Avastin/Cytoxan
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avastin/cytoxin
I have also had multiple rounds of chemotherapy and it has been common for me to find out at chemotherapy number 4 if something is working or not. I find that other cases don't help much in figuring out what might happen with me. I have had a good response to avastin and cytoxin but have had poor responses to many combinations that seemed like sure fire winners with others. I wish your mother (and you) well. I was diagnosed at stage 4 in 2006 and have never been out of chemo. I am happy to be alive, though and that my son is now 11 and not 5 1/2.0 -
defining response
Like Rhondana, I have had multiple recurrences and probably will never be off treatment, other than short breaks. I had responded to carboplatin/taxol with CA 125 going down to 9 and scans NED. had 3 different radiations and after 2nd recurrence, I had 6 months of Cisplatin/Adriamycin which I found brutal. When my onc told me the tumors had shrunk 30%, I cried thinking that was terrible and he assured me it was an excellent response.He did explain to me that I would never show NEd on a scan again- some tumors disappeared but most just shrunk.Now six months later they are growing again and we are discussing drugs to slow growth,etc. I have learned to quiz him on the expectations for the drugs and what does define success. Right now I am on tamoxifen as we hope to hold disease stable and give my body a break before we decide which of the remaining drugs-quite possibly Avastin- we choose next.
But I do intend to keep fighting for as long as I can have quality of life and continue to be inspired by my sisters on this website.0 -
Avastinnancygt said:defining response
Like Rhondana, I have had multiple recurrences and probably will never be off treatment, other than short breaks. I had responded to carboplatin/taxol with CA 125 going down to 9 and scans NED. had 3 different radiations and after 2nd recurrence, I had 6 months of Cisplatin/Adriamycin which I found brutal. When my onc told me the tumors had shrunk 30%, I cried thinking that was terrible and he assured me it was an excellent response.He did explain to me that I would never show NEd on a scan again- some tumors disappeared but most just shrunk.Now six months later they are growing again and we are discussing drugs to slow growth,etc. I have learned to quiz him on the expectations for the drugs and what does define success. Right now I am on tamoxifen as we hope to hold disease stable and give my body a break before we decide which of the remaining drugs-quite possibly Avastin- we choose next.
But I do intend to keep fighting for as long as I can have quality of life and continue to be inspired by my sisters on this website.
Hi: I thought Avastin had come off the market in the States for treatment of ovarian cancer. It is coming off in Canada based on results in the States that basically found that the side effects were so bad with it and it wasn't really doing the job expected.
Cheryl0
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