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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Did your tail tumor size decrease significantly? Did they find it in the lungs because they were looking for it or did you have symptoms?
I’m always afraid it’s going somewhere and we won’t realize unless he has other symptoms. It had metastasized to the liver when he started.
Our oncologist intends to keep him on the gemabraxane with pamrevulab as long as he has stable disease and no bad side effects. Then the current plan is for Fulforinox, then there is hope that the KRAS studies will pan out- they are very promising but not currently being tested in his lab articulation variant.
I am with you - I wouldn’t stop - cancer is very aggressive- I wouldn’t take a chance if it were up to us.
@markymatkfl;
Where is your metastises?
Gem/abraxane has shrunk my 2 tumors and brought CA19-9 to normal range. Surgery next week to remove them One is a definite, one is very very small and not in a sweet spot. But back up plan is to manipulate the area so it can be radiated. This time I WILL go back on chemo. I have not developed resistance to Fulfurinox or Gemzar so will be listening to recommendations from docs here and elsewhere. But, I will not delay for long!
@gamaryanne and @ncteacher -- Your comments are right on, LOL! I have chemo on Fridays and get home feeling OK, relax on the weekend, then crash and have to take Monday off work.
I did reduce the decadron in my pre-meds by about 1/3 several months ago because of its impact on my blood sugar. That and a long drive home might be suppressing my insomnia. I do have dexamethasone tablets at home as a backup to Zofran. I rarely take them, but if so, only in the morning because of the insomnia.
@sprinter345 and @199 -- You are true marathon champions. Have your oncologists discussed switching treatments or reducing/eliminating any of your chemo meds?
I've heard the Gem/Abrax (+/- cisplatin) is usually only good for 6-9 months before it either becomes intolerable (neuropathy) or ineffective (cancer develops resistance). My docs have said they have an answer for every side effect but neuropathy, which I accept as a tradeoff for the other positives of treatment.
My CA19-9 leveled off around 40 for about 8 weeks, and two oncologists both started discussing "maintenance therapies" for me, suggesting the Abraxane/cisplatin had done all they were going to do. This would mean reducing/eliminating one/other/both and likely going to nothing but Gem. And then, my CA19-9 this week dropped to 33 -- two points inside the normal range! (Previous week's scans still report "stable disease" and Signatera detects no ctDNA.)
I don't think this regimen has run out of gas yet. I fear if I back off of anything it will give the cancer a chance to regroup and spread. 19 treatments haven't killed me yet. I was ruled out as a candidate for HIPEC, and I might be a candidate for some trials in the distant future, but I don't see anything on the horizon with more promise than what I'm currently on.
Would love and appreciate your insights on this.
Yes! First night(Friday) I’m ready to go out to dinner stay up all night! But Saturday afternoon when the Onpro shot goes off it’s downhill for two days. Very predictable. I guess the steroid gets us out of the doctor’s office with no complaints until Monday!
The Decadron dose was reduced due to the thinking that the swelling in my feet & ankles & whole body might be related to it as it is a steroid. Not sure if that changed much for the swelling. I too have insomnia the first and sometimes second nights of getting the Decadron. That did not change when I got the lower dose. I was still "wired" the night of chemo and the next. Lack of sleep & steroid equals one cranky person 🙂 Try to stay away from people who do not get it & that ends up being most people 🙂
Ty I did read through those (one was one of my own post lol) and it was interesting reading some others... the Gemzar/abraxane has definitely been easier for him to tolerate and he's at least eating a little more. My biggest issue ATM is making him realize he's diabetic and needs to take insulin regularly..
This week's treatment wasn't terrible on him so we'll see how he does
Ty for sharing thise
@mommacandy, I think you'll appreciate these related discussions:
- Anyone on Gemcitabine with Abraxane? How long? Effective?
https://connect.mayoclinic.org/discussion/gemcitabine-and-abraxane/
- Changing chemo regimen after 4 cycles of Folfirinox?
https://connect.mayoclinic.org/discussion/changing-chemo-regimen-after-4-cycles-of-folfirinox/
Regarding wild fluctuations in CA-19, see these discussions:
- Pancreatic cancer and CA19-9
https://connect.mayoclinic.org/discussion/pancreatic-cancer-and-ca19-9/
- CEA and CA19-9 Results as Predictors of Treatment Outcome
https://connect.mayoclinic.org/discussion/cea-and-ca19-9-results-as-predictors-of-treatment-outcome/
- CA-19 has elevated even more
https://connect.mayoclinic.org/discussion/ca-19-has-elevated-even-more/
On those sleep-deprived nights, I just camp out on the living room couch with the TV on. I drift in and out as needed. It also helps that my daughter is a night ER nurse, so she's often either awake at work or awake at home, and we can chat while I'm awake.
ncteacher - Like you (and Ken20), I'm convinced Decadron (dexamethasone) causes insomnia following Gem/Abrax infusions. After my last infusion one week ago I slept only 2 hours that night. Sleeplessness happens every time. No hiccups here however.