Welcome to the Prostate Cancer Support Federation, the only UK-wide patient-led charity that acts and speaks for prostate cancer patients and their families. Click to find out more about us.
  • Home
  • Members
    • Find a Support Group near you
    • How to Join the Federation
    • Member Organisations
    • Partner Organisations
  • News
    • The Great PSA Debate
  • What we do
    • Aims
    • Campaign to re-examine screening
    • RISKMAN — Prostate Cancer Risk-based Screening Trial
    • Newsletters - Prostate Matters
    • Prostate Matters — Latest edition
    • Real PCRMP
    • Achievements to Date
    • Research Priority Setting Partnership
    • Information Sheets
    • History
  • Conferences
    & Workshops
    • Annual Conference 2012 — “Screening for prostate cancer - are we making progress?”
    • Workshop: “Lifestyle and Prostate Cancer” Oct 2011
    • Annual Conference 2011 — “Clinical Trials - Hope for the Future”
    • Workshop: “Research in Prostate Cancer – Patients Lead” Nov 2010
    • Annual Conference 2010 — “Living Well with Prostate Cancer”
    • You had your say — The Great PSA Debate — Nov 2009
    • Annual Conference 2009 — April 2009
    • Promoting Patient Power Workshop — Oct 2008
    • Inaugural Conference — April 2008
  • Prostate Action
    Grants
  • Contacts
    & Credits
    • Who's who in the Federation
    • Acknowedgements
    • Send us an email
 

PSA Screening for prostate cancer

Prostate cancer patients face huge problems in getting an early detection programme established for prostate cancer. Biased judgements, deliberate mis-use of evidence, questionable value judgements, sloppy research and arrogance all played their part to ensure that the National Screening Committee made the recommendation that the Department of Health wanted to hear.

But the recommendation is unsafe and some of us have had enough of this; So, to mark National Prostate Cancer Awareness Month last March, we launched a campaign, with widest possible publicity, to get the process re-opened immediately. First shot in this campaign was to send a letter to everyone we could think of who professes to have at heart the interests of men at risk of prostate cancer, inviting them to sign up to support us. It includes an Annex listing the fundamental flaws in the process that has been followed, under the following headings:

  • evidence has been ignored that clearly shows the benefits of screening;
  • the decision is based on out of date assumptions about prostate cancer treatment;
  • the decision is based on demonstrably false assumptions about the quality of life impact of prostate cancer detection and treatment;
  • and finally, and most gallingly for us, the report of the decision falsely implied a level of consensus that does not exist.

Full details of the shortcomings of the work can be found in a report written by Richard Firth of the Prospect group in Bristol, and published in Issue 11 of Prostate Matters. The report itself can be downloaded from here and details of the specific arithmetic errors it reports can be found here. These matters have been brought to the attention of the Prostate Cancer Advisory Group, and it is hoped that an early update of the National Screening Coomittee recommendation will result.

If you know of any particular individuals that you would like to see targeted by this letter, for example local medical policy makers and clinicians, please send them the letter and invite them to join the campaign.

If you, yourself, wish to support the campaign, please go to the petition website, and record your support, AND TELL YOUR FRIENDS!


The Prostate Cancer Support Federation is a member of
 Link to Europa Uomo
This page was updated on 11th July 2011

 
 
The Prostate Cancer Support Federation, Mansion House Chambers, 22 High Street, Stockport, Cheshire, SK1 1EG
Tel: 0161 474 8222.
Registered Charity Nº: 1123373