IXEMPRA
Comments
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My triple neg sister had her first Ixempra treatment 2 weeks ago and it was horrible severe abdominal pain and swelling, disabled for 2 weeks and in hospital for 1, Anyone have a reduced dosage of this? Cant seem to get answers from the drug company.
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I just got info this week on this protocal. It had a lot of info on all the reasons to redues dosage. Shocking amount at that.
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I had my first Ixempra treatment 12/11/07. Days 1 and 2 no problems, days 3, 4, 5, and 6 ---abdominal cramping, jaw pain, neuropathy of toes and fingers, severe fatigue, more than any other chemo I have ever been on. I complained to my onc when I saw him. He had just returned from the San Antonio symposium attended by over 8,000 in the medical field. He said there was a lot of talk of Ixempra. He heard that by reducing the dose to weekly injection (instead of every 3 weeks) the side effects are much less and better tolerated. I will have the smaller dose weekly starting 01/03/08. After day 7 went by, I felt much better, but those first 4 to 5 days were horrible. This stuff better be working! :-) I know the stats are not so good on this drug, but I am willing to give it a try because nothing I have been on has stopped my cancer in its tracks.
Good luck to us all.
Lauralynne
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Hi Lauralynne,
What is your onc trying to accomplish with Ixempra? Is it an IV treatment?
Tay -
Tay-
I have stage IV inflammatory breast cancer diagnosed in February 2006. I have been on 8 different chemos and nothing has been able to destroy my cancer. Ixempra is another one for me to try. Yes, it is given intravenously.
Lauralynne
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I was told Ixempra is the next big "hope" for triple negs. I have not seen alot of trial results yet. I'm hoping I will get to by pass this one. Laural what other chemo have you taken? Were you true IBC or spread to skin like mine did? I did Gemzar, carbo & avastan and took the herb curcumin and got good results. I'm one year from skin mets. But I still have other local bc.
Living in hope,
Flalady
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