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Old 03-12-2009, 09:00 AM   #8
fullofbeans
Senior Member
 
Join Date: Jan 2007
Location: UK
Posts: 617
Well there is something quite illogical in simply saying that more clinical trial results need to be carried out in that:

Are you saying that all the other countries such as France for example are simply making Tykerb available on no scientific background ??

Because if that it to you a satisfactory answer, well I beleive that what was said about Herceptin.. when an independent court reviewed the evidence they found that NICE was wrong.

So the real question that is emerging really is: Is NICE an independent body capable of reviewing scientific evidence??
__________________

35 y/o
June 06: BC stage I
Grade 3; ER/PR neg
Her-2+++; lumpectomies

Aug 06: Stage IV
liver mets: 6 tumours
July 06 to Jan 07: 2*FEC+6*Taxotere; 3*TACE; LITT
March 07- Sept 07: Vaccination trial (phase 2, peptide based) at the UW (Seattle).
Herceptin since 2006
NED til Oct 09
Recurrence Oct 2009: to internal mammary gland since October 2009 missed on Oct and March 2010 scan.. palpable nodes in May 2010 when I realised..
Nov 2011:7 mets to lungs progressing fast failed hercp/tykerb/xeloda combo..

superior vena cava blocked: stent but face remains puffy

April 2012: Teresa Trial, randomised to TDM1
Nov 2012 progressing on TDM1
Dec 2012 blockage of my airways by tumours, obliteration of these blocking tumours breathing better but hoping for more- at mo too many tumours to count in the lungs and nodes.

Dec 2012 Starting new trial S-222611 phase 1b dual egfr her2+ inhibitor.



'Under no circumstances should you lose hope..' Dalai Lama
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