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?
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When I started Gem/Abraxane my WBC dropped and my neutrophils count was 1.07 They reduced the following session to 85% strength. That was the only time when they reduced the strength of the dose. Since then I am on full 100%
What wonderful news news about your count !!! I truly feel that working is the best remedy Your boss sounds like a wonderful guy. My cousins boss is the sane. Maryann had treatment
on Monday and yesterday she had to leave early. Now she is fine again. Please keep me updated. I am glad that you are doing so well with few side effects 😊😊😊😊
Sincerely Susan
Thank you Helenar. They say he cannot go back up but it’s because of the trial he is in. There have been a lot of trial restrictions but his Dr still wants him to stay in it- no shrinkage but no growth. When his WBC was low he got the Neulasta patch but didn’t have to miss any cycles. Can I ask how old you are? He is 71 and was in really great health when this came out of nowhere. Hope your next scan shows continued improvement and so glad to see the 19-9 down.
Hi, I am 51 and was diagnosed a week after my 51st birthday. Also out of nowhere! The only time I was in hospital in all of my life, was when I had my c-sections for the births of my 2 girls. I RARELY went to a doctor, can count on my two hands the times I was off sick from work, was on no chronic medication, all and all I was in excellent health.
Then my right leg became sore with swelling, and they suspected cellulitis and treated me for that for 2 weeks. It did not get better and they started with other test and did a CT scan, and whola! - there's a tumor on you pancreas and it has spread to the liver! (2 small lesions)
I had chemo that didn’t work for Pancreatic cancer- so the just put me in this and after the first treatment I still had horrendous side effects and the white blood cells were so low they put me in every other week
Omg I feel exactly the same and they just switched me telling me side effects wouldn’t be as bad- same horrible effects but add hair loss after ine treatment! I git switched to every other week because blood count and side effects... had anyone had sore eyes eye pain or photo sensitivity ??? They said it hardly happens but it’s killing me
Very low dose of steroids with the infusion and also anti nausea meds with the infusion helped my husband’s side effects tremendously. When he didn’t have the steroids he was sick for days after each treatment. Now we go home and have dinner and the rest of his week is pretty good.
I hope you get some relief from the side effects. The Neulasta helped with the white blood cell counts so treatments could still be 3 times, then one off. The platelets are the new challenge.
Yes after first treatment so I had to change to every other week
Had to lower my husbands dose after first session. He is on his 6 session of 2 on 1 off. He started with C-19-9 of 16,000. Now down to 187. It went up last month by 70 points