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Old 08-05-2006, 01:47 PM   #1
sassy
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muga trends

My onc has agreed to keep me on herceptin into the second year (completed first year June 10) until new data is released or my muga drops. I had been having echos staying at 60 until May 06 when my onc switched to muga. My muga was 55 and I am now due for another muga. I assumed the difference between the 60 on echo and 55 on muga could have been a variance of the tests. I am hoping my next muga is at least 55.

Has anyone experience a drop in muga after one year on herceptin? I was under the impression that a drop was more likely to occur during the first few months of treatment.

Thanks for any info.
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Old 08-05-2006, 04:31 PM   #2
KathyA
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Sassy,
I've had several MUGA's and they fluctuate in a 7 point range. I've been on herceptin since May 2005.

I've ranged between 58, 65. My onc is fine with this.

God bless
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Old 08-05-2006, 06:09 PM   #3
Becky
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A drop in heart function can happen at any time in the process. However, you need to take into consideration that you used 2 different tests and the only way to compare is to compare Echo to Echo or Muga to Muga. So... there probably is absolutely no different between the 2 readings.


Kind regards

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Old 08-05-2006, 06:11 PM   #4
Bev
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Hi Sassy,

Started Herceptin last November and my scores have been creeping up. I did switch from MUGA to Echo recently, and had a 70! Higher than the baseline of 65 on MUGA. So I think there may be some subjectivity in how these tests are read. I didn't ask so I can't say for sure. I prefer the Echo because you don't need to do the nuclear IV. I would be interested in anything members have to say regarding these tests. Will stick with Echo if they let me. Bev
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Old 08-05-2006, 07:46 PM   #5
Maggie
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Hi Sassy, I started Herceptin in November for 1 year. My Muga scans have been going down gradually, and this last one showed it has dropped 11% since I started. My onco feels I should stop. I am stage 1. ER/PR neg/Her2 3+strong..
I have been very sad these last two weeks and haven't been on the board since last night. Feeling a bit better now!
I would be interested as to why your doctor switched to a Muga scan.
I hope you continue to do well on Herceptin..
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Old 08-05-2006, 08:03 PM   #6
sassy
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Maggie,


I have not asked my onc why he switched to muga from echo. I assumed it was because I was getting close to end of one year of treatment and he wanted accuracy of muga. I will ask him for sure next time.

I give this board credit for my being able to continue treatment into my second year. I have learned so much from everyone here. My onc respects the knowledge that I have gained and discusses everything with me to great lengths. I feel he is willing to continue because of my high risk and my understanding of my treatment and prognosis. This week we talked about the tykerb compassionate use and use of zometa for early stage women on AI's. He has told me for several months that approval for the Zometa is in the offing and I should be able to get it soon. My insurance has declined to pay since I do not have bone mets, but we both want me to get on it as soon as possible, both for bone loss (I am on Lupron and Arimidex) and the possibility of prevention of bone mets.

I am thankful to be NED and plan to stay that way thru faith, prayer and the miracle of medicine!

Sassy
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Old 08-06-2006, 07:56 AM   #7
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Have you had a bone scan for osteoporosis? I had evidence of osteoporosis so I have been on Zometa every four months (they run it the same time as my Herceptin). Insurance pays for it.
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