Anti-proliferative Effects of Vitamin D and Melatonin in Breast Cancer (MELO-D)
Primary Purpose
Early Stage Breast Cancer
Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Melatonin
Vitamin D
Placebo (melatonin)
Placebo (vitamin D)
Sponsored by

About this trial
This is an interventional treatment trial for Early Stage Breast Cancer focused on measuring Breast cancer, melatonin, vitamin d, ki67
Eligibility Criteria
Inclusion Criteria:
- Woman with histologically confirmed invasive breast cancer (ductal, lobular, or mixed)
- Planned to undergo definitive surgery, either lumpectomy or mastectomy in 3 or more weeks
Exclusion Criteria:
- Less than 18 years of age
- Stage IIIB or IV disease
- Inoperable locally advanced or metastatic breast cancer
- Neoadjuvant chemotherapy is intended
- Currently taking vitamin D supplements
- Currently taking melatonin supplements
- Previously taking vitamin D or melatonin supplements within the last 3 months
- Currently taking a multivitamin and not willing to discontinue for the duration of the study
- Hyperparathyroid disease or other calcium disturbance in the past five years
- Active renal stones in the last six months
- Renal failure (creatinine > 190 mmol/L)
- Hypercalcemia (serum calcium > 2.6 mmol/L)
- Known pregnancy
- Participation in another clinical trial where the patient receives any other investigational product
- Unwilling or unable to provide informed consent
Sites / Locations
- St Joseph's Healthcare Hamilton
- Juravinski Cancer Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Placebo Comparator
Arm Label
Melatonin and Vitamin D
Placebo and Vitamin D
Melatonin and Placebo
Placebo and Placebo
Arm Description
Outcomes
Primary Outcome Measures
Ki67
The primary outcome is the difference in proliferation rate of Ki67 in the tumour (expressed as the percentage of tumour cells expressing Ki67). Ki67 will be measured on the original core biopsy (pre-treatment) and on the lumpectomy/mastectomy specimen (post-treatment).
Secondary Outcome Measures
microRNA
Change in serum profile of microRNA at the time of surgery (lumpectomy or mastectomy, post-treatment) will be compared to the time of initial biopsy (pre-treatment).
Full Information
NCT ID
NCT01965522
First Posted
October 11, 2013
Last Updated
June 14, 2017
Sponsor
Juravinski Cancer Center
1. Study Identification
Unique Protocol Identification Number
NCT01965522
Brief Title
Anti-proliferative Effects of Vitamin D and Melatonin in Breast Cancer
Acronym
MELO-D
Official Title
Anti-proliferative Effects of Vitamin D and Melatonin in Breast Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
October 2013 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
May 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Juravinski Cancer Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Investigators plan to carry out a study to investigate two different pills, Vitamin D and melatonin, and whether they can reduce the spread of cancer cells in the tumors of women with breast cancer. These pills are inexpensive and have very few side effects. A large number of studies using cell cultures and animals have shown that both vitamin D and melatonin can help destroy breast cancer cells. However thoughtful and well-designed studies are necessary on humans to see if they can decrease the spread of breast cancer, and possibly even prevent breast cancer. The proposed study aims to understand the anti-cancer activity of vitamin D and melatonin. This knowledge will assist in creating efficient cancer prevention strategies for Canadians. This study will include women with breast cancer who are being planned for surgery, and will assess whether treatment with vitamin D (dose of 2000 IU per day) in a group of 36 women, or melatonin (dose of 20mg per day) in another group of 36 women, or both pills together in yet another group of 36 women, reduces the spread of cancer cells when compared to a fourth group of 36 women who are treated with sugar pills. To do this we will measure a substance in the blood called Ki67, which provides information about the spread of cancer. Investigators will compare the Ki67 levels in the 4 groups, and all women will receive identical appearing pills so they will not know which treatment they received.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Early Stage Breast Cancer
Keywords
Breast cancer, melatonin, vitamin d, ki67
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Melatonin and Vitamin D
Arm Type
Experimental
Arm Title
Placebo and Vitamin D
Arm Type
Experimental
Arm Title
Melatonin and Placebo
Arm Type
Experimental
Arm Title
Placebo and Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Melatonin
Intervention Description
Melatonin 20mg taken orally once daily. This is in the form of one capsule which contains two pills of melatonin, 10 mg each.
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Intervention Description
Vitamin D 2000 IU taken orally once daily. This is in the form of one capsule which contains two pills of vitamin D, 1000 IU each.
Intervention Type
Drug
Intervention Name(s)
Placebo (melatonin)
Intervention Description
Overencapsulated placebo capsule which contains an inert substance. The capsule appears identical to the capsule which contains melatonin tablets.
Intervention Type
Drug
Intervention Name(s)
Placebo (vitamin D)
Intervention Description
Overencapsulated placebo capsule which contains an inert substance. The capsule appears identical to the capsule which contains vitamin D tablets.
Primary Outcome Measure Information:
Title
Ki67
Description
The primary outcome is the difference in proliferation rate of Ki67 in the tumour (expressed as the percentage of tumour cells expressing Ki67). Ki67 will be measured on the original core biopsy (pre-treatment) and on the lumpectomy/mastectomy specimen (post-treatment).
Time Frame
From time of initial biopsy to the final surgery, which is on average 4 weeks
Secondary Outcome Measure Information:
Title
microRNA
Description
Change in serum profile of microRNA at the time of surgery (lumpectomy or mastectomy, post-treatment) will be compared to the time of initial biopsy (pre-treatment).
Time Frame
At the time of surgery compared to time of biopsy, which is on average 4 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Woman with histologically confirmed invasive breast cancer (ductal, lobular, or mixed)
Planned to undergo definitive surgery, either lumpectomy or mastectomy in 3 or more weeks
Exclusion Criteria:
Less than 18 years of age
Stage IIIB or IV disease
Inoperable locally advanced or metastatic breast cancer
Neoadjuvant chemotherapy is intended
Currently taking vitamin D supplements
Currently taking melatonin supplements
Previously taking vitamin D or melatonin supplements within the last 3 months
Currently taking a multivitamin and not willing to discontinue for the duration of the study
Hyperparathyroid disease or other calcium disturbance in the past five years
Active renal stones in the last six months
Renal failure (creatinine > 190 mmol/L)
Hypercalcemia (serum calcium > 2.6 mmol/L)
Known pregnancy
Participation in another clinical trial where the patient receives any other investigational product
Unwilling or unable to provide informed consent
Facility Information:
Facility Name
St Joseph's Healthcare Hamilton
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 1Y3
Country
Canada
Facility Name
Juravinski Cancer Center
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8V 1C3
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
Anti-proliferative Effects of Vitamin D and Melatonin in Breast Cancer
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