Research Regarding Vitamin C and Prostate Cancer Management

Using The Search Bar

The "Search Bar" is divided into three sections: 1 - The search argument section; 2 - The search submit button; 3 - The search site selection dropdown.

The current (hidden) search engine that is hard coded is the Bing.com/search site. This will eventually change to allow selection of different search engine.

The "site selection" dropdown allows the selection of several different sites on which to focus the search argument.

The search argument can be tailored to your specific needs. As an example your search argument will end up looking something like "site:nih.gov cancer vitamin c prostate." You can select another site and try your argument again and get different results.

I'm providing this tool, because it eliminates a lot of the SPOAFStating Personal Opinion As Fact websites that are popping up, and are filled with ads, and are just there to make money off the ads.

On some some sites you may have to reply to the simple CAPTCHA to continue. It's their way to prevent BOTSBOTS is short for roBOTSF7-1 from doing massive searches.

If you would like to format your own search argument for a different site here is an example you can use: (it will require you to respond to the CAPTCHA.)

Quick Summaries

Comments & Notes

Quick Summaries

Abbreviations

AAAscorbic Acid
ADAGA1C-Derived Average Glucose

References:

  1. Top
    Added May 17 2024:
    2015 Apr; Elimination of ascorbic acid after high-dose infusion in prostate cancer patients: a pharmacokinetic evaluation
    • Purpose of this study was to assess the basic kinetic variables in human beings over a relevant AA dosing interval for proper design of future clinical trials.
    • Ten patients with metastatic prostate cancer were treated for 4 weeks with fixed AA doses of 5, 30 and 60 g.
    • The target dose of 60 g AA IV produced a peak plasma AA concentration of 20.3 mM.
    • Elimination half-life was 1.87 hr (mean, S.D. ± 0.40), volume of distribution 0.19 L/kg (S.D. ±0.05) and clearance rate 6.02 L/hr (100 mL/min).
    • No differences in pharmacokinetic parameters were observed between weeks/doses.
    • A relatively fast first-order elimination with half-life of about 2 hr makes it impossible to maintain AA concentrations in the potential cytotoxic range after infusion stop in prostate cancer patients with normal kidney function.
    • Full text of study (free)
  2. Top
    Added December 1, 2024:
    2024 Oct.; Cancer Care The Role of Repurposed Drugs and Metabolic Interventions In Treating Cancer 2nd Edition
    • This is a PDF download
    • Chapter 1: Introduction
    • Chapter 2: What is cancer: understanding its pathogenetic causes
    • Chapter 3: Preventing cancer
    • Chapter 4: The metabolic approach to treating cancer
      • Glucose management and the ketogenic diet
    • Chapter 5: Metabolic and lifestyle interventions for cancer treatment
    • Chapter 6: Repurposed drugs
    • Chapter 7: Tier one repurposed drugs – strong recommendation
    • Chapter 8: Tier two repurposed drugs – weak recommendation
    • Chapter 9: Tier three repurposed drugs -insuficient data
    • Chapter 10: Tier four repurposed drugs – recommend against
    • Chapter 11: Potential adjunctive therapies
    • Chapter 12: Chemotherapy: a basic primer
  3. Top
    Added December 4, 2024:
    2022 Oct.; High dose intravenous vitamin c treatment in a patient with lung cancer: A case report
    • A 56-year-old Hispanic male patient diagnosed with lung cancer. After undergoing surgery and chemotherapy, he started a high dose intravenous Vitamin C protocol
    • A maximum of 75 gr of Vitamin C in 1,000 cc lactated Ringer’s was given three times a week in a period over a year and a half.
    • CEACarcinoembryonic antigen (CEA) is a protein that can be found in the blood and is used as a tumor marker to help monitor cancer treatment and recurrence:CC-1 levels continued to be within normal levels while high doses of Vitamin C infusions were given.
    • It has been reported that a vitamin C plasma level above 400 mg/dL is toxic to tumor cellsPRHSJ-1