HonCode

Go Back   HER2 Support Group Forums > her2group
Register Gallery FAQ Members List Calendar Search Today's Posts Mark Forums Read

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 03-26-2009, 12:55 PM   #17
julierene
Senior Member
 
julierene's Avatar
 
Join Date: Dec 2005
Location: Illinois
Posts: 327
I think it's just the theory that Herceptin and Tykerb block all the receptors, the immune system kills off all those cells, then you are left with whatever is left. They theorize that at microscopic levels, you can have many different types of cells, some having less receptors than others. Once you have effectively cleared out all the cancer with receptors, you can end up with cells that have different receptors. As receptors change to evade the immune system, so does the nature of the cancer. It's like the part of the cellular structure that works against people who have cancer. In normal healthy cells, this process is survival. But the natural programmed cellular structure, is now cancerous, and working against what we want. That's why Tykerb works when Herceptin fails. It's a new way to target when the receptors on the outside of the cell seem to not respond to Herceptin anymore. Then when Tykerb clears out the receptors that are on the inside, then there are cells left that don't respond to either... At that point, you start running out of targeted therapies. Avastin is a monoclonal antibody against vascular endothelial growth factor-A (VEGF-A).[1] It is used to inhibit tumor growth by blocking the formation of new blood vessels (angiogenesis). Since HER2 disease has shown trend to being very vascular, this makes sense. P53 targeted therapy also makes a lot of sense. But figuring out whichever direction you go after Tykerb and Herceptin fail, is a mystery to me.
__________________
Jan04: Bilateral Mastectomy at age 28
Initial DX: Left Breast: IDC 2cm, Grade 3, HER2+3, 0 Nodes +, ER/PR-. Right Breast: Extensive DCIS ER-/PR+; Stage 1-2a
Feb04-Apr04: 4 AC, dose dense
Aug 04: 4 Taxotere
Dec 05: Bone and Liver METS; Stage 4. Carboplatin/Taxol/Herceptin. DX with Li-Fraumeni Syndrome
Apr 06: NED, maintenance Herceptin
Apr 07: CA1503=14; masses in liver; Xeloda/Tykerb
Nov 07: NED, Tykerb maintenance
Sept 08: Liver mets again, on Tykerb/Xeloda again, CA=19 and 27
Nov 08: Progression, Tykerb/Gemzar, CA=25
Dec 08: Progression, Herceptin/Navelbine, CA=40, 57, and 130
Jan 09: Progression in bone, recession in liver, Herceptin/Carbo/Abraxane CA=135
June 09: CA27/29=24, chemo break
Sept 09: Progression, CA=24, waiting on clinical trial (4 weeks no treatment)
Nov 09: now have brain mets, trial "on hold", getting 14 WBR treatments starting 11/2/09
Dec 09: possible start on p53 trial
julierene is offline   Reply With Quote
 

Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Forum Jump


All times are GMT -7. The time now is 02:20 PM.


Powered by vBulletin® Version 3.8.7
Copyright ©2000 - 2026, vBulletin Solutions, Inc.
Copyright HER2 Support Group 2007 - 2021
free webpage hit counter