taoofpooh Posted September 26, 2020 Posted September 26, 2020 Hello everyone.I would like to hear from anyone that has completed 12 rounds of folfirinox then at some point later had further rounds. Or from anyone that has completed 12 rounds then requested more but been refused. I completed 12 rounds in Nov 19, have had no treatment since and am now requesting more fol from my Oncologist who seems quite reluctant to offer it, citing increased neuropathy and chances of sepsis as a risk ( I have inoperable PC). I have stated I am willing to take my chances.Any advice from your experience would be grateful.Thanks everyone.
PCUK Nurse Nicola Posted October 2, 2020 Posted October 2, 2020 Hi taoofpooh, It’s Nicci, one of the support line nurses here. Thank you for your post, I’m sorry you haven’t had any responses as yet from other forum users but hopefully you will soon. Please do feel free to contact us also on the support line to talk this through in more detail. Our support line is open Monday-Friday 10am-4pm 0808 801 0707. Thanks,Nicci Nicci Murphy Pancreatic Cancer Specialist NurseSupport TeamPancreatic Cancer UK
Marta Posted October 9, 2020 Posted October 9, 2020 Hi! I had about 46? Rounds of folfirinox. No, I am not joking. Every patient is of course different and this was thoroughly discussed with my medical team. I was diagnosed with metastasis after my surgery in 2018 and got almost two full years on it with some blips due to low blood counts, a CMV infection and one diarrea bout (and a couple of holidays). I got 10 rounds, then dichted off oxaliplatin due to the peripheral neuropathy but continued with the rest of the treatment for over 10 months, progressed slightly, got another 10 rounds with oxaliplatin, stopped it again at 10 rounds due to neuropathy, got three months without it and am now switching to Gem+abraxane. The points my doctors considered to make the decision was the response I had and the toxicity (minimal), so this Is decided on patients characteristics and might vary a lot from one person to the other. I am not in any way giving medical advice, but in my particular case that option was fecommended by my doctors and I accepted. I hope this helps and best of luck with tour treatment.
taoofpooh Posted October 10, 2020 Author Posted October 10, 2020 Thank you Marta. It is great to hear you have done so well on the chemo.Paul.
RoyBoy Posted October 12, 2020 Posted October 12, 2020 Paul, I cannot help with chemo but sending you extra strength and good luck to keep fighting
Vasil Posted October 31, 2020 Posted October 31, 2020 Dear Paul, may I ask you something. What comes after the 12th round? A break or one has to continue on the same regimen. I am asking because my father is on this treatment, done 7 rounds so far and a scan has been scheduled after finishing the whole cycle.
taoofpooh Posted November 9, 2020 Author Posted November 9, 2020 Hi Vasil.I think each case is different, but from what I can gather the Oncologist have a 'wait and see' approach. I finished my 12 rounds in Nov 2019 and have had CT scans every 3 months. The Oncologist feels more Folfirinox would be more harmful than beneficial due to its toxicity. Hope this helps.Paul.
Theresa Upton Posted November 11, 2020 Posted November 11, 2020 Hi. I was diagnosed in Sept 2018 and have mets in my liver. I did 19 rounds of folfirinox, a lot of it was at 80% with the oxaliplatin being reduced to 60%. I enjoyed a 14 month chemo break but my last scan showed that the tumour in my pancreas has grown very slightly. Tomorrow I start on folfirinox again, we are looking at 6 more infusions followed by a scan and we will go from there.
faylemv Posted March 22, 2021 Posted March 22, 2021 I completed 12 gruelling rounds in February and my oncologist said because I’ve responded well to the treatment that he may consider giving me more further down the road
JayneP Posted March 23, 2021 Posted March 23, 2021 HelloI finished 12 rounds on 9th February 2021. I have inoperable PC. At the halfway scan my tumour had shrunk by about a third. It measured 2.7x2.4 cm. On my final scan it had shrunk a bit more but not given the exact measurements and the oncologist said it wasn’t written down - a bit strange I thought.I had my CT scan results and way forward discussion with my oncologist 2 weeks ago, and my next course of treatment is Radiotherapy with chemotherapy (chemo either through pump/PICC line or tablet form). 5 weeks of Radiotherapy Monday to Friday. My break is only really the waiting time between the last treatment of FOLFIRINOX and setting up the next. Best wishes
Recommended Posts
Create an account or sign in to comment
You need to be a member in order to leave a comment
Create an account
Sign up for a new account in our community. It's easy!
Register a new accountSign in
Already have an account? Sign in here.
Sign In Now