Vitamin C as an Anti-cancer Drug
Primary Purpose
Prostatic Neoplasms
Status
Completed
Phase
Phase 2
Locations
Denmark
Study Type
Interventional
Intervention
Ascorbic Acid (Vitamin C)
Sponsored by

About this trial
This is an interventional treatment trial for Prostatic Neoplasms focused on measuring Prostate cancer, palliative care, antioxidants, ascorbic acid, rna expression
Eligibility Criteria
Inclusion Criteria:
- Castration resistant metastatic prostate cancer (bony or visceral metastases)
- Gleason sum > 6
- PSA > 10 ng/ml
- ECOG < 3
- Prior orchidectomy or LHRH antagonist/agonist treatment
- Must give informed content
Exclusion Criteria:
- Synchronous active cancer (skin cancer excluded)
- Prior chemotherapy
- History of oxalate renal stones
- Glucose-6-phosphate dehydrogenase deficiency
- Impaired renal function (creatinine > 200micromoles/L
- Haemochromatosis
- Cardiac disease (NYHA > 2, CSS > 2, recent AMI (less than 6 months)
- Recent major surgery (less than 4 weeks before inclusion and more than 2 days of admittance time)
- Prior intended curative treatment of prostate cancer
Sites / Locations
- Departmen of Urology, Copenhagen University Hospital at Herlev
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Vitamin C treatment
Arm Description
Each subjects receive 12 weeks of 1 weekly treatment with intravenous vitamin c. 5grams are given at week 1, 30 grams at week 2 and 60 grams at week 3-12. If eligibility criteria are met the subject may continue with 1 weekly vitamin c treatment of 60 grams at week 13-20.
Outcomes
Primary Outcome Measures
PSA changes after 12-20 weeks of treatment
Secondary Outcome Measures
Bone metastases changes
bALP changes
NTX changes
PINP changes
8-oxo-guanine changes
Full Information
NCT ID
NCT01080352
First Posted
March 3, 2010
Last Updated
March 25, 2015
Sponsor
Copenhagen University Hospital at Herlev
Collaborators
Rigshospitalet, Denmark, University of Copenhagen
1. Study Identification
Unique Protocol Identification Number
NCT01080352
Brief Title
Vitamin C as an Anti-cancer Drug
Official Title
Evaluation of Cytotoxicity and Genetic Changes of High Dose Vitamin C Infusions in Castration Resistant Metastatic Human Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
November 2010 (undefined)
Primary Completion Date
September 2014 (Actual)
Study Completion Date
March 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Copenhagen University Hospital at Herlev
Collaborators
Rigshospitalet, Denmark, University of Copenhagen
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Can high dose, intravenous Vitamin C prolong life for patients with metastatic prostate cancer?
Prostate cancer is the most common cancer (excluding skin cancer) in men in Denmark and the Unites States. When metastatic disease is present cure is no longer possible. The main treatment at this stage is castration, either surgical or medical, ending the patients testosterone production and causing a temporary regression in disease activity.
Eventually, the cancer will progress, usually within 2 years from the castration, with a more aggressive course and a survival of 2-3 years.
The current treatment option for the patients, who have undergone castration and have disease progression, is chemotherapy with only limited gains in quality of life and survival.
This clinical study is a phase 2 study to evaluate the effects of high dose intravenous vitamin c in subjects with early castration resistant prostate cancer.
Primary endpoint:
Prostate specific antigen (PSA) changes after 12 to 20 weekly vitamin c infusions
Secondary endpoints:
Bone metastases changes after 12 to 20 weekly vitamin c infusions
Changes in bone specific alkaline phosphates, oxidative DNA-damage, PINP, NTX after 12 to 20 weekly vitamin c infusions
RNA-expression changes in prostatic tumor tissue after 12 to 20 weekly vitamin c infusions
RNA-expression changes in lymphocytes after 12 to 20 weekly vitamin c infusions
Tertiary endpoints:
Pharmacokinetics of vitamin c in the elderly cancer patients
Methods and material:
80 subjects are included (efficacy evaluation when 20 subjects have been evaluated for extension arm)
Each subject receives a weekly infusion of 60 grams vitamin c (in the form of ascorbate) for 12 to 20 weeks
Detailed Description
Vitamin C for palliative treatment:
Intravenous vitamin C has been used since the 1970's for terminally ill cancer patients claiming big increases in survival time. The efficacy of the drug is questioned and no randomized, controlled trial of Vitamin C's efficacy on cancer patients survival has been made.
