Anyone on Gemcitabine with Abraxane? How long? Effective?
Hi, I'm Helena from South Africa. I have been diagnosed with PC, stage 4, in March. Tumour between body and tail and with one lesion on my liver.
I have been on Folfirinox for 3months, but it had no effect, allthough my markers came down from 3091 to 357, the tumour increased in size and there is another lesion on my liver.
I have started Gemcitabine with Abraxane.
Has anyone been on Gemcitabine/Abraxane?
If so, how long and how effective is this treatment?
Interested in more discussions like this? Go to the Pancreatic Cancer Support Group.
@pam79, are you and your sister still at Mayo Clinic? In Rochester? There are many things to do. I encourage you to check out the Cancer Education Center if you haven't already in the lobby of the Gonda building. Here's more information:
- General https://connect.mayoclinic.org/blog/cancer-education-center/
- Classes https://connect.mayoclinic.org/blog/cancer-education-center/tab/offerings/#ch-tab-navigation
They have kind people to greet you and offer support where you may need it.
Be sure to also stop in to Concierge Services in Mayo Building (lobby level, in the International Center)
https://www.mayoclinic.org/patient-visitor-guide/minnesota/concierge-services
They can tell you more about what is going on in Rochester, Mayo Clinic, and make recommendations from activities to restaurants to quiet places to visit to art tours and more.
How is she doing on radiation? How are YOU doing?
That is so awesome @199! And a 4-month break at that! I think with our diligence (57 treatments) and stamina we are showing PC who’s the boss! The longer we survive the more researchers will learn about this disease.
Ok, actionable? - that’s a new term for me - I’ll have to look it up!
I've been on it since July 2022 (gemcitabine & Abraxane). I had a four-month break from Jan to July of this year.
Last treatment made it 57 in all! This time my CA 19-9 just got within normal limits after 12 treatments: 29.4 🙂
Does anyone know of any in person meetings , activities or events in the Mayo area today or this week that we could attend?
I am my sisters caregiver. She was also diagnosed February, March. She started the same treatment in May and finished first round in October. It helped shrink her tumor and is very stable. We are now at Mayo for 3 weeks while she is doing radiation. She is very active and doing things that she enjoys.
Without treatment the prediction was 2 months.
My husband was stage 4 metastasis to liver when he started.
He has an ATM, KRAS G12V and a BRACA 2 that may or may not be actionable.
They are considering a KRAS study when tumor starts to grow.
Great news! Doctors are now being able to predict which standard of care recipe will work best . I believe it’s based on mutations. Wouldn’t it be great if they all knew this and implemented this strategy to save the wear and tear on our bodies! So glad GA is stabilizing and and working. I’ve never heard of anyone tolerating it for two years!
I was on it for awhile but they removed the abraxane and shortly after my marker was on the rise and a liver tumor appeared.
All good now
so happy to hear of the long time positive effects of GA for marienewland and gracect! My husband is just starting this journey after nearly a year on various forms of 5FU. Yesterday he felt fine. Today, tired and achy. We'll see what tomorrow brings. Thanks for the hope and help.