Efficacy of Vitamin D in Colorectal Cancer Chemoprevention

• ClinicalTrials.gov Identifier: NCT01574027
• Recruitment Status: Completed
• First Posted: April 10, 2012
• Last Update Posted: April 10, 2012
• Sponsor: University of Illinois at Chicago
• Information provided by (Responsible Party): Richard Benya, M.D., University of Illinois at Chicago

Tracking Information

• First Submitted Date: March 30, 2012
• First Posted Date: April 10, 2012
• Last Update Posted Date: April 10, 2012
• Study Start Date: April 2008
• Actual Primary Completion Date: October 2011 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: April 5, 2012)

Reduction in ACF biomarkers [ Time Frame: 6 months ]

The investigators propose giving patient's with 10 or more ACF's 25(OH)D3 (calcifediol) or placebo, and determining if there is a drug-dependant decrease in ACF number. The primary objective is to determine whether 25(OH)D3 (calcifediol) supplementation, compared to placebo, causes significant reduction of ACF number from baseline levels. The primary endpoint will be change in ACF number.

• Original Primary Outcome Measures: Same as current
• Change History: No Changes Posted
• Current Secondary Outcome Measures: Not Provided
• Original Secondary Outcome Measures: Not Provided
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Efficacy of Vitamin D in Colorectal Cancer Chemoprevention
• Official Title: Not Provided

Brief Summary

Vitamin D's ability to prevent colorectal cancer (CRC) has been suspected for nearly 30 years, but has never been directly studied in humans. The biologically active version of vitamin D, 1,25(OH)2D3, cannot be readily used in humans because of its tendency to cause serum calcium levels to rise. In contrast, 25(OH)D3 (ie calcifediol) does not have this side effect. The investigators previous research suggests that the enzyme necessary to convert 25(OH)D3 (calcifediol) into active 1,25(OH)D3 is present in cells lining the large intestine (colon).

Aberrant crypt foci (ACF) are very small (ie microscopic) collections of abnormally shaped cells that are a commonly used marker of CRC risk. Screening colonoscopy at UIC routinely uses methods that allow ACF counting to be done as a part of standard practice. ACF's are not fixed, like polyps or cancers, but can disappear as a person's risk for developing CRC decreases.

The investigators propose giving patient's with 10 or more ACF's 25(OH)D3 (calcifediol) or placebo, and determining if there is a drug-dependant decrease in ACF number. The primary objective is to determine whether 25(OH)D3 (calcifediol) supplementation, compared to placebo, causes significant reduction of ACF number from baseline levels. The primary endpoint will be change in ACF number.

Detailed Description

Patients will be offered participation in this study at the time of their regularly scheduled visit to the UIC Colorectal Cancer Screening Clinic. Those agreeing will have indicated their understanding that participation will be conditional upon their having 10+ ACF at the time of their screening colonoscopy. If at screening colonoscopy 10+ ACF are found patients will:

• undergo 3 endoscopic mucosal biopsies of the distal colon; and
• undergo a blood draw from an i.v. already in place for sedative-narcotic administration for serum 25(OH)D3 and serum ionized calcium; and
• be given either placebo or calcifediol and instructed to take daily for 6 months.
• provide urine for calcium/creatine spot ratio.

At 7 and 14 days after the screening colonoscopy patients will be called on the telephone by the clinical research nurse assigned to this study to follow-up and note 25(OH)D3 (calcifediol) toxicity, if any (note that toxicity has not been described except in the case of overdose). Signs specifically looked for will include: headache, increased urination, nausea, vomiting, abdominal pain, weakness, constipation, and anorexia. If present, patient will be advised to present immediately to the UIC GCRC for physical and serological evaluation.

At 30, 90 and 120 days the patient will have agreed to present to the GCRC clinic for:

• Capsule retrieval/count (80% compliance will be required to remain in study); and
• Detailed history and physical, focusing specifically on signs and symptoms of hypercalcemia.
• At day 90 only - provide urine for calcium/creatine spot ratio.

Evidence on exam, or laboratory, of hypercalcemia will result in an adverse event reporting and immediate patient discharge from this study. Signs specifically looked for include: headache, increased urination, nausea, vomiting, abdominal pain, weakness, constipation, and anorexia.

At 180 days the patient will have agreed to undergo:

• Repeat endoscopic exam limited to the recto-sigmoid colon, also known as a "flexible sigmoidoscopy"; and
• repeat blood draw for serum 25(OH)D3 and serum ionized calcium

• Study Type: Interventional
• Study Phase: Phase 2
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: Triple (Participant, Care Provider, Investigator); Primary Purpose: Prevention
• Condition: Colorectal Cancer

Intervention

• Drug: Vitamin D3 (cholecalciferol)
  One capsule per day for six months
• Drug: Placebo
  One capsule per day for six months

Study Arms

• Placebo Comparator: Placebo
  Some participants were given a placebo pill to take daily for the length of the study. The placebo patients were used as a control group to compare against those taking the Vitamin D supplement.
  Intervention: Drug: Placebo
• Experimental: Vitamin D3 (cholecalciferol)
  Other participants were administered Vitamin D3 (cholecalciferol) for the six month study duration to determine if it would decrease the number of aberrant crypt foci in the colon as compared to the baseline number.
  Intervention: Drug: Vitamin D3 (cholecalciferol)

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Completed
• Actual Enrollment (submitted: April 5, 2012): 55
• Original Actual Enrollment: Same as current
• Actual Study Completion Date: October 2011
• Actual Primary Completion Date: October 2011 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• All non-pregnant patients 50 years of age or older with 10 or more ACFs.

Exclusion Criteria:

• The following will be specifically looked for, and result in patients not being eligible for study enrollment:
• Use of non-steroidal anti-inflammatory drugs or glucocorticosteroids within 60 days of study entry.
• History of chronic IBD or prior pelvic radiation (inflammation distorts crypt pattern).
• Intake of any vitamin D or calcium supplements within 60 days of study entry.
• Patients with increased bleeding risk from biopsy protocol (i.e. renal failure, decompensated cirrhosis, blood dyscrasia

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 50 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: United States

Administrative Information

• NCT Number: NCT01574027
• Other Study ID Numbers: R01CA122299( U.S. NIH Grant/Contract )
• Has Data Monitoring Committee: Not Provided
• U.S. FDA-regulated Product: Not Provided
• IPD Sharing Statement: Not Provided
• Responsible Party: Richard Benya, M.D., University of Illinois at Chicago
• Study Sponsor: University of Illinois at Chicago
• Collaborators: Not Provided

Investigators

• Principal Investigator: Richard V Benya, M.D.; University of Illinois at Chicago

• PRS Account: University of Illinois at Chicago
• Verification Date: April 2012