Recent results from in vitro and xenograft studies in mice has shown some promise for vitamin c as a cytotoxic agent against cancer cells.
The following parameters are recorded for baseline:
Biomarkers (PSA, bALP, NTX, PINP)
Routine blood work (hgb, creatinine, p-vitamin c etc.)
Radio nucleotide bone scintigraphy
Prostate biopsies for later microarray (Affymetrix ST1.0)
Urine samples 8-oxo-guanine(for oxidative DNA-damage measurements)
These parameters are repeated after treatment, usually after 12 to 26 weeks after the first vitamin c infusion.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatic Neoplasms
Keywords
Prostate cancer, palliative care, antioxidants, ascorbic acid, rna expression
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
31 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vitamin C treatment
Arm Type
Experimental
Arm Description
Each subjects receive 12 weeks of 1 weekly treatment with intravenous vitamin c.
5grams are given at week 1, 30 grams at week 2 and 60 grams at week 3-12. If eligibility criteria are met the subject may continue with 1 weekly vitamin c treatment of 60 grams at week 13-20.
Intervention Type
Drug
Intervention Name(s)
Ascorbic Acid (Vitamin C)
Intervention Description
60grams of ascorbate given intravenous infusion in 1000ml sterile water.
Primary Outcome Measure Information:
Title
PSA changes after 12-20 weeks of treatment
Time Frame
12, 20 and 26 weeks
Secondary Outcome Measure Information:
Title
Bone metastases changes
Time Frame
12, 26 and 52 weeks
Title
bALP changes
Time Frame
12, 20, 26 and 52 weeks
Title
NTX changes
Time Frame
12, 20, 26 and 52 weeks
Title
PINP changes
Time Frame
12, 20, 26 and 52 weeks
Title
8-oxo-guanine changes
Time Frame
12 weeks
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Castration resistant metastatic prostate cancer (bony or visceral metastases)
Gleason sum > 6
PSA > 10 ng/ml
ECOG < 3
Prior orchidectomy or LHRH antagonist/agonist treatment
Must give informed content
Exclusion Criteria:
Synchronous active cancer (skin cancer excluded)
Prior chemotherapy
History of oxalate renal stones
Glucose-6-phosphate dehydrogenase deficiency
Impaired renal function (creatinine > 200micromoles/L
Haemochromatosis
Cardiac disease (NYHA > 2, CSS > 2, recent AMI (less than 6 months)
Recent major surgery (less than 4 weeks before inclusion and more than 2 days of admittance time)
Prior intended curative treatment of prostate cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kari J Mikines, MD, DsMC
Organizational Affiliation
Copenhagen University Hospital at Herlev
Official's Role
Principal Investigator
Facility Information:
Facility Name
Departmen of Urology, Copenhagen University Hospital at Herlev
City
Herlev
State/Province
DK
ZIP/Postal Code
2730
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
28725594
Citation
Nielsen TK, Hojgaard M, Andersen JT, Jorgensen NR, Zerahn B, Kristensen B, Henriksen T, Lykkesfeldt J, Mikines KJ, Poulsen HE. Weekly ascorbic acid infusion in castration-resistant prostate cancer patients: a single-arm phase II trial. Transl Androl Urol. 2017 Jun;6(3):517-528. doi: 10.21037/tau.2017.04.42.
Results Reference
derived
PubMed Identifier
25220574
Citation
Nielsen TK, Hojgaard M, Andersen JT, Poulsen HE, Lykkesfeldt J, Mikines KJ. Elimination of ascorbic acid after high-dose infusion in prostate cancer patients: a pharmacokinetic evaluation. Basic Clin Pharmacol Toxicol. 2015 Apr;116(4):343-8. doi: 10.1111/bcpt.12323. Epub 2014 Oct 7.
Results Reference
derived
Learn more about this trial
Vitamin C as an Anti-cancer Drug
We'll reach out to this number within 24 hrs