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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So sorry to hear of your loss. Condolences to you and your family
My dads Dr. Said that this wouldn’t be an option. He did folfurinox which didn’t work- then gem/Abrax which also didn’t work. He just passed away august 5th after a 7 month battle.
Thank you. So far so good. She had her second treatment of G/A yesterday and is starting to lose her hair. She’s a little tired, but continues to have zero nausea and vomiting. She uses Tylenol as well and says it seems to work. She will have scans after two more treatments. I pray this is helping her. Best wishes to you.
Thank you. I know there are so many variables to the CA19-9, but seeing a jump to 50k just made me sick to my stomach. Best wishes to you.
Curious. I hear of stage iv people having the whipple or pancreaectomy. Many doctors claim to work on cases that were deemed inoperable with massive vein involvement, liver, Mets, lymph nodes, etc.
if chemo shrinks the pan mass and the metastatic spots are gone or necrotic, will surgeons still do the surgery? I’ve spoken to many stage iv survivors who have had this chance…why is that some can and some can’t? Look forward to some insight. Inspiration. I know some are even many years out with no evidence of disease or in remission with chemo alone.
I am also on Gemzar. Initially my numbers jumped but are now trending downward. My history shows that the CA19-9 tracks with the tumor activity in me; however my doctors say that is not the case with everyone. It has been explained to me that it is reasonable to see the numbers jump initially if the treatment is new to your body and causes the tumors to shed. For me that is the case as the scans do show shrinkage. This was true also with Fulfurinox in 2021-2022.
However, I would have raised a flag if the numbers rose more than 2 times. My blood work is every other week. Had my numbers continued to rise, I would have insisted that Cisplatin be added to my “recipe”.
From my experience of one year of pancreatic cancer, and what my oncologist tells me, is that CA numbers in and of themselves do not tell full stories. Accompanying scans will shed more light. I had a jump in CA when I switched from Folferinox to Gemzar Abraxane treatment, that consequently decreased, so there are lot of variables in that blood test. Best wishes. I hope this is somewhat helpful.
Hi Helena
How are you doing with your treatment ? Glad to hear that you are not experiencing any nausea. My cousin Maryann was on Gemcitabine Abraxane for almost 2 years and she did really well. Her tumor is also in the tail and near a main vein so they cannot operate. Now Maryann is on 5 Fluorourcil She is doing fine on this chemo. Will go for cat scan next month. Keep positive. We are all in this together.
Sincerely Susan
My husband and I were discussing my cancer markers going up after having a CT scan. My doctor said he has seen patients that have very high marker counts and are physically doing well. He has also seen patients have low marker counts and are physically doing poorly. I guess we just have to take it as it comes. It bothers me seeing my numbers going up but I don't know if it's good or bad. Will just have to deal with it as it comes. I'm glad to hear she didn't have any nausea or vomiting. This is my 3rd day after getting the G-A. I have been very tired the past few days & I have been taking naps. I also have joint & body aches but I take Tyenol & it helps. It is positive that your mom wants to fight her cancer. I did seem to notice the week after treatment I didn't feel as tired. I hope this goes for your mom too. Take care.
My mom is 71 years old and was just diagnosed in late July with stage 4 pan can with nodules to her lungs that are growing. She just started G-A two weeks ago. She will get it every other week due to her being extremely weak and tired. She did get a rash possibly from the Gem which was cleared up with prednisone. She has been tired but had zero nausea or vomiting. Tomorrow will be her second treatment. I hope she continues to tolerate. She really wants to fight this , but she’s awfully tired. Her last CA19-9 was up to 50k. We haven’t told her that, as she was worried when it hit 20.000. Has anyone heard of this number being so high? Back in April before she was diagnosed it was 1500 and we were worried then. Now I don’t know what to think!!!