Questions about maintenance chemotherapy
After 6 rounds of chemo and my gallbladder surgery, my pancan stats are looking good--so of course, now I have more questions! As a reminder, I'm stage 4 adenocarcinoma in the body of the pancreas, inoperable due to blood vessel involvement. I have the ATM genetic mutation.
I've been off chemo since 7/5/23 due to a gallbladder attack and laparoscopic removal. CA 19-9 has dropped from 1736 in March to 271 per blood test on 7/24, and a CT scan taken 7/25 when I was admitted to the hospital shows that my main tumor is stable when compared with scans taken in March and June. At my appointment today, my oncologist said he wants to do two more rounds of modified Folfirinox, then get new CT scans and CA 19-9 results. Depending on those results, he said I might be a candidate for maintenance therapy.
He said there are two main approaches. One is Folfiri (no oxaliplatin) at a lower dose; I don't know the frequency or dosage. The other would be using olaparib (Lynparza), an oral chemo agent (PARP inhibitor) that is FDA-approved for BRCA-related cancers. He said he wasn't happy with the way the olaparib clinical trial was constructed; he also said the drug is extremely expensive and not specifically approved for ATM-related cancer.
While we wait for my new data, I need to research these two possibilities. Can anyone out there talk about your experience with maintenance therapy? Which one did you use, results, side effects, how long did your tumor remain stable, etc.? Is olaparib covered by insurance for ATM-linked cancers? Thanks in advance for any info you can provide.
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Hi,
I am responding to your private message you sent to me, after I shared my ca19 was 35.
This is my first private message. I hope I am doing it right.
I too have had 6 rounds of chemo - fulfirnox.
I was diagnosed june 8th 2023,with stage 2b.
A 2.5-3cm tumor on the head and spread to one lymph node by liver.
I had a CT and pet after 4 chemos-at that time they said tumor was stable. In June they said their goal for me was a cure - 12 chemo treatments, 1 month rest, the Whipple, 3 months surgery recuperation.
Recently I had problems w my gallbladder. The gallbladder duct was blocked w sludge. They did an ercp- the duct is still blocked but they made a new pathway from gallbladder to small intestine and included a stent in the new pathway. I had to skip chemo for 3 weeks. Tomorrow I have followup for the ercp.
I will have another CT and pet on Nov 12 -13, after my 8th chemo.
@katiegrace, you can find instructions on how to send a private message in the Help Center https://connect.mayoclinic.org/help-center/
How are you doing? What did you learn at the follow-up after the endoscopic retrograde cholangiopancreatography (ERCP) ?
At my follow up for the ercp, everything checked out fine.
Bloodwork looked good. Overall I have been feeling better since the ERCP.
I had chemo last Thursday and have not been feeling well. I've had jaw pain from the oxaliplaten. In the beginning of my chemo treatment I had jaw pain from the oxaliplaten, so they lowered my dose down to 50%. The jaw pain went away, but now it is back. So I will ask my Dr if we can lower the dose again.
@stageivsurvivor : Apologies for not quite understanding, but do you attribute your "I'm cured" status to your 46 cycles of Folfirinox, to this clinical-trial drug, or to the combo?
I'm asking bc I'm not yet at the point of looking for a clinical trial, but I'm worried that I wouldn't be able to participate in one if I wanted to (I'm broke and I'd be unable to pay for travel to, and lodging near, a clinical-trial site). I'm hoping that lots and lots of IV chemo will bring me to remission.
Thank you for the enormous amount of info and expertise that you share with us; best wishes.