Cholecalciferol and Calcium Carbonate in Treating Patients With Colon Cancer That Has Been Removed by Surgery

Roswell Park Comprehensive Cancer Center

Status: Terminated

Conditions: Colorectal Cancer

Treatments: Dietary Supplement: calcium carbonate; Other: laboratory biomarker analysis; Other: pharmacological study; Other: immunohistochemistry staining method; Procedure: biopsy; Dietary Supplement: cholecalciferol

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00470353

I 78706

RPCI-I-78706

Details and patient eligibility

About

RATIONALE: The use of cholecalciferol and calcium carbonate may keep colon cancer from coming back in patients with colon cancer that has been removed by surgery.

PURPOSE: This randomized clinical trial is studying two different doses of cholecalciferol to compare how well they work when given together with calcium carbonate in treating patients with colon cancer that has been removed by surgery.

Full description

OBJECTIVES:

Primary

• Compare the antiproliferative effects of 2 different doses of cholecalciferol (i.e., vitamin D3) in combination with calcium carbonate on the proliferative labeling index in patients with resected colon cancer.

Secondary

• Compare the effects of these doses on serum levels of 25-OH-D3, 1,25-OH-D3, 24,25-OH-D3, calcium, and parathyroid hormone in these patients.
• Determine the safety of high-dose cholecalciferol in these patients over 2 years.
• Compare the effects of these doses on several biological markers (i.e., cyclin D1, protein kinase C, vitamin D receptor, p21, and p27) in the rectal mucosa of these patients.

OUTLINE: This is a randomized, pilot study. Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive oral low-dose cholecalciferol once daily and oral calcium carbonate twice daily.
• Arm II: Patients receive oral high-dose cholecalciferol once daily and calcium carbonate as in arm I.

Treatment in both arms continues for up to 2 years in the absence of disease progression or unacceptable toxicity. All patients undergo sigmoidoscopy or colonoscopy with 4 quadrant mucosal biopsies at baseline and after 6 months of study treatment. After their 6-month mucosal biopsy, patients in arm I switch to high-dose cholecalciferol as in arm II.

Patients undergo blood, urine, and tissue collection periodically during study for pharmacokinetic, pharmacodynamic, and/or histopathological analysis. Serum is collected monthly for 3 months and then once every 3 months to assess changes in serum levels of vitamin D and vitamin D metabolites (i.e., 1,25-OH-D3; 25-OH-D3; 24,25-OH-D3), as well as changes in calcium and parathyroid hormone, BUN, creatinine, electrolytes, and phosphorus levels. Urine is collected once every 3 months to assess changes in urine calcium and creatinine levels for hypercalciuria. Tissue biopsies of normal endorectal mucosa collected at baseline and after 6 months of study treatment are evaluated by IHC for proliferative index, vitamin D receptor staining, p21, p27, cyclin D1, and protein kinase C.

PROJECTED ACCRUAL: A total of 20 patients will be accrued for this study.

Enrollment: 8 patients

Sex: All

Ages: 18 to 120 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• History of colon cancer

  • Underwent resection and has been in clinical remission for ≥ 1 year

• No inflammatory bowel disease

• No familial adenomatous polyposis

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2
• Life expectancy > 1 year
• No genitourinary stones within the past 5 years
• No severe comorbid conditions, such as uncompensated heart failure or active uncontrolled infection
• No history of hypercalcemia
• No active colostomy
• No contraindications to sigmoidoscopy or mucosal biopsies

PRIOR CONCURRENT THERAPY:

• No prior rectal surgery or abdominoperineal resection

• At least 1 month since prior vitamin D or calcium supplementation

  • Prior vitamin D supplemental intake ≤ 800 IU per day

• At least 1 year since prior chemotherapy

• No prior radiotherapy to the pelvis

• No concurrent active anticoagulation

  • Patients who stop anticoagulation therapy at the time of mucosal biopsy are eligible

• No other concurrent supplemental calcium or vitamin D