Began folfirinox treatment - have a few questions

Posted by lisn @lisn, Sep 16, 2023

My husband started his folfirinox regimen on Tuesday. I'm thinking that Tuesday is counted as day 1?

Many thanks to all who've posted information about what to expect. During the irinotectan, I noticed he was clearing his throat excessively, and he spoke up because he started to feel very warm. They stopped it immediately and gave him Atropine. The nurse was happy he spoke up when he did, because she said it was definitely a reaction, and what was going to happen next was stomach pain and distress.

Wednesday was the first full day with the pump (day 2?), and he had the pump disconnected Thursday afternoon (day 3?) By the time we got home Thursday, he was exhausted. He was very tired Friday (day 4?). Today, Saturday (day 5?), He says he feels off, tired and achy. I think this is normal from what I've read.

I'm also wondering if I'm counting the days correctly. If I have, then I'm thinking that he may start feeling a little bit more like himself starting tomorrow?

Thank you.

Interested in more discussions like this? Go to the Pancreatic Cancer Support Group.

@lisn

Thank you for this information. I hope you're doing well on this treatment. It's so different for everyone.

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After 6 treatments, my CA 19 cancer markers are down to 35 ( from 142 in June 23.).
Has anyone else had their cancer markers go down to normal (0-35), and what did it mean for them? I know cancer markers can't be used by themselves to diagnose anything. But I'm encouraged my markers are down.

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@katiegrace

After 6 treatments, my CA 19 cancer markers are down to 35 ( from 142 in June 23.).
Has anyone else had their cancer markers go down to normal (0-35), and what did it mean for them? I know cancer markers can't be used by themselves to diagnose anything. But I'm encouraged my markers are down.

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Wow! Congratulations! I'm now at 70 after 10 rounds of Folfirinox. I'm hoping to reach normal range, while realizing that scans show the tumor is still there and I'm not cured or NED by any standard. In my case, my oncologist is discussing maintenance chemo, depending on what new scans and CA 19-9 show. I would be interested in sharing ideas on that. He mentioned three possibilities--Lynparza (olaparib, a PARP inhibitor, which is approved for BRCA mutations but not my ATM mutation), continued 5FU pump (but no other chemo drugs), and some other oral med (my notes are unfortunately sketchy). No radiation treatment because of the small-volume lesions outside of the main tumor, and no surgery or Whipple because of blood vessel involvement. What has your MD discussed with you?

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@katiegrace

When I get the saline flush it smells like alcohol to me and makes me feel sick to my stomach. The last time I had the flush , I told them to give me heads up so I could hold my breath- after the flush I then exhaled, and it worked better for me so I didn't have to breathe in during the flush. Have had 6/12 treatments.

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Oh wow, thanks for that tip, I'll let him know to try that!

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@katiegrace

Medical cannibas has helped me with my nausea. I take a tincture of 1:1 ratio , one part thc and one part cbd. It's called Harmony. I've had 6 fulfirnox treatments and I have been able to stop Zofran completely and just use cannibas for nausea. It has worked for me.

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We'll have to look into this because the nausea is relentless and Reglan wasn't working. The doctor prescribed Zofran but he's not going to be able to continue with it due to the side effects. He had difficulty getting a full breath, stomach pains, was very anxious, shaky and weak. His system is very sensitive to so many things, but we'll look into this because even one of the nurses suggested medical cannabis. Thank you.

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@mayoconnectuser1

lien,

I may have missed it, but are you at a center of excellence?

If you are not, my consistent input it to get to one and stay there - for chemo and any other follow-on treatment.

Relocation is difficult, but there is a difference in knowledge, focus and care.

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How do I find or identify a "center of excellence?" Who lays that title on the center and what is their criteria?

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@rfherald

How do I find or identify a "center of excellence?" Who lays that title on the center and what is their criteria?

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The National Cancer Institute also has its own list. Its list and the pancan.org list are not exactly the same.
https://www.cancer.gov/research/infrastructure/cancer-centers

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@katiegrace

After 6 treatments, my CA 19 cancer markers are down to 35 ( from 142 in June 23.).
Has anyone else had their cancer markers go down to normal (0-35), and what did it mean for them? I know cancer markers can't be used by themselves to diagnose anything. But I'm encouraged my markers are down.

