physician.

Time frame:
3 to 5 years after baseline colonoscopy
Reported as:
Number · Adenomas
Number of Recurrent Adenomas at Surveillance Colonoscopy
AdenomasSeleniumPlacebo
Number of Recurrent Adenomas at Surveillance Colonoscopy302295
PrimaryMedian Selenium Blood Levels at One Year.

Adequate adherence to long-term selenium treatment as measured by blood selenium levels (ng/mL) at one year.

Time frame:
One year
Reported as:
Median · ng/mL
Median Selenium Blood Levels at One Year.
ng/mLSeleniumPlacebo
Median Selenium Blood Levels at One Year.205.4 (100.7 to 367.6)140.0 (84.9 to 270.2)
Statistical analysis
  • Selenium · Negative binomial regression · p = 0.68 · Risk ratio (rr): 1.03 · 95% CI 0.91 to 1.16

Adverse events

Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Selenium11/685 (1.6%)228/685 (33.3%)0/685 (0%)
Placebo10/689 (1.5%)226/689 (32.8%)0/689 (0%)
Most frequent serious events
Showing 10 of 41
Most frequent serious events
EventSeleniumPlacebo
CancerNeoplasms benign, malignant and unspecified (incl cysts and polyps)48/68567/689
Misc. cardiac disordersCardiac disorders17/68526/689
Arthritis/Degenerative joint diseaseMusculoskeletal and connective tissue disorders18/68516/689
Misc. renal and urinary disordersRenal and urinary disorders9/68514/689
Atrial fibrillation/arrhythmiaCardiac disorders13/6859/689
Misc. GI disordersGastrointestinal disorders8/68513/689
AnginaCardiac disorders12/68512/689
FractureMusculoskeletal and connective tissue disorders11/6856/689
Chest painCardiac disorders10/68511/689
Misc. vascular disordersVascular disorders8/68511/689

Baseline characteristics

Age, Continuous
Age, Continuous(years)SeleniumPlaceboTotal
Mean63.6 ± 8.963.1 ± 8.763.4 ± 8.8
Sex: Female, Male
Sex: Female, Male(Participants)SeleniumPlaceboTotal
Female242234476
Male443455898
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)SeleniumPlaceboTotal
Hispanic or Latino253964
Not Hispanic or Latino6606501310
Unknown or Not Reported000
Race (NIH/OMB)
Race (NIH/OMB)(Participants)SeleniumPlaceboTotal
American Indian or Alaska Native011
Asian8816
Native Hawaiian or Other Pacific Islander000
Black or African American171633
White6526501302
More than one race71320
Unknown or Not Reported112
Region of Enrollment
Region of Enrollment(participants)SeleniumPlaceboTotal
United States6856891374
08

Study locations

7 sites
  • Veterans Affairs Medical Center - Phoenix
    Phoenix, Arizona 85012, United States
  • Virginia G. Piper Cancer Center at Scottsdale Healthcare - Shea
    Scottsdale, Arizona 85258-4512, United States
  • Mayo Clinic Scottsdale
    Scottsdale, Arizona 85259-5499, United States
  • Arizona Cancer Center - Tucson Clinic
    Tucson, Arizona 85724-5024, United States
  • University of Colorado Cancer Center at UC Health Sciences Center
    Denver, Colorado 80220, United States
  • Endoscopy Center of Western New York
    Williamsville, New York 14221, United States
  • Baylor University Medical Center - Dallas
    Dallas, Texas 75246, United States
09

References and documents

Publications

  • Trejo MJ, Batai K, Chen Y, Brezina S, Chow HS, Ellis N, Lance P, Hsu CH, Pogreba-Brown K, Bishop M, Gsur A, Jacobs ET. Genome-Wide Association Study of Metachronous Colorectal Adenoma Risk among Participants in the Selenium Trial. Nutr Cancer. 2023;75(1):143-153. doi: 10.1080/01635581.2022.2096910. Epub 2022 Jul 9. PubMed 35815403 ↗
  • Jacobs ET, Lance P, Mandarino LJ, Ellis NA, Chow HS, Foote J, Martinez JA, Hsu CP, Batai K, Saboda K, Thompson PA. Selenium supplementation and insulin resistance in a randomized, clinical trial. BMJ Open Diabetes Res Care. 2019 Feb 7;7(1):e000613. doi: 10.1136/bmjdrc-2018-000613. eCollection 2019. PubMed 30899530 ↗
  • Thompson P, Roe DJ, Fales L, Buckmeier J, Wang F, Hamilton SR, Bhattacharyya A, Green S, Hsu CH, Chow HH, Ahnen DJ, Boland CR, Heigh RI, Fay DE, Martinez ME, Jacobs E, Ashbeck EL, Alberts DS, Lance P. Design and baseline characteristics of participants in a phase III randomized trial of celecoxib and selenium for colorectal adenoma prevention. Cancer Prev Res (Phila). 2012 Dec;5(12):1381-93. doi: 10.1158/1940-6207.CAPR-12-0204. Epub 2012 Oct 11. PubMed 23060037 ↗
  • Solomon SD, Wittes J, Finn PV, Fowler R, Viner J, Bertagnolli MM, Arber N, Levin B, Meinert CL, Martin B, Pater JL, Goss PE, Lance P, Obara S, Chew EY, Kim J, Arndt G, Hawk E; Cross Trial Safety Assessment Group. Cardiovascular risk of celecoxib in 6 randomized placebo-controlled trials: the cross trial safety analysis. Circulation. 2008 Apr 22;117(16):2104-13. doi: 10.1161/CIRCULATIONAHA.108.764530. Epub 2008 Mar 31. PubMed 18378608 ↗

Related links

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 24, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT00078897
Lead sponsor
University of Arizona
Collaborators
National Cancer Institute (NCI)
Responsible party
Sponsor
First posted
Mar 9, 2004
Start date
Jan 20, 2005
Primary completion
Jan 7, 2014
Completion
May 17, 2018
Results posted
Sep 24, 2019
Last update
Sep 24, 2019

Study contacts

M. Peter Lance, MD
principal investigator · University of Arizona

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Sep 2019. You cannot join it, but the record below documents what was studied.

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