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Vitamin C as an Anti-cancer Drug

Evaluation of Cytotoxicity and Genetic Changes of High Dose Vitamin C Infusions in Castration Resistant Metastatic Human Prostate Cancer

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01080352
Enrollment
31
Registered
2010-03-04
Start date
2010-11-30
Completion date
2015-03-31
Last updated
2015-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostatic Neoplasms

Keywords

Prostate cancer, palliative care, antioxidants, ascorbic acid, rna expression

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.

Interventions

60grams of ascorbate given intravenous infusion in 1000ml sterile water.

Sponsors

Rigshospitalet, Denmark
CollaboratorOTHER
University of Copenhagen
CollaboratorOTHER
Copenhagen University Hospital at Herlev
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
PSA changes after 12-20 weeks of treatment12, 20 and 26 weeks

Secondary

MeasureTime frame
Bone metastases changes12, 26 and 52 weeks
bALP changes12, 20, 26 and 52 weeks
NTX changes12, 20, 26 and 52 weeks
PINP changes12, 20, 26 and 52 weeks
8-oxo-guanine changes12 weeks

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026