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Before distal surgery I was at 91 and after surgery I was 8. Following 12 sessions of chemo I’m at 6. My drs tell me nobody at 0. I feel fantastic and am back to working part-time! I had metastasis to 1 lymph node out of 25 that were tested. CAT scans and symptoms must be paired with your cancer antigen. I was also with the Hoag Medical PANCAN support group and we did have at least a couple of people who were stage 4 and had antigen in the 2000 range. They were in clinical trials and were told their tumors were no longer detectable in scans so even a high antigen paired with clinical trials can also mean you are “cancer free”.

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@katiegrace

After 6 treatments, my CA 19 cancer markers are down to 35 ( from 142 in June 23.).
Has anyone else had their cancer markers go down to normal (0-35), and what did it mean for them? I know cancer markers can't be used by themselves to diagnose anything. But I'm encouraged my markers are down.

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@katiegrace ,

My CA19-9 was at 677 when I began chemo (Gem+Abrax+Cisplatin) for the post-Whipple recurrence. It came down fairly fast, hovered in the low-mid 40's for a couple months, then teased me with a 33 two weeks ago (ULN < 35 at my lab) before going back to 43 yesterday at my 20th round of this regimen. Even my Signatera ctDNA tests still show no cancer detected.

I take it happily but with a grain of salt, knowing that my scans continue to show live tumors.

Celebrating NED status prematurely after Whipple (3 months after surgery with clean margins, clean lymph nodes, CA19-9 of 12 and 3 ctDNA tests clean), then discovering the recurrence 6 weeks later on MRI was a real downer and a reality check on the nature of this disease.

What is means for me is that I have to keep looking into clinical trials that I qualify for and can realistically participate in. Having all the right "conditions" to qualify for a trial is only one part. Being able to travel if required is another, and then the time factor -- how long will it actually take you to get in, and what if that delay is too long?

After 9 months on my current chemo, there is discussion of whether it has run its course (disease becoming resistant) or how much more neuropathy and fatigue I can take before jumping to a maintenance therapy or new treatment. It's a challenge getting all the clinical trial ducks in a row so I can make the switch quickly if the right study opens up. Being pre-enrolled as a patient at multiple centers is somewhat helpful with that.

I guess it's worth enjoying the freedom, but having a backup plan and a lot of "sleeping with one eye open." 😉

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@ncteacher

Wow! Congratulations! I'm now at 70 after 10 rounds of Folfirinox. I'm hoping to reach normal range, while realizing that scans show the tumor is still there and I'm not cured or NED by any standard. In my case, my oncologist is discussing maintenance chemo, depending on what new scans and CA 19-9 show. I would be interested in sharing ideas on that. He mentioned three possibilities--Lynparza (olaparib, a PARP inhibitor, which is approved for BRCA mutations but not my ATM mutation), continued 5FU pump (but no other chemo drugs), and some other oral med (my notes are unfortunately sketchy). No radiation treatment because of the small-volume lesions outside of the main tumor, and no surgery or Whipple because of blood vessel involvement. What has your MD discussed with you?

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@ncteacher ,

Since we share the ATM mutation, I'll send you a direct message with some trials that were proposed / recommended for me.

My primary oncologist was not impressed with the study results of PARP inhibitors on BRCA-mutated tumors, and perceived less applicability for PARP-i on ATM-mutated tumors.

The more directed research for ATM mutations seems to be focused on ATR inhibitors.

In both cases, I think the intent is to prevent the cancer cells from figuring out how to repair their own DNA in order to survive.

I'm not aware (yet) of studies that pair an ATR inhibitor with a conventional cytotoxic chemo like Folfirinox or Gem/Abrax/Cis. Knowing that the latter (GAC) is doing a decent job controlling my current disease, presumably damaging some DNA in the process, I would like to pile an ATR inhibitor on top of that, but apparently can't. One researcher I spoke with suggested his belief that an ATR inhibitor he was studying did double duty (damaging DNA as well as preventing repair) so that might offer some relief from treatment overload.

I've also read (but didn't save the links) that ATR inhibitors may also help reverse the platinum resistance that patients (ATM-mutated in particular) eventually develop on that therapy, so there might be hope for combining the two (legally in the USA) as a more aggressive therapy in the future.

I can't remember if a similar response (reversing platinum resistance) was suspected for PARP inhibitors in BRCA-mutated patients, but it's worth researching for those affected. My brain was full before chemo-brain settled in on top of that, so I apologize for not having more details.

I hope this helps a little.

--mm